Blood Flashcards

(53 cards)

1
Q

What is the typical composition of blood (plasma and formed elements)?

A

55% plasma and 45% formed elements

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2
Q

What is the composition of plasma?

A

7% proteins, 2% other solutes, and 91% water

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3
Q

What is the composition of the proteins in plasma

A

58% albumins, 38% globulins, and 4% fibrinogen

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4
Q

Where is albumin produced? What does it do?

A

It is produced in the liver and functions to draw water into the blood

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5
Q

Where is globulin produced? What is its function?

A

It is produced by white blood cells and it functions to transport vitamins, minerals, hormones, fats, and clotting factors.

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6
Q

What is the function of fibrinogen?

A

It creates fibrin

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7
Q

What is the function of fibrin?

A

It creates plugs with platelets and white cells

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8
Q

What are platelets?

A

Fragments of cells that contain substance for clotting surrounded by plasma membrane

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9
Q

What are the six types of white blood cells? What are their relative percentages?

A

Neutrophils (60-70%), lymphocytes (20-25%), monocytes (3-8%), eosinophils (2-4%), and basophils (0.5-1%)

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10
Q

What are the three types of granulocytes?

A

Neutrophils, Eosinophils, and Basophils

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11
Q

What are the two types of agranulocytes?

A

Lymphocytes and monocytes

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12
Q

What is the word for the formation of formed elements?

A

Hematopoiesis

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13
Q

What does a hemocytoblast need to bind to to make a red blood cell? Where is that made?

A

Erythropoietin from the kidneys

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14
Q

What does a hemocytoblast need to bind to to make a white blood cell? Where is that made?

A

Colony stimulating factor from the bone marrow and white blood cells

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15
Q

Where are hemocytoblasts made?

A

The red bone marrow

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16
Q

What does a hemocytoblast need to bind to to make a platelet? Where is that made?

A

Thrombopoietin which is made in the liver

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17
Q

What percentage of formed elements is made up of RBCs

A

95%

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18
Q

What is the average hematocrit for men? Women?

A

42-52 for men and 37-47 for women

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19
Q

What is the structure of a RBC?

A

Each RBC is like a bag filled with 250 million hemoglobin molecules

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20
Q

What is the structure of hemoglobin?

A

Each hemoglobin is made up of 4 heme molecules

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21
Q

How many O2 molecules can each heme bind?

A

1

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22
Q

How does hemoglobin react in areas of high and low O2?

A

In areas with low O2 oxygen is more likely to be released, the opposite is true in areas with high O2

23
Q

What are the ingredients for RBCs?

A

Iron, Protein, B12, and Folic Acid

24
Q

How are the components in RBCs recycled?

A

The proteins are broken down into amino acids | Heme is broken into iron and bilirubin which is recycled directly

25
How long does a RBC last?
110-120 days
26
How many RBCs are created and destroyed in a day?
20-25 million
27
What does anemia mean?
Anemia is an issue were blood becomes ineffective and can be caused in many different ways including low #, irregular shape, and low iron which leads to low hemoglobin
28
What are some major symptoms of anemia
Fatigue, cold, shortness of breath, dizziness
29
What are some types of iron deficiency?
Iron deficiency, folate deficiency, pernicious (Vit B12 or intrinsic factor), sickle cell, hemorrhagic
30
What is erythrocytosis?
Too many red blood cells - 80% hematocrit
31
What is the problem with erythrocytosis?
Blood becomes viscous increasing stress on the heart which can lead to a heart attack
32
What causes primary erythrocytosis?
Abnormality in the red bone marrow increases the production of RBCs
33
What causes secondary erythrocytosis?
Increase in erythropoietin either because of an abnormality or doping.
34
What are the main characteristics of leukocytes?
They perform chemotaxis (follow chemical signals), diapedesis (squeeze through vessel walls), and have ameboid movement
35
What are some features/qualities of neutrophils?
Secrete neutrophilic extracellular traps (NETs) Secrete anti-microbial compounds Good at phagocytosis First to arrive at the location Multi-lobed nucleus (2-5)
36
What are some features/qualities of basophils?
Secrete inflammatory compounds (histamines) and cause inflammation pain
37
What are some features/qualities of eosinophils?
Bilobed nucleus Bright red granules Anti-parasitic Secrete anti-inflammatory compounds battling with basophils They don't secrete anti-inflammatory compounds in the lungs (eosinophilic asthma)
38
What are the three kinds of lymphocytes?
B-cells T-cells (helper T and cytotoxic T)
39
How can lymphocytes be identified?
They have a single large nucleus and are agranular
40
What do B cell do?
They are antibody factories that stimulate an immune response
41
What do cytotoxic T cells do?
Destroys specific bacteria/virus/unhealthy (cancer) cells
42
What do helper T cells do?
They activate B cells and toxic T cells
43
What is the unique about monoxytes?
They are the largest WBC They become macrophages when in tissue They have a kidney bean nucleus The love phagocytosis They are fashionably late They phagocytize large things
44
What is the pneumonic for the white blood cells?
Never let monkeys eat bananas
45
Where are leukocytes made?
They are made in the red bone marrow but are activated in the spleen (giant lymph nodes) and lymph nodes
46
What is leukemia?
Excess white blood cells which are immature and incapable of mobilizing an immune response
47
What does leukemia cause?
It decreases the RBC count --> Anemia It decreases platelets --> Hemorrhaging
48
What is DIV?
Irregular internal clotting caused by trauma, bacterial toxins, or venoms
49
What clotting factor does hemophilia type A not have?
8
50
What clotting factor does hemophilia type B not have?
9
51
What is Von Willebrand's disease?
Irregular Von Willebrand factor preventing platelets from sticking to the wound
52
What causes thrombocytopenia?
Too few platelets
53
Why is vitamin K insufficiency a problem?
It is needed to make most of the clotting factors