This presentation is an overview of the description of the 4 stages of the cardiac cycle (atrial diastole, atrial systole, ventricular systole, ventricular diastole) as well as explaining the mechanism of the cardiac cycle.
Cardiac myocytes are short
branched striated muscle cells
Connected with gap junctions
gap junctions transmit
electrical activity between cells
So, cardiac myocytes act as
a single functional unit
(syncitium)1. Rhythmicity
2. Excitability
3. Conductivity
4. Contractility
Right Atrium of human heart
This PPT help to understand the external and internal structures of right atrium.
sulcus terminalis on external surface of rt atrium,
crista terminalis on internal side of rt. atrium,
interior is divided into rough anterior part and smooth posterior part ( sinus venarum)
superior and inferior venae cavae drains deoxygenated blood into rt. atrim
there is Eustachian valve to guard the opening of IVC and Thebesian valve to guard the opening of coronary sinus
septal wall presents fossa ovalis with its border limbus fossa ovalis
This presentation is an overview of the description of the 4 stages of the cardiac cycle (atrial diastole, atrial systole, ventricular systole, ventricular diastole) as well as explaining the mechanism of the cardiac cycle.
Cardiac myocytes are short
branched striated muscle cells
Connected with gap junctions
gap junctions transmit
electrical activity between cells
So, cardiac myocytes act as
a single functional unit
(syncitium)1. Rhythmicity
2. Excitability
3. Conductivity
4. Contractility
Right Atrium of human heart
This PPT help to understand the external and internal structures of right atrium.
sulcus terminalis on external surface of rt atrium,
crista terminalis on internal side of rt. atrium,
interior is divided into rough anterior part and smooth posterior part ( sinus venarum)
superior and inferior venae cavae drains deoxygenated blood into rt. atrim
there is Eustachian valve to guard the opening of IVC and Thebesian valve to guard the opening of coronary sinus
septal wall presents fossa ovalis with its border limbus fossa ovalis
This presentation is a combination of different slides which I re-purposed. I included a reference of all the slides I used at the end of my presentation.
Cardiovascular physiology for university studentsItsOnyii
A detailed pdf document on cardiovascular physiology for university students including structure and functions of heart, Electrocardiogram, echocardiography, chest and limb leads, Diseases and disorders of the heart.
✓Heart
✓Anatomy of heart
✓Blood circulation
✓Blood Vessels
✓Structure and function of artery, vein and capillaries
✓Elements of conduction system of heart and heart beat
✓Its regulation by nervous system
✓Cardiac output
✓Cardiac cycle
✓Regulation of bood pressure
✓Pulse
✓Electrocardiogram
✓Disorder of heart
Model Attribute Check Company Auto PropertyCeline George
In Odoo, the multi-company feature allows you to manage multiple companies within a single Odoo database instance. Each company can have its own configurations while still sharing common resources such as products, customers, and suppliers.
Ethnobotany and Ethnopharmacology:
Ethnobotany in herbal drug evaluation,
Impact of Ethnobotany in traditional medicine,
New development in herbals,
Bio-prospecting tools for drug discovery,
Role of Ethnopharmacology in drug evaluation,
Reverse Pharmacology.
The Indian economy is classified into different sectors to simplify the analysis and understanding of economic activities. For Class 10, it's essential to grasp the sectors of the Indian economy, understand their characteristics, and recognize their importance. This guide will provide detailed notes on the Sectors of the Indian Economy Class 10, using specific long-tail keywords to enhance comprehension.
For more information, visit-www.vavaclasses.com
Students, digital devices and success - Andreas Schleicher - 27 May 2024..pptxEduSkills OECD
Andreas Schleicher presents at the OECD webinar ‘Digital devices in schools: detrimental distraction or secret to success?’ on 27 May 2024. The presentation was based on findings from PISA 2022 results and the webinar helped launch the PISA in Focus ‘Managing screen time: How to protect and equip students against distraction’ https://www.oecd-ilibrary.org/education/managing-screen-time_7c225af4-en and the OECD Education Policy Perspective ‘Students, digital devices and success’ can be found here - https://oe.cd/il/5yV
This is a presentation by Dada Robert in a Your Skill Boost masterclass organised by the Excellence Foundation for South Sudan (EFSS) on Saturday, the 25th and Sunday, the 26th of May 2024.
