16-4: Thrombocytes and Hemostasis Flashcards

1
Q

thrombocytes

A

tiny round or oval discs without nuclei

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2
Q

Platelets are produced in the __ as ___.

A

red bone marrow; large megakaryocytes break off fragments that enter the blood and become platelets

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3
Q

Thrombocytopenia

A

“clotting cell deficiency” - deficiency of platelets leading to spontaneous bleeding from small vessels and petechiae on the skin

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4
Q

Platelets have a ___ lifespan of about ___.

A

short; 10 days (less if involved in clotting)

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5
Q

function of platelets

A

initiate a chain of reactions causing blood to clot

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6
Q

What are the relative frequencies of the various blood cells, starting with the most?

A
Erythrocytes
Thrombocutes
Leukocytes: (Never Let Monkeys Eat Bananas)
neutrophils
lymphocytes
monocytes
eosinophils
basophils
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7
Q

hemostasis

A

the stoppage of bleeding - when a blood vessel is damaged or ruptured, a series of events takes place to stop blood loss. There are three major phases which occur in rapid sequence

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8
Q

What are the three major phases of hemostasis?

A
  1. vascular spasm
  2. platelet plug formation
  3. coagulation
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9
Q

vascular spasm

A

the smooth muscle in the wall of a damaged vessel contracts immediately to slow blood loss; this lasts 20-30 minutes

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10
Q

platelet plug formation

A

when platelets come in contact with a torn (rough) blood vessel, they stick to the exposed collagen fibers in the torn surface and clump together, temporary plugging the whole and further reducing blood loss (occurs w/in a minute)

Example of positive feedback - they release chemicals to attract more platelets

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11
Q

coagulation

A

the formation of a blood clot. The platelets in the plug release a variety of factors which stimulate a chain of reactions, where the activation of 1 factor catalyzes the activation of the next factor in the sequence.

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12
Q

What are the three main steps in coagulation?

A
  1. Formation of prothrombin activator
  2. prothrombin (plasma protein formed by liver, always present but inactive) —> thrombin (active enzyme)
  3. fibrinogen (soluble plasma protein) —> fibrin (insoluble threads)
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13
Q

Fibrin

A

insoluble threads - molecules clump together forming a network to trap RBCs and platelets, and pull the damaged edges of the vessel closer together

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14
Q

What is the last stage of blood clotting?

A

once the clot plugs the ruptured area, permanent repair can take place and new endothelial cells restore the torn lining. Once repaired, the unneeded clot is removed by fibrinolysis

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15
Q

hemophilia

A

a heredictary bleeding disorder; due to a mutation on the X chromosome, the person lacks one of the platelet clotting factors needed to form prothrombin activator. As a result, their blood fails to clot properly and small cuts cause serious bleeding that can be life-threating

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16
Q

Hemophilia A lacks factor __, B lacks __, and C lacks ___.

A

A VIII; B IX; C XI

17
Q

What is the treatment for hemophilia?

A

transfusions of fresh plasma or injections of the missing clotting factor (only lasts a few days - needs continuous administration)