• All living cells require nutrients, O2 and other
essential substances to generate energy.
• The waste or harmful substances produced,
have to be removed continuously for healthy
functioning of tissues.
• It is very essential to have efficient
mechanisms for the removal of these
substances to the cells and from the cells.
WHAT IS CIRCULATION?
• Circulation is the transport of nutrients,
oxygen, CO2 and excretory products to the
concerned tissues or organs.
• For circulation, simple organisms (sponges,
coelenterates etc) use water from their
surroundings.
• However the higher organisms (complex
organisms) use special fluids called body fluids
for transport of substances
• Body fluids include blood & lymph (tissue
fluids) .
WHAT IS CIRCULATION?
55%
Straw-coloured and
slightly alkaline (pH 7.4)
fluid matrix.
1. BLOOD VASCULAR SYSTEM
bankofbiology.blogspot.com
A. BLOOD
45%
Include cells
(RBC, WBC and Platelets )
COMPOSITION OF BLOOD
a. Plasma b. Formed elements
bankofbiology.blogspot.com
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Constituents of
plasma
Functions
Water (90-92%)
Solvent. Transports vitamins, hormones,
enzymes, nutrients etc.
Plasma
proteins
(6-8 %)
Fibrinogen For blood coagulation (clotting)
Globulins Act as antibodies (for defense of the body)
Albumins
Osmotic balance & regulation of blood
pressure.
Glucose, amino acids,
lipids, cholesterol
For energy production and growth
Inorganic: (Na+
, K+
,
Mg2+
, Cl-
, HCO3
-
, Ca2+
)
Regulation of osmosis etc.
Ca2+
For blood clotting and muscle
contraction
Gases (CO2, O2, N2 etc) For transport
Plasma
without
clotting
factors is
called
Serum.
1. BLOOD VASCULAR SYSTEM
A. BLOOD
•FORMED ELEMENTS
•Red Blood Cells (RBC) or
Erythrocytes
•White Blood Cells (WBC) or
Leucocytes
•Platelets (Thrombocytes)
Normal Hb level in blood:
12-16 gm/ 100 ml
Worn-out RBCs are destroyed
in spleen (graveyard of RBCs)
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Features of RBC (Erythrocytes)
Colour Red (due to haemoglobin)
Lifespan 120 days
Count 5 - 5.5 millions/mm-3
Formed in Red bone marrow
Structure
Biconcave in shape.
No nucleus, mitochondria
etc.
Functions CO2 and O2 transport
RBCs are destroyed in the spleen (graveyard of RBCs).
A healthy individual has 12-16 gms of haemoglobin in every 100 ml of blood.
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Features of WBC (Leucocytes)
Colour Colourless
Lifespan 1-15 days
Count 6000-8000 /mm-3
Formed in
Bone marrow, lymph
glands, spleen
Structure
Nucleated. Different
types
Functions Part of immune system
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Types of WBC % Functions
Gran
ulocy
tes
Neutrophils (Heterophils) 60-65% Phagocytosis. Soldier of the body.
Eosinophils (Acidphils) 2-3% Resist infections.
Cause allergic reactions.
Basophils (Cyanophils) 0.5-1%
Secrete histamine, serotonin, heparin.
Cause inflammatory reactions.
Agra
nuloc
ytes
Monocytes (Largest WBC) 6-8% Phagocytosis
Lymphocytes
(Smallest WBC,
largest nucleus)
B-
lymphocytes
20-25%
Immune responses of the body.
Secrete antibodies.
T-
lymphocytes
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Features of Platelets (Thrombocytes)
Colour Colourless
Lifespan 7 days
Count 1.5 - 3.5 lakhs/mm-3
Formed in
Megakaryocytes in Bone
marrow
Structure
Non-nucleated cell fragments.
Release clotting substances.
Functions Blood clotting or coagulation
Activated platelets
• Blood groups were discovered by
Carl Land Steiner.
• It includes ABO grouping & Rh
Grouping.
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Blood Grouping
A+
A-
B+
B-
AB+
AB-
O+
O-
• It is based on presence or absence
of 2 surface antigens (chemicals
that induce immune response) on
RBCs namely A & B.
• Similarly, plasma contains 2
antibodies (proteins produced in
response to antigens) namely anti-
A & anti-B.
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Blood Grouping 1. ABO grouping
bankofbiology.blogspot.com
1. BLOOD VASCULAR SYSTEM
A. BLOOD
ABO Blood Grouping
Blood
group
Antigens
on RBC
Antibodies in
plasma
Can donate
blood to
Can receive
blood from
(Donor’s
group)
A A Anti-B A and AB A, O
B B Anti-A B and AB B, O
AB A, B Nil AB only A, B, AB & O
O Nil
Anti-A & Anti-
B
A, B, AB & O O only
• Antigen A reacts with anti-A.
• Antigen B reacts with anti-B.
• Mixing of bloods with interactive
antigens & antibodies causes
clumping (agglutination) of RBCs.
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Blood Grouping 1. ABO grouping
• O group persons are called
Universal donors as they can
donate blood to persons with any
blood group.
• AB group persons are called
Universal recipients because they
can accept blood from all groups.
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Blood Grouping
O-group:
Universal
Donor
AB-
group:
1. ABO grouping
• Rhesus (Rh) factor is an antigen
found on RBC.
• Rh+ve means the presence of Rh
factor or antigen and Rh-ve means
absence of Rh factor or antigen.
• Nearly 80% of humans are Rh+ve.
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Blood Grouping 2. Rh grouping
• Anti-Rh antibodies are not naturally
found. So Rh-ve person can receive
Rh+ve blood only once but it causes
the development of anti-Rh
antibodies in his blood. So a second
transfusion of Rh+ve blood causes
agglutination.
• Therefore, Rh-group should be
matched before transfusion.
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Blood Grouping 2. Rh grouping
• Rh factor plays important role in
pregnancy.