He discussed the concept of quality improvement, emphasizing its applicability to various aspects of life, including personal, project, and program improvements. He defined quality as doing the right thing at the right time in the right way to achieve the best possible results and discussed the concept of the "gap" between what we know and what we do, and how this gap represents the areas we need to improve. He explained the scientific approach to quality improvement, which involves systematic performance analysis, testing and learning, and implementing change ideas. He also highlighted the importance of client focus and a team approach to quality improvement.
Synthetic Fiber Construction in lab .pptxPavel ( NSTU)
Synthetic fiber production is a fascinating and complex field that blends chemistry, engineering, and environmental science. By understanding these aspects, students can gain a comprehensive view of synthetic fiber production, its impact on society and the environment, and the potential for future innovations. Synthetic fibers play a crucial role in modern society, impacting various aspects of daily life, industry, and the environment. ynthetic fibers are integral to modern life, offering a range of benefits from cost-effectiveness and versatility to innovative applications and performance characteristics. While they pose environmental challenges, ongoing research and development aim to create more sustainable and eco-friendly alternatives. Understanding the importance of synthetic fibers helps in appreciating their role in the economy, industry, and daily life, while also emphasizing the need for sustainable practices and innovation.
The Art Pastor's Guide to Sabbath | Steve ThomasonSteve Thomason
What is the purpose of the Sabbath Law in the Torah. It is interesting to compare how the context of the law shifts from Exodus to Deuteronomy. Who gets to rest, and why?
Welcome to TechSoup New Member Orientation and Q&A (May 2024).pdfTechSoup
In this webinar you will learn how your organization can access TechSoup's wide variety of product discount and donation programs. From hardware to software, we'll give you a tour of the tools available to help your nonprofit with productivity, collaboration, financial management, donor tracking, security, and more.
4. Functions of cardiovascular
system
• Circulates OXYGEN and removes Carbon
Dioxide.
• Provides cells with NUTRIENTS.
• Removes the waste products of
metabolism to the excretory organs for
disposal.
• Transports HORMONES to target cells
and organs.
• Helps regulate body temperature.
6. What Are the Parts of the Circulatory
System?
• Two pathways come from the heart:
• The pulmonary circulation is a short loop
from the heart to the lungs, where blood is
oxygenatedand.
• The systemic circulation carries blood
from the heart to all the other parts of the
body.
7. Pulmonary circulation
• In pulmonary circulation:
• The pulmonary artery is
a big artery that comes
from the heart. It brings
blood from the heart to
the lungs. At the lungs,
the blood picks up
oxygen and drops off
carbon dioxide. The
blood then returns to the
heart through the
pulmonary veins.
8. Systemic circulation
The left side of the heart
pumps blood to the rest of the
tissues of the body through the
systemic circulation: Blood
pumped from left ventricle
passes through a series of
blood vessels, arterial system
and reaches the tissues.
Exchange of various
substances between blood and
the tissues occurs at the
capillaries. After exchange of
materials, blood enters the
venous system and returns to
right atrium of the heart. From
right atrium, blood enters the
right ventricle.
10. HEART
• The heart is a muscular organ about
the size of a closed fist that functions
as a body’s circulatory pump.
11. Functional anatomy of the heart
The heart is located in
the center of the thoracic
cavity. It sits directly
above the muscles of the
diaphragm, which
separates the thorax from
the abdomen, and lies
beneath the sternum
between the two lungs.
12. The heart is enclosed
and anchored in place
by a double-walled
fibrous sac referred to
as the pericardium.
The membranes of
the pericardium produce
a small amount
of pericardial fluid
that minimizes friction
produced by the movement
of the heart when it beats.
FUNCTIONAL ANATOMY OF THE HEART
13. Functional Anatomy of the Heart
CARDIAC MUSCLE
• Characteristics:
– Striated
– Short branched cells
– Uninucleate
– Intercalated discs
14. Functional Anatomy of the Heart
CHAMBERS
Human heart
has 4 chambers
– 2 Atria
– 2 Ventricles
Chambers
are separated
by septum…
Due to separate
chambers,
heart functions as double pump
15. Functional Anatomy of the Heart
VALVES
Two sets of valves in the heart maintain the
one-way flow of blood as it passes through
the heart chambers:
• Atrioventricular (AV) valves
• Semilunar valves
16. Functional Anatomy of the Heart
VALVES
Each of these valves consists of
thin flaps of flexible but tough
fibrous tissue whose movements
are passive.
