SlideShare a Scribd company logo
1 of 25
Download to read offline
CHAPTER NO:09
CARDIO-VASCULAR
SYSTEM
Prepared by,
RAMDAS BHAT
Asst. Professor
Karavali college of Pharmacy
Mangalore
7795772463
Ramdas21@gmail.com
INTRODUCTION:
Cardiovascular is the system which includes the study of the heart, blood vessels and blood. This
system is some time known as circularly system because it circulates or transport the nutrients,
oxygen, carbon dioxide and essential molecules from environment to cells and cells to
environment. It is involuntary in nature and gives continuous work. The heart propelling or
impelling blood around 100,000 km of blood vessels and it pumps 14000 liters blood in day and
10 million liters in year.
LOCATION OF HEART:
▪ Cone shaped heart is relatively small, about the same size of closed fist of person.
▪ It is 12 cm (5 in.) long, 9 cm (3.5 in.) wide and 6 cm (2.5 in.) thick.
▪ In an adult, average weight of heart is 300gm.
▪ The heart consists four chambers:
a) Two atria or atrium
b) Two ventricles
▪ It is located near to the middle of thoracic cavity in the mediastinum (the space between the
lungs) and it rest on to the diaphragm.
▪ About two third of the mass of the heart lies to the left of the body’s midline.
▪ Pointed end portion which is formed by the tip of left ventricle is known as apex and opposite
to apex the wide superior and posterior margin is known as base.
CARDIOVASCULAR SYSTEM
LAYER OF THE HEART:
▪ Heart layer is formed by pericardium ("around the heart”) which is triple-layered fluid-
filled sac that surrounds and protects the heart.
▪ The pericardium consists of two principal portions
Layer of Heart (Pericardium)
Fibrous Pericardium Serous Pericardium
Parietal Layer (Outer Layer) Visceral Layer (Inner Layer)
(Epicardium)
a) Fibrous pericardium:
▪ It is a strong layer of dense connective tissue.
▪ It adheres to the diaphragm inferiorly, and superiorly it is fused to the roots of the great
vessels that leave and enter the heart.
▪ The fibrous pericardium acts as a tough outer coat that holds the heart in place and keeps it
from overfilling with blood.
▪ It prevents overstretching of the heart, provides protection and fix the heart in mediastinum.
b) Serous pericardium:
▪ It is a Deep to the fibrous pericardium and form double layer around the heart.
▪ The outer layer is known as parietal layer which is fused to the fibrous pericardium.
▪ The inner layer is known as visceral layer also known as epicardium.
▪ Between the outer layer (parietal layer) and inner layer (visceral layer) is gap known as
pericardial cavity filled by fluid is known as pericardial fluid.
▪ This fluid ac as lubricant and reduces friction between the layer during contraction and
relaxation.
WALL OF THE HEART:
▪ The wall of the heart is formed by three layers:
a) Epicardium (External layer):
▪ It is also known as the visceral layer of the serous pericardium.
▪ It is composed of mesothelium and delicate connectivetissue.
▪ It is the outer or external wall of the heart.
b) Myocardium (Middle layer):
▪ Myo means muscles so it is made up by cardiac muscles tissue.
▪ It provides the bulkiness to the heart and it is responsible for the pumping action of heart.
c) Endocardium (Inner layer):
▪ The endocardium is an innermost, thin, smooth layer of epithelial tissue that lines the inner
surface of the heart chambers and valves.
INTERIOR OF THE HEART:
▪ The heart is divided in to right and left side by partition known as the septum which is made
up by myocardium covered by epithelium
a) Chamber of heart:
▪ Heart consists of four chambers;
i) Two atria:
▪ The two superior chambers are known as right atrium and left atrium.
▪ The posterior wall of the atrium is smooth surface while the anterior wall of the atrium is
rough surface.
▪ On the surface of the atrium is wrinkle pouch like structure is known as auricle because it
resembles like dog ear.
ii) Two ventricles
▪ The two inferiors are known as right ventricle and left ventricles.
▪ On the surface of heart grooves like structures known as coronary sulcus which separate the
atria to ventricle.
▪ The thickness of the wall of the four chambers varies according to their function.
▪ Example: The wall of the atria is thin and it pumps blood in to ventricles & the ventricle wall
is thick in which right ventricle pumps blood in to lungs and left ventricle pumps blood in to aorta
so the work load on left ventricle is high because of that the wall of left ventricle is two to four
times thicker than right ventricle.
b) Valve of the heart:
▪ In the heart blood passes from various compartment and finally it enters in to the artery.
▪ During these circulations for the prevention of back flow of blood there is special type of
structure in heart which is known as valve.
▪ These special types of structures or valves are composed by dense connective tissue which is
covered by endocardium.
▪ Valves are opened and closed in response to the contraction or relaxation of heart.
It is classified into 2 types:
a) Atrioventricular valve:
▪ Its names indicate the location of valves that means these valves located between the atria
and ventricle or it moves blood from atrium to ventricle.
▪ Inner surface of the ventricle contains the papillary muscles which is connected with the end
or tip part of valve.
▪ Blood moves atrium to ventricle when the pressure in to the ventricle is lower than the atrium
that time valves get opened and papillary muscles are in relaxed condition.
▪ When the AV valve is open the point end of the valve project in to the ventricle.
▪ So, pressure in to the ventricle get increased at a same time ventricles start to contraction
due to this contraction blood produce pressure on to the cups of valve and they move upward
until their edge meet and close the opening.
▪ During the ventricle contraction blood may not goes from ventricle to atrium because valve
have special type of opening and closing structure and during the closing time papillary muscles
are also contracted so it prevents the back flow of blood from ventricles to atrium.
▪ It is mainly subdivided in to two types:
i) Tricuspid Valves:
ii) Bicuspid Valves (mitral valve):
▪ This valve located between the left atrium and left ventricle.
▪ It consists two cups so it is known as bicuspid valves also known as mitral valve.
b) Semilunar valve:
▪ These valves consist three Semilunar (half-moon like) cups.
▪ It is further subdivided in to:
i) Pulmonary Semilunar valve:
▪ It passes the blood from right ventricle to lungs during opening stage.
ii) Aortic Semilunar valve:
▪ It passes the blood from left ventricle to aorta during opening condition.
CIRCULATRY SYSTEM OF BLOOD THROUGH HEART:
1) Pulmonary circulation:
▪ In the body system cells receive O2 from blood and give CO2 in to blood so blood become
deoxygenate.
▪ These Deoxygenated blood by the help of Superior venacava, Inferior venacava and
coronary sinus transfer in to the right atrium.
▪ Right atrium flows this deoxygenated blood in to right ventricle with the help of tricuspid
valves.
▪ Right ventricle pumps blood in to pulmonary trunk via pulmonary Semilunar valve.
▪ The pulmonary trunk divided in to right pulmonary artery and left pulmonary artery, the right
pulmonary artery gives blood to right lungs and left pulmonary artery gives blood to left lungs.
2) Systemic Circulation:
▪ In the lungs blood become oxygenated means it gains O2 and loss CO2.
▪ Now, the oxygenated blood returns in to heart through pulmonary veins.
▪ Then pulmonary veins pass blood in to left atrium which pumps blood in to left ventricle
with the help of bicuspid valve.
▪ Finally, bloods flows in systemic circulation from aorta and reach near to each and every cell
of the body and gives O2 and take CO2.
▪ Again, the deoxygenated blood flow through pulmonary circulation.
3) Coronary circulation:
▪ It supplies the oxygenated blood to the heart.
▪ It arises from the ascending aorta and divided in to left and right coronary branches.
i) The left coronary artery:
▪ The left coronary artery pass inferior to left auricle and divided in to the anterior
interventricular and circumflex branches.
▪ The anterior interventricular branch or left anterior descending (LAD) arteries enter in to the
anterior interventricular sulcus and supplies oxygenated blood to the walls of both ventricles and
the interventricular septum.
▪ The circumflex branch lies in the coronary sulcus and distributes oxygenated blood to the
walls of the left ventricle and left atrium.
ii) The right coronary artery:
▪ The right coronary arteries branches supply blood to the right atrium.
▪ It continues inferior to the right auricle and divided in to the posterior interventricular and
marginal branches.
▪ The posterior interventricular branches enter in to the posterior interventricular sulcus and
supply the oxygenated blood in to two ventricles and the interventricular septum.
The marginal branch in the coronary sulcus transports oxygenated blood to the myocardium of
the right ventricle.
a) Coronary Vein:
▪ After delivering the oxygen and nutrients to the heart, the blood receives waste and carbon
dioxide.
▪ It then drains in to a large vascular sinus or coronary sinus on the posterior surface of the
heart.
▪ Coronary sinus empties deoxygenated bloods into the right atrium.
HUMAN ANATOMY AND PHYSIOLOGY NOTES
RAMDAS BHAT
KARAVALI COLLEGE OF PHARMACY 11
CONDUCTING SYSTEM OF HEART:
Action Potentials in Cardiac Muscle (Ventricular Muscle)
1. SA Nodal Action Potential – Pace Maker potential
2. Ventricular Muscle Action Potential
3. Atrial Muscle Action Potential
4. Purkinje System Action Potential
Phases of Ventricular Muscle Action Potential
1. Phase 0 – Up Stroke
2. Phase I – Initial Repolarization
3. Phase II – Plateau Phase • Phase III – Repolarization
4. Phase IV – Resting Membrane Potential
PHASE 0 - UPSTROKE
• It is the Upstroke of Action Potential
• Opening of Voltage Gated Sodium Channels at -70 to -80 mV
• There is transient increase in Sodium Conductance leading to rapid influx of Sodium Ions
causing membrane Depolarization.
• At the peak of Upstroke, the membrane potential approaches the sodium Equilibrium
Potential.
HUMAN ANATOMY AND PHYSIOLOGY NOTES
RAMDAS BHAT
KARAVALI COLLEGE OF PHARMACY 12
PHASE I – Initial Repolarization
• It is a brief period of initial repolarization
• This phase results from – Closure of voltage gated sodium channels leading to Decreased
sodium influx – Opening of potassium channels leading to potassium efflux.
PHASE II – Plateau Phase
• It is the plateau phase of the action potential
• There is slow opening of voltage gated calcium channels at -30 to -40 mV
• There is excessive calcium influx during this phase because of transient increase in calcium
conductance
• This calcium influx is balanced by the Potassium efflux leading to the production of plateau
i.e., delay in the repolarization
• During the plateau, outward and inward currents are nearly equal so that the membrane
potential is stable in this phase.
• Plateau phase is not part of repolarization. It is sustained depolarization.
PHASE III – Repolarization
• During this phase, the calcium conductance decreases due to closure of slow calcium