• When a Rh + man marries Rh –
woman .The baby may be Rh- or
Rh +.
• Suppose the foetus is Rh + and
mother Rh - ,this causes Rh
incompatibility.
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Blood Grouping 2. Rh grouping
• It is an Rh incompatibility between
the Rh-ve blood of a pregnant
mother and Rh+ve blood of the
foetus.
• Rh antigens do not get mixed with
maternal blood in first pregnancy
because placenta separates the two
bloods.
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Blood Grouping Erythroblastosis foetalis
• But at the time of first delivery,
there is a possibility of exposure of
the maternal blood to small
amounts of the Rh+ve blood from
the foetus.
• This induces the formation of Rh
antibodies in maternal blood.
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Blood Grouping Erythroblastosis foetalis
• In case of her subsequent
pregnancies, Rh antibodies from
mother leak into the foetal blood
(Rh+ve) and destroy the foetal
RBCs. This is fatal to foetus or cause
severe anaemia and jaundice to the
baby. This condition is called
Erythroblastosis foetalis.
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Blood Grouping Erythroblastosis foetalis
• Erythroblastosis foetalis can be
avoided by administering anti-Rh
antibodies( RhoGAM) to the
mother immediately after the
delivery of first child.
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Blood Grouping Erythroblastosis foetalis
• Coagulation or clotting-It is a
mechanism for haemostasis
(prevention of excess loss of blood
through injuries).
• Clot is –a network of threads of
fibrin, in which dead and damaged
formed elements of blood are
trapped.
• It involves the following events:
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Blood coagulation
1. BLOOD VASCULAR SYSTEM
A. BLOOD
Blood coagulation
1. BLOOD VASCULAR SYSTEM
Blood coagulation
• A tissue factor called thrombokinase from injured tissue converts
inactive prothrombin (produced by liver) in the presence of ca2+
into
active thrombin.
ca2+
(Inactive)Prothrombin thrombin(active)
Thrombokinase
(insoluble)fibrin
• The reaction is a series of enzyme linked reaction called (cascade process).
• Platelets also release factor called Serotonin for coagulation.
Fibrinogen(solu
ble)
• It includes Lymph, Lymph vessels & Lymph
nodes.
• As the blood passes through the capillaries
in tissues, some water or plasma and
water soluble substances are filtered out
from plasma to the intercellular spaces, to
form tissue (interstitial) fluid. It has the
same mineral distribution as that in
plasma.
2. LYMPHATIC SYSTEM
• Exchange of nutrients, gases,
etc between the blood & cells
occur through this fluid.
• Some tissue fluid enters
lymphatic system (a system of
lymph vessels and lymph
glands) and the tissue fluid in
them is called lymph.
• Lymph drains back to the
major veins.
2. LYMPHATIC SYSTEM
• Lymph is a colourless fluid contain
lymphocytes ,nutrients and hormones.
• It is the middleman between blood & tissues.
• It carries plasma proteins synthesized in liver to
the blood.
• Transports digested fats (through lacteals in the
intestinal villi), fat soluble vitamins, hormones etc.
• Filtration of bacteria and foreign particles.
• Lymph nodes produce WBC (lymphocytes) &
antibodies, helps in the defensive mechanism of
body.
2. LYMPHATIC SYSTEM
FUNCTIONS OF LYMPH
1. Open circulatory system
• Here, the blood pumped by the heart passes
through large vessels into open spaces or
cavities called sinuses.
• E.g. Arthropods and molluscs.
2. Closed circulatory system
• Here, the blood pumped by the heart is
circulated through blood vessels.
• It is more advantageous as the flow of fluid can
be precisely regulated.
• E.g. Annelids and chordates.
CIRCULATORY PATHWAYS
HEART OF VERTEBRATES
• All vertebrates have a muscular chambered
heart.
•Fishes -2-chambered (an atrium + a ventricle).
•Amphibians -3-chambered (2 atria + a ventricle).
•Reptiles (except crocodiles)-3-chambered
•(incomplete partition for ventricle).
•Crocodiles, birds & mammals-4-chambered.
• (2 atria + 2 ventricle).
CIRCULATORY PATHWAYS
Patterns of Circulation in Vertebrates
• Single circulation
• Incomplete double circulation
• Double circulation
• It is seen in fishes.
• Heart receives impure blood only (venous
heart).
• Deoxygenated blood from heart → oxygenated
by gills → supplied to body parts →
deoxygenated blood → to heart.
CIRCULATORY PATHWAYS
Patterns of Circulation in Vertebrates
1. Single circulation
• It is seen amphibians & reptiles.
• Left atrium receives oxygenated blood from
gills/lungs/skin. Right atrium gets deoxygenated
blood from other body parts. However, they get
mixed up in the single ventricle.
• Ventricle pumps out mixed blood.
CIRCULATORY PATHWAYS
Patterns of Circulation in Vertebrates
2. Incomplete double circulation
• It is seen in birds & mammals.
• Left atrium receives Oxygenated blood. It passes
on to left ventricle.
• Right atrium receives Deoxygenated blood. It
passes on to right ventricle.
• Ventricles pump it out separately without any
mixing up.
CIRCULATORY PATHWAYS
Patterns of Circulation in Vertebrates
3. Double circulation
Human circulatory system consists of
-muscular chambered heart
-Blood vessels and Blood.
Blood circulation in man discovered by William
Harvey.
Human circulatory system consists of
-muscular chambered heart
-Blood vessels and
- Blood.
CIRCULATORY PATHWAYS
HUMAN CIRCULATORY SYSTEM
1. BLOOD VASCULAR SYSTEM
B. BLOOD VESSELS
Types of Blood vessels
•Arteries
•Veins
•Capillaries
• They carry blood from heart to
other tissues.
• They contain oxygenated
blood (except pulmonary
artery).
• Their smaller branches are
called arterioles.
