blood Flashcards

(45 cards)

1
Q

vol of blood in normal adult

A

5.5L

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2
Q

how much of blood is haematocrit

A

45%

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3
Q

polycythaemia

A

bone marrow tumours

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4
Q

symptoms of polycythaemia

A
  1. red complexion
  2. headache
  3. blurred vision
  4. confusion
  5. stroke/coma
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5
Q

what is absolute erythrocytosis

A

raised RBC mass, normal plasma volume

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6
Q

what is apparent erythrocytosis

A

normal RBC mass, reduced plasma volume

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7
Q

plasma components

A
  1. water
  2. solutes
    3, proteins
  3. albumin
  4. globulins
  5. fibrinogen
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8
Q

what do albumins do and where are they made

A

made in liver, contribute to colloid osmotic pressure

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9
Q

what do globulins do and where are they made

A

made in liver and lymphoid tissue, clotting factors, enzymes and antibodies

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10
Q

what do fibrinogens do and where are they made

A

liver, forms fibrin strands for blood clotting

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11
Q

what does transferrin do and where are they made

A

liver, iron transport

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12
Q

erythrocytes size and conc

A

7-8 µm, 5 million/µl

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13
Q

why can erythrocytes easily pass through capillaries

A

they are highly flexible

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14
Q

how many Hb molecules in a single RBC

A

250,000,000

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15
Q

how long to RBCs survive

A

120 days

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16
Q

sites of haematopoiesis

A

yolk sac, liver/spleen, bone marrow

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17
Q

where is red bone marrow in adults

A

sternum, ribs and upper ends of long limb bones

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18
Q

how is erythropoiesis controlled

A
  1. kidneys detect reduced O2- carrying capacity of blood
  2. less O2 delivered to kidney so erythropoietin secreted
  3. erythropoietin triggers erythropoiesis by bone marrow
  4. additional RBCs increase O2-carrying capacity of blood
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19
Q

CO2 effect on RBCs

A

binds irreversibly to polypeptide chains, carbonic anhydrase found in RBCs

20
Q

CO effect on RBCs

A

occupies O2 binding sites, leads to CO poisoning, Hb has 4x more affinity for CO than O2

21
Q

NO effect on RBCs

A

vasodilator, allows blood to circulate

22
Q

Fe in diet effect on blood

A
  1. absorbed by active transport
  2. transferrin transports Fe in plasma
  3. liver stores Fe as ferrin
  4. bone marrow uses Fe to make Hb
  5. spleen converts Hb to bilirubin
  6. liver metabolises bilirubin and excretes it as bile
23
Q

3 steps of haemostasis

A
  1. vascular spasm
  2. formation of thrombus
  3. formation of blood clot
24
Q

what do platelets (thrombocytes) contain

A
  1. mitochondria
  2. SER
  3. cytoplasmic granules
25
what secretes vWf
megakaryocytes, platelets and endothelial cells
26
what does vWf do upon damage
1. binds to collagen 2. platelets binds to it and trigger stickiness 3. secretion
27
what do platelets secrete after binding to vWf
serotonin, ADP, epinephrine
28
what halts clot formation
prostacyclin, nitric acid
29
how does clot formation halt
1. exposed collagen binds and activates platelets 2. platelet factors released 3. attracts more platelets 4. platelets aggregate into plug
30
platelet function factors: Collagen
from subendothelial extracellular matrix, injury exposes platelets to collagen
31
platelet function factors: vWf
activated by exposure to collagen, links platelets to collagen
32
platelet function factors: serotonin
from secretory vesicles of platelets, activated by platelet activation, aggregates platelets
33
platelet function factors: ADP
from platelet mitochondria, activated by platelet activation and thrombin, aggregates platelets
34
platelet function factors: platelet activating factor (PAF)
from platelets/neutrophils, activated by platelet activation, aggregates platelets
35
platelet function factors: Thromboxane A2
from phospholipids, activated by PAF, aggregates platelets
36
platelet function factors: platelet-derived growth factor (PDGF)
from platelets, activated by platelet activation
37
what triggers fibrinogen
coagulation cascade
38
how do anticoagulants work
1. inhibit platelet adhesion 2. inhibit coagulation cascade + fibrin production
39
causes of coaggulation disorders
1. liver disease 2. cirrhosis 3. vit K deficiency 4. haemophilia 5. low blood platelets
39
examples of anticoagulants
heparin, antithrombin II
39
how does warfarin work as an anticoagulant
blocks vitamin K which is a cofactor in factor II, VII, IX, and X synthesis
40
type A haemophilia
factor VIII deficiency, 80% of cases
41
type B haemophilia
factor IX deficiency, treated w gene therapy
42
4 key players in lymphatic system
1. histamines 2. interleukins 3. bradykinin 4. complement cascade
43
function of antibodies
1. activate B lymphocytes 2. act as opsonins 3. cause antigen clumping 4. activate antibody dependent cellular activity 5. trigger mast cell degeneration 6. activate compliment