channels
• There is increase in the potassium conductance leading to excessive efflux of potassium
and this is the only dominant current during this phase.
• This results in the repolarization till the potassium equilibrium potential is reached.
PHASE IV – Resting Membrane Potential
• During this phase the Membrane is in resting state.
• RMP is -85 to -90 mv
• Activation of Na+/K + ATPase pump
HUMAN ANATOMY AND PHYSIOLOGY NOTES
RAMDAS BHAT
KARAVALI COLLEGE OF PHARMACY 13
Sinoatrial node (SA node)
Specialized region in right atrial wall near opening of superior vena cava.
Atrioventricular node (AV node)
Small bundle of specialized cardiac cells located at base of right atrium near septum
Bundle of His (atrioventricular bundle)
Cells originate at AV node and enters interventricular septum Divides to form right and left
bundle branches which travel down septum, curve around tip of ventricular chambers,
travel back toward atria along outer walls
Purkinje fibers
Small, terminal fibers that extend from bundle of His and spread throughout ventricular
myocardium
▪ Electrical impulses generated in the SAN cause the right and left atria to contract first.
Depolarization (heart muscle contraction caused by electrical stimulation) occurs nearly
simultaneously in the right and left ventricles 1-2 tenths of a second after atrial
depolarization. The entire sequence of depolarization, from beginning to end (for one
heart beat), takes 2-3 tenths of a second.
▪ All heart cells muscle and conducting tissue are capable of generating electrical impulses
that can trigger the heart to beat. Under normal circumstances all parts of the heart
conducting system can conduct over 140-200 signals (and corresponding heart beats) per
minute.
▪ The SAN is known as the "heart's pacemaker" because electrical impulses are normally
generated here. At rest the SAN usually produces 60-70 signals a minute. It is the SAN that
increases its' rate due to stimuli such as exercise, stimulant drugs, or fever.
▪ Should the SAN fail to produce impulses the AVN can take over. The resting rate of the
AVN is slower, generating 40-60 beats a minute. The AVN and remaining parts of the
conducting system are less capable of increasing heart rate due to stimuli previously
HUMAN ANATOMY AND PHYSIOLOGY NOTES
RAMDAS BHAT
KARAVALI COLLEGE OF PHARMACY 14
mentioned than the SAN.
▪ The atrioventricular node delays impulses by approximately 0.09s. This delay in the
cardiac pulse is extremely important: It ensures that the atria have ejected their blood
into the ventricles first before the ventricles contract.
▪ The Bundle of HIS can generate 30-40 signals a minute. Ventricular muscle cells may
generate 20-30 signals a minute.
▪ Heart rates below 35-40 beats a minute for a prolonged period usually cause problems
due to not enough blood flow to vital organs.
▪ Problems with signal conduction, due to disease or abnormalities of the conducting
system, can occur anyplace along the heart's conduction pathway. Abnormally conducted
signals, resulting in alterations of the heart's normal beating, are called arrhythmias or
dysrhythmia.
▪ By analysing an EKG, a doctor is often able to tell if there are problems with specific parts
of the conducting system or if certain areas of heart muscle may be injured.
PROPERTIES OF CARDIAC MUSCLE:
1. Excitability (Bathmotropic action)
2. Auto rhythmicity
3. Conductivity (Dromotropic action)
4. Contractility (Inotropic action)
5. Refractory period
6. All or none phenomenon
7. Franks-Starlings law
8. Functional syncytium.
9. Role of calcium.
10. Resistance to fatigue.
1. EXCITIBILITY
• Cardiac muscle shows the property of excitability.
• Presence of SA node that acts as a pacemaker undergoes self-excitation under the
influence of the sodium and thus causes the transmission of the impulses to the nearby
muscles.
• Heart responds to electrical, mechanical and chemical stimuli.
2. AUTO RHYTHMICITY
• Spontaneous generation of action potential in heart without external stimulation is called
Automaticity. Self-Generation.
• It occurs at regular intervals so it is called Rhythmicity.
• Automaticity in heart is Myogenic and not neurogenic.
• SA NODE: 70 -80 Impulses/minute
• AV NODE: 40-60 / min
• AV Bundle/Purkinje system/Ventricles 15-40 /min
• SA Node having the highest rate of impulse formation is called PACE MAKER.
HUMAN ANATOMY AND PHYSIOLOGY NOTES
RAMDAS BHAT
KARAVALI COLLEGE OF PHARMACY 15
3. CONDUCTIVITY (DROMOTROPIC ACTION)
• Ability to conduct AP or cardiac impulses.
• The property of conductivity varies in different parts of the heart.
Velocity of conduction in:
• Atrial Muscle: 0.3 m/sec
• Inter nodal pathway: 1 m/sec
• AV Node: 0.1 m/sec (slowest)
• Purkinje System: 1.5 – 4 m/sec
Conductivity is affected by autonomic stimulation. Sympathetic increase the velocity of
conduction. Vagal stimulation Slows down. Ischemia slows the velocity of conduction
4. CONTRACTILITY
• Property to undergo shortening.
• The tension developed during cardiac muscle contraction is less than that developed in
Skeletal muscle contraction.
5. REFRACTORY PERIOD:
• It is that period during which a second stimulus fails to evoke a response.
• Absolute Refractory Period: It is that period during which a second stimulus however
high it is fails to evoke a response.
• Relative Refractory Period: It is that period during which a second stimulus evokes a
response if it is sufficiently high.
• Refractory period in cardiac muscle is much larger compared to any other muscles.
• Cardiac muscles have refractory period of 250 ms where as the skeletal muscles shows
1-3 ms.
6. ALL OR NONE PHENOMENON
• In order for the cardiac muscle to undergo the depolarization, the potential inside the
cardiac muscle should reach the threshold potential of -55mV
• If the potential is reached cardiac muscle shows complete or maximal depolarization and
if the threshold is not reached cardiac muscle shows no depolarization.
• This is termed as All or None phenomenon.
7. FRANKS-STARLING LAW:
• Greater the initial or resting length, greater will be the force of contraction.
• In heart the initial or resting length depends upon end diastolic volume or pressure.
• End diastolic volume depends upon the venous return.
8. FUNCTIONAL SYNCYTIUM
• Cardiac myocytes are closely packed.
• Cardiac myocytes are connected to the adjacent myocytes with the help of the GAP
junction.
• Transmission of the impulses from one myocyte to the another happens rapidly within a
shorter duration compared to any other muscle.
HUMAN ANATOMY AND PHYSIOLOGY NOTES
RAMDAS BHAT
KARAVALI COLLEGE OF PHARMACY 16
9. ROLE OF CALCIUM
• Calcium plays an important role in the contraction of cardiac muscle.
• Calcium ions in the ECF are taken up by the cardiac myocytes through the transverse
tubular system are not enough for the contraction of cardiac muscle and hence the
calcium stored in the Longitudinal tubular system (Sarcoplasmic reticulum) are utilized
for contraction.
10. RESISTANCE TO FATIGUE
Cardiac muscle has longer refractory period hence are not prone to fatigue.
ELECTROCARDIOGRAPHY
▪ Electrocardiography (ECG or EKG from the German Elektrokardiogramm) is a
transthoracic interpretation of the electrical activity of the heart over time captured and
externally recorded by skin electrodes.
▪ It is a non-invasive recording produced by an electrocardiographic device.
▪ The ECG works mostly by detecting and amplifying the tiny electrical changes on the skin
that are caused when the heart muscle "depolarizes" during each heartbeat.
▪ At rest, each heart muscle cell has a charge across its outer wall, or cell membrane.
Reducing this charge towards zero is called de-polarization, which activates the
mechanisms in the cell that cause it to contract.
▪ During each heartbeat a healthy heart will have an orderly progression of a wave of
depolarization that is triggered by the cells in the sinoatrial node, spreads out through the
atrium, passes through "intrinsic conduction pathways" and then spreads all over the
ventricles. This is detected as tiny rises and falls in the voltage between two electrodes
placed either side of the heart which is displayed as a wavy line either on a screen or on
paper. This display indicates the overall rhythm of the heart and weaknesses in different
parts of the heart muscle.
▪ Usually more than 2 electrodes are used and they can be combined into a number of
pairs. (For example: Left arm (LA), right arm (RA) and left leg (LL) electrodes form the
pairs: LA+RA, LA+LL, RA+LL) The output from each pair is known as a lead. Each lead is
said to look at the heart from a different angle.
▪ Different types of ECGs can be referred to by the number of leads that are recorded, for
example 3-lead, 5-lead or 12-lead ECGs (sometimes simply "a 12-lead").
▪ A 12-lead ECG is one in which 12 different electrical signals are recorded at approximately
the same time and will often be used as a one-off recording of an ECG, typically printed
out as a paper copy. 3- and 5-lead ECGs tend to be monitored continuously and viewed
only on the screen of an appropriate monitoring device, for example during an operation
or whilst being transported in an ambulance.
▪ There may, or may not be any permanent record of a 3- or 5-lead ECG depending on the
equipment used.
HUMAN ANATOMY AND PHYSIOLOGY NOTES
RAMDAS BHAT
KARAVALI COLLEGE OF PHARMACY 17
Electrode
label (in
the USA)
Electrode placement
RA On the right arm, avoiding bony prominences.
LA In the same location that RA was placed, but on the left arm this time.
RL On the right leg, avoiding bony prominences.
LL In the same location that RL was placed, but on the left leg this time.
V1 In the fourth intercostal space (between ribs 4 & 5) just to the right of
the sternum (breastbone).
V2 In the fourth intercostal space (between ribs 4 & 5) just to the left of the
sternum.
V3 Between leads V2 and V4.
V4 In the fifth intercostal space (between ribs 5 & 6) in the mid-clavicular
line (the imaginary line that extends down from the midpoint of the
clavicle (collarbone)).
V5 Horizontally even with V4, but in the anterior axillary line. (The anterior
axillary line is the imaginary line that runs down from the point midway
between the middle of the clavicle and the lateral end of the clavicle; the
lateral end of the collarbone is the end closer to the arm.)
V6 Horizontally even with V4 and V5 in the midaxillary line. (The midaxillary
line is the imaginary line that extends down from the middle of the
patient's armpit.)
➢ Waves and intervals:
▪ A typical ECG tracing of the cardiac cycle (heartbeat) consists of a P wave, a QRS complex,
a T wave, and a U wave which is normally visible in 50 to 75% of ECGs.
▪ The baseline voltage of the electrocardiogram is known as the isoelectric line.
▪ Typically, the isoelectric line is measured as the portion of the tracing following the T wave
and preceding the next P wave.
HUMAN ANATOMY AND PHYSIOLOGY NOTES
RAMDAS BHAT
KARAVALI COLLEGE OF PHARMACY 18
Feature Description Duration
RR interval The interval between an R wave and the next R wave is the
inverse of the heart rate. Normal resting heart rate is between 50
