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

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
Basophils residence
When basophils are mature they are called mast cells. They reside in intestine skin lungs mucosa in nose
26
Monocytes
Circulate for a day or two then mature into macrophages or histocytes. They then migrate into tissue spaces
27
Cytokines
Glycoproteins that cause pluripotential cells to replicate or differentiate, regulates immune response, involved with inflammation, aids in function of mature blood cells
28
Hematopoiesis
Production of mature blood cells from stem cells
29
Cytokines are released by
Endothelial cells monocytes macrophages fibroblasts and lymphocytes
30
Types of hematopoietic growth factors
Interleukins 1-13, colony stimulating factors (G-CSF) and (GM-CSF) m means macrophage, thrombopoietins, erythropoietin
31
Thrombopoietins
All molecules responsible for the development if platelets from Megakaryocytes
32
Erythropoietin
Renal hormone that controls RBC production
33
Other factors required for Hematopoiesis
Vitamins B-12 and folio acid, metals like iron cobalt and manganese, amino acids, hormones like thyroxin