#32 Flashcards

(42 cards)

1
Q

3 Functions of blood

A

Transport
Defence
Regulation

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2
Q

What does blood contain?

A

plasma [aqueous matrix], cells, platelets and proteins

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3
Q

What cells are in blood?

A

Red Blood Cells and White Blood Cells

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4
Q

What does plasma consist of?

A

water, dissolved substances and proteins

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5
Q

Why does plasma have high BCOP

A

because it has far more protein than other exracellular fluids

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6
Q

Haematocrit

A

packed red blood cell volume

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7
Q

Formed elements

A

cells or cell fragments found in blood which help carry out its varios functions

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8
Q

What do platelets do?

A

Defence against fluid loss

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9
Q

What does White Blood Cells do? (Leukocytes)

A

Defence ahainst pathogens and toxins

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10
Q

What do red blood cells (erythrocytes) do?

A

Transport of dissolved gases and wastes

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11
Q

What are notable features of RBCs?

A

bioconcave shape
lack of nucleus
lack of mitochondria
no other organelles

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12
Q

Why are RBCs shaped like that?

A

for flexibility and stackability for flow

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13
Q

Why do RBCs lack organelles?

A

more space for storage

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14
Q

What is responsible for oxygen transport in mature RBCs?

A

protein haemoglobin

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15
Q

What does each haemoglobin have?

A

4 globin chains, 4 haem units, 4 iron ions

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16
Q

What can each haem and iron do?

A

carry 1 molecule of oxygen

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17
Q

What happens to oxygen in the blood?

A

almost all oxygen is carried by haemoglobin and the rest is dissolved in plasma

18
Q

The carbonic acid-bicarbonate

A

critical buffer system that maintains the pH of human blood and bodily fluids within a narrow healhy range

19
Q

How does The carbonic acid-bicarbonate work?

A

When hydrogen ions increase, pH lowers, bicarbonate acts as a base to bind them forming carbonic acid. When pH is too high, carbonic acid releases hydrogen ions

20
Q

How does buffering against changes in pH happen?

A
  • bicarnonate from blood and other body fluids binds to and buffer hydrogen generated from production of metabolic acids
  • haemoglobin can bine a significant fraction of the hydrogren ions
21
Q

Haemostasis

A

physiological processes that limit/halt blood loss through damaged bloos vessels

22
Q

Serum

A

fluid that is left after blood clotting. contains water solute and blood proteins that are not related to clot formation

23
Q

Whole blood

A

contains specialized cell fragments, platelets and proteins that give it the bility to form clots

24
Q

Plasma

A

aqueous component of undistributed blood and contains protein clotting factors

25
What's a major part of haemostasis?
clotting/coagulation
26
Vascular phase of haemostasis
cells in the blood vessel wall undergo rapid changes - 1. contraction (vascular spasm) 2. increased endothelial 'stickiness'
27
Platelet phase of haemostasis
platelets combine at exposed endothelial surfaces to plug the broken vessel - platelets attach to the sticky endothelial cells and basement membrane and become activated - activated platelets change shape and release chemicals that attract other platelets and help them stick to each other
28
What part of blood clotting is a positive feedback loop?
platelet phase
29
Coagulation phase on haemostasis
bibrin mesh netwrok forms around platelets producing a clot
30
Fibrin
protein which binds aggregated platelets and blood cells into a clot
31
What is the ultimate ffect of coagulation?
create strands of insoluble fibrin
32
What is involved in the coagulation phase?
cascade of enzymes that catalyze the formation of fibrin from soluble fibrinogen
33
What do platelets release when they stick to the collagen wall?
Release prothrombin activator (something produced in the liver and requires vitamin K)
34
Thrombin
molecular scissors that cut protein. cuts fibronogen into fibrin
35
Factor X
enzyme in blood coagulation cascade
36
How is prothrombinase complex formation formed?
Activated Factor Xa along with cofactor FVa, calcium ions and platelet phospholipids form prothrombinase complex
37
What does the prothrombinase complex do?
convert prothombin (Factor II) into active thrombin (Factor IIa)
38
What does thrombin do to fibrinogen
converts fibrinogen (factor I) into insoluble fibrin (Factor Ia)
39
Fibrinolysis
opposing process to coagulation that breaks down the fibrin clot to restore blood flow and prevent excessive clotting
40
What does thrombin also activate?
Factor XIII TO XIIIa, with calcium it cross-links the fibrin polymers to form a stable, unsoluble fibrin mesh
41
Tissue plasminogen activator
released from injured endothelial cells, tPA acts as an activator it binds to the fibrin clot and converts the inactive zymogen plasminogen in to the active enzyme plasmin
42
Plasmin
primary protease responsible for degrading the fibrin networld into soluble fragments called fibrin degradation products or fibrin splot products