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AP 2 Chapter 17 Blood

front 1

What are the three main distribution functions of blood?

back 1

Delivery of O2 (from lungs) and nutrients (digestive tract) to all body tissues

Transport metabolic wastes from cells to lungs (CO2) or kidneys (urine)

Transport hormones (from glands to target organ)

front 2

What are the three regulatory functions of blood?

back 2

Regulate body temperature, pH balance, and fluid volume.

front 3

How does blood help regulate body temperature?

back 3

Via absorption and distribution of heat

front 4

How does blood help regulate pH balance?

back 4

RBC and other substances in plasma help to prevent sudden changes in pH.

front 5

How does blood help regulate fluid volume?

back 5

Substances (such as Na+ and Cl-; proteins) help to retain water to maintain proper balance between blood volume and tissue cells.

front 6

What are the protective functions of blood?

back 6

Protects against blood loss via clotting mechanisms

Protects against infection via antibodies, WBC, and other immune proteins.

front 7

What is the optimal pH range for blood?

back 7

Between 7.35-7.45

front 8

At what pH level does acidosis occur?

back 8

Below 7.35

front 9

At what pH level does alkalosis occur?

back 9

Above 7.45

front 10

How much does blood compose of the total body weight?

back 10

Approximately 8%

front 11

What is the average volume of blood in the body?

back 11

Males: 5-6L

Females: 4-5L

front 12

What percentage does solvents compose in plasma composition?

back 12

90% water

front 13

What are the dissolved solutes in plasma?

back 13

Nutrients, wastes, salts, respiratory gases and proteins.

front 14

What proteins compose plasma?

back 14

Albumin (60%), Globulins (36%), Clotting Proteins (4%)

front 15

What is the function of Albumin?

back 15

Transport lipids and is the main contributor of osmotic pressure.

front 16

How much of plasma protein does Albumin account for?

back 16

Some 60%

front 17

What is the function of globulins?

back 17

Transport lipids and are released during immune responses

front 18

What are the functions of clotting proteins?

back 18

Forms fibrin threads of blood clots.

front 19

What do the formed elements of blood consist of?

back 19

Erythrocytes, leukocytes, and platelets.

front 20

Of erythrocytes, leukocytes, and platelets, which ones are true cells?

back 20

Only leukocytes.

Erythrocytes lack a nucleus and platelets are cell fragments.

front 21

Most types of formed elements survive in the bloodstream for how long?

back 21

Only a few days.

front 22

Small cells, about 7.5 µm in diameter, biconcave discs with depressed centers

back 22

Erythrocytes

front 23

Mature erythrocytes are anucleate (lack nucleus) and represent bags of ____?

back 23

hemoglobin.

front 24

What percentage does hemoglobin make up an erythrocyte?

back 24

97%

front 25

What is the purpose of erythrocytes?

back 25

They transport respiratory gases via hemoglobin (Hb)

front 26

What is the structural composition of hemoglobin?

back 26

Red heme pigment bound to globular protein.

Globin consists of 4 polypeptide chains (2 alpha, 2 beta) with the heme pigment molecule located at the center.

front 27

What does the heme molecule bind to?

back 27

Binds reversibly to oxygen molecules

front 28

When oxygen binds to iron (heme molecule), the hemoglobin assumes a three-dimensional shape and becomes ruby red. This is called

back 28

oxyhemoglobin

front 29

When oxygen detaches from iron and resumes its former shape. This occurs in body tissue.

back 29

Deoxyhemoglobin.

front 30

About 20% of the carbon dioxide transported in the blood combines with hemoglobin, but it binds to globin's amino acids instead of the heme group. This is called

back 30

Carbaminohemoglobin

front 31

Blood cell formation is called

back 31

hematopoiesis

front 32

Red blood cell formation is called

back 32

Erythropoiesis

front 33

Where does erythropoiesis occur?

back 33

Largely in red marrow of bones (head of humerus, femur, sternum, and pelvin girdles)

front 34

Precursor cells that reside in red bone marrow and give rise to erythrocytes

back 34

Hemocytoblasts (stem cells)

front 35

How does red blood cell production occur?

back 35

Via hormonal control.

The kidneys produce erythropoietin which stimulate production.

front 36

What are the steps for EPO production?

back 36

1. Kidney cells become hypoxic (O2 availability is inadequate)

2. Increased EPO production circulates to red marrow

3. Increased RBC production

front 37

What are the causes for hypoxia?

back 37

1. Exercise induced

2. Hemorrhage

3. High altitude

4. Respiratory distress (ex., pneumonia, emphysema)

front 38

What controls the rate of erythopoiesis?

back 38

The ability to transport enough oxygen to meet tissue demands.

front 39

What are the nutritional requirements for erythropoiesis?

back 39

Iron, B complex vitamins (B12, folic acid), amino acids

front 40

What is the lifespan of new erythrocytes in the bloodstream?

back 40

100 to 120 days.

front 41

Aged and damaged RBC are engulfed by what?

back 41

Macrophages in the liver, spleen, and bone marrow.

