Blood categories and functions Flashcards

1
Q

what does blood do

A

transport: raw materials,metabolic waste, function modulators. protection: wbc, antibody/ complement, platelet/ coag proteins. temperature control

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2
Q

plasma protein function

A

maintain osmotic pres. / fluid balance, transport other mol., provide immune functions, hemostasis, act as blood buffers,enzymes

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3
Q

albumin role

A

principle protein responsible for colloid osmotic pressure, transport free fatty acids and bilirubin, binds competitively with other drugs

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4
Q

complement system function

A

approx 20 proteins, immune response mediates defense and inflammatory events on cell surface, forms surface membrane attach complex,

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5
Q

kinin system function

A

forms bradykinin by kallikreins

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6
Q

blood coag system function

A

cascade initiated by extrinsic and intrinsic factors, thrombin formed which converts fibrinogen into fibrin

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7
Q

plasma protease inhibitors

A

inhibit proteolytic system

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8
Q

a2 macroglobulin inhibits

A

plasmin,thrombin,kallikrein 250mg/dl 3.5umol

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9
Q

antithrombin 3 inhibits

A

thrombin factor Xa IXa 15 mg/dl 2.5 umol

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10
Q

C1 inhibitor inhibits

A

activated C1r, C1s, Kallikrein 18mg/dl 1.5 u mol

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11
Q

a2 plasmin inhibitor

A

inhibits plasmin 7mg/dl 1umol

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12
Q

haptoglobin

A

protein that binds with plasma hemoglobin from lysed RBC

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13
Q

Hemopexin

A

protein that binds with free heme from plasma hemoglobin

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14
Q

haptoglobin plasma concentration and function

A

130 mg/dl produced by liver binds with up to 3 gm of Hb which is 5 x the amount released on a daily basis combo binds to liver where iron is processed

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15
Q

hemopexin concentration and function

A

50-100 mg/dl complex removed circulation and iron reprocessed, binds with heme. if capacity exceeded metheme bind with albumin but complex is not filtered

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16
Q

methemoglobin

A

Fe 3+. normal state of iron component of heme Fe2+ but methemoglobin reductase keeps iron in reduced state. Methemoglobin does not bind with O2

17
Q

causes of methemoglobin

A

oxidation by nitrites or sulfonamides, congenital deficiency of methemoglobin reductase

18
Q

Hg F production time and site

A

4th month, immature rbc in bone marrow

19
Q

Neutrophil life span

A

10-12 hours in blood 5-6 days in tissue

20
Q

Immature neutrophils released into circulation are called

A

Bands

21
Q

Eosinophil function

A

Attack foreign proteins and parasite and are common in allergic reaction

22
Q

Chemical that eosinophils release

A

MBP major basic protein. Attaches to antigen and causes antigen to lyse. Toxic to all antigens. If no antigen it will attack endothelium

23
Q

Life span of eosinophils

A

12-24 hours. Mature in bone marrow circulate for a day then come to rest in skin,bronchi ,bronchioles

24
Q

Basophil function

A

Exhibit chemotaxis and release histamine and heparin at site of antigen

25
Q

Basophils residence

A

When basophils are mature they are called mast cells. They reside in intestine skin lungs mucosa in nose

26
Q

Monocytes

A

Circulate for a day or two then mature into macrophages or histocytes. They then migrate into tissue spaces

27
Q

Cytokines

A

Glycoproteins that cause pluripotential cells to replicate or differentiate, regulates immune response, involved with inflammation, aids in function of mature blood cells

28
Q

Hematopoiesis

A

Production of mature blood cells from stem cells

29
Q

Cytokines are released by

A

Endothelial cells monocytes macrophages fibroblasts and lymphocytes

30
Q

Types of hematopoietic growth factors

A

Interleukins 1-13, colony stimulating factors (G-CSF) and (GM-CSF) m means macrophage, thrombopoietins, erythropoietin

31
Q

Thrombopoietins

A

All molecules responsible for the development if platelets from Megakaryocytes

32
Q

Erythropoietin

A

Renal hormone that controls RBC production

33
Q

Other factors required for Hematopoiesis

A

Vitamins B-12 and folio acid, metals like iron cobalt and manganese, amino acids, hormones like thyroxin