Chapter 11: The Cardiovascular System(Blood) Flashcards

1
Q

what is the first system that develops in an embryo and at how many weeks is it developed?

A

the cardiovascular system; 3 weeks

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2
Q

a baby grows 2x its size by week _______ once the cardiovascular system is developed and can provide nutrients for growth

A

4

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3
Q

what are the 3 requirements for the cardiovascular system?

A

-fluid(blood)
-pump(heart)
-tubes(blood vessels)

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4
Q

what are the 5 functions of blood?

A

-transportation
-regulation of pH/composition of ions
-ability to form clots
-defense against pathogens
-regulate body temperature

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5
Q

what is transported in blood? (4)

A

-dissolved gases(O2, CO2)
-nutrients(glucose, amino acids, nucleotides, fatty acids)
-wastes
-minerals/ions

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6
Q

what is caused by too low of pH?

A

coma

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7
Q

what is caused by too high of pH?

A

convulsions

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8
Q

what are the 3 characteristics of blood?

A

-100.4 temp
-pH of 7.35-7.45
-viscosity 5x more than water

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9
Q

what is viscosity

A

thickness

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10
Q

what type of blood vessel must almost always be used in drawing blood and which specific one is most commonly used?

A

vein; medial cubital vein

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11
Q

what is it called when blood is taken from a vein for a test or to be donated?

A

venipuncture

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12
Q

what is one of the only scenarios where an artery is used to draw blood and what precautions must be taken?

A

the person’s gas O2 or CO2 levels need to be tested; a surgeon must be present in case of needing emergency surgery to avoid bleeding out

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13
Q

what artery is used to draw blood if needed?

A

radial artery

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14
Q

why is it so dangerous to draw blood from an artery?

A

an artery brings blood from the heart and moves with more power, causing more of a chance of bleeding out

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15
Q

how much of blood is made up of plasma and what color is it?

A

55%; straw-colored

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16
Q

what 4 things make up plasma?

A

-albumins
-globulins
-fibrinogen
-regulatory proteins

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17
Q

60% of plasma; moves water in blood; carries/transports some lipids/hormones

A

albumins

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18
Q

35% of plasma; carry/transport lipids/hormones; immunoglobin antibodies(immune function)

A

globulins

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19
Q

4% of plasma; inactive clotting proteins

A

fibrinogen

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20
Q

<1% of plasma; ex. angiotension II

A

regulatory proteins

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21
Q

what makes up only 1% of plasma?

A

dissolved solutes(ions, glucose, hormones, nutrients, wastes)

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22
Q

what are the 3 formed elements in blood?

A

RBCs, WBCs, and platelets

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23
Q

how much of blood is formed elements?

A

45%

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24
Q

what is another name for RBCs?