The atrioventricular (AV)
valves are found between the
atria and the ventricles.
The right AV valve is a tricuspid
valve and has three cusps or
leaflets. The left AV valve (also
referred to as the mitral valve) is
a bicuspid valve because it has
two cusps.
17. Functional Anatomy of the Heart
VALVES
The semilunar valves
separate the ventricles from
their associated arteries.
The pulmonary valve is found
between the right ventricle and
the pulmonary artery and the
aortic valve is found between
the left ventricle and the aorta.
These valves prevent
backward flow of blood from
the pulmonary artery or the
aorta into their preceding
ventricles when the ventricles
relax. The semilunar valves
also have three cusps.
18.
19. Functional Anatomy of the Heart
The wall of the heart
The wall of the heart has three layers:
• Epicardium
• Endocardium
• Myocardium
The outermost layer, the epicardium, is the thin membrane
on the external surface of the heart. The innermost layer,
the endocardium, consists of a thin delicate layer of cells
lining the chambers of the heart and the valve leaflets.
The endocardium is continuous with the endothelium ,
which lines the blood vessels.
The middle layer is the myocardium, which is the
muscular layer of the heart. This is the thickest
layer, although the thickness varies from one
chamber to the next. Thickness of the myocardium
is related to the amount of work that a given
chamber must perform when pumping blood.
20. Properties of myocardium
• Different cells within the heart are
specialized for different functional roles. In
general, these specializations are for
1.automaticity
2.excitability
3. conduction
4. contraction
21. Automaticity
• The specialized (pacemaker) cells of heart
spontaneously depolarize to threshold and
generate action potential. They are located in
• Sinoatrial (SA) node
This cells have the highest intrinsic rhythm (rate), making
them the pacemaker in the normal heart. Their intrinsic
rate is 60- 100beats/min.
• Atrioventricular (AV) node
Its cells have the second highest intrinsic rhythm (40-
60beats/min). Often, these cells become the pacemaker
if SA node cells are damaged.
• Purkinje fibers
They exhibit spontaneous depolarization with a rate of – 35
beats/min.
22. Myocardial Physiology
Autorhythmic Cells (Pacemaker Cells)
• Characteristics of
Pacemaker Cells
– Smaller than
contractile cells
– Don’t contain many
myofibrils
– No organized
sarcomere structure
• do not contribute to
the contractile force
of the heart
normal contractile
myocardial cell
conduction myofibers
SA node cell
AV node cells
23. Automaticity
Autorhythmic Cells (Pacemaker Cells)
•Characteristics of Pacemaker Cells: They
have unstable membrane potential
•“bottoms out” at -60mV
•“drifts upward” to -40mV, forming
a pacemaker potential
•The upward “drift” allows the membrane
to reach threshold potential (-40mV) by
itself
•This is due to:
1.Leakage Na+ causes slow depolarization
2.Ca2+ voltage-gated channels opening as
membrane approaches threshold (Ca2+
goes in)
At threshold additional Ca2+ voltage-gated
channels open causing more rapid
depolarization
3. Slow K+ voltage-gated channels open
causing an efflux of K+ (K+ goes out) and
Ca2+ in K+out
Ca2+ in
Na+in
25. Excitability
Contractile Cells
• Special aspects
– Intercalated discs
•Highly convoluted and
interdigitated junctions
–Joint adjacent cells with
»Desmosomes & fascia adherens
–Allow for synticial activity
»With gap junctions
–More mitochondria than skeletal
muscle
–Less sarcoplasmic reticulum
•Ca2+ also influxes from ECF reducing
storage need
–Larger t-tubules
•Internally branching
–Myocardial contractions are
graded!
27. Excitability
Action potential of contractile cells
• Phase 0
(depolarization)begins when
the membrane potential
reaches threshold (–40 mV).
Similar to nerve and skeletal
muscle, mediated by the
opening of voltage-gated, fast
Na+ channels
• Phase 1 (initial
repolarization) Slight
repolarization mediated by a
transient potassium current.
Sodium channels are in the
inactivated state.