1. BLOOD VASCULAR SYSTEM
B. BLOOD VESSELS
1. Arteries
Arteries have 3 layers:
▪Tunica intima: Squamous
endothelium. Inner layer.
▪Tunica media: Smooth
muscles & elastic fibres.
Middle layer.
▪Tunica externa: Fibrous
connective tissue with
collagen fibres. Outer layer.
1. BLOOD VASCULAR SYSTEM
B. BLOOD VESSELS
1. Arteries
• They carry blood towards
heart.
• They contain deoxygenated
blood (except pulmonary vein)
• Their smaller branches are
called venules.
• Veins are also 3-layered but
tunica media is comparatively
thin.
1. BLOOD VASCULAR SYSTEM
B. BLOOD VESSELS
2. Veins
• In tissues, arterioles divide
into thin walled and single
layered vessels. They are
called capillaries.
• They unite into venules.
1. BLOOD VASCULAR SYSTEM
B. BLOOD VESSELS
3. Capillaries
• Heart is a mesodermally derived
organ located in
mediastinum(thoracic cavity).
• It is protected by double-layered
pericardium.
• The pericardial space (between
pericardial membranes) is filled
with pericardial fluid. It reduces the
friction between the heart walls,
and surrounding tissues.
1. BLOOD VASCULAR SYSTEM
Structure of Heart
• Heart is 4 chambered- 2 upper
atria (auricles) & 2 lower
ventricles.
• The walls (cardiac muscles) of the
ventricles are much thicker than
that of the atria.
• Atria are separated by inter-atrial
septum.
• Ventricles are separated by inter-
ventricular septum.
1. BLOOD VASCULAR SYSTEM
C. HEART
Structure of Heart
• In b/w atrium and ventricle there is
a thick fibrous atrio-ventricular
septum with an opening.
• A tricuspid valve (3 muscular flaps
or cusps) guards the opening
between right atrium and right
ventricle.
• A bicuspid (mitral) valve guards the
opening between left atrium and
left ventricle.
1. BLOOD VASCULAR SYSTEM
C. HEART
Structure of Heart
• These valves allow the flow of blood
only in one direction, i.e. from atria to
ventricles.
• The right ventricles are opened into
pulmonary artery which supplies
deoxygenated blood to lungs.
• The left ventricles are opened to
aorta(largest artery)supplies
oxygenated blood to body parts.
• Both Pulmonary artery and aorta are
provided with the semi-lunar valves.
They prevent backwards flow of
blood.
1. BLOOD VASCULAR SYSTEM
Structure of Heart
• Heart is made up of cardiac muscles.
• Human heart is myogenic, i.e. normal activities
of heart are auto regulated by nodal tissues (a
specialized cardiac musculature present in heart
wall).
• It consists of
o Sino-atrial node (SAN)-A patch of nodal tissue
in the right upper corner of the right atrium.
Which produces signal or action potential (70-
80/min) initiates heart beat.
o Hence called pacemaker.
o Atrio-ventricular node (AVN) in the lower left
corner of the right atrium close to the atrio-
ventricular septum.
1. BLOOD VASCULAR SYSTEM
Conducting System
• From the AVN, a bundle of fibrous atrio-
ventricular bundle (AV bundle) passes
through atrio-ventricular septa and divides
into a right & left branches.
• Each branch passes through the ventricular
walls of its side.
• In the ventricular wall, it breaks up into
minute fibres (Purkinje fibres). These fibres
along with the bundles are known as
bundle of His.
1. BLOOD VASCULAR SYSTEM
C. HEART
Conducting System
• Nodal tissues generate action potential
without any external stimuli, i.e. it is
autoexcitable.
• SAN initiates and maintains contraction
of heart by generating action potentials
(70-80/min). So it is called the
pacemaker.
1. BLOOD VASCULAR SYSTEM
C. HEART
Conducting System
1. BLOOD VASCULAR SYSTEM
C. HEART
•Phases of Cardiac cycle
• Joint diastole
• Atrial systole
• Ventricular systole
• Firstly, all chambers of heart are in
relaxed state (joint diastole).
• When the tricuspid & bicuspid valves
open, blood from pulmonary vein and
vena cava flows into left & right ventricles
respectively through left & right atria.
• Semilunar valves are closed at this stage.
1. BLOOD VASCULAR SYSTEM
C. HEART
Cardiac Cycle 1. Joint Diastole
• The SAN generates an action potential.
It stimulates both the atria to undergo
contraction (atrial systole).
• This increases the flow of blood into the
ventricles by about 30%.
1. BLOOD VASCULAR SYSTEM
C. HEART
2. Atrial (Auricular) systole
Cardiac Cycle
• Action potential is conducted to
ventricular side by AVN & AV bundle
from where bundle of His transmits it
through the ventricular musculature.
• It causes contraction of ventricles
(ventricular systole). During this, the
atria undergo diastole.
1. BLOOD VASCULAR SYSTEM
C. HEART
Cardiac Cycle 3. Ventricular Systole
Ventricular systole increases the ventricular
pressure. It causes the following events:
• Closure of tricuspid and bicuspid valves
due to attempted backflow of blood into
the atria.
• Semilunar valves open. So deoxygenated
blood enters the pulmonary artery from
right ventricle and oxygenated blood
enters the aorta from left ventricle.
1. BLOOD VASCULAR SYSTEM
C. HEART
Cardiac Cycle 3. Ventricular Systole
The ventricles now relax (ventricular
diastole) and the ventricular pressure
falls. It causes the following events:
▪ Closure of the semilunar valves. It
prevents the backflow of blood into
the ventricles.
▪ Tricuspid & bicuspid valves are
opened by the pressure in the atria.
1. BLOOD VASCULAR SYSTEM
C. HEART
Cardiac Cycle
• Ventricles & atria again undergo joint
diastole and the above processes are
repeated. This is called cardiac cycle.
• A cardiac cycle= atrial systole +
ventricular systole + diastole
• A cardiac cycle is completed in 0.8
seconds.