front 42

Abnormal excess of RBC which increases blood viscosity is called

back 42

Polycythemia

front 43

Polycythemia vera results from

back 43

Bone marrow cancer

front 44

Secondary polycythemia occurs if

back 44

There is a decrease is O2 in the atmosphere (as in high altitudes) or an increase in EPO (either naturally or artificially)

front 45

A condition in which the blood's oxygen-carrying capacity is too low to support normal metabolism

back 45

Anemia

front 46

Hemorrhagic anemia results from

back 46

Blood loss

front 47

Hemolytic anemia results from

back 47

Red blood cell rupture

front 48

Iron-deficiency anemia results from

back 48

Hemorrhage (secondary result of) or low Fe (iron) in diet

front 49

Pernicious anemia results from

back 49

Vitamin B12 deficiency (not absorbed in GI tract)

front 50

Sickle-cell anemia results from

back 50

Genetically altered hemoglobin molecules create sickle-shaped RBCs under conditions of low oxygen availability.

front 51

Thalassemia anemia results from

back 51

Genetically one hemoglobin chain is absent or faulty and causes RBCs to be thin and delicate.

front 52

Aplastic anemia results from

back 52

Failure of RBC production.

front 53

The only formed elements that are complete cells, with nuclei and the usual organelles; White blood cells

back 53

Leukocytes

front 54

How much of total blood volume do leukocytes account for?

back 54

1%.

front 55

Unlike RBC, WBCs are not confined to the bloodstream and are able to be transported across the body in a process called

back 55

Diapedesis

front 56

What are the two major categories of leukocytes?

back 56

Granulocytes and agranulocytes.

front 57

What are the difference between granulocytes and agranulocytes?

back 57

Granulocytes contain obvious membrane-bound cytoplasmic granules.

front 58

List leukocytes in the order of most abundant to least abundant.

back 58

Neutrophils, lymphocytes, monocytes, eosinophils, basophils.

Never Let Monkeys Eat Bananas

front 59

Which leukocytes are considered granulocytes?

back 59

Neutrophils, eosinophils, basophils.

front 60

What percentage do neutrophils make up of WBC population?

back 60

Roughly 50-70%.

front 61

How many nuclei do neutrophils typically have?

back 61

3-6.

front 62

What is the function of neutrophils?

back 62

Phagocytize bacteria

Attracted to inflammation

front 63

What percentage do eosinophils account for?

back 63

2-4%.

front 64

What are some characteristics of eosinophils?

back 64

Nucleus usually has two lobes connected by a broad band of nuclear material (resembles ear muffs); Stain brick red to crimson with acid dyes;

front 65

What is the main function of eosinophils?

back 65

Kills parasitic worms and play a complex role in allergies and asthma.

Reduce allergy reactions via breakdown of antibody complexes.

front 66

Rarest of WBC, accounting for only .5-1% of the leukocyte population

back 66

Basophils

front 67

Characteristics of basophils

back 67

Cytoplasm contains large, course, histamine-containing granules that have an affinity for the basic dyes (basophil = base loving) and stain purplish-black. The deep purple nucleus is generally U or S shaped with one or two constrictions.

front 68

What is the function of basophils?

back 68

Release histamine and other mediators of inflammation; contain heparin, an anticoagulant.

front 69

Accounting for 25% or more of WBC population (1500-3000 ul), these are the second most numerous leukocytes in the blood

back 69

Lymphocytes

front 70

Characteristics of lymphocytes

back 70

Large, dark-purple nucleus that occupies most of the cell volume; nucleus is normally spherical; surrounded by a thin rim of pale-blue cytoplasm; classified by size as small, medium, or large.

front 71

What is the function of lymphocytes?

back 71

Play a crucial role in immunity. T cells function in the immune response by acting directly against virus-infected cells and tumor cells. B cells give rise to plasma cells, which produce antibodies that are released in the blood.

front 72

What percentage of WBCs do monocytes account for?

back 72

3-8% (100-700 ul)

front 73

Characteristics of monocytes?

back 73

Largest of leukocytes (average diameter of 18 um); an abundant pale-blue cytoplasm and a darkly staining purple nucleus, which is often U shaped or kidney shaped.

front 74

What is the main function of monocytes?

back 74

Phagocytosis

Help activate lymphocytes.

front 75

Literally "white blood," refers to a group of cancerous conditions involving overproduction of abnormal white blood cells.

back 75

Leukemia

front 76

With leukemia, what happens to the white blood cells?

back 76

They remain unspecialized and proliferate out of control, impairing normal red bone marrow function.

front 77

An abnormally low white blood cell count, commonly induced by drugs, particularly glucocorticoids and anticancer drugs.

back 77

Leukopenia

front 78

What are platelets?

back 78

Cytoplasmic packets of enzymes.

front 79

What is the function of platelets?

back 79

Clot formation.

front 80

What happens during the first step in homeostasis?

back 80

Damaged blood vessel responds to the injury by constricting, exposing collagen fibers.

front 81

What occurs during the second step in homeostasis?

back 81

Platelets stick together forming a plug that temporarily seals the break in the vessel wall. A plasma protein causes platelets to swell, form spiked processes, and become stickier. This allows for a bridge to form between platelets and collagen fibers.

front 82

What occurs during the third step in homeostasis?

back 82

Coagulation occurs. It reinforces the platelet plug with fibrin threads that act as a "molecular glue" for the aggregated platelets.

front 83

Blood is transformed from a liquid to a gel in a multistep process that involves a series of substances called

back 83

Clotting factors, or procoagulants.

front 84

Process of enzymatic clot breakdown once healing has occurred; this "clean-up" is continual.

back 84

Fibrinolysis.

front 85

What types of hemophilia exist?

back 85

A, B, and C; These are linked to X-chromosome genetic disorders that result in inadequate clotting mechanisms.

front 86

What is the management for hemophilia?

back 86

Transfusions and control over activity to prevent injury. Can be treated with genetically engineered clotting factors IX or VII.