Ch. 13/14 Cardiovascular (CV) Physiology Flashcards

1
Q

What are the functions of the circulatory system?

A
  1. Transport of respiratory gases, nutrients, and wastes
  2. Communication/regulation of hormones and temperature
  3. Defense/protection - clotting and immunity
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2
Q

CV System Components

A

Blood - fluid medium
–cells and plasma

Heart - pump (primary motive force)
–septum divides left and right halves

Blood vessels - conduit/delivery system (plumbing)

  • -arteries, arterioles, capillaries, post capillary venules, veins
  • -pulmonary and systemic circulation

Lymphatic system

  • -lymphatic vessels, lymphoid tissues, lymphatic organs (spleen, thymus, tonsils, lymph nodes)
  • -return fluid leaked from CV system back to CV system
  • -immune functions/system
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3
Q

Why do we need a CV system?

A

Bulk transport! Diffusion has limitations over long distances

Diffusion is fast over short distances, but slow over greater distances

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4
Q

What is diffusion?

A

Simple method for moving things down a concentration gradient

Equation: t = x^2/2D
(x = distance traveled, D = diffusion coefficient [different for each solute])
–note: time varies w/ the square of the distance

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5
Q

Overview of CV System

A

Right and left hearts are in series - so output from each side matches the other

Pulmonary circulation: blood from body –> heart –> lungs

Systemic circulation: blood from heart –> body

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6
Q

Arrangement of circulation to different organs is?

A

Parallel

Exception: GI in series w/ liver

Parallel arrangement prevents blood flow changes in one organ from affecting flow to others

W/ every heartbeat lungs get 100% of cardiac output; all other organs share 100% cardiac output

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7
Q

Blood

A

Fluid medium

Average adult volume: 5L

45% formed elements (cells/platelets); 55% plasma (by volume)

Arterial blood: leaving heart, bright red, oxygenated [except for pulmonary artery]

Venous blood: entering the heart, dark red, deoxygenated [except for pulmonary veins]

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8
Q

In a centrifuged blood sample, what is the layer in between the blood plasma and formed elements?

A

“Buffy coat”

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9
Q

Plasma Volume

A

Regulated to maintain BP [CV/renal/hypothalamo-anterior pituitary-adrenal axis]

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10
Q

Plasma Osmolality

A

Regulated to maintain solute (Na+) concentration [CV/renal/hypothalamo-posterior pituitary axis]

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11
Q

Plasma constituents

A

Plasma is made up of lots of things, ranging from water, ions, organic molecules (proteins, AAs, fibrinogen), trace elements/vitamins, and gases (CO2 and O2)

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12
Q

Plasma Proteins make up what percentage of total plasma?

A

7-8% of plasma

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13
Q

What is the most important plasma protein?

A

Albumin

Made in liver (lack of it during liver failure)

Fxn: major contributions to colloid osmotic pressure of plasma, carriers for various substances

Holds fluid in CV system, determines volume

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14
Q

Formed Elements (cells)

A

RBCs

Platelets

WBCs
–lymphocytes, monocytes, neutrophils, eosinophils, basophils

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15
Q

RBCs

A

“Erythrocyte”

Oxygen transport

Flattened, biconcave discs, NO NUCLEI OR MITOCHONDRIA

120-day lifespan

% of blood volume (hematocrit) - index of O2 carrying capacity

Anemia: abnormally low hematocrit or HB count

Heme (contains iron molecule) carries O2
–each heme can carry a maximum of 4 oxygen molecules

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16
Q

Blood Count

A

58% plasma volume

17
Q

WBCs

A

“Leukocytes”

Granular (granulocytes): neutrophils, eosinophils, basophils

Agranular: monocytes, lymphocytes (T and B cells)

Have nuclei, mitochondria

Move in amoeboid fashion - can move from capillaries, post-capillary venules into tissues (diapedesis/extravasation)

Major role in innate and adaptive immune systems and inflammatory response

18
Q

Platelets

A

“Thrombocytes”

Smallest formed element, fragments of megakaryocytes

No nuclei

Short-lived (5-9 days)

Clot w/ several other chemicals and fibrinogen

Release serotonin (stimulate vasoconstriction)

19
Q

Hematopoiesis

A

Development of blood cells and platelets - begin in bone marrow

20
Q

Erythropoiesis

A

Production of RBCs

Red bone marrow produces about 2.5 million RBCs/sec

Stimulated by erythropoietin (EPO) from kidneys in response to low blood O2

Most iron recycled from old RBCs, the rest comes from diet

21
Q

Thrombopoiesis

A

Production of platelets

The cytokine, thrombopoietin stimulates growth of megakaryocytes and maturation into platelets

22
Q

Leukopoiesis

A

Production of WBCs

Begins in bone marrow, final development requires maturation in lymphoid tissues (lymph nodes, tonsils, spleen, thymus)

As cells differentiate, they express membrane receptors to cytokines, which have both general and specific effects in determining the final subtype:

  • -multipotent growth factor-1 (general effects on all subtypes)
  • -interleukin-1 (general effects on all subtypes)
  • -interleukin-3 (general effects on all subtypes)
  • -granulocyte colony stimulating factor (G-CSF) - neutrophils
  • -granulocyte-monocyte colony-stimulating factor (GM-CSF) - monocytes, eosinophils
23
Q

Cytokine

A

Signaling molecule (peptide), usually, but not exclusively, secreted by cells of the immune system (e.g. EPO comes from kidney). Have effects on development and function of leukocytes and other cell types. May operate as autocrine, paracrine, and endocrine signals

24
Q

Blood Clotting

A

Hemostasis: cessation of bleeding when a blood vessel is damaged

Damage exposes collagen fibers to blood, producing:

a) Formation of platelet plug
- -platelets stick to collagen fibers –> activate –> stick to each other
b) Vasoconstriction
c) Formation of fibrin protein web –> mature clot

25
Q

Platelets and Blood Vessel Walls

A

Intact endothelium secrete prostacyclin and nitric oxide, which:

  • -vasodilate
  • -inhibit platelet aggregation (keeps them from sticking)

AND CD39, which:

  • -breaks down ADP into AMP and Pi to inhibit platelet aggregation further
  • ->ADP makes endothelial cells sticky; converting ADP to AMP and Pi retains stickiness of platelets
26
Q

Intact Endothelium

A

Expresses/secretes platelet inhibitory factors

Barrier function - prevents exposure of platelets to sub-endothelial extracellular matrix molecules

27
Q

Damaged Endothelium

A

Exposes collagen

Platelets bind to exposed collagen and Von Willebrand Factor which hold them in place

Activated platelets recruit more platelets and form plug by secreting (platelet release reaction - all starts w/ platelets)

  • -a) ADP (sticky platelets)
  • -b) Serotonin (vasoconstriction - acts upstream to close arteriole so less blood is lost)
  • -c) Thromboxane A2 (sticky platelets and vasoconstriction)

Activated platelets also activate and bind to soluble plasma clotting factors

28
Q

Formation of Platelet Plug and Clot

A

Platelets bind to fibrin –> reinforces mass of aggregated platelets which effectively plugs the defect

RBCs become entwined in the plug –> solid clot

29
Q

Coagulation Cascade

A

Both intrinsic and extrinsic pathways converge on formation of THROMBIN

Thrombin converts fibrinogen to fibrin (aids on cross linkages of platelets in blood clotting)

30
Q

Clot Formation and Dissolution

A

Thrombin involved in BOTH

Formation of clot: making fibrin

Dissolution of clot: breakdown of fibrin

As vessel heals, factors are released which digest fibrin polymers