• One heartbeat = a cardiac cycle.
• So number of normal heartbeat:
70-75 times/min (average: 72/min).
1. BLOOD VASCULAR SYSTEM
C. HEART
Cardiac Cycle
• Stroke volume: Volume of blood pumped
out by each ventricle during a cardiac
cycle. It is about 70 ml.
• Cardiac output: Volume of blood pumped
out by each ventricle per minute, i.e.
stroke volume x heart rate (70 x 72). It is
about 5000 ml (5 litres).
• Cardiac output of an athlete is very high.
1. BLOOD VASCULAR SYSTEM
C. HEART
Cardiac Cycle Stroke volume & Cardiac output
• During each cardiac cycle, 2 prominent
sounds are produced.
• First sound (lub) is due to the closure of
tricuspid & bicuspid valves.
• Second sound (dub) is due to the
closure of the semilunar valves.
• One heartbeat = a lub + a dub.
1. BLOOD VASCULAR SYSTEM
C. HEART
Cardiac Cycle Heart Sounds
• Human heart is myogenic because
normal activities of heart are auto
regulated by nodal tissues.
• Medulla oblongata regulates
cardiac activity through ANS.
• Sympathetic nerves of ANS
increase the rate of heartbeat,
the strength of ventricular
contraction and cardiac output.
1. BLOOD VASCULAR SYSTEM
C. HEART
Regulation of Cardiac activity
• Parasympathetic nerves of ANS
decrease the heart beat,
conduction of action potential
and the cardiac output.
• Adrenal medullary hormones
increase the cardiac output.
1. BLOOD VASCULAR SYSTEM
C. HEART
Regulation of Cardiac activity
• In man, blood flows through the heart
twice for completing its circuit. This is
called double circulation.
• It includes,
➢ Pulmonary circulation
➢ Systemic circulation
1. BLOOD VASCULAR SYSTEM
DOUBLE CIRCULATION
• It is the circulation b/w lungs and
heart.
• Deoxygenated blood pumped into
the pulmonary artery is passed on
to lungs from where oxygenated
blood is carried by pulmonary
veins into the left atrium.
1. BLOOD VASCULAR SYSTEM
DOUBLE CIRCULATION
1. Pulmonary Circulation
• It is the circulation b/w heart & various
body parts.
• Oxygenated blood is passed through
aorta, arteries, arterioles & capillaries
and is reached the tissues.
• Deoxygenated blood collected from
tissues by venules, veins & vena cava is
carried to the right atrium.
• Systemic circulation provides nutrients,
O2 and other substances to the tissues
and takes CO2 and other harmful
substances away for elimination.
1. BLOOD VASCULAR SYSTEM
DOUBLE CIRCULATION
2. Systemic Circulation
1. BLOOD VASCULAR SYSTEM
DOUBLE CIRCULATION
Pulmonary & Systemic
circulations
• It is a system which includes the
hepatic portal vein that carries
blood from intestine to the liver
before it is delivered to the
systemic circulation.
1. BLOOD VASCULAR SYSTEM
HEPATIC PORTAL SYSTEM
It is a system of coronary vessels that circulate blood to and from the
cardiac musculature.
1. BLOOD VASCULAR SYSTEM
CORONARY CIRCULATORY SYSTEM
Coronary
Arteries
Coronary
Veins
• It is an instrument used to obtain
electrocardiogram (it is a graphical
representation of the electrical activity of
the heart during a cardiac cycle).
• To get an ECG, a patient is connected to the
machine with 3 electrical leads (one to
each wrist and to left ankle) that monitor
heart activity. For a detailed evaluation of
heart’s function, multiple leads are
attached to the chest region.
ELECTROCARDIOGRAPH (ECG)
An ECG consists of the following waves:
• P-wave: Represents the excitation
(depolarization) of atria which causes
atrial systole.
• QRS-complex: Represents depolarization
of ventricles (Ventricular systole).
• T-wave: Represents the repolarisation of
ventricles.
ELECTROCARDIOGRAPH (ECG)
Deviation in the ECG indicates the abnormality or disease. So ECG has
great clinical significance.
• Here, the blood pressure is higher than
normal systolic (pumping) pressure (120
mm Hg) and normal diastolic (resting)
pressure (80 mm Hg), i.e. above 120/80
mm Hg.
• If the BP is 140/90 or above, it is
hypertension.
• It leads to heart diseases and affects
vital organs (brain, kidney etc).
DISORDERS OF CIRCULATORY SYSTEM
1. Hypertension (High Blood Pressure)
• It is the deposition of Ca, fat,
cholesterol and fibrous tissue in
coronary arteries.
• It makes the lumen of arteries
narrower and thereby affect the
blood supply.
DISORDERS OF CIRCULATORY SYSTEM
2. Coronary Artery Disease (CAD) or Atherosclerosis
• An acute chest pain due to O2
deficiency to heart muscles.
• It occurs due to improper blood
flow.
• It is common among middle-aged
and elderly.
DISORDERS OF CIRCULATORY SYSTEM
3. Angina (angina pectoris)
• It is the condition in which heart is not
pumping blood enough to meet the
needs of the body.
• Congestion of the lungs is the main
symptom.
• Heart failure is not same as cardiac
arrest (heart stops beating) or a heart
attack (sudden damage of heart muscle
due to inadequate blood supply).
DISORDERS OF CIRCULATORY SYSTEM
4. Heart Failure (congestive heart failure)
THE END

body fluids and its circulation for puc students

  • 2.
    • All livingcells require nutrients, O2 and other essential substances to generate energy. • The waste or harmful substances produced, have to be removed continuously for healthy functioning of tissues. • It is very essential to have efficient mechanisms for the removal of these substances to the cells and from the cells. WHAT IS CIRCULATION?
  • 3.