and 100 bpm
0.6 to
1.2s
P wave During normal atrial depolarization, the main electrical vector is
directed from the SA node towards the AV node, and spreads
from the right atrium to the left atrium. This turns into the P wave
on the ECG.
80ms
PR interval The PR interval is measured from the beginning of the P wave to
the beginning of the QRS complex. The PR interval reflects the
time the electrical impulse takes to travel from the sinus node
through the AV node and entering the ventricles. The PR interval
is therefore a good estimate of AV node function.
120 to
200ms
PR segment The PR segment connects the P wave and the QRS complex. This
coincides with the electrical conduction from the AV node to the
bundle of His to the bundle branches and then to the Purkinje
Fibers. This electrical activity does not produce a contraction
directly and is merely traveling down towards the ventricles and
this shows up flat on the ECG. The PR interval is more clinically
relevant.
50 to
120ms
QRS
complex
The QRS complex reflects the rapid depolarization of the right and
left ventricles. They have a large muscle mass compared to the
atria and so the QRS complex usually has a much larger
amplitude than the P-wave.
80 to
120ms
J-point The point at which the QRS complex finishes and the ST
segment begins. Used to measure the degree of ST elevation or
depression present.
N/A
ST segment The ST segment connects the QRS complex and the T wave. The
ST segment represents the period when the ventricles are
80 to
120ms
HUMAN ANATOMY AND PHYSIOLOGY NOTES
RAMDAS BHAT
KARAVALI COLLEGE OF PHARMACY 19
➢ Some pathological entities which can be seen on the ECG:
Shortened QT interval Hypercalcemia, some drugs, certain genetic abnormalities.
Prolonged QT interval Hypocalcemia, some drugs, certain genetic abnormalities.
Elevated ST segment Myocardial infraction
Depressed ST
segment
The heart muscles receive insufficient oxygen
Prolonged PQ intervals Coronary artery disease, Rheumatic fever and Scar tissue may
be form in the heart.
Flattened or inverted T
Waves
Coronary ischemia, left ventricular hypertrophy, digoxin
effect, some drugs.
Hyper acute T Waves Possibly the first manifestation of acute myocardial
infarction.
Prominent U Waves Hypokalemia.
Larger P Wave Indicate enlargement of an Atrium, as may occur in mitral
stenosis in which blood back up in to the left atrium.
Enlarge Q Wave Indicates myocardium infraction.
Enlarge R Wave Indicates enlarged ventricles
▪ The ECG cannot reliably measure the pumping ability of the heart, for which ultrasound-
based (echocardiography) or nuclear medicine tests are used. It is possible to be in cardiac
arrest with a normal ECG signal (a condition known as pulseless electrical activity).
CARDIAC CYCLES:
“A cardiac cycle includes all the events associated within one heart beat”
▪ The normal heart beats in healthy adult is 75 beats/min and cardiac cycle last for 0.8 sec.
▪ In the cardiac cycle due to the pressure changes atria and ventricles alternately contract
and relax, and blood flows from areas of higher blood pressure to areas of lower blood
depolarized. It is isoelectric.
T wave The T wave represents the repolarization (or recovery) of the
ventricles. The interval from the beginning of the QRS complex to
the apex of the T wave is referred to as the absolute refractory
period. The last half of the T wave is referred to as the relative
refractory period (or vulnerable period).
160ms
ST interval The ST interval is measured from the J point to the end of the T
wave.
320ms
QT interval The QT interval is measured from the beginning of the QRS
complex to the end of the T wave. A prolonged QT interval is a
risk factor for ventricular tachyarrhythmias and sudden death. It
varies with heart rate and for clinical relevance requires a
correction for this, giving the QTc.
300 to
430ms
U wave The U wave is not always seen. It is typically low amplitude, and,
by definition, follows the T wave.
J wave The J wave, elevated J-Point or Osborn Wave appears as a late
delta wave following the QRS or as a small secondary R wave. It
is considered path gnomic of hypothermia or hypocalcemia.
HUMAN ANATOMY AND PHYSIOLOGY NOTES
RAMDAS BHAT
KARAVALI COLLEGE OF PHARMACY 20
pressure.
▪ The term systole is used for the contraction and diastole used for the relaxation.
▪ In a normal cardiac cycle, the two atria contract while the two ventricles relax. Then, while
the two-ventricle contract, the two atria relax.
▪ Cardiac cycle is described by the following phase:
1) Atrial systole
▪ In this phase Atrial contraction is begins which is last about 0.1 sec at same time ventricle
are relaxed.
▪ So, the Right and Left AV valves are open and Atria send blood
into the relaxed ventricles.
▪ Atrial systole pushes 25 ml of blood in to ventricles which already contain 105 ml blood
so at the end of atrial systole means end of ventricle diastole Ventricles contain maximum
blood volume which is 130 ml known as end-diastolic volume (EDV).
▪ In the ECG or EKG, it is noted as P wave.
2) Ventricular Systole
▪ In this phase ventricles begin contraction which is last for 0.3 sec.
▪ Pressure in ventricles rises due to contraction and shut the AV valves which is heard by
“Lubb” Sound.
▪ For about 0.05 sec all four valve are closed which is known as isovolumetric contraction.
▪ Ventricular contraction pushes blood out of the ventricles and opens the both Semilunar
valve and ejected 70 ml blood in to aorta and same amount of blood in to pulmonary trunk
by respectively left and right ventricles so the 60 ml of blood remains in each ventricle out
of 130 ml.
▪ This is known as ventricular ejection which last for 0.25 sec
Ventricular systole = isovolumetric contraction + ventricular ejection
= (0.05) + (0.25)
= 0.3 sec.
▪ The blood volume in the Ventricles at the end of ventricle systole is 60 ml known as end-
systolic volume (ESV).
▪ The blood ejection per beat from each ventricle is known as stroke volume.
Stroke volume = EDV – ESV
= 130 ml – 60 ml
= 70 ml
▪ It is noted as QRS wave in ECG or EKG.
3. Ventricular Diastole or Relaxation period:
▪ In this phase both ventricles and atria are in relaxation.
▪ Relaxation which is last for 0.4 sec.
▪ Pressure in the ventricles drops so blood in the Pulmonary Trunk and aorta backflows
closing the Semilunar Valves.
▪ This is heard by “Dubb” sound.
▪ In this period, ventricular pressure is higher than atrial pressure hence all heart valves
are closed again and this period is known as isovolumetric.
▪ It is noted as T wave in ECG or EKG.
▪ Again, the AV valves open and fill up the ventricle and complete the one Cardiac cycle.
HUMAN ANATOMY AND PHYSIOLOGY NOTES
RAMDAS BHAT
KARAVALI COLLEGE OF PHARMACY 21
4. Atrial diastole
• During atrial diastole, blood enters the right atrium through the superior and inferior
vena cava and the left atrium via the pulmonary veins.
• In the early part of this phase, the atrioventricular valves are closed and blood pools in
the atria.
• It lasts about 0.7 seconds - relaxation of the atria, during which the atria fill with blood
from the large veins (the vena cava)
CARDIAC OUTPUT:
▪ Cardiac output is the amount of blood ejected from the left ventricle (or the right
ventricle) in to the aorta (or pulmonary trunk) each minute and it is equal to the product
of stroke volume and heart rate.
Thus,
Cardiac Output = Stroke volume (ml/beat) * Heart rate (beats/min)
= 70 ml/beat * 75 beats/min
= 5250 ml/min or 5.25 liters/min.
HUMAN ANATOMY AND PHYSIOLOGY NOTES
RAMDAS BHAT
KARAVALI COLLEGE OF PHARMACY 22
Factor affecting on Stroke volume:
▪ Three important factors regulate the stroke volume in different circumstances and ensure
that the left and right ventricles pump equal volume of blood.
i) Preload:
▪ The blood supply to the ventricle is often referred to as preload. Technically, the
definition of preload is the volume or pressure in the ventricle at the end of diastole or
refers as end-diastolic volume.
▪ According to Frank-Starling law of the heart, more the heart is filling during diastole, the
greater the force of contraction during systole.
▪ The duration of ventricular diastole and venous pressure are the two key factors that
determine EDV.
▪ When the heart rate is increase, the duration of diastole is shorter so it takes smaller
filling times means smaller EDV.
▪ On the other hand, when venous pressure increase, a greater volume of blood is forced
into the ventricles and the EDV is increased.
For example:
▪ When heart rate exceeds about 160 beats/min, stroke volumes usually decrease. At such
rapid heart rate decrease the ventricular filling time so decrease the EDV and thus the
preload is lower.
▪ People, who have slow resting heart rate, usually have large stroke volumes because
filling time is prolonged and preload thus is larger.
ii) Contractility:
▪ The second factor that influences stroke volume is myocardial contractility, which is the
strength of contraction at any given preload.
▪ Increases the contractility are called positive inotropic agents and decreases the
contractility are called negative inotropic agents.
▪ Thus, for a constant preload, stroke volume is larger when positive inotropic agent is
present and it promotes the forceful contraction.
iii) Afterload:
▪ The resistance to the ejection of blood by the ventricle is called afterload. For example:
▪ In the atherosclerosis condition arteries are narrowed so they resist the blood flow from
ventricles to out of heart and it decrease the stroke volume, and more blood remains in
the ventricles at the end of systole.
Other factors are:
Sympathetic stimulation
▪ Increase the Epinephrine (E) and Non-Epinephrine (NE) level
▪ Causes ventricles to contract with more force and increases ejection fraction and
decreases ESV and increase the stroke volume.
Parasympathetic activity
▪ Increases the Acetylcholine (Ach) released by vagus nerves
▪ Reduces force of cardiac contractions
BLOOD PRESSURE:
• Lateral pressure exerted by the column of the blood flowing on the walls of blood
vessels
• They are divided into 2 types on which blood vessel they are exerted:
1. ARTERIAL BLOOD PRESSURE(ABP)
2. VENTRICULAR BLOOD PRESSURE(VBP)
HUMAN ANATOMY AND PHYSIOLOGY NOTES
RAMDAS BHAT
KARAVALI COLLEGE OF PHARMACY 23
SYSTOLIC BP:
• Maximum pressure exerted during the flow of the blood following ventricular systole
• The normal value is 120mmHG
• It ranges from 110-130mmHG depending on the Physiological condition of the body.
DIASTOLIC BP:
• Minimum pressure exerted during the flow of the blood following ventricular diastole.
• The normal value is 80mmHG
• It ranges from 70-90mmHG depending on the Physiological condition of the body.
Device used to measure Systolic and Diastolic BP is called as SPHYGMOMANOMETER
REGULATION OF BLOOD PRESSURE:
Nervous regulation:
SHORT TERM REGULATION OF BLOOD PRESSURE:
a) Baroreceptor regulation:
HUMAN ANATOMY AND PHYSIOLOGY NOTES
RAMDAS BHAT
KARAVALI COLLEGE OF PHARMACY 24
b) Chemoreceptor regulation:
HUMAN ANATOMY AND PHYSIOLOGY NOTES
RAMDAS BHAT
KARAVALI COLLEGE OF PHARMACY 25
LONG TERM REGULATION OF BLOOD PRESSURE
HORMONAL REGULATION OF BLOOD PRESSURE:

More Related Content

What's hot (20)

Anatomy and physiology of Lymphatic System
Anatomy and physiology of Lymphatic SystemAnatomy and physiology of Lymphatic System
Anatomy and physiology of Lymphatic System
 
Structure of heart
Structure of heartStructure of heart
Structure of heart
 
Lymphatic system
Lymphatic systemLymphatic system
Lymphatic system
 
ANATOMY AND PHYSIOLOGY OF HEART
ANATOMY AND PHYSIOLOGY OF HEARTANATOMY AND PHYSIOLOGY OF HEART
ANATOMY AND PHYSIOLOGY OF HEART
 
Tissues of Human body.pdf
Tissues of Human body.pdfTissues of Human body.pdf
Tissues of Human body.pdf
 
Cell anatomy
Cell anatomyCell anatomy
Cell anatomy
 
LYMPHATIC SYSTEM
LYMPHATIC SYSTEMLYMPHATIC SYSTEM
LYMPHATIC SYSTEM
 
Unit III, chapter-1-Body fluids and Blood
Unit III, chapter-1-Body fluids and BloodUnit III, chapter-1-Body fluids and Blood
Unit III, chapter-1-Body fluids and Blood
 
BLOOD CIRCULATION
BLOOD CIRCULATIONBLOOD CIRCULATION
BLOOD CIRCULATION
 
Blood anatomy
Blood anatomyBlood anatomy
Blood anatomy
 
Anatomy of the Cardiovascular system
Anatomy of the Cardiovascular systemAnatomy of the Cardiovascular system
Anatomy of the Cardiovascular system
 
THE CARDIOVASCULAR SYSTEM CHAPTER 4
THE CARDIOVASCULAR SYSTEM CHAPTER 4THE CARDIOVASCULAR SYSTEM CHAPTER 4
THE CARDIOVASCULAR SYSTEM CHAPTER 4
 
Circulatory System.ppt
Circulatory System.pptCirculatory System.ppt
Circulatory System.ppt
 
Cardiac muscle tissue
Cardiac muscle tissueCardiac muscle tissue
Cardiac muscle tissue
 
Structure of blood vessels
Structure of blood vesselsStructure of blood vessels
Structure of blood vessels
 
Structure of human heart
Structure of human heartStructure of human heart
Structure of human heart
 
Cardiovascular system
Cardiovascular systemCardiovascular system
Cardiovascular system
 
ANATOMY OF THE LYMPHATIC SYSTEM
ANATOMY OF THE LYMPHATIC SYSTEMANATOMY OF THE LYMPHATIC SYSTEM
ANATOMY OF THE LYMPHATIC SYSTEM
 
Lymphatic system-----(Physiology)
Lymphatic system-----(Physiology)Lymphatic system-----(Physiology)
Lymphatic system-----(Physiology)
 
The heart walls
The heart wallsThe heart walls
The heart walls
 

Similar to CVS and its Physiology.pdf

L2 location and general description
L2 location and general descriptionL2 location and general description
L2 location and general descriptionReach Na
 
Cardiovascular system by Yogesh patel
Cardiovascular system by Yogesh patelCardiovascular system by Yogesh patel
Cardiovascular system by Yogesh patelPrabhat Kumar
 
cardiovascular system
cardiovascular systemcardiovascular system
cardiovascular systemAkashsagar22
 
Anatomy and physiology of heart, lung ,
Anatomy and physiology of heart, lung ,Anatomy and physiology of heart, lung ,
Anatomy and physiology of heart, lung ,ligi xavier
 
9.circulatory system ppt by miss sejal m. khuman
9.circulatory system ppt by miss sejal m. khuman9.circulatory system ppt by miss sejal m. khuman
9.circulatory system ppt by miss sejal m. khumanSejalkhumam
 
general physiology- the physiology of the heart
general physiology- the physiology of the heartgeneral physiology- the physiology of the heart
general physiology- the physiology of the heartjanine543943
 
The cardiovascular system.pptx
The cardiovascular system.pptxThe cardiovascular system.pptx
The cardiovascular system.pptxJagruti Marathe
 
anatomy and physiology of human heart BY DEEPIKA.R
anatomy and physiology of human heart BY DEEPIKA.Ranatomy and physiology of human heart BY DEEPIKA.R
anatomy and physiology of human heart BY DEEPIKA.RDeepikaLingam2
 
Cardiovascular system (blood vessels, anatomy)
Cardiovascular system (blood vessels, anatomy) Cardiovascular system (blood vessels, anatomy)
Cardiovascular system (blood vessels, anatomy) Pharmacy Universe
 
CVS ANATOMY- The Heart.pptx
CVS ANATOMY- The Heart.pptxCVS ANATOMY- The Heart.pptx
CVS ANATOMY- The Heart.pptxShaly Jose
 
Johny's A&P Structure and Function of Heart
Johny's A&P Structure and Function of HeartJohny's A&P Structure and Function of Heart
Johny's A&P Structure and Function of HeartJohny Kutty Joseph
 
Lecture 3 the cardiovascular system
Lecture 3 the cardiovascular systemLecture 3 the cardiovascular system
Lecture 3 the cardiovascular systemBilalHoushaymi
 
anatomy and physiology of cardiovascular 1 (1).pptx
anatomy and physiology of cardiovascular 1 (1).pptxanatomy and physiology of cardiovascular 1 (1).pptx
anatomy and physiology of cardiovascular 1 (1).pptxEricsonKiprono
 
Transport in animals
Transport in animalsTransport in animals
Transport in animalsSian Ferguson
 

Similar to CVS and its Physiology.pdf (20)

L2 location and general description
L2 location and general descriptionL2 location and general description
L2 location and general description
 
The heart
The heartThe heart
The heart
 
Cardiovascular system by Yogesh patel
Cardiovascular system by Yogesh patelCardiovascular system by Yogesh patel
Cardiovascular system by Yogesh patel
 
cardiovascular system
cardiovascular systemcardiovascular system
cardiovascular system
 
Anatomy and physiology of heart, lung ,
Anatomy and physiology of heart, lung ,Anatomy and physiology of heart, lung ,
Anatomy and physiology of heart, lung ,
 
Anatomy of heart
Anatomy of heartAnatomy of heart
Anatomy of heart
 
9.circulatory system ppt by miss sejal m. khuman
9.circulatory system ppt by miss sejal m. khuman9.circulatory system ppt by miss sejal m. khuman
9.circulatory system ppt by miss sejal m. khuman
 
general physiology- the physiology of the heart
general physiology- the physiology of the heartgeneral physiology- the physiology of the heart
general physiology- the physiology of the heart
 
Heart
HeartHeart
Heart
 
The cardiovascular system.pptx
The cardiovascular system.pptxThe cardiovascular system.pptx
The cardiovascular system.pptx
 
anatomy and physiology of human heart BY DEEPIKA.R
anatomy and physiology of human heart BY DEEPIKA.Ranatomy and physiology of human heart BY DEEPIKA.R
anatomy and physiology of human heart BY DEEPIKA.R
 
Cardiovascular ststem
Cardiovascular ststemCardiovascular ststem
Cardiovascular ststem
 
Cardiovascular system (blood vessels, anatomy)
Cardiovascular system (blood vessels, anatomy) Cardiovascular system (blood vessels, anatomy)
Cardiovascular system (blood vessels, anatomy)
 
CVS ANATOMY- The Heart.pptx
CVS ANATOMY- The Heart.pptxCVS ANATOMY- The Heart.pptx
CVS ANATOMY- The Heart.pptx
 
Johny's A&P Structure and Function of Heart
Johny's A&P Structure and Function of HeartJohny's A&P Structure and Function of Heart
Johny's A&P Structure and Function of Heart
 
Body fluids and circulation
Body fluids and circulationBody fluids and circulation
Body fluids and circulation
 
Lecture 3 the cardiovascular system
Lecture 3 the cardiovascular systemLecture 3 the cardiovascular system
Lecture 3 the cardiovascular system
 
Heart anatomy
Heart anatomyHeart anatomy
Heart anatomy
 
anatomy and physiology of cardiovascular 1 (1).pptx
anatomy and physiology of cardiovascular 1 (1).pptxanatomy and physiology of cardiovascular 1 (1).pptx
anatomy and physiology of cardiovascular 1 (1).pptx
 
Transport in animals
Transport in animalsTransport in animals
Transport in animals
 

More from RAMDAS BHAT

CHEMOTHERAPY INTRODUCTION.pdf
CHEMOTHERAPY INTRODUCTION.pdfCHEMOTHERAPY INTRODUCTION.pdf
CHEMOTHERAPY INTRODUCTION.pdfRAMDAS BHAT
 
CELL DIVISION AND ITS REGULATION.pdf
CELL DIVISION AND ITS REGULATION.pdfCELL DIVISION AND ITS REGULATION.pdf
CELL DIVISION AND ITS REGULATION.pdfRAMDAS BHAT
 
TOXICOPHARMACOLOGY.pdf
TOXICOPHARMACOLOGY.pdfTOXICOPHARMACOLOGY.pdf
TOXICOPHARMACOLOGY.pdfRAMDAS BHAT
 
IMMUNOPHARMACOLOGY.pdf
IMMUNOPHARMACOLOGY.pdfIMMUNOPHARMACOLOGY.pdf
IMMUNOPHARMACOLOGY.pdfRAMDAS BHAT
 
IMMUNOPHARMACOLOGY.pdf
IMMUNOPHARMACOLOGY.pdfIMMUNOPHARMACOLOGY.pdf
IMMUNOPHARMACOLOGY.pdfRAMDAS BHAT
 
Drugs acting on Urinary system.pdf
Drugs acting on Urinary system.pdfDrugs acting on Urinary system.pdf
Drugs acting on Urinary system.pdfRAMDAS BHAT
 
SPORTS PHYSIOLOGY.pdf
SPORTS PHYSIOLOGY.pdfSPORTS PHYSIOLOGY.pdf
SPORTS PHYSIOLOGY.pdfRAMDAS BHAT
 
Endocrine system.pdf
Endocrine system.pdfEndocrine system.pdf
Endocrine system.pdfRAMDAS BHAT
 
Digestive system.pdf
Digestive system.pdfDigestive system.pdf
Digestive system.pdfRAMDAS BHAT
 
Reproductive system.pdf
Reproductive system.pdfReproductive system.pdf
Reproductive system.pdfRAMDAS BHAT
 
Urinary system.pdf
Urinary system.pdfUrinary system.pdf
Urinary system.pdfRAMDAS BHAT
 
PC of Blood and Blood forming agents.pdf
PC of Blood and Blood forming agents.pdfPC of Blood and Blood forming agents.pdf
PC of Blood and Blood forming agents.pdfRAMDAS BHAT
 
Respiratory system.pdf
Respiratory system.pdfRespiratory system.pdf
Respiratory system.pdfRAMDAS BHAT
 
Nervous system.pdf
Nervous system.pdfNervous system.pdf
Nervous system.pdfRAMDAS BHAT
 
Lymphatic system.pdf
Lymphatic system.pdfLymphatic system.pdf
Lymphatic system.pdfRAMDAS BHAT
 
Bones and Joints.pdf
Bones and Joints.pdfBones and Joints.pdf
Bones and Joints.pdfRAMDAS BHAT
 
Sense Organs.pdf
Sense Organs.pdfSense Organs.pdf
Sense Organs.pdfRAMDAS BHAT
 

More from RAMDAS BHAT (20)

CHEMOTHERAPY INTRODUCTION.pdf
CHEMOTHERAPY INTRODUCTION.pdfCHEMOTHERAPY INTRODUCTION.pdf
CHEMOTHERAPY INTRODUCTION.pdf
 
CELL DIVISION AND ITS REGULATION.pdf
CELL DIVISION AND ITS REGULATION.pdfCELL DIVISION AND ITS REGULATION.pdf
CELL DIVISION AND ITS REGULATION.pdf
 
TOXICOPHARMACOLOGY.pdf
TOXICOPHARMACOLOGY.pdfTOXICOPHARMACOLOGY.pdf
TOXICOPHARMACOLOGY.pdf
 
IMMUNOPHARMACOLOGY.pdf
IMMUNOPHARMACOLOGY.pdfIMMUNOPHARMACOLOGY.pdf
IMMUNOPHARMACOLOGY.pdf
 
IMMUNOPHARMACOLOGY.pdf
IMMUNOPHARMACOLOGY.pdfIMMUNOPHARMACOLOGY.pdf
IMMUNOPHARMACOLOGY.pdf
 
Drugs acting on Urinary system.pdf
Drugs acting on Urinary system.pdfDrugs acting on Urinary system.pdf
Drugs acting on Urinary system.pdf
 