28. Excitability
Action potential of contractile cells
• Phase 2 (plateau)
Depolarization opens voltage-gated Ca2+ channels
and voltage-gated K+ channels
• Phase 3 (repolarization)
At this point, the Ca++ channels close and K+
channels open. The resulting efflux of K+ ions
causes the repolarization phase of the action
potential.
• Phase 4 Resting membrane potential
29. Excitability
Action potential of contractile cells
• As in neurons, cardiac muscle
cells undergo an absolute or
effective refractory period in
which, at the peak of the action
potential, the voltage-gated fast
Na+ channels become inactivated
and incapable of opening
regardless of further stimulation.
As a result, the absolute refractory
period lasts almost as long as the
duration of the associated
contraction — about 250 msec.
The physiological significance of
this phenomenon is that it
prevents the development of
tetanus or spasm of the
ventricular myocardium.
The effective refractory period is followed by
a relative refractory period that lasts for the
remaining 50 msec of the ventricular action
potential. During this period, action
potentials may be generated; however, the
myocardium is more difficult than normal to
excite.
32. Contractility
• Initiation
– Action potential via pacemaker
cells to conduction fibers
• Excitation-Contraction Coupling
1. AP spreads along sarcolemma
• T-tubules contain voltage gated L-
type Ca2+ channels which open upon
depolarization
• Ca2+ entrance into myocardial cell
and opens RyR (ryanodine receptors)
Ca2+ release channels
2. Ca2+ (Ca2+ from SR and ECF) binds
to troponin to initiate myosin head
attachment to actin
• Contraction
33. Contractility
• Relaxation
– Ca2+ is transported back
into the SR and
– Ca2+ is transported out of
the cell by a facilitated
Na+/Ca2+ exchanger (NCX)
– As ICF Ca2+ levels drop,
interactions between
myosin/actin are stopped
– Sarcomere lengthens
34. Electrocardiography
• is the recording of the electrical activity
of the heart.
• It is based on recording of
electric potentials generated by heart on
different body parts (mostly on body
surface)
Electrocardiogram is graphic record
of the electrocardiography
36. Elements of ECG
• Waves are parts of ECG, which are
located above or below the isoline.
• Segments are parts of ECG, which are
located on the isoline.
• Intervals include waves and segments.
38. Waves of ECG
• P wave represents atrial depolarization
• QRS complex represents ventricular
depolarization
• T wave represents ventricular
repolarization
• U wave represents repolarization of the
papillary muscles or Purkinje fibers.
39. Blood Vessels
Over 80,000 miles of blood vessels transport your blood throughout your body.
There are 3 types of blood vessels.
• Arteries: Blood vessels
that carry blood away
from the heart to other
parts of the body.
• Veins: Blood vessels
that carry blood from
the body back to the
heart.
• Capillaries: Tiny tubes
that carry blood from
the arteries to the
body’s cells, and then
back to the veins.
40. Arteries:
carries blood Away from heart
– Large
– Thick-walled, Muscular
– Elastic
– Oxygenated blood
Exception Pulmonary Artery
– Carried under great pressure
– Steady pulsating
Arterioles: smaller vessels, enter tissue
42. Veins:
Carries blood to heart
– Carries blood that contains
waste and CO2
• Exception pulmonary vein
– Blood not under much
pressure
– Valves to prevent much
gravity pull
Venules: larger than capillaries
44. Blood Components
Blood is made up of plasma and
formed elements
Plasma: It transports blood solids,
nutrients, hormones, and other
materials.
Formed elements:
–Erythrocytes (Red blood cells)
–Leukocytes (White blood cells)
–Platelets (thrombocytes)
45. Red blood cells
1. Made up about 99%
of the blood’s cellular
component
2. Small, disk-like shape
3. No nucleus
4. Cannot reproduce
5. Last 4 months then
rupture
6. Produced by red bone
marrow
7. Contain hemoglobin
8. Carry oxygen
46. Hemoglobin
• Hemoglobin is a
complex protein
made up of four
protein strands, plus
iron-rich heme
groups.
• Each hemoglobin
molecule can carry
four oxygen atoms.
The presence of
oxygen turns
hemoglobin bright
red.
47. White blood cells
• Nucleus present
• Types of leukocytes:
• most are neutrophils
that engulf
microorganisms
• Basophils
• Eosinophils
• Lymphocytes
Active in immune system.
Help fight disease and infection by
attacking germs that enter the body.