    • Circulation isthe transport of nutrients, oxygen, CO2 and excretory products to the concerned tissues or organs. • For circulation, simple organisms (sponges, coelenterates etc) use water from their surroundings. • However the higher organisms (complex organisms) use special fluids called body fluids for transport of substances • Body fluids include blood & lymph (tissue fluids) . WHAT IS CIRCULATION?
  • 4.
    55% Straw-coloured and slightly alkaline(pH 7.4) fluid matrix. 1. BLOOD VASCULAR SYSTEM bankofbiology.blogspot.com A. BLOOD 45% Include cells (RBC, WBC and Platelets ) COMPOSITION OF BLOOD a. Plasma b. Formed elements
  • 5.
    bankofbiology.blogspot.com 1. BLOOD VASCULARSYSTEM A. BLOOD Constituents of plasma Functions Water (90-92%) Solvent. Transports vitamins, hormones, enzymes, nutrients etc. Plasma proteins (6-8 %) Fibrinogen For blood coagulation (clotting) Globulins Act as antibodies (for defense of the body) Albumins Osmotic balance & regulation of blood pressure. Glucose, amino acids, lipids, cholesterol For energy production and growth Inorganic: (Na+ , K+ , Mg2+ , Cl- , HCO3 - , Ca2+ ) Regulation of osmosis etc. Ca2+ For blood clotting and muscle contraction Gases (CO2, O2, N2 etc) For transport Plasma without clotting factors is called Serum.
  • 6.
    1. BLOOD VASCULARSYSTEM A. BLOOD •FORMED ELEMENTS •Red Blood Cells (RBC) or Erythrocytes •White Blood Cells (WBC) or Leucocytes •Platelets (Thrombocytes)
  • 7.
    Normal Hb levelin blood: 12-16 gm/ 100 ml Worn-out RBCs are destroyed in spleen (graveyard of RBCs) 1. BLOOD VASCULAR SYSTEM A. BLOOD Features of RBC (Erythrocytes) Colour Red (due to haemoglobin) Lifespan 120 days Count 5 - 5.5 millions/mm-3 Formed in Red bone marrow Structure Biconcave in shape. No nucleus, mitochondria etc. Functions CO2 and O2 transport RBCs are destroyed in the spleen (graveyard of RBCs). A healthy individual has 12-16 gms of haemoglobin in every 100 ml of blood.
  • 8.
    1. BLOOD VASCULARSYSTEM A. BLOOD Features of WBC (Leucocytes) Colour Colourless Lifespan 1-15 days Count 6000-8000 /mm-3 Formed in Bone marrow, lymph glands, spleen Structure Nucleated. Different types Functions Part of immune system
  • 9.
    1. BLOOD VASCULARSYSTEM A. BLOOD Types of WBC % Functions Gran ulocy tes Neutrophils (Heterophils) 60-65% Phagocytosis. Soldier of the body. Eosinophils (Acidphils) 2-3% Resist infections. Cause allergic reactions. Basophils (Cyanophils) 0.5-1% Secrete histamine, serotonin, heparin. Cause inflammatory reactions. Agra nuloc ytes Monocytes (Largest WBC) 6-8% Phagocytosis Lymphocytes (Smallest WBC, largest nucleus) B- lymphocytes 20-25% Immune responses of the body. Secrete antibodies. T- lymphocytes
  • 10.
    1. BLOOD VASCULARSYSTEM A. BLOOD Features of Platelets (Thrombocytes) Colour Colourless Lifespan 7 days Count 1.5 - 3.5 lakhs/mm-3 Formed in Megakaryocytes in Bone marrow Structure Non-nucleated cell fragments. Release clotting substances. Functions Blood clotting or coagulation Activated platelets
  • 11.
    • Blood groupswere discovered by Carl Land Steiner. • It includes ABO grouping & Rh Grouping. 1. BLOOD VASCULAR SYSTEM A. BLOOD Blood Grouping A+ A- B+ B- AB+ AB- O+ O-
  • 12.
    • It isbased on presence or absence of 2 surface antigens (chemicals that induce immune response) on RBCs namely A & B. • Similarly, plasma contains 2 antibodies (proteins produced in response to antigens) namely anti- A & anti-B. 1. BLOOD VASCULAR SYSTEM A. BLOOD Blood Grouping 1. ABO grouping
  • 13.
    bankofbiology.blogspot.com 1. BLOOD VASCULARSYSTEM A. BLOOD ABO Blood Grouping Blood group Antigens on RBC Antibodies in plasma Can donate blood to Can receive blood from (Donor’s group) A A Anti-B A and AB A, O B B Anti-A B and AB B, O AB A, B Nil AB only A, B, AB & O O Nil Anti-A & Anti- B A, B, AB & O O only
  • 14.
    • Antigen Areacts with anti-A. • Antigen B reacts with anti-B. • Mixing of bloods with interactive antigens & antibodies causes clumping (agglutination) of RBCs. 1. BLOOD VASCULAR SYSTEM A. BLOOD Blood Grouping 1. ABO grouping
  • 15.
    • O grouppersons are called Universal donors as they can donate blood to persons with any blood group. • AB group persons are called Universal recipients because they can accept blood from all groups. 1. BLOOD VASCULAR SYSTEM A. BLOOD Blood Grouping O-group: Universal Donor AB- group: 1. ABO grouping
  • 16.
    • Rhesus (Rh)factor is an antigen found on RBC. • Rh+ve means the presence of Rh factor or antigen and Rh-ve means absence of Rh factor or antigen. • Nearly 80% of humans are Rh+ve. 1. BLOOD VASCULAR SYSTEM A. BLOOD Blood Grouping 2. Rh grouping
  • 17.
    • Anti-Rh antibodiesare not naturally found. So Rh-ve person can receive Rh+ve blood only once but it causes the development of anti-Rh antibodies in his blood. So a second transfusion of Rh+ve blood causes agglutination. • Therefore, Rh-group should be matched before transfusion. 1. BLOOD VASCULAR SYSTEM A. BLOOD Blood Grouping 2. Rh grouping
  • 18.
    • Rh factorplays important role in pregnancy. • When a Rh + man marries Rh – woman .The baby may be Rh- or Rh +. • Suppose the foetus is Rh + and mother Rh - ,this causes Rh incompatibility. 1. BLOOD VASCULAR SYSTEM A. BLOOD Blood Grouping 2. Rh grouping
  • 19.
    • It isan Rh incompatibility between the Rh-ve blood of a pregnant mother and Rh+ve blood of the foetus. • Rh antigens do not get mixed with maternal blood in first pregnancy because placenta separates the two bloods. 1. BLOOD VASCULAR SYSTEM A. BLOOD Blood Grouping Erythroblastosis foetalis
  • 20.
    • But atthe time of first delivery, there is a possibility of exposure of the maternal blood to small amounts of the Rh+ve blood from the foetus. • This induces the formation of Rh antibodies in maternal blood. 1. BLOOD VASCULAR SYSTEM A. BLOOD Blood Grouping Erythroblastosis foetalis
  • 21.
    • In caseof her subsequent pregnancies, Rh antibodies from mother leak into the foetal blood (Rh+ve) and destroy the foetal RBCs. This is fatal to foetus or cause severe anaemia and jaundice to the baby. This condition is called Erythroblastosis foetalis. 1. BLOOD VASCULAR SYSTEM A. BLOOD Blood Grouping Erythroblastosis foetalis
  • 22.
    • Erythroblastosis foetaliscan be avoided by administering anti-Rh antibodies( RhoGAM) to the mother immediately after the delivery of first child. 1. BLOOD VASCULAR SYSTEM A. BLOOD Blood Grouping Erythroblastosis foetalis
  • 23.
    • Coagulation orclotting-It is a mechanism for haemostasis (prevention of excess loss of blood through injuries). • Clot is –a network of threads of fibrin, in which dead and damaged formed elements of blood are trapped. • It involves the following events: 1. BLOOD VASCULAR SYSTEM A. BLOOD Blood coagulation
  • 24.
    1. BLOOD VASCULARSYSTEM A. BLOOD Blood coagulation
  • 25.
    1. BLOOD VASCULARSYSTEM Blood coagulation • A tissue factor called thrombokinase from injured tissue converts inactive prothrombin (produced by liver) in the presence of ca2+ into active thrombin. ca2+ (Inactive)Prothrombin thrombin(active) Thrombokinase (insoluble)fibrin • The reaction is a series of enzyme linked reaction called (cascade process). • Platelets also release factor called Serotonin for coagulation. Fibrinogen(solu ble)
  • 26.
    • It includesLymph, Lymph vessels & Lymph nodes. • As the blood passes through the capillaries in tissues, some water or plasma and water soluble substances are filtered out from plasma to the intercellular spaces, to form tissue (interstitial) fluid. It has the same mineral distribution as that in plasma. 2. LYMPHATIC SYSTEM
  • 27.
    • Exchange ofnutrients, gases, etc between the blood & cells occur through this fluid. • Some tissue fluid enters lymphatic system (a system of lymph vessels and lymph glands) and the tissue fluid in them is called lymph. • Lymph drains back to the major veins. 2. LYMPHATIC SYSTEM
  • 28.
    • Lymph isa colourless fluid contain lymphocytes ,nutrients and hormones. • It is the middleman between blood & tissues. • It carries plasma proteins synthesized in liver to the blood. • Transports digested fats (through lacteals in the intestinal villi), fat soluble vitamins, hormones etc. • Filtration of bacteria and foreign particles. • Lymph nodes produce WBC (lymphocytes) & antibodies, helps in the defensive mechanism of body. 2. LYMPHATIC SYSTEM FUNCTIONS OF LYMPH
  • 29.
    1. Open circulatorysystem • Here, the blood pumped by the heart passes through large vessels into open spaces or cavities called sinuses. • E.g. Arthropods and molluscs. 2. Closed circulatory system • Here, the blood pumped by the heart is circulated through blood vessels. • It is more advantageous as the flow of fluid can be precisely regulated. • E.g. Annelids and chordates. CIRCULATORY PATHWAYS
  • 30.
    HEART OF VERTEBRATES •All vertebrates have a muscular chambered heart. •Fishes -2-chambered (an atrium + a ventricle). •Amphibians -3-chambered (2 atria + a ventricle). •Reptiles (except crocodiles)-3-chambered •(incomplete partition for ventricle). •Crocodiles, birds & mammals-4-chambered. • (2 atria + 2 ventricle).
  • 31.
    CIRCULATORY PATHWAYS Patterns ofCirculation in Vertebrates • Single circulation • Incomplete double circulation • Double circulation
  • 32.
    • It isseen in fishes. • Heart receives impure blood only (venous heart). • Deoxygenated blood from heart → oxygenated by gills → supplied to body parts → deoxygenated blood → to heart. CIRCULATORY PATHWAYS Patterns of Circulation in Vertebrates 1. Single circulation
  • 33.
    • It isseen amphibians & reptiles. • Left atrium receives oxygenated blood from gills/lungs/skin. Right atrium gets deoxygenated blood from other body parts. However, they get mixed up in the single ventricle. • Ventricle pumps out mixed blood. CIRCULATORY PATHWAYS Patterns of Circulation in Vertebrates 2. Incomplete double circulation
  • 34.
    • It isseen in birds & mammals. • Left atrium receives Oxygenated blood. It passes on to left ventricle. • Right atrium receives Deoxygenated blood. It passes on to right ventricle. • Ventricles pump it out separately without any mixing up. CIRCULATORY PATHWAYS Patterns of Circulation in Vertebrates 3. Double circulation
  • 36.
    Human circulatory systemconsists of -muscular chambered heart -Blood vessels and Blood.
  • 37.