SPORTS PHYSIOLOGY.pdf
SPORTS PHYSIOLOGY.pdfSPORTS PHYSIOLOGY.pdf
SPORTS PHYSIOLOGY.pdf
 
ENERGETICS.pdf
ENERGETICS.pdfENERGETICS.pdf
ENERGETICS.pdf
 
Endocrine system.pdf
Endocrine system.pdfEndocrine system.pdf
Endocrine system.pdf
 
Digestive system.pdf
Digestive system.pdfDigestive system.pdf
Digestive system.pdf
 
GENETICS.pdf
GENETICS.pdfGENETICS.pdf
GENETICS.pdf
 
Reproductive system.pdf
Reproductive system.pdfReproductive system.pdf
Reproductive system.pdf
 
Urinary system.pdf
Urinary system.pdfUrinary system.pdf
Urinary system.pdf
 
PC of Blood and Blood forming agents.pdf
PC of Blood and Blood forming agents.pdfPC of Blood and Blood forming agents.pdf
PC of Blood and Blood forming agents.pdf
 
Respiratory system.pdf
Respiratory system.pdfRespiratory system.pdf
Respiratory system.pdf
 
Nervous system.pdf
Nervous system.pdfNervous system.pdf
Nervous system.pdf
 
Lymphatic system.pdf
Lymphatic system.pdfLymphatic system.pdf
Lymphatic system.pdf
 
Blood.pdf
Blood.pdfBlood.pdf
Blood.pdf
 
Bones and Joints.pdf
Bones and Joints.pdfBones and Joints.pdf
Bones and Joints.pdf
 
Sense Organs.pdf
Sense Organs.pdfSense Organs.pdf
Sense Organs.pdf
 

Recently uploaded

All Time Service Available Call Girls Marine Drive 📳 9820252231 For 18+ VIP C...
All Time Service Available Call Girls Marine Drive 📳 9820252231 For 18+ VIP C...All Time Service Available Call Girls Marine Drive 📳 9820252231 For 18+ VIP C...
All Time Service Available Call Girls Marine Drive 📳 9820252231 For 18+ VIP C...Arohi Goyal
 
Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...
Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...
Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...narwatsonia7
 
Call Girl Coimbatore Prisha☎️ 8250192130 Independent Escort Service Coimbatore
Call Girl Coimbatore Prisha☎️  8250192130 Independent Escort Service CoimbatoreCall Girl Coimbatore Prisha☎️  8250192130 Independent Escort Service Coimbatore
Call Girl Coimbatore Prisha☎️ 8250192130 Independent Escort Service Coimbatorenarwatsonia7
 
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...narwatsonia7
 
Artifacts in Nuclear Medicine with Identifying and resolving artifacts.
Artifacts in Nuclear Medicine with Identifying and resolving artifacts.Artifacts in Nuclear Medicine with Identifying and resolving artifacts.
Artifacts in Nuclear Medicine with Identifying and resolving artifacts.MiadAlsulami
 
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night EnjoyCall Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoybabeytanya
 
(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...
(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...
(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...indiancallgirl4rent
 
VIP Mumbai Call Girls Hiranandani Gardens Just Call 9920874524 with A/C Room ...
VIP Mumbai Call Girls Hiranandani Gardens Just Call 9920874524 with A/C Room ...VIP Mumbai Call Girls Hiranandani Gardens Just Call 9920874524 with A/C Room ...
VIP Mumbai Call Girls Hiranandani Gardens Just Call 9920874524 with A/C Room ...Garima Khatri
 
Call Girl Number in Vashi Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Vashi Mumbai📲 9833363713 💞 Full Night EnjoyCall Girl Number in Vashi Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Vashi Mumbai📲 9833363713 💞 Full Night Enjoybabeytanya
 
Call Girls Ludhiana Just Call 9907093804 Top Class Call Girl Service Available
Call Girls Ludhiana Just Call 9907093804 Top Class Call Girl Service AvailableCall Girls Ludhiana Just Call 9907093804 Top Class Call Girl Service Available
Call Girls Ludhiana Just Call 9907093804 Top Class Call Girl Service AvailableDipal Arora
 
The Most Attractive Hyderabad Call Girls Kothapet 𖠋 6297143586 𖠋 Will You Mis...
The Most Attractive Hyderabad Call Girls Kothapet 𖠋 6297143586 𖠋 Will You Mis...The Most Attractive Hyderabad Call Girls Kothapet 𖠋 6297143586 𖠋 Will You Mis...
The Most Attractive Hyderabad Call Girls Kothapet 𖠋 6297143586 𖠋 Will You Mis...chandars293
 
Bangalore Call Girls Hebbal Kempapura Number 7001035870 Meetin With Bangalor...
Bangalore Call Girls Hebbal Kempapura Number 7001035870  Meetin With Bangalor...Bangalore Call Girls Hebbal Kempapura Number 7001035870  Meetin With Bangalor...
Bangalore Call Girls Hebbal Kempapura Number 7001035870 Meetin With Bangalor...narwatsonia7
 
♛VVIP Hyderabad Call Girls Chintalkunta🖕7001035870🖕Riya Kappor Top Call Girl ...
♛VVIP Hyderabad Call Girls Chintalkunta🖕7001035870🖕Riya Kappor Top Call Girl ...♛VVIP Hyderabad Call Girls Chintalkunta🖕7001035870🖕Riya Kappor Top Call Girl ...
♛VVIP Hyderabad Call Girls Chintalkunta🖕7001035870🖕Riya Kappor Top Call Girl ...astropune
 
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...CALL GIRLS
 
Night 7k to 12k Chennai City Center Call Girls 👉👉 7427069034⭐⭐ 100% Genuine E...
Night 7k to 12k Chennai City Center Call Girls 👉👉 7427069034⭐⭐ 100% Genuine E...Night 7k to 12k Chennai City Center Call Girls 👉👉 7427069034⭐⭐ 100% Genuine E...
Night 7k to 12k Chennai City Center Call Girls 👉👉 7427069034⭐⭐ 100% Genuine E...hotbabesbook
 
High Profile Call Girls Coimbatore Saanvi☎️ 8250192130 Independent Escort Se...
High Profile Call Girls Coimbatore Saanvi☎️  8250192130 Independent Escort Se...High Profile Call Girls Coimbatore Saanvi☎️  8250192130 Independent Escort Se...
High Profile Call Girls Coimbatore Saanvi☎️ 8250192130 Independent Escort Se...narwatsonia7
 
Premium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort Service
Premium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort ServicePremium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort Service
Premium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort Servicevidya singh
 
Best Rate (Hyderabad) Call Girls Jahanuma ⟟ 8250192130 ⟟ High Class Call Girl...
Best Rate (Hyderabad) Call Girls Jahanuma ⟟ 8250192130 ⟟ High Class Call Girl...Best Rate (Hyderabad) Call Girls Jahanuma ⟟ 8250192130 ⟟ High Class Call Girl...
Best Rate (Hyderabad) Call Girls Jahanuma ⟟ 8250192130 ⟟ High Class Call Girl...astropune
 

Recently uploaded (20)

All Time Service Available Call Girls Marine Drive 📳 9820252231 For 18+ VIP C...
All Time Service Available Call Girls Marine Drive 📳 9820252231 For 18+ VIP C...All Time Service Available Call Girls Marine Drive 📳 9820252231 For 18+ VIP C...
All Time Service Available Call Girls Marine Drive 📳 9820252231 For 18+ VIP C...
 
Escort Service Call Girls In Sarita Vihar,, 99530°56974 Delhi NCR
Escort Service Call Girls In Sarita Vihar,, 99530°56974 Delhi NCREscort Service Call Girls In Sarita Vihar,, 99530°56974 Delhi NCR
Escort Service Call Girls In Sarita Vihar,, 99530°56974 Delhi NCR
 
Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...
Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...
Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...
 
Call Girl Coimbatore Prisha☎️ 8250192130 Independent Escort Service Coimbatore
Call Girl Coimbatore Prisha☎️  8250192130 Independent Escort Service CoimbatoreCall Girl Coimbatore Prisha☎️  8250192130 Independent Escort Service Coimbatore
Call Girl Coimbatore Prisha☎️ 8250192130 Independent Escort Service Coimbatore
 
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...
 
Artifacts in Nuclear Medicine with Identifying and resolving artifacts.
Artifacts in Nuclear Medicine with Identifying and resolving artifacts.Artifacts in Nuclear Medicine with Identifying and resolving artifacts.
Artifacts in Nuclear Medicine with Identifying and resolving artifacts.
 
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night EnjoyCall Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoy
 
(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...
(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...
(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...
 
VIP Mumbai Call Girls Hiranandani Gardens Just Call 9920874524 with A/C Room ...
VIP Mumbai Call Girls Hiranandani Gardens Just Call 9920874524 with A/C Room ...VIP Mumbai Call Girls Hiranandani Gardens Just Call 9920874524 with A/C Room ...
VIP Mumbai Call Girls Hiranandani Gardens Just Call 9920874524 with A/C Room ...
 
Call Girl Number in Vashi Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Vashi Mumbai📲 9833363713 💞 Full Night EnjoyCall Girl Number in Vashi Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Vashi Mumbai📲 9833363713 💞 Full Night Enjoy
 
Call Girls Ludhiana Just Call 9907093804 Top Class Call Girl Service Available
Call Girls Ludhiana Just Call 9907093804 Top Class Call Girl Service AvailableCall Girls Ludhiana Just Call 9907093804 Top Class Call Girl Service Available
Call Girls Ludhiana Just Call 9907093804 Top Class Call Girl Service Available
 
Russian Call Girls in Delhi Tanvi ➡️ 9711199012 💋📞 Independent Escort Service...
Russian Call Girls in Delhi Tanvi ➡️ 9711199012 💋📞 Independent Escort Service...Russian Call Girls in Delhi Tanvi ➡️ 9711199012 💋📞 Independent Escort Service...
Russian Call Girls in Delhi Tanvi ➡️ 9711199012 💋📞 Independent Escort Service...
 
The Most Attractive Hyderabad Call Girls Kothapet 𖠋 6297143586 𖠋 Will You Mis...
The Most Attractive Hyderabad Call Girls Kothapet 𖠋 6297143586 𖠋 Will You Mis...The Most Attractive Hyderabad Call Girls Kothapet 𖠋 6297143586 𖠋 Will You Mis...
The Most Attractive Hyderabad Call Girls Kothapet 𖠋 6297143586 𖠋 Will You Mis...
 
Bangalore Call Girls Hebbal Kempapura Number 7001035870 Meetin With Bangalor...
Bangalore Call Girls Hebbal Kempapura Number 7001035870  Meetin With Bangalor...Bangalore Call Girls Hebbal Kempapura Number 7001035870  Meetin With Bangalor...
Bangalore Call Girls Hebbal Kempapura Number 7001035870 Meetin With Bangalor...
 