A

erythrocytes

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25
measure of the amount of formed elements in blood; equal to the number of RBCs
hematocrit
26
what is the average male's hematocrit?
4.6(meaning that 46% of blood is RBCs)
27
what is the average female's hematocrit?
4.2
28
why do males have more RBCs/a higher hematocrit?
they have testosterone and androgens, which stimulate RBC production
29
what is the name of the shape of an RBC?
biconcave
30
why do RBCs have a biconcave shape?
so they have more surface area to exchange O2 and CO2 and so they have flexibility and can bend in tight places
31
does a fully mature RBC have organelles?
no
32
why do RBCs have no nucleus?
there is more space for hemoglobin and we do not want the RBC to control whether or not it divides
33
why do RBCs have no mitochondria?
we do not want the RBC to use any of the oxygen that it is supposed to be carrying
34
what percent of the proteins in the cytosol of an RBC is hemoglobin?
95%
35
what is 1 hemoglobin made up of? (3)
-4 polypeptide chains(2 sets of twins) -4 heme units(1 per polypeptide) -4 Fe+2 units(1 per polypeptide)
36
how many hemoglobins does each RBC have?
250 million
37
when body cells are not receiving enough oxygen; skeletal muscles are fatigued without exercising and brain has a hard time staying awake/alert even after sleeping
anemia
38
how long is the life span of an RBC?
90-120 days/3-4 months
39
what percent of RBCs will burst on their own and lose all protein chains in urine?
10%
40
what is it called when more than 10% of RBCs are bursting on their own, causing a orange-ish/red-ish tint to blood
hemoglobinuria
41
about what percent of RBCs are engulfed by phagocytes/macrophages in the spleen, liver, and bone marrow?
90%
42
what happens to polypeptide chains after RBC is engulfed?
they are broken down into their amino acids and placed into the bloodstream to be used
43
what happens to the heme units after RBC is engulfed?
they are converted into biliverdin, which is then converted into bilirubin, and then is placed into blood biliverdin-->bilirubin-->into blood
44
black/green color; day 1 bruise
biliverdin
45
yellowish-brown color; day 2 bruise
bilirubin
46
when bilirubin leaks back into blood and goes into body tissues, causing skin and scleras to turn yellow
jaundice
47
iron in phagocytes are transported in blood on ___________-->taken into bone marrow(ferrin)
transferrin
48
how much extra iron do females store?
.5g (less than males, this is why anemia is more common)
49
how much extra iron do males store?
1g
50
production of RBCs
erythropoesis
51
what hormone controls erythropoesis?
EPO(erythropoetin)
52
what 2 things control the release of EPO?
kidney and hair cells
53
what are the 2 functions of EPO?
-stimulate production of more RBCs -speed up maturation of RBCs
54
name for antigens in blood
agglutinogens
55
name for antibodies in blood
agglutinins
56
has Rh antigen
Rh+
57
does not have Rh antigen
Rh-
58
what do agglutinins/antibodies do in blood?
agglutination
59
the clumping of RBCs and clogging of capillaries
agglutination
60
antigens: A, Rh antibodies: B
A+
61
antigens: A antibodies: B, Rh
A-
62
antigens: B, Rh antibodies: A
B+
63
antigens: B antibodies: A, Rh
B-
64
antigens: A, B, Rh antibodies: none(universal recipient)
AB+
65
antigens: A, B antibodies: Rh
AB-
66
antigens: Rh antibodies: A, B
O+
67
antigens: none(universal donor) antibodies: A, B, Rh
O-
68
when the mom attacks the baby's blood at birth(mom=Rh-, baby=Rh+)
hemolytic disorders of the newborn(HDN)
69
Rh- mom and Rh+ 2nd baby
erythroblastosis fetalis
70
larger; contains a nucleus and other organelles; does not have hemoglobin; defends against pathogens, removes toxins and wastes, and destroys damaged/abnormal cells
WBCs/leukocytes
71
secretory vesicles and lysosomes
granules
72
WBCs that contain granules that can be seen with a microscope
granulocytes
73
WBCs that contain granules that are too small to be seen with a light microscope
agranulocytes
74
what are the 3 granulocytes?
neutrophils, eosinophils, and basophils
75
what are the 2 agranulocytes?
monocytes and lymphocytes
76
about how many WBCs are in circulation per mL?
6000-9000
77
what are the 4 characteristics of WBCs?
-amoeboid movement -diapedesis -positive chemotaxis -phagocytosis
78
-50%-70% of circulating WBCs -granules are chemically neutral and difficult to stain -dense nucleus with 2-5 lobes looking like beads on a string -1st to arrive at an injury site -phagocyte(specializes in attacking bacteria) -lifespan is 10 hrs -engulf 1-2 dozen bacteria, dies, and releases chemicals to attract other ______________ to the site
neutrophils
79
-granules stain with red dye -2%-4% of circulating WBCs -similar in size to neutrophils -red color and 2-lobed nucleus -attack objects coated with antibodies -primarily attack by performing exocytosis with nitric oxide and cytotoxic enzymes that deteriorate but will also engulf the antibody marked bacteria, protezea
eosinophils
80
-numerous granules that stain purple/blue -smaller than neutrophils or eosinophils -less than 1% of circulating WBCs -migrate to injury site and release heparin and/or histamine and attract more eosinophils and ______________ to the site
basophils
81
-largest WBC -nucleus is largest and oval or kidney bean shaped -2%-8% of circulating WBCs -release chemicals that attract or stimulate other neutrophils, _____________, or phagocytes and bring fibroblasts to that area to from scar tissue -can become either free or fixed macrophages
monocytes
82
-large and contain a very large nucleus -20%-30% of circulating WBCs -migrate from bloodstream-->tissue-->bloodstream -no phagocytes(use perforin or antibodies) -protect against specific pathogens -produced in bone marrow and lymphoid tissues(only WBC produced outside of this)
lymphocytes
83
chemical that prevents blood clotting
heparin
84
chemical that inflames tissue surrounding a cut
histamine
85
macrophages that migrate and are very active; take on pathogens 2x its size
free macrophages
86
macrophages stationed in connective tissue
fixed macrophages
87
number of WBCs found in blood smear; determines a variety of infections, inflammatory, and allergic reactions
differential count
88
low number of WBCs
leukopenia
89
high number of WBCs
leukocytosis
90
indicated by extreme leukocytosis; cancer of blood-forming tissues; also have abnormal/immature WBCs in blood; fatal unless treated
leukemia
91
a group of 4(so far) hormones used to control all WBCs except lymphocytes
CSF(colony-stimulating factor)
92
what controls lymphocytes?
exposure to antigens
93
formed by megakaryocytes (pockets of cytosol that start the clotting process); lifespan of about 9-12 days; destroyed by phagocytes if not used
platelets
94
number of platelets is too low; caused by internal bleeding
thrombocytopenia
95
number of platelets is too high; caused by bone cancer or infection
thrombocytosis
96
maintenance of constant blood vessels; used with blood loss; has 3 stages
hemostasis
97
what are the 3 stages of hemostasis?
-vascular stage -platelet phase -clotting process
98
innermost layer of blood vessel is simple squamous and 2nd layer is smooth muscle; cut=bleeding; smooth muscle does vascular spasms for about 20-30 mins, this closes the damaged opening of the blood vessel; damaged simple squamous releases sticky substances
vascular stage
99
platelets release 2 substances(another sticky substance that brings in other platelets, which also releases sticky substances: platelet plug OR chemicals that stimulate clotting process)
platelet phase
100
uses 11 or 12 clotting proteins; clotting factor-->activates 1st plasma protein-->2nd-->eventually get to Factor X(10th; prothrombinase)--> 11th(thrombin; activates 12th)--> 12th(fibrinogen which turns into fibrin)
clotting process
101
web-like protein forming in clot
fibrin
102
pathway in which the clot is formed from the inside of the wall of the blood vessel outward(until next pathway)
intrinsic pathway
103
pathway in which clot is formed from the outside of the blood vessel wall toward the blood vessel wall
extrinsic pathway
104
what is the main function of thrombin?
activates another enzyme that dissolves the clot
105
the inability to form clots
hemophilia
106
what are the 2 requirements to clot blood?
-clotting proteins -Ca+2 and Vitamin K