Anatomy & Physiology: Cardiovascular System - Blood Vessels and Blood Flow
Terms in this set (28)
Tissue perfusion is the blood flow through body tissues, essential for delivering O2 and nutrients, removing wastes, gas exchange in lungs, nutrient absorption in the digestive tract, and urine formation in kidneys.
Blood flow rate is controlled by extrinsic factors (sympathetic nervous system and hormones) and intrinsic factors (autoregulation/local control by tissues).
Extrinsic control involves nerves and hormones acting on arteriolar smooth muscle to reduce blood flow to less needed regions, regulating flow through the whole body.
Intrinsic control or autoregulation is local adjustment of blood flow by tissues themselves, modifying arteriole diameter to meet specific tissue needs.
During exercise, skeletal muscle arterioles dilate (intrinsic control) increasing blood flow to muscles, while extrinsic controls reduce flow to organs like kidneys and digestive system.
The two intrinsic mechanisms are metabolic controls and myogenic controls, both determining the autoregulatory response.
Increased tissue metabolism lowers O2 and raises metabolic products (H+, K+, adenosine, prostaglandins), causing arteriole relaxation and nitric oxide release for vasodilation.
Endothelins are potent vasoconstrictors released by endothelium, balanced with nitric oxide; when blood flow is inadequate, nitric oxide predominates causing vasodilation.
Myogenic controls respond to changes in mean arterial pressure (MAP): increased stretch causes vasoconstriction, decreased stretch causes vasodilation to maintain constant perfusion.
Long-term autoregulation occurs when short-term control fails, involving angiogenesis and vessel enlargement to increase blood supply over weeks or months.
At rest, myogenic and neural mechanisms maintain flow (~1 L/min); during activity, local controls override sympathetic vasoconstriction, increasing flow up to 10 times.
Brain blood flow is tightly regulated by metabolic controls (pH, CO2 levels) and myogenic controls responding to MAP changes to prevent ischemia or edema.
Skin blood flow is neurally controlled; vasodilation occurs with heat to radiate warmth, vasoconstriction occurs with cold to conserve heat, also serving as a blood reservoir.
Pulmonary arteries have low pressure and resistance; low O2 causes vasoconstriction, high O2 causes vasodilation, directing blood to oxygen-rich lung areas.
During systole, coronary vessels are compressed stopping flow; during diastole, high aortic pressure forces blood through coronary circulation.
Blood flow velocity is fastest in the aorta, slows down in capillaries due to large cross-sectional area, then increases again in veins.
Vasomotion is the intermittent flow of blood through capillaries caused by the opening and closing of precapillary sphincters.
Molecules cross capillaries by diffusion through endothelial membranes, passing through intercellular clefts, fenestrations, or active transport via pinocytotic vesicles.
Bulk flow is driven by hydrostatic pressure (fluid pushing out) and colloid osmotic pressure (protein pulling fluid in), determining fluid movement at arterial and venous ends.
NFP is the net force driving fluid out or into capillaries: \(NFP = (HP_c + OP_{if}) - (HP_{if} + OP_c)\).
Edema is caused by increased capillary hydrostatic pressure, increased interstitial osmotic pressure, decreased capillary osmotic pressure, or lymphatic blockage, leading to excess interstitial fluid.
The vascular system has pulmonary circulation (heart to lungs and back) and systemic circulation (heart to body and back).
Arteries run deep only, while veins can be deep or superficial; superficial veins do not correspond to arteries by name.
Venous pathways are more interconnected, can have multiple names, and include special drainage systems like dural venous sinuses and the hepatic portal system.
The hepatic portal system is a vein connecting two capillary beds, transporting blood from digestive organs to the liver for filtering before systemic circulation.
Blood from digestive organs is filtered in the liver to remove toxins and microorganisms using hepatocytes and phagocytes in sinusoid capillaries.
The hepatic portal vein carries nutrient-rich blood from digestive organs to the liver for processing before it enters the general circulation.
At the arterial end, NFP causes fluid to move out (filtration); at the venous end, NFP causes fluid to move in (reabsorption).