♛VVIP Hyderabad Call Girls Chintalkunta🖕7001035870🖕Riya Kappor Top Call Girl ...
♛VVIP Hyderabad Call Girls Chintalkunta🖕7001035870🖕Riya Kappor Top Call Girl ...♛VVIP Hyderabad Call Girls Chintalkunta🖕7001035870🖕Riya Kappor Top Call Girl ...
♛VVIP Hyderabad Call Girls Chintalkunta🖕7001035870🖕Riya Kappor Top Call Girl ...
 
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...
 
Night 7k to 12k Chennai City Center Call Girls 👉👉 7427069034⭐⭐ 100% Genuine E...
Night 7k to 12k Chennai City Center Call Girls 👉👉 7427069034⭐⭐ 100% Genuine E...Night 7k to 12k Chennai City Center Call Girls 👉👉 7427069034⭐⭐ 100% Genuine E...
Night 7k to 12k Chennai City Center Call Girls 👉👉 7427069034⭐⭐ 100% Genuine E...
 
High Profile Call Girls Coimbatore Saanvi☎️ 8250192130 Independent Escort Se...
High Profile Call Girls Coimbatore Saanvi☎️  8250192130 Independent Escort Se...High Profile Call Girls Coimbatore Saanvi☎️  8250192130 Independent Escort Se...
High Profile Call Girls Coimbatore Saanvi☎️ 8250192130 Independent Escort Se...
 
Premium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort Service
Premium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort ServicePremium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort Service
Premium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort Service
 
Best Rate (Hyderabad) Call Girls Jahanuma ⟟ 8250192130 ⟟ High Class Call Girl...
Best Rate (Hyderabad) Call Girls Jahanuma ⟟ 8250192130 ⟟ High Class Call Girl...Best Rate (Hyderabad) Call Girls Jahanuma ⟟ 8250192130 ⟟ High Class Call Girl...
Best Rate (Hyderabad) Call Girls Jahanuma ⟟ 8250192130 ⟟ High Class Call Girl...
 