48. Platelets
• Platelets are cell
fragments used in
blood clotting.
• Platelets are derived
from egakaryocites.
Help blood form a clot at the
site of a wound. A clot seals a
cut and prevents excessive
blood loss.
50. • He developed the
modern criteria of
phase analysis of
the cardiac cycle
(1921).
21st APS President (1949-1950)
Carl J. Wiggers
(1883-1963)
51. • Cardiac cycle refers to all events associated
with blood flow through the heart. A single
cycle of cardiac activity can be divided into
two basic phases:
–Systole – contraction of heart muscle
–Diastole – relaxation of heart muscle
The Cardiac Cycle
55. Phase 1. Asynchronous contraction
• The beginning of this phase
= the end of Presystole (phase 9) = the end of diastole
• The end of this phase
= the beginning of Isovolumic contraction (phase 2)
The beginning of phase
AV valves are open
SL valves are closed
The end of phase
AV valves are closed
SL valves are closed
During this phase:
•Ventricular contraction
•The ventricular cavity volume
doesn't change
•The ventricular cavity pressure
doesn't change
56. Phase 2. Isovolumic contraction
• The beginning of this phase
= the end of Asynchronous contraction (phase 1)
• The end of this phase
= the beginning of Rapid ejection phase (phase 3)
During this phase,
Ventricular contraction
The ventricular cavity volume doesn't change
The ventricular cavity pressure increases
The beginning of phase
AV valves are closed
SL valves are closed
The end of phase
AV valves are
closed
SL valves are open
57. Phase 3. Rapid ejection
• The beginning of this phase
= the end of Isovolumic contraction (phase 2)
• The end of this phase
= the beginning of Reduced ejection (phase 4)
The beginning of phase
AV valves are closed
• SL valves are open
The end of phase
AV valves are
closed
SL valves are
openDuring this phase:
Ventricular contraction
2/3rd of stroke volume rapid ejected
The ventricular cavity volume decreases
The pressure inside the ventricles rises
to 120 mmHg
58. Phase 4. Reduced ejection
• The beginning of this phase
= the end of Rapid ejection (phase 3)
• The end of this phase
= the beginning of Protodiastole (phase 5)
= the end of Systole = the beginning of Diastole
The beginning of phase
• AV valves are closed
• SL valves are open
• The end of phase
• AV valves are closed
• SL valves are open
During this phase:
• Ventricular contraction
• 1/3rd of stroke volume slow ejected
• The ventricular cavity volume decreases
59. Phase 5. Protodiastole
• The beginning of this phase
= the end of Reduced ejection (phase 4)
• The end of this phase
= the beginning of . Isovolumic relaxation (phase 6)
The beginning of phase
• AV valves are closed
• SL valves are open
The end of phase
• AV valves are closed
• SL valves are closed
During this phase:
• The ventricles are relaxing
• The ventricles aren’t filling
• The ventricular cavity volume doesn't change
60. Phase 6. Isovolumic relaxation
The beginning of this phase
= the end of Protodiastole (phase 5)
• The end of this phase = the beginning
of Rapid filling (phase 7)
The beginning of phase
• AV valves are closed
• SL valves are closed
The end of phase
• AV valves are open
• SL valves are closed
During this phase,
The ventricles are relaxing
The ventricles aren’t filling
The ventricular cavity volume
doesn't chan
The pressure inside the
ventricles increases
significantly
61. Phase 7. Rapid filling
• The beginning of this phase
= the end of Isovolumic relaxati (phase 6)
• The end of this phase
= the beginning of Reduced ventricular filling (phase 8)
The beginning of
phase
AV valves are open
SL valves are
closed
The end of phase
AV valves are open
SL valves are
closed
During this phase:
The ventricles are relaxing
The ventricles are rapid filling
The ventricular cavity volume increases
The pressure inside the ventricles increases
slightly
62. Phase 8. Reduced filling
The beginning of this phase
= the end of Rapid filling (phase 7)
The end of this phase
= the beginning of Presystole (phase 9)
The beginning of phase
• AV valves are open
• SL valves are closed
• The end of phase
• AV valves are open
• SL valves are closed
During this phase,
The ventricles are relaxing
The ventricles are slow
filling
The ventricular cavity
volume increases
The pressure inside the
ventricles increases slightly
63. Phase 9. Presystole
• The beginning of this phase
= the end of Reduced filling (phase 8)
• The end of this phase
= the beginning of ventricular systole (phase 1)
= the beginning of ventricular systole
= the end of ventricular diastole
The beginning of phase
• AV valves are open
• SL valves are closed
The end of phase
• AV valves are open
• SL valves are closed
64. Phase 9. Presystole
During this phase,
•During ventricular relaxation blood flows from
atria to ventricles. When both atria contracts
almost simultaneously and pupms remaining 25%
of blood flows in respective ventricles (therefore
even when if atrial fails to function it is unlikely to
be noticed unless a person exercises).
•The ventricles are rapid filling
•The ventricular cavity volume increases
•The pressure inside the ventricles increases
slightly
67. Cardiac Output
• Cardiac Output (CO) is the volume pumped by
the left ventricle each minute
– influenced by
• Stroke Volume (SV)
EDV – ESV = SV
135ml – 65ml = 70ml
• Heart Rate (HR) bpm
– CO = SV x HR
(70ml/b x 72bpm = 5040 ml/min
=5.04L/min)
68. Blood Vessel Structure
• enables specific functions
– Aorta
• absorb pulse pressure
(systolic pressure – diastolic
pressure) and release
energy creating diastolic
pulse
– Large arteries
• conduct and distribute blood
to regional areas
– Arterioles
• Regulate flow to tissues and
regulate MAP (mean arterial
pressure)
69. – Capillaries
• Allow for exchange
– Venules
• Collect and direct
blood to the veins
– Veins
• Return blood to heart
and act as a blood
reservoir
Blood Vessel Structure
71. • Hemodynamics is the description of the
laws which govern blood flow within the
vasculature.
• Ultimately, all blood flow between two
points within the vasculature is actuated
by differences in the pressure of blood
between those two points.
73. Blood flow through a vessel is
determined by 2 factors:
• pressure gradient along the vessel
(pressure difference of the blood between
the two ends of the vessel)
• vascular resistance (impediment to blood
flow through the vessel)
74. The flow through the vessel can be
calculated by the following formula, which is
called Ohm’s law :
Q = (P1 - P2) / R
•in which Q is blood flow,
•(P1 - P2) is the pressure difference
between the two ends of the vessel,
•R is the resistance.
75. Blood Pressure
– Systolic Pressure
• The pressure that is created when the ventricles
contract
• Usually around 120 mm Hg
76. Blood Pressure
– Diastolic Pressure
• The pressure that is created by the recoil of the
aorta AND the closure of the aortic semilunar valve
• Usually around 80 mm Hg
77. Blood Pressure
Pulse Pressure
• Pulse Pressure=Systolic Pressure - Diastolic
Pressure
• The difference between the systolic and diastolic
pressures
– Usually 40 mm Hg (120 mm Hg – 80 mm Hg)
• Only applies to arteries
Mean Arterial Pressure
• We can determine the average pressure within the
arterial system = Mean Arterial Pressure (MAP)
MAP = Diastolic Pressure + 1/3 Pulse
Pressure
MAP = 80 mm Hg + 1/3( 120 mm Hg – 80 mm
Hg)
MAP = 93 mm Hg
78. QUESTIONS
1. The cardiovascular system. Functions. The pulmonary and systemic circuits.
2. The heart muscle cells. Structure.
3. Properties of the cardiac muscle.
4. Automaticity of the heart. Pasemaker cells.
5. Conductivity of the heart. Conductive system of the heart.
6. Excitability of the heart. Cardiac Action potential . The refractory periods of the cardiac muscle.
7. Contractility of the heart. Mechanism of cardiac muscle cell contraction.
8. The normal electrocardiogram.
9. Elements of ECG.
10. Mechanical events in the heart: cardiac cycle . Steps of the cardiac cycle .
11. Electrical events of cardiac cycle.
12. The origin of the heart sounds.
13. Ventricular volume-pressure loop.
14. Stroke volume. Control of stroke volume. Ejection fraction.
15. Cardiac output (CO). Regulation of CO .
16. Types and characteristics of blood vessels.
17. Relationship between blood flow, pressure and resistance.
18. Pressures in the cardiovascular system. Arterial pressure in the systemic circulation: diastolic,
systolic, pulse and mean arterial pressures.
19. Neural Regulation of Blood Pressure.