Ch.17 Flashcards

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1
Q

Blood travels:

A

leaves arteries that branch until they become capillaries.

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2
Q

Bloods function:

A

carry oxygen, removes waste, transport metabolic waste, releases CO2. (Distribution, Regualtion, Body protection)

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3
Q

Blood pumped through:

A

pulmonary circuit (going to lungs) and systemic circuit (rest of body)

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4
Q

blood leaving heart is what type of blood vessels?

A

arteries. Returning to heart is veins.

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5
Q

Composition of blood:

A

plasma, formed elements (erythrocytes, leukocytes, platelets) and hematocrit

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6
Q

hematocrit

A

percentage of RBCs out of total blood volume

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7
Q

erythrocytes

A

red blood cells

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8
Q

leukocytes

A

white blood cells (buffy coat)

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9
Q

Blood structure:

A

sticky, opaque, scarlet (oxygen-rich) to dark red (oxygen poor)

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10
Q

blood distribution: (transportation)

A

oxygen to lungs, nutrients from digest. tract., metabolic wastes

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11
Q

regulation:

A

body temp by absorbing and distrib. heat, normal pH (7.45) in tissues, adequate water content in circulatory syst.

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12
Q

body protection

A

prevent blood loss, activating plasma proteins, clot formation, prevent infection (activating WBCs to fight against foreign material)

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13
Q

blood plasmsa:

A

protiens, albumin, globulins, fibrinogen (clotting proteins), hormones

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14
Q

gamma

A

immunity for defense

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15
Q

albumin

A

contributor to osmotic pressure. 60% plasma proteins

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16
Q

globulins (2):

A

(alpha, beta, gamma) transport proteins that bind to lipids. 36% plasma proteins.

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17
Q

formed elements (3):

A

erythrocytes, leukocytes, platelets

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18
Q

Erythrocytes :

A

(RBCs) No nuclei or organelles. (not complete) Filled with hemoglobin 97% (protein that functions in gas transport). Plasma membrane protein spectrin (felxibilty to change shape).

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19
Q

Erythrocytes function:

A

transporting gas, composed of protein globin (two alpha/ two beta chains) bound to heme group. Heme group bind to oxygen molecule.

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20
Q

Hemoglobin:

A

(transport up to 4 oxygen molecules.) O2 loading in lungs Produces Oxyhemoglobin (ruby red). O2 unload in tissues produce deoxyhemoglobin (dark red). Carbaminohemoglobin (CO2 loading in tissues)

21
Q

Hematopoiesis

A

produce Red Bone Marrow of: Axial skeleton, Epiphyses. Hemocytoblasts give rise to form elemnts. Eventually form to RBC’s.

22
Q

Erythropoiesis:

A

Production of blood cells. (homeostasis of RBCs). Balance of RBC.

23
Q

Balance of RBC’s:

A

hormonal controls, adequate Iron, amino acids, B Vit.

24
Q

Erythropoietin:

A

hormone, stimulating RBCs, Hypoxia (not enough RBCs)

25
Q

RBCs die:

A

after 4 months. Lose shape, macrophages engulf them, spit them out, cellular debris. (can reuse) Heme and globin seperate. (Iron reuse).

26
Q

Heme

A

degrade to bilirubin. Liver secretes into intestines where it metabolizes into Uribilinogen.

27
Q

Globin

A

metabolized into amino acids and released into circulation.

28
Q

never let monkeys eat bananas (most abundant)

A

neutrophils, lymphocytes, monocytes, eosinophils, basophils.

29
Q

granulocytes (3):

A

neutrophils, eosinophils, basophils.

30
Q

neutrophils:

A

pink, multiple lobes leukocytes. (PMNs). Hydrolizing enzymes and defensins. Bacteria slayers.

31
Q

eosinophils:

A

red, lysosome like. specialize on infections from parasitic worms. lessen severity of allergies.

32
Q

basophils:

A

U or S shaped. Histamine.

33
Q

lymphocytes:

A

close to RBC size, nucleus take up most of cell. B lymphocytes give off antibodies.

34
Q

Monocytes:

A

horse shoe shaped. Macrophages digest/ engulf. protect against parasites and infections.

35
Q

platelets

A

blue staining outer region. HMPMP hemocyto-blast, megakaryoblast, promegakaryocyte, megakarocyte. –> platelets. Clotting mechanism.

36
Q

hemostasis

A

forming blood clot. 3 steps: Vascular Spasm, Platelet plug formation, coagulation. (VPC)

37
Q

vascular spasm (1):

A

smooth muscle contracts causing vasonstriction.

38
Q

Platelet plug (2):

A

platelets release chemicals that make nearby platelets sticky and platelet plug fomrs.

39
Q

coagulation (3):

A

(blood clotting). Fibrin forms a mesh that traps RBCs and platelets forming the clot.

40
Q

coagulation:

A

prothrombin activator leads to clot formation. (after platelets/ mesh network). INTRINSIC (factors present inside blood) EXTRINSIC (factors outside blood). –> lead to prothrombin -> thrombin -> fibronogen ->fibrin-> cross linked fibrin mesh.

41
Q

clot retraction:

A

stabilizes clot. Actin & myosin in platelets contract. (PDGF), fibrinolysis

42
Q

Platelet-derive growth factor (PDGF):

A

rebuild blood vessel wall.

43
Q

fibronolysis:

A

removes unneeded clot after healing.

44
Q

thromboembolic disorders:

A

undesirable clot formation. (thrombus, embolus, embolism). Aspirin/ Heparin (blood thinners)

45
Q

thrombus:

A

clot that develops unbroken blood vessels

46
Q

embolus:

A

thrombus freely floating in blood stream

47
Q

embolism:

A

embolus obstructing a vessel.

48
Q

Thrombocytopenia:

A

deficient # of circulating platelets. (Petechiae -> hemorrhage due to destruction of red bone marrow)

49
Q

Hemophilia:

A

Hereditary bleeding disorder, can’t generate platelets.