CVS and its Physiology.pdf

  • 1. CHAPTER NO:09 CARDIO-VASCULAR SYSTEM Prepared by, RAMDAS BHAT Asst. Professor Karavali college of Pharmacy Mangalore 7795772463 Ramdas21@gmail.com
  • 2. INTRODUCTION: Cardiovascular is the system which includes the study of the heart, blood vessels and blood. This system is some time known as circularly system because it circulates or transport the nutrients, oxygen, carbon dioxide and essential molecules from environment to cells and cells to environment. It is involuntary in nature and gives continuous work. The heart propelling or impelling blood around 100,000 km of blood vessels and it pumps 14000 liters blood in day and 10 million liters in year. LOCATION OF HEART: ▪ Cone shaped heart is relatively small, about the same size of closed fist of person. ▪ It is 12 cm (5 in.) long, 9 cm (3.5 in.) wide and 6 cm (2.5 in.) thick. ▪ In an adult, average weight of heart is 300gm. ▪ The heart consists four chambers: a) Two atria or atrium b) Two ventricles ▪ It is located near to the middle of thoracic cavity in the mediastinum (the space between the lungs) and it rest on to the diaphragm. ▪ About two third of the mass of the heart lies to the left of the body’s midline. ▪ Pointed end portion which is formed by the tip of left ventricle is known as apex and opposite to apex the wide superior and posterior margin is known as base. CARDIOVASCULAR SYSTEM
  • 3. LAYER OF THE HEART: ▪ Heart layer is formed by pericardium ("around the heart”) which is triple-layered fluid- filled sac that surrounds and protects the heart. ▪ The pericardium consists of two principal portions Layer of Heart (Pericardium) Fibrous Pericardium Serous Pericardium Parietal Layer (Outer Layer) Visceral Layer (Inner Layer) (Epicardium) a) Fibrous pericardium: ▪ It is a strong layer of dense connective tissue. ▪ It adheres to the diaphragm inferiorly, and superiorly it is fused to the roots of the great vessels that leave and enter the heart. ▪ The fibrous pericardium acts as a tough outer coat that holds the heart in place and keeps it from overfilling with blood. ▪ It prevents overstretching of the heart, provides protection and fix the heart in mediastinum. b) Serous pericardium: ▪ It is a Deep to the fibrous pericardium and form double layer around the heart. ▪ The outer layer is known as parietal layer which is fused to the fibrous pericardium.
  • 4. ▪ The inner layer is known as visceral layer also known as epicardium. ▪ Between the outer layer (parietal layer) and inner layer (visceral layer) is gap known as pericardial cavity filled by fluid is known as pericardial fluid. ▪ This fluid ac as lubricant and reduces friction between the layer during contraction and relaxation. WALL OF THE HEART: ▪ The wall of the heart is formed by three layers: a) Epicardium (External layer): ▪ It is also known as the visceral layer of the serous pericardium. ▪ It is composed of mesothelium and delicate connectivetissue. ▪ It is the outer or external wall of the heart. b) Myocardium (Middle layer): ▪ Myo means muscles so it is made up by cardiac muscles tissue. ▪ It provides the bulkiness to the heart and it is responsible for the pumping action of heart. c) Endocardium (Inner layer): ▪ The endocardium is an innermost, thin, smooth layer of epithelial tissue that lines the inner surface of the heart chambers and valves. INTERIOR OF THE HEART: ▪ The heart is divided in to right and left side by partition known as the septum which is made up by myocardium covered by epithelium
  • 5. a) Chamber of heart: ▪ Heart consists of four chambers; i) Two atria: ▪ The two superior chambers are known as right atrium and left atrium. ▪ The posterior wall of the atrium is smooth surface while the anterior wall of the atrium is rough surface. ▪ On the surface of the atrium is wrinkle pouch like structure is known as auricle because it resembles like dog ear. ii) Two ventricles ▪ The two inferiors are known as right ventricle and left ventricles. ▪ On the surface of heart grooves like structures known as coronary sulcus which separate the atria to ventricle. ▪ The thickness of the wall of the four chambers varies according to their function. ▪ Example: The wall of the atria is thin and it pumps blood in to ventricles & the ventricle wall is thick in which right ventricle pumps blood in to lungs and left ventricle pumps blood in to aorta so the work load on left ventricle is high because of that the wall of left ventricle is two to four times thicker than right ventricle. b) Valve of the heart: ▪ In the heart blood passes from various compartment and finally it enters in to the artery. ▪ During these circulations for the prevention of back flow of blood there is special type of structure in heart which is known as valve. ▪ These special types of structures or valves are composed by dense connective tissue which is covered by endocardium. ▪ Valves are opened and closed in response to the contraction or relaxation of heart.
  • 6. It is classified into 2 types: a) Atrioventricular valve: ▪ Its names indicate the location of valves that means these valves located between the atria and ventricle or it moves blood from atrium to ventricle. ▪ Inner surface of the ventricle contains the papillary muscles which is connected with the end or tip part of valve. ▪ Blood moves atrium to ventricle when the pressure in to the ventricle is lower than the atrium that time valves get opened and papillary muscles are in relaxed condition. ▪ When the AV valve is open the point end of the valve project in to the ventricle. ▪ So, pressure in to the ventricle get increased at a same time ventricles start to contraction due to this contraction blood produce pressure on to the cups of valve and they move upward until their edge meet and close the opening. ▪ During the ventricle contraction blood may not goes from ventricle to atrium because valve have special type of opening and closing structure and during the closing time papillary muscles are also contracted so it prevents the back flow of blood from ventricles to atrium. ▪ It is mainly subdivided in to two types:
  • 7. i) Tricuspid Valves: ii) Bicuspid Valves (mitral valve): ▪ This valve located between the left atrium and left ventricle. ▪ It consists two cups so it is known as bicuspid valves also known as mitral valve. b) Semilunar valve: ▪ These valves consist three Semilunar (half-moon like) cups. ▪ It is further subdivided in to: i) Pulmonary Semilunar valve: ▪ It passes the blood from right ventricle to lungs during opening stage. ii) Aortic Semilunar valve: ▪ It passes the blood from left ventricle to aorta during opening condition. CIRCULATRY SYSTEM OF BLOOD THROUGH HEART: 1) Pulmonary circulation: ▪ In the body system cells receive O2 from blood and give CO2 in to blood so blood become deoxygenate. ▪ These Deoxygenated blood by the help of Superior venacava, Inferior venacava and coronary sinus transfer in to the right atrium.
  • 8. ▪ Right atrium flows this deoxygenated blood in to right ventricle with the help of tricuspid valves. ▪ Right ventricle pumps blood in to pulmonary trunk via pulmonary Semilunar valve. ▪ The pulmonary trunk divided in to right pulmonary artery and left pulmonary artery, the right pulmonary artery gives blood to right lungs and left pulmonary artery gives blood to left lungs. 2) Systemic Circulation: ▪ In the lungs blood become oxygenated means it gains O2 and loss CO2. ▪ Now, the oxygenated blood returns in to heart through pulmonary veins. ▪ Then pulmonary veins pass blood in to left atrium which pumps blood in to left ventricle with the help of bicuspid valve. ▪ Finally, bloods flows in systemic circulation from aorta and reach near to each and every cell of the body and gives O2 and take CO2. ▪ Again, the deoxygenated blood flow through pulmonary circulation. 3) Coronary circulation: ▪ It supplies the oxygenated blood to the heart. ▪ It arises from the ascending aorta and divided in to left and right coronary branches. i) The left coronary artery: ▪ The left coronary artery pass inferior to left auricle and divided in to the anterior interventricular and circumflex branches. ▪ The anterior interventricular branch or left anterior descending (LAD) arteries enter in to the anterior interventricular sulcus and supplies oxygenated blood to the walls of both ventricles and the interventricular septum. ▪ The circumflex branch lies in the coronary sulcus and distributes oxygenated blood to the walls of the left ventricle and left atrium. ii) The right coronary artery: ▪ The right coronary arteries branches supply blood to the right atrium. ▪ It continues inferior to the right auricle and divided in to the posterior interventricular and marginal branches. ▪ The posterior interventricular branches enter in to the posterior interventricular sulcus and supply the oxygenated blood in to two ventricles and the interventricular septum. The marginal branch in the coronary sulcus transports oxygenated blood to the myocardium of the right ventricle.
  • 9. a) Coronary Vein: ▪ After delivering the oxygen and nutrients to the heart, the blood receives waste and carbon dioxide. ▪ It then drains in to a large vascular sinus or coronary sinus on the posterior surface of the heart. ▪ Coronary sinus empties deoxygenated bloods into the right atrium.
  • 10.
  • 11. HUMAN ANATOMY AND PHYSIOLOGY NOTES RAMDAS BHAT KARAVALI COLLEGE OF PHARMACY 11 CONDUCTING SYSTEM OF HEART: Action Potentials in Cardiac Muscle (Ventricular Muscle) 1. SA Nodal Action Potential – Pace Maker potential 2. Ventricular Muscle Action Potential 3. Atrial Muscle Action Potential 4. Purkinje System Action Potential Phases of Ventricular Muscle Action Potential 1. Phase 0 – Up Stroke 2. Phase I – Initial Repolarization 3. Phase II – Plateau Phase • Phase III – Repolarization 4. Phase IV – Resting Membrane Potential PHASE 0 - UPSTROKE • It is the Upstroke of Action Potential • Opening of Voltage Gated Sodium Channels at -70 to -80 mV • There is transient increase in Sodium Conductance leading to rapid influx of Sodium Ions causing membrane Depolarization. • At the peak of Upstroke, the membrane potential approaches the sodium Equilibrium Potential.
  • 12. HUMAN ANATOMY AND PHYSIOLOGY NOTES RAMDAS BHAT KARAVALI COLLEGE OF PHARMACY 12 PHASE I – Initial Repolarization • It is a brief period of initial repolarization • This phase results from – Closure of voltage gated sodium channels leading to Decreased sodium influx – Opening of potassium channels leading to potassium efflux. PHASE II – Plateau Phase • It is the plateau phase of the action potential • There is slow opening of voltage gated calcium channels at -30 to -40 mV • There is excessive calcium influx during this phase because of transient increase in calcium conductance • This calcium influx is balanced by the Potassium efflux leading to the production of plateau i.e., delay in the repolarization • During the plateau, outward and inward currents are nearly equal so that the membrane potential is stable in this phase. • Plateau phase is not part of repolarization. It is sustained depolarization. PHASE III – Repolarization • During this phase, the calcium conductance decreases due to closure of slow calcium channels • There is increase in the potassium conductance leading to excessive efflux of potassium and this is the only dominant current during this phase. • This results in the repolarization till the potassium equilibrium potential is reached. PHASE IV – Resting Membrane Potential • During this phase the Membrane is in resting state. • RMP is -85 to -90 mv • Activation of Na+/K + ATPase pump
  • 13. HUMAN ANATOMY AND PHYSIOLOGY NOTES RAMDAS BHAT KARAVALI COLLEGE OF PHARMACY 13 Sinoatrial node (SA node) Specialized region in right atrial wall near opening of superior vena cava. Atrioventricular node (AV node) Small bundle of specialized cardiac cells located at base of right atrium near septum Bundle of His (atrioventricular bundle) Cells originate at AV node and enters interventricular septum Divides to form right and left bundle branches which travel down septum, curve around tip of ventricular chambers, travel back toward atria along outer walls Purkinje fibers Small, terminal fibers that extend from bundle of His and spread throughout ventricular myocardium ▪ Electrical impulses generated in the SAN cause the right and left atria to contract first. Depolarization (heart muscle contraction caused by electrical stimulation) occurs nearly simultaneously in the right and left ventricles 1-2 tenths of a second after atrial depolarization. The entire sequence of depolarization, from beginning to end (for one heart beat), takes 2-3 tenths of a second. ▪ All heart cells muscle and conducting tissue are capable of generating electrical impulses that can trigger the heart to beat. Under normal circumstances all parts of the heart conducting system can conduct over 140-200 signals (and corresponding heart beats) per minute. ▪ The SAN is known as the "heart's pacemaker" because electrical impulses are normally generated here. At rest the SAN usually produces 60-70 signals a minute. It is the SAN that increases its' rate due to stimuli such as exercise, stimulant drugs, or fever. ▪ Should the SAN fail to produce impulses the AVN can take over. The resting rate of the AVN is slower, generating 40-60 beats a minute. The AVN and remaining parts of the conducting system are less capable of increasing heart rate due to stimuli previously
  • 14. HUMAN ANATOMY AND PHYSIOLOGY NOTES RAMDAS BHAT KARAVALI COLLEGE OF PHARMACY 14 mentioned than the SAN. ▪ The atrioventricular node delays impulses by approximately 0.09s. This delay in the cardiac pulse is extremely important: It ensures that the atria have ejected their blood into the ventricles first before the ventricles contract. ▪ The Bundle of HIS can generate 30-40 signals a minute. Ventricular muscle cells may generate 20-30 signals a minute. ▪ Heart rates below 35-40 beats a minute for a prolonged period usually cause problems due to not enough blood flow to vital organs. ▪ Problems with signal conduction, due to disease or abnormalities of the conducting system, can occur anyplace along the heart's conduction pathway. Abnormally conducted signals, resulting in alterations of the heart's normal beating, are called arrhythmias or dysrhythmia. ▪ By analysing an EKG, a doctor is often able to tell if there are problems with specific parts of the conducting system or if certain areas of heart muscle may be injured. PROPERTIES OF CARDIAC MUSCLE: 1. Excitability (Bathmotropic action) 2. Auto rhythmicity 3. Conductivity (Dromotropic action) 4. Contractility (Inotropic action) 5. Refractory period 6. All or none phenomenon 7. Franks-Starlings law 8. Functional syncytium. 9. Role of calcium. 10. Resistance to fatigue. 1. EXCITIBILITY • Cardiac muscle shows the property of excitability. • Presence of SA node that acts as a pacemaker undergoes self-excitation under the influence of the sodium and thus causes the transmission of the impulses to the nearby muscles. • Heart responds to electrical, mechanical and chemical stimuli. 2. AUTO RHYTHMICITY • Spontaneous generation of action potential in heart without external stimulation is called Automaticity. Self-Generation. • It occurs at regular intervals so it is called Rhythmicity. • Automaticity in heart is Myogenic and not neurogenic. • SA NODE: 70 -80 Impulses/minute • AV NODE: 40-60 / min • AV Bundle/Purkinje system/Ventricles 15-40 /min • SA Node having the highest rate of impulse formation is called PACE MAKER.
  • 15. HUMAN ANATOMY AND PHYSIOLOGY NOTES RAMDAS BHAT KARAVALI COLLEGE OF PHARMACY 15 3. CONDUCTIVITY (DROMOTROPIC ACTION) • Ability to conduct AP or cardiac impulses. • The property of conductivity varies in different parts of the heart. Velocity of conduction in: • Atrial Muscle: 0.3 m/sec • Inter nodal pathway: 1 m/sec • AV Node: 0.1 m/sec (slowest) • Purkinje System: 1.5 – 4 m/sec Conductivity is affected by autonomic stimulation. Sympathetic increase the velocity of conduction. Vagal stimulation Slows down. Ischemia slows the velocity of conduction 4. CONTRACTILITY • Property to undergo shortening. • The tension developed during cardiac muscle contraction is less than that developed in Skeletal muscle contraction. 5. REFRACTORY PERIOD: • It is that period during which a second stimulus fails to evoke a response. • Absolute Refractory Period: It is that period during which a second stimulus however high it is fails to evoke a response. • Relative Refractory Period: It is that period during which a second stimulus evokes a response if it is sufficiently high. • Refractory period in cardiac muscle is much larger compared to any other muscles. • Cardiac muscles have refractory period of 250 ms where as the skeletal muscles shows 1-3 ms. 6. ALL OR NONE PHENOMENON • In order for the cardiac muscle to undergo the depolarization, the potential inside the cardiac muscle should reach the threshold potential of -55mV • If the potential is reached cardiac muscle shows complete or maximal depolarization and if the threshold is not reached cardiac muscle shows no depolarization. • This is termed as All or None phenomenon. 7. FRANKS-STARLING LAW: • Greater the initial or resting length, greater will be the force of contraction. • In heart the initial or resting length depends upon end diastolic volume or pressure. • End diastolic volume depends upon the venous return. 8. FUNCTIONAL SYNCYTIUM • Cardiac myocytes are closely packed. • Cardiac myocytes are connected to the adjacent myocytes with the help of the GAP junction. • Transmission of the impulses from one myocyte to the another happens rapidly within a shorter duration compared to any other muscle.
