exam deck 10 Flashcards

1
Q

What are the three main steps in haemostasis?

A

Vasoconstriction, Platelet Plug Formation, Clotting Cascade.

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2
Q

Why is thrombin crucial in haemostasis?

A

It converts fibrinogen to fibrin, activates Factor XIII for clot stabilization, and promotes clot retraction.

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3
Q

What role does von Willebrand Factor (vWF) play?

A

vWF mediates platelet adhesion to the damaged site.

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4
Q

What substances are released by platelets to promote aggregation?

A

ADP, Thromboxane A2 (TXA2), and Serotonin (5-HT).

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5
Q

What distinguishes the intrinsic and extrinsic pathways?

A

The intrinsic pathway is activated by internal vessel damage, while the extrinsic pathway is triggered by external trauma exposing tissue factor.

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6
Q

What is the common endpoint of both pathways in the clotting cascade?

A

Activation of thrombin, which converts fibrinogen to fibrin.

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7
Q

How does calcium contribute to clotting?

A

It facilitates the activation of clotting factors in the cascade.

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8
Q

How is a clot stabilized after fibrin formation?

A

Factor XIIIa cross-links fibrin strands, and platelet actin and myosin retract the clot edges.

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9
Q

What happens during clot retraction?

A

Platelet contraction reduces the wound size by drawing the edges together.

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10
Q

What enzyme is responsible for clot breakdown in fibrinolysis?

A

Plasmin.

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10
Q

How is plasmin formed?

A

Tissue plasminogen activator (t-PA) converts plasminogen to plasmin.

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11
Q

What inhibits t-PA activity?

A

Plasmin Activator Inhibitor (PAI-1).

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12
Q

Name two vasodilators released by intact endothelial cells.

A

Prostacyclin and Nitric Oxide (NO).

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13
Q

How does heparin prevent clotting?

A

By activating antithrombin, which neutralizes clotting factors IX-XII.

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14
Q

What is the role of thrombomodulin in anti-coagulation?

A

It binds thrombin, aiding Protein C and S in inactivating Factors V and VIII.

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15
Q

What does Tissue Factor Pathway Inhibitor (TFPI) do?

A

Inhibits the Factor VII/tissue factor complex.

16
Q

How does aspirin affect haemostasis?

A

It inhibits thromboxane A2 synthesis, reducing platelet aggregation.

17
Q

What is the mechanism of action of warfarin?

A

It inhibits Vitamin K-dependent synthesis of clotting factors II, VII, IX, and X.

17
Q

What are the risks associated with aspirin and warfarin?

A

Increased bleeding time.

18
Q

What are the two arms of the immune system?

A

Innate and Adaptive immunity.

19
Q

How do innate immune cells recognize pathogens?

A

Through Pathogen-Associated Molecular Patterns (PAMPs) detected by Pattern Recognition Receptors (PRRs), like Toll-like receptors (TLRs).

20
Q

Name two key phagocytic cells.

A

Neutrophils and Macrophages.

21
Q

What is the function of the complement system?

A

Tagging pathogens (opsonization), recruiting immune cells, and lysing pathogens with the Membrane Attack Complex (MAC).

22
Q

What is the role of T helper cells (Th)?

A

They secrete cytokines to modulate immune responses and help B cells produce antibodies.

23
Q

What happens during the secondary immune response?

A

Memory B cells recognize the same pathogen, leading to a faster and stronger response.

24
Q

What are the main classes of antibodies?

A

IgM, IgG, IgA, IgE, and IgD.

25
Q

Which antibody is associated with mucosal immunity?

A

IgA.

26
Q

What is a cytokine storm?

A

A life-threatening overproduction of cytokines in response to infection.

27
Q

What triggers anaphylactic shock?

A

Mast cells releasing histamines and other mediators during an extreme allergic reaction.