    Blood circulation inman discovered by William Harvey. Human circulatory system consists of -muscular chambered heart -Blood vessels and - Blood. CIRCULATORY PATHWAYS HUMAN CIRCULATORY SYSTEM
  • 38.
    1. BLOOD VASCULARSYSTEM B. BLOOD VESSELS Types of Blood vessels •Arteries •Veins •Capillaries
  • 39.
    • They carryblood from heart to other tissues. • They contain oxygenated blood (except pulmonary artery). • Their smaller branches are called arterioles. 1. BLOOD VASCULAR SYSTEM B. BLOOD VESSELS 1. Arteries
  • 40.
    Arteries have 3layers: ▪Tunica intima: Squamous endothelium. Inner layer. ▪Tunica media: Smooth muscles & elastic fibres. Middle layer. ▪Tunica externa: Fibrous connective tissue with collagen fibres. Outer layer. 1. BLOOD VASCULAR SYSTEM B. BLOOD VESSELS 1. Arteries
  • 41.
    • They carryblood towards heart. • They contain deoxygenated blood (except pulmonary vein) • Their smaller branches are called venules. • Veins are also 3-layered but tunica media is comparatively thin. 1. BLOOD VASCULAR SYSTEM B. BLOOD VESSELS 2. Veins
  • 42.
    • In tissues,arterioles divide into thin walled and single layered vessels. They are called capillaries. • They unite into venules. 1. BLOOD VASCULAR SYSTEM B. BLOOD VESSELS 3. Capillaries
  • 43.
    • Heart isa mesodermally derived organ located in mediastinum(thoracic cavity). • It is protected by double-layered pericardium. • The pericardial space (between pericardial membranes) is filled with pericardial fluid. It reduces the friction between the heart walls, and surrounding tissues. 1. BLOOD VASCULAR SYSTEM Structure of Heart
  • 44.
    • Heart is4 chambered- 2 upper atria (auricles) & 2 lower ventricles. • The walls (cardiac muscles) of the ventricles are much thicker than that of the atria. • Atria are separated by inter-atrial septum. • Ventricles are separated by inter- ventricular septum. 1. BLOOD VASCULAR SYSTEM C. HEART Structure of Heart
  • 45.
    • In b/watrium and ventricle there is a thick fibrous atrio-ventricular septum with an opening. • A tricuspid valve (3 muscular flaps or cusps) guards the opening between right atrium and right ventricle. • A bicuspid (mitral) valve guards the opening between left atrium and left ventricle. 1. BLOOD VASCULAR SYSTEM C. HEART Structure of Heart
  • 46.
    • These valvesallow the flow of blood only in one direction, i.e. from atria to ventricles. • The right ventricles are opened into pulmonary artery which supplies deoxygenated blood to lungs. • The left ventricles are opened to aorta(largest artery)supplies oxygenated blood to body parts. • Both Pulmonary artery and aorta are provided with the semi-lunar valves. They prevent backwards flow of blood. 1. BLOOD VASCULAR SYSTEM Structure of Heart
  • 47.
    • Heart ismade up of cardiac muscles. • Human heart is myogenic, i.e. normal activities of heart are auto regulated by nodal tissues (a specialized cardiac musculature present in heart wall). • It consists of o Sino-atrial node (SAN)-A patch of nodal tissue in the right upper corner of the right atrium. Which produces signal or action potential (70- 80/min) initiates heart beat. o Hence called pacemaker. o Atrio-ventricular node (AVN) in the lower left corner of the right atrium close to the atrio- ventricular septum. 1. BLOOD VASCULAR SYSTEM Conducting System
  • 48.
    • From theAVN, a bundle of fibrous atrio- ventricular bundle (AV bundle) passes through atrio-ventricular septa and divides into a right & left branches. • Each branch passes through the ventricular walls of its side. • In the ventricular wall, it breaks up into minute fibres (Purkinje fibres). These fibres along with the bundles are known as bundle of His. 1. BLOOD VASCULAR SYSTEM C. HEART Conducting System
  • 49.
    • Nodal tissuesgenerate action potential without any external stimuli, i.e. it is autoexcitable. • SAN initiates and maintains contraction of heart by generating action potentials (70-80/min). So it is called the pacemaker. 1. BLOOD VASCULAR SYSTEM C. HEART Conducting System
  • 50.
    1. BLOOD VASCULARSYSTEM C. HEART •Phases of Cardiac cycle • Joint diastole • Atrial systole • Ventricular systole
  • 51.
    • Firstly, allchambers of heart are in relaxed state (joint diastole). • When the tricuspid & bicuspid valves open, blood from pulmonary vein and vena cava flows into left & right ventricles respectively through left & right atria. • Semilunar valves are closed at this stage. 1. BLOOD VASCULAR SYSTEM C. HEART Cardiac Cycle 1. Joint Diastole
  • 52.
    • The SANgenerates an action potential. It stimulates both the atria to undergo contraction (atrial systole). • This increases the flow of blood into the ventricles by about 30%. 1. BLOOD VASCULAR SYSTEM C. HEART 2. Atrial (Auricular) systole Cardiac Cycle
  • 53.
    • Action potentialis conducted to ventricular side by AVN & AV bundle from where bundle of His transmits it through the ventricular musculature. • It causes contraction of ventricles (ventricular systole). During this, the atria undergo diastole. 1. BLOOD VASCULAR SYSTEM C. HEART Cardiac Cycle 3. Ventricular Systole
  • 54.
    Ventricular systole increasesthe ventricular pressure. It causes the following events: • Closure of tricuspid and bicuspid valves due to attempted backflow of blood into the atria. • Semilunar valves open. So deoxygenated blood enters the pulmonary artery from right ventricle and oxygenated blood enters the aorta from left ventricle. 1. BLOOD VASCULAR SYSTEM C. HEART Cardiac Cycle 3. Ventricular Systole
  • 55.
    The ventricles nowrelax (ventricular diastole) and the ventricular pressure falls. It causes the following events: ▪ Closure of the semilunar valves. It prevents the backflow of blood into the ventricles. ▪ Tricuspid & bicuspid valves are opened by the pressure in the atria. 1. BLOOD VASCULAR SYSTEM C. HEART Cardiac Cycle
  • 56.
    • Ventricles &atria again undergo joint diastole and the above processes are repeated. This is called cardiac cycle. • A cardiac cycle= atrial systole + ventricular systole + diastole • A cardiac cycle is completed in 0.8 seconds. • One heartbeat = a cardiac cycle. • So number of normal heartbeat: 70-75 times/min (average: 72/min). 1. BLOOD VASCULAR SYSTEM C. HEART Cardiac Cycle
  • 57.
    • Stroke volume:Volume of blood pumped out by each ventricle during a cardiac cycle. It is about 70 ml. • Cardiac output: Volume of blood pumped out by each ventricle per minute, i.e. stroke volume x heart rate (70 x 72). It is about 5000 ml (5 litres). • Cardiac output of an athlete is very high. 1. BLOOD VASCULAR SYSTEM C. HEART Cardiac Cycle Stroke volume & Cardiac output
  • 58.
    • During eachcardiac cycle, 2 prominent sounds are produced. • First sound (lub) is due to the closure of tricuspid & bicuspid valves. • Second sound (dub) is due to the closure of the semilunar valves. • One heartbeat = a lub + a dub. 1. BLOOD VASCULAR SYSTEM C. HEART Cardiac Cycle Heart Sounds
  • 59.
    • Human heartis myogenic because normal activities of heart are auto regulated by nodal tissues. • Medulla oblongata regulates cardiac activity through ANS. • Sympathetic nerves of ANS increase the rate of heartbeat, the strength of ventricular contraction and cardiac output. 1. BLOOD VASCULAR SYSTEM C. HEART Regulation of Cardiac activity
  • 60.
    • Parasympathetic nervesof ANS decrease the heart beat, conduction of action potential and the cardiac output. • Adrenal medullary hormones increase the cardiac output. 1. BLOOD VASCULAR SYSTEM C. HEART Regulation of Cardiac activity
  • 61.
    • In man,blood flows through the heart twice for completing its circuit. This is called double circulation. • It includes, ➢ Pulmonary circulation ➢ Systemic circulation 1. BLOOD VASCULAR SYSTEM DOUBLE CIRCULATION
  • 62.
    • It isthe circulation b/w lungs and heart. • Deoxygenated blood pumped into the pulmonary artery is passed on to lungs from where oxygenated blood is carried by pulmonary veins into the left atrium. 1. BLOOD VASCULAR SYSTEM DOUBLE CIRCULATION 1. Pulmonary Circulation
  • 63.
    • It isthe circulation b/w heart & various body parts. • Oxygenated blood is passed through aorta, arteries, arterioles & capillaries and is reached the tissues. • Deoxygenated blood collected from tissues by venules, veins & vena cava is carried to the right atrium. • Systemic circulation provides nutrients, O2 and other substances to the tissues and takes CO2 and other harmful substances away for elimination. 1. BLOOD VASCULAR SYSTEM DOUBLE CIRCULATION 2. Systemic Circulation
  • 64.
    1. BLOOD VASCULARSYSTEM DOUBLE CIRCULATION Pulmonary & Systemic circulations
  • 65.
    • It isa system which includes the hepatic portal vein that carries blood from intestine to the liver before it is delivered to the systemic circulation. 1. BLOOD VASCULAR SYSTEM HEPATIC PORTAL SYSTEM
  • 66.
    It is asystem of coronary vessels that circulate blood to and from the cardiac musculature. 1. BLOOD VASCULAR SYSTEM CORONARY CIRCULATORY SYSTEM Coronary Arteries Coronary Veins
  • 67.
    • It isan instrument used to obtain electrocardiogram (it is a graphical representation of the electrical activity of the heart during a cardiac cycle). • To get an ECG, a patient is connected to the machine with 3 electrical leads (one to each wrist and to left ankle) that monitor heart activity. For a detailed evaluation of heart’s function, multiple leads are attached to the chest region. ELECTROCARDIOGRAPH (ECG)
  • 68.
    An ECG consistsof the following waves: • P-wave: Represents the excitation (depolarization) of atria which causes atrial systole. • QRS-complex: Represents depolarization of ventricles (Ventricular systole). • T-wave: Represents the repolarisation of ventricles. ELECTROCARDIOGRAPH (ECG) Deviation in the ECG indicates the abnormality or disease. So ECG has great clinical significance.
  • 70.
    • Here, theblood pressure is higher than normal systolic (pumping) pressure (120 mm Hg) and normal diastolic (resting) pressure (80 mm Hg), i.e. above 120/80 mm Hg. • If the BP is 140/90 or above, it is hypertension. • It leads to heart diseases and affects vital organs (brain, kidney etc). DISORDERS OF CIRCULATORY SYSTEM 1. Hypertension (High Blood Pressure)
  • 71.
    • It isthe deposition of Ca, fat, cholesterol and fibrous tissue in coronary arteries. • It makes the lumen of arteries narrower and thereby affect the blood supply. DISORDERS OF CIRCULATORY SYSTEM 2. Coronary Artery Disease (CAD) or Atherosclerosis
  • 72.
    • An acutechest pain due to O2 deficiency to heart muscles. • It occurs due to improper blood flow. • It is common among middle-aged and elderly. DISORDERS OF CIRCULATORY SYSTEM 3. Angina (angina pectoris)
  • 73.
    • It isthe condition in which heart is not pumping blood enough to meet the needs of the body. • Congestion of the lungs is the main symptom. • Heart failure is not same as cardiac arrest (heart stops beating) or a heart attack (sudden damage of heart muscle due to inadequate blood supply). DISORDERS OF CIRCULATORY SYSTEM 4. Heart Failure (congestive heart failure)
  • 74.