  • 16. HUMAN ANATOMY AND PHYSIOLOGY NOTES RAMDAS BHAT KARAVALI COLLEGE OF PHARMACY 16 9. ROLE OF CALCIUM • Calcium plays an important role in the contraction of cardiac muscle. • Calcium ions in the ECF are taken up by the cardiac myocytes through the transverse tubular system are not enough for the contraction of cardiac muscle and hence the calcium stored in the Longitudinal tubular system (Sarcoplasmic reticulum) are utilized for contraction. 10. RESISTANCE TO FATIGUE Cardiac muscle has longer refractory period hence are not prone to fatigue. ELECTROCARDIOGRAPHY ▪ Electrocardiography (ECG or EKG from the German Elektrokardiogramm) is a transthoracic interpretation of the electrical activity of the heart over time captured and externally recorded by skin electrodes. ▪ It is a non-invasive recording produced by an electrocardiographic device. ▪ The ECG works mostly by detecting and amplifying the tiny electrical changes on the skin that are caused when the heart muscle "depolarizes" during each heartbeat. ▪ At rest, each heart muscle cell has a charge across its outer wall, or cell membrane. Reducing this charge towards zero is called de-polarization, which activates the mechanisms in the cell that cause it to contract. ▪ During each heartbeat a healthy heart will have an orderly progression of a wave of depolarization that is triggered by the cells in the sinoatrial node, spreads out through the atrium, passes through "intrinsic conduction pathways" and then spreads all over the ventricles. This is detected as tiny rises and falls in the voltage between two electrodes placed either side of the heart which is displayed as a wavy line either on a screen or on paper. This display indicates the overall rhythm of the heart and weaknesses in different parts of the heart muscle. ▪ Usually more than 2 electrodes are used and they can be combined into a number of pairs. (For example: Left arm (LA), right arm (RA) and left leg (LL) electrodes form the pairs: LA+RA, LA+LL, RA+LL) The output from each pair is known as a lead. Each lead is said to look at the heart from a different angle. ▪ Different types of ECGs can be referred to by the number of leads that are recorded, for example 3-lead, 5-lead or 12-lead ECGs (sometimes simply "a 12-lead"). ▪ A 12-lead ECG is one in which 12 different electrical signals are recorded at approximately the same time and will often be used as a one-off recording of an ECG, typically printed out as a paper copy. 3- and 5-lead ECGs tend to be monitored continuously and viewed only on the screen of an appropriate monitoring device, for example during an operation or whilst being transported in an ambulance. ▪ There may, or may not be any permanent record of a 3- or 5-lead ECG depending on the equipment used.
  • 17. HUMAN ANATOMY AND PHYSIOLOGY NOTES RAMDAS BHAT KARAVALI COLLEGE OF PHARMACY 17 Electrode label (in the USA) Electrode placement RA On the right arm, avoiding bony prominences. LA In the same location that RA was placed, but on the left arm this time. RL On the right leg, avoiding bony prominences. LL In the same location that RL was placed, but on the left leg this time. V1 In the fourth intercostal space (between ribs 4 & 5) just to the right of the sternum (breastbone). V2 In the fourth intercostal space (between ribs 4 & 5) just to the left of the sternum. V3 Between leads V2 and V4. V4 In the fifth intercostal space (between ribs 5 & 6) in the mid-clavicular line (the imaginary line that extends down from the midpoint of the clavicle (collarbone)). V5 Horizontally even with V4, but in the anterior axillary line. (The anterior axillary line is the imaginary line that runs down from the point midway between the middle of the clavicle and the lateral end of the clavicle; the lateral end of the collarbone is the end closer to the arm.) V6 Horizontally even with V4 and V5 in the midaxillary line. (The midaxillary line is the imaginary line that extends down from the middle of the patient's armpit.) ➢ Waves and intervals: ▪ A typical ECG tracing of the cardiac cycle (heartbeat) consists of a P wave, a QRS complex, a T wave, and a U wave which is normally visible in 50 to 75% of ECGs. ▪ The baseline voltage of the electrocardiogram is known as the isoelectric line. ▪ Typically, the isoelectric line is measured as the portion of the tracing following the T wave and preceding the next P wave.
  • 18. HUMAN ANATOMY AND PHYSIOLOGY NOTES RAMDAS BHAT KARAVALI COLLEGE OF PHARMACY 18 Feature Description Duration RR interval The interval between an R wave and the next R wave is the inverse of the heart rate. Normal resting heart rate is between 50 and 100 bpm 0.6 to 1.2s P wave During normal atrial depolarization, the main electrical vector is directed from the SA node towards the AV node, and spreads from the right atrium to the left atrium. This turns into the P wave on the ECG. 80ms PR interval The PR interval is measured from the beginning of the P wave to the beginning of the QRS complex. The PR interval reflects the time the electrical impulse takes to travel from the sinus node through the AV node and entering the ventricles. The PR interval is therefore a good estimate of AV node function. 120 to 200ms PR segment The PR segment connects the P wave and the QRS complex. This coincides with the electrical conduction from the AV node to the bundle of His to the bundle branches and then to the Purkinje Fibers. This electrical activity does not produce a contraction directly and is merely traveling down towards the ventricles and this shows up flat on the ECG. The PR interval is more clinically relevant. 50 to 120ms QRS complex The QRS complex reflects the rapid depolarization of the right and left ventricles. They have a large muscle mass compared to the atria and so the QRS complex usually has a much larger amplitude than the P-wave. 80 to 120ms J-point The point at which the QRS complex finishes and the ST segment begins. Used to measure the degree of ST elevation or depression present. N/A ST segment The ST segment connects the QRS complex and the T wave. The ST segment represents the period when the ventricles are 80 to 120ms
  • 19. HUMAN ANATOMY AND PHYSIOLOGY NOTES RAMDAS BHAT KARAVALI COLLEGE OF PHARMACY 19 ➢ Some pathological entities which can be seen on the ECG: Shortened QT interval Hypercalcemia, some drugs, certain genetic abnormalities. Prolonged QT interval Hypocalcemia, some drugs, certain genetic abnormalities. Elevated ST segment Myocardial infraction Depressed ST segment The heart muscles receive insufficient oxygen Prolonged PQ intervals Coronary artery disease, Rheumatic fever and Scar tissue may be form in the heart. Flattened or inverted T Waves Coronary ischemia, left ventricular hypertrophy, digoxin effect, some drugs. Hyper acute T Waves Possibly the first manifestation of acute myocardial infarction. Prominent U Waves Hypokalemia. Larger P Wave Indicate enlargement of an Atrium, as may occur in mitral stenosis in which blood back up in to the left atrium. Enlarge Q Wave Indicates myocardium infraction. Enlarge R Wave Indicates enlarged ventricles ▪ The ECG cannot reliably measure the pumping ability of the heart, for which ultrasound- based (echocardiography) or nuclear medicine tests are used. It is possible to be in cardiac arrest with a normal ECG signal (a condition known as pulseless electrical activity). CARDIAC CYCLES: “A cardiac cycle includes all the events associated within one heart beat” ▪ The normal heart beats in healthy adult is 75 beats/min and cardiac cycle last for 0.8 sec. ▪ In the cardiac cycle due to the pressure changes atria and ventricles alternately contract and relax, and blood flows from areas of higher blood pressure to areas of lower blood depolarized. It is isoelectric. T wave The T wave represents the repolarization (or recovery) of the ventricles. The interval from the beginning of the QRS complex to the apex of the T wave is referred to as the absolute refractory period. The last half of the T wave is referred to as the relative refractory period (or vulnerable period). 160ms ST interval The ST interval is measured from the J point to the end of the T wave. 320ms QT interval The QT interval is measured from the beginning of the QRS complex to the end of the T wave. A prolonged QT interval is a risk factor for ventricular tachyarrhythmias and sudden death. It varies with heart rate and for clinical relevance requires a correction for this, giving the QTc. 300 to 430ms U wave The U wave is not always seen. It is typically low amplitude, and, by definition, follows the T wave. J wave The J wave, elevated J-Point or Osborn Wave appears as a late delta wave following the QRS or as a small secondary R wave. It is considered path gnomic of hypothermia or hypocalcemia.
  • 20. HUMAN ANATOMY AND PHYSIOLOGY NOTES RAMDAS BHAT KARAVALI COLLEGE OF PHARMACY 20 pressure. ▪ The term systole is used for the contraction and diastole used for the relaxation. ▪ In a normal cardiac cycle, the two atria contract while the two ventricles relax. Then, while the two-ventricle contract, the two atria relax. ▪ Cardiac cycle is described by the following phase: 1) Atrial systole ▪ In this phase Atrial contraction is begins which is last about 0.1 sec at same time ventricle are relaxed. ▪ So, the Right and Left AV valves are open and Atria send blood into the relaxed ventricles. ▪ Atrial systole pushes 25 ml of blood in to ventricles which already contain 105 ml blood so at the end of atrial systole means end of ventricle diastole Ventricles contain maximum blood volume which is 130 ml known as end-diastolic volume (EDV). ▪ In the ECG or EKG, it is noted as P wave. 2) Ventricular Systole ▪ In this phase ventricles begin contraction which is last for 0.3 sec. ▪ Pressure in ventricles rises due to contraction and shut the AV valves which is heard by “Lubb” Sound. ▪ For about 0.05 sec all four valve are closed which is known as isovolumetric contraction. ▪ Ventricular contraction pushes blood out of the ventricles and opens the both Semilunar valve and ejected 70 ml blood in to aorta and same amount of blood in to pulmonary trunk by respectively left and right ventricles so the 60 ml of blood remains in each ventricle out of 130 ml. ▪ This is known as ventricular ejection which last for 0.25 sec Ventricular systole = isovolumetric contraction + ventricular ejection = (0.05) + (0.25) = 0.3 sec. ▪ The blood volume in the Ventricles at the end of ventricle systole is 60 ml known as end- systolic volume (ESV). ▪ The blood ejection per beat from each ventricle is known as stroke volume. Stroke volume = EDV – ESV = 130 ml – 60 ml = 70 ml ▪ It is noted as QRS wave in ECG or EKG. 3. Ventricular Diastole or Relaxation period: ▪ In this phase both ventricles and atria are in relaxation. ▪ Relaxation which is last for 0.4 sec. ▪ Pressure in the ventricles drops so blood in the Pulmonary Trunk and aorta backflows closing the Semilunar Valves. ▪ This is heard by “Dubb” sound. ▪ In this period, ventricular pressure is higher than atrial pressure hence all heart valves are closed again and this period is known as isovolumetric. ▪ It is noted as T wave in ECG or EKG. ▪ Again, the AV valves open and fill up the ventricle and complete the one Cardiac cycle.
  • 21. HUMAN ANATOMY AND PHYSIOLOGY NOTES RAMDAS BHAT KARAVALI COLLEGE OF PHARMACY 21 4. Atrial diastole • During atrial diastole, blood enters the right atrium through the superior and inferior vena cava and the left atrium via the pulmonary veins. • In the early part of this phase, the atrioventricular valves are closed and blood pools in the atria. • It lasts about 0.7 seconds - relaxation of the atria, during which the atria fill with blood from the large veins (the vena cava) CARDIAC OUTPUT: ▪ Cardiac output is the amount of blood ejected from the left ventricle (or the right ventricle) in to the aorta (or pulmonary trunk) each minute and it is equal to the product of stroke volume and heart rate. Thus, Cardiac Output = Stroke volume (ml/beat) * Heart rate (beats/min) = 70 ml/beat * 75 beats/min = 5250 ml/min or 5.25 liters/min.
  • 22. HUMAN ANATOMY AND PHYSIOLOGY NOTES RAMDAS BHAT KARAVALI COLLEGE OF PHARMACY 22 Factor affecting on Stroke volume: ▪ Three important factors regulate the stroke volume in different circumstances and ensure that the left and right ventricles pump equal volume of blood. i) Preload: ▪ The blood supply to the ventricle is often referred to as preload. Technically, the definition of preload is the volume or pressure in the ventricle at the end of diastole or refers as end-diastolic volume. ▪ According to Frank-Starling law of the heart, more the heart is filling during diastole, the greater the force of contraction during systole. ▪ The duration of ventricular diastole and venous pressure are the two key factors that determine EDV. ▪ When the heart rate is increase, the duration of diastole is shorter so it takes smaller filling times means smaller EDV. ▪ On the other hand, when venous pressure increase, a greater volume of blood is forced into the ventricles and the EDV is increased. For example: ▪ When heart rate exceeds about 160 beats/min, stroke volumes usually decrease. At such rapid heart rate decrease the ventricular filling time so decrease the EDV and thus the preload is lower. ▪ People, who have slow resting heart rate, usually have large stroke volumes because filling time is prolonged and preload thus is larger. ii) Contractility: ▪ The second factor that influences stroke volume is myocardial contractility, which is the strength of contraction at any given preload. ▪ Increases the contractility are called positive inotropic agents and decreases the contractility are called negative inotropic agents. ▪ Thus, for a constant preload, stroke volume is larger when positive inotropic agent is present and it promotes the forceful contraction. iii) Afterload: ▪ The resistance to the ejection of blood by the ventricle is called afterload. For example: ▪ In the atherosclerosis condition arteries are narrowed so they resist the blood flow from ventricles to out of heart and it decrease the stroke volume, and more blood remains in the ventricles at the end of systole. Other factors are: Sympathetic stimulation ▪ Increase the Epinephrine (E) and Non-Epinephrine (NE) level ▪ Causes ventricles to contract with more force and increases ejection fraction and decreases ESV and increase the stroke volume. Parasympathetic activity ▪ Increases the Acetylcholine (Ach) released by vagus nerves ▪ Reduces force of cardiac contractions BLOOD PRESSURE: • Lateral pressure exerted by the column of the blood flowing on the walls of blood vessels • They are divided into 2 types on which blood vessel they are exerted: 1. ARTERIAL BLOOD PRESSURE(ABP) 2. VENTRICULAR BLOOD PRESSURE(VBP)
  • 23. HUMAN ANATOMY AND PHYSIOLOGY NOTES RAMDAS BHAT KARAVALI COLLEGE OF PHARMACY 23 SYSTOLIC BP: • Maximum pressure exerted during the flow of the blood following ventricular systole • The normal value is 120mmHG • It ranges from 110-130mmHG depending on the Physiological condition of the body. DIASTOLIC BP: • Minimum pressure exerted during the flow of the blood following ventricular diastole. • The normal value is 80mmHG • It ranges from 70-90mmHG depending on the Physiological condition of the body. Device used to measure Systolic and Diastolic BP is called as SPHYGMOMANOMETER REGULATION OF BLOOD PRESSURE: Nervous regulation: SHORT TERM REGULATION OF BLOOD PRESSURE: a) Baroreceptor regulation:
  • 24. HUMAN ANATOMY AND PHYSIOLOGY NOTES RAMDAS BHAT KARAVALI COLLEGE OF PHARMACY 24 b) Chemoreceptor regulation:
  • 25. HUMAN ANATOMY AND PHYSIOLOGY NOTES RAMDAS BHAT KARAVALI COLLEGE OF PHARMACY 25 LONG TERM REGULATION OF BLOOD PRESSURE HORMONAL REGULATION OF BLOOD PRESSURE: