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The cardiovascular system serves as the principal transportation and distribution network of the body, allowing:
Delivery of several essential substances (e.g., glucose and oxygen) to the tissues
Removal of by-products of metabolism (e.g., carbon dioxide, lactate, and heat)
In its simplest formulation, the system is composed of three parts:
Pump (the heart)
Series of distributing and collecting tubes (the arterial and venous systems)
Transport medium (the blood)
The physiology of the vasculature may be understood as blood flow through the vessels, on blood pressure in various parts of the vascular network, and on vascular resistance to flow.
The relation between these three variables is expressed in an analogy to Ohm’s law.
Further discussion of the regulation of systemic blood pressure appears in one of the renal physiology chapters (see Ch. 19 ) because the renal and cardiovascular systems govern the blood pressure in concert. Chapters 10 and 11 discuss the mechanical action and electrophysiology of the heart. Chapter 12 discusses cardiovascular adaptations to exercise.
The heart is comprised of two hollow muscular pumps in series, dividing the circulation into pulmonary and systemic components ( Fig. 9.1 ).
The right ventricle propels deoxygenated blood from the systemic veins → the pulmonary arteries and on to the lungs.
Exchange of oxygen and carbon dioxide in the pulmonary capillaries, and the pulmonary veins return the oxygenated blood to the heart via the left atrium.
The left ventricle propels oxygenated blood received from the pulmonary veins to the remaining tissues of the body through the aorta and its branches.
Deoxygenated blood eventually returns to the heart in the vena cava via the right atrium.
The circuit from left ventricle to right atrium is the systemic circulation. The circuit from the right ventricle to the left atrium is the pulmonary circulation.
In systemic circulation, the organ systems are connected in parallel, allowing arterial blood flow to shunt between vascular beds based on moment-to-moment need (see Fig. 9.1 ).
Regurgitant flow (backward flow) in the heart is prevented by a series of unidirectional cardiac valves that guard the entrance and exit of each cardiac ventricle.
The valves will be discussed in further detail in Chapter 10 .
The slamming shut of the cardiac valves create the “lub-dub” sound heard through the stethoscope over the precordium (the area of the chest over the heart).
In the cardiovascular circuit, different vessels are adapted to transport blood at different pressures. The differences between the two main types, arteries and veins, are summarized in Table 9.1 , as well as Figs. 7.1 and 9.2 .
Arteries
↑ elastic tissue and smooth muscle.
Arterial pressure is created not only by the heart but also by smooth muscle in the walls of the arteries, which squeezes the arterial blood.
This squeezes blood into the high-capacity veins, leaving only around 20% of total blood volume in systemic arteries at any given time.
The high proportion of elastin in the walls of large arteries gives them elastic recoil, the tendency to shrink back down once stretched.
Under high pressure.
Relatively low compliance.
Arterioles
Smallest branches of arteries.
Highest total resistance in the vascular system.
Arterioles are critical for the control of blood pressure and blood flow.
By constricting some or all of the body’s arterioles, the vasculature can direct the flow of blood to the organs that most need it, or it can elevate blood pressure throughout the cardiovascular circuit.
Regulated by the autonomic nervous system.
Capillaries
Highest total cross-sectional and surface area in the vascular system
Thin-walled
Sites of nutrient and gas exchange
Single layer of endothelial cells → facilitates transport
Veins
The vein walls have low muscle content and are highly distensible.
Veins and venules have high compliance when pressure is low, whereas arterioles are of low compliance at low pressures.
This property of veins allows for the accommodation of large volumes of blood in the circulation before development of high venous pressure.
The high blood volume in the veins is available to return to the heart and lungs when needed, as in the case of exercise or other demand on cardiac output (see Fast Fact Box 9.1 and Fast Fact Box 9.2 ).
Arteries | Veins | |
---|---|---|
Pressure of transported blood | High-pressure | Low-pressure |
Smooth muscle content | +++ | + |
Blood volume (%) | 20 | 80 |
Elasticity | +++ | − |
Compliance | + | +++ (low-pressure) + (high-pressure) |
If the normal blood volume is rapidly expanded (e.g., by blood transfusion) or contracted (e.g., through hemorrhage), most of the volume change is accommodated in the low-pressure portion of the circulation rather than in the arterial high-pressure circulation, whose volume remains relatively constant.
Compliance is the distensibility of the vessel, or change in volume in the vessel per change in pressure (C = ΔV/ΔP). Compliance is high when a large volume (ΔV) can be accommodated with small pressure changes (ΔP), and low when small volume changes result in large pressure differences or, stated differently, a large pressure change is required to make a small change in the volume.
The venous pressure is also a driving force for movement of blood from vein back to heart, a flow known as venous return.
Normal gravitational forces oppose venous return and need to be overcome by developed venous pressures, particularly in the lower extremities.
Recalling the relationship between compliance and pressure (C = ΔV/ΔP), venous pressure may be increased by:
Reduced compliance
Compression of peripheral veins by muscular contractions of the legs
Increased tone of vessels (i.e., by sympathetic nervous system)
Increased volume
From the cardiac perspective, venous return is an important component of preload, a topic covered in Chapter 10 .
The contraction of the cardiac ventricles, an event called systole, drives blood into the pulmonary arteries and into the aorta. The ventricles then relax, an event called diastole.
Systole expands the highly elastic aorta, and elastic recoil occurs during diastole.
This drives the blood out of the aorta and into the smaller arterial branches.
Because both systole and diastole drive the blood forward, blood never stops moving.
Flow is very pulsatile in the aorta and becomes less pulsatile as blood moves down the arterial system.
Pulsatility is still measured well in small arteries.
From the aorta, the blood travels through a branching network of vessels of progressively smaller caliber.
Just before the level of the capillaries are the highly muscular arterioles.
The flow of blood into a given capillary bed may be controlled by muscular contraction in structures known as precapillary sphincters.
When constricted, these sphincters result in a diversion through thoroughfare channels directly into the venous sinusoids, bypassing the capillary bed.
Arterial circulation terminates in the capillaries.
Site of nutrient and gas exchange.
To understand blood pressure, blood flow, and vessel resistance, it is useful to review some basic concepts in physics.
Recall from basic gas laws that the pressure, P, of a gas in a container is proportional to the number of moles (n) in the container per volume (V) of the container:
(because P = nRT/V, where R is the gas constant and T is temperature in Kelvin).
This implies that ↓ volume (V) → molecules forced together → more frequent collisions → ↑ force per area → pressure (P).
This holds true for fluids in a tube (i.e., vessel).
Systole: contraction of cardiac muscles → shrinking vessel (ventricle) size → ↑ P
Diastole: blood emptied into systemic circulation → ↑ V available in aorta → ↓ P
To shrink the ventricle or the aorta, work (W) must be done on the vessel walls (force, F, must be applied over a distance, d):
Thus work or energy is necessary to drive the contraction of the vessels.
In the heart, the energy of muscular contraction is derived from adenosine triphosphate (ATP).
In the aorta, the kinetic energy of the blood entering from the heart pushes the aortic walls out. That energy is stored as potential energy in the aortic elastin fibers. This is released during vessel contraction during diastole.
Because the work is being done in three dimensions, the work equation can be rewritten for three dimensions:
Note: Because pressure is force per area (P = F/A) and volume is equal to distance times area (Δ = d × A), the equation W = P(ΔV) can be reduced to W = (F/A) × (d × A), which is the same as the more familiar W = F × d.
Two types of pressure need be considered in the cardiovascular system ( Fig. 9.4 ):
Transmural pressure refers to a pressure gradient felt across the vascular wall, at one particular point in the vascular tree.
This creates the driving pressure forward through circulation.
It requires an opportunity for outflow (i.e., pressure gradient) to move fluid.
Perfusion pressure or driving pressure, which is the gradient of pressures between two places within the circulation.
The Ohm’s law analogy (I=V/R, where the current I is analogous to blood flow, voltage V is analogous to the pressure gradient) describes the flow of blood (Q) in liters per minute from point A to point B:
where ΔP is the difference in pressure between point A and point B and R is the resistance (mm Hg/mL/min) to flow along the way from A to B.
From this relationship, we see that blood flow is inversely proportional to blood vessel resistance.
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