exam 1 Flashcards

1
Q

plasma membrane make up

A

lipid bilayer
hydrophobic ends oriented inward
hydrophilic ends oriented outward

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2
Q

constituents of plasma membrane

A

phospholipids
glycolipids
cholesterol

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3
Q

what will freely pass through cell membrane

A

hydrophobic (lipophilic)

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4
Q

secondary transport: symport

A

when the second substance being moved goes in the same direction

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5
Q

secondary transport: antiport

A

when the second substance being moved goes in the opposite direction

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6
Q

G protein coupled receptors

A

interact with other membrane bound proteins that activate second messenger systems. Initiate transduction pathways

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7
Q

protein kinase

A

enzyme catalyzing the transfer of phosphate to from ATP to a protein substrate.

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8
Q

uncontrolled entry of calcium into cytosol

A

destructive agent
activates enzymes
important final pathway in many causes of cell death.

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9
Q

increased capillary hydrostatic pressure

A

venous obstruction
Na and water retention
heart failure
- fluids move into tissue

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10
Q

decreased capillary oncotic pressure

A

decrease production of plasma proteins

  • cirrhosis
  • malnutrition
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11
Q

Increased tissue oncotic pressure

A

related to increased capillary permeability
- proteins move into tissues
burns
allergic inflammation reactions

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12
Q

lymph obstruction

A

unable to move proteins out of interstitial fluid

  • tumor
  • parasites
  • removal of lymph nodes
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13
Q

pernicious anemia s/s

A

cognitive dysfunction
paresthesias of feet and hands
wt loss
nerve degeneration

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14
Q

iron deficiency anemia s/s

A
pallor
weakness/fatigue
palpitations
irritability
headaches
pica
spoon-shaped nails
blue sclerae
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15
Q

thalassemia major

A
bone deformities
bowing  of long bones
icterus
hepatomegaly
spleenomegaly
cardiac failure
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16
Q

Thalessema intermeda

A

deforming b one and joint disease

chronic leg ulcerations

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17
Q

acute blood loss anemia s/s

A

tachycardia with exercise
postural drop in BP
cold clammy skin

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18
Q

HIT

A

heparin induced thromobcytopenia

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19
Q

ITP

A

immune/idiopathic thrombocytopenia
increased platelet destruction (autoimmune)
can be seen after an illness

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20
Q

transfusion and platelets

A

platelets degrade in stored blood after 24 hours so when transfused there is no platelets; dilution

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21
Q

endothelial cells and platelets

A

endothelial cells prevent adhesion by releasing nitric oxide and prostaglandin I2 which increases platelet cGMP and cAMP -> decrease in activation of platelets.

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22
Q

antibodies at birth

A

maternal IgG: will be gone around 10 months

small amounts of fetal IgA and IgM

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23
Q

antibodies at 6 months of age

A

fetal IgG, IgA, IgM

declining maternal IgG

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24
Q

mother and baby with different blood types

A

Fc receptor on placenta only lets IgG antibodies through.
IgG attacks Rh factor
IgM attacks ABO factor

25
chorioamnionitis
infection from mother passes to fetus | potential for preterm labor and sick baby
26
bradykinin
responsible for pain in the inflammatory process.
27
kinin and platelet systems linked by
C1 complement
28
nonspecific immunity
first and second line of defense
29
first line of defense immunity
``` chemical barriers -GI lining -Tears mechanical barriers - skin reflexes - coughing - sneezing ```
30
innate immunity
born with it fast and non-specific myeloid cells and NK-cells
31
adaptive immunity
specific: developed cells | B-cells, antibodies, T-cells
32
humoral immunity
humors= body fluids myeloid cells B-cells, antibodies, helper-T cells
33
Cell-mediated immunity
does not involve antibodies NK-cells cytotoxic T cells
34
neutrophils and inflammation
first to arrive after injury
35
monocytes/macrophages and inflammation
phagocytosis
36
eosinophils and inflammation
respond to parasitic and allergic | release inflammatory cytokines
37
basophils
release histamine | allergic and hypersensitivity
38
immature neutrophils
bands
39
MHC1 found on
nucleated cells
40
variable region on antibody
allows for specificity of an antibody mediated response
41
hallmarks of inflammation
swelling pain heat redness
42
What activates the classical cascade
Ab-Ag complexes | - Factor X
43
What activates the lectin pathway
Binding of lectin | - C1
44
what activates the alternative patheway
foreign material | -C3b protein
45
generation of clonal diversity
born with specificity in utero | - lymphocytes are differentiated in utero
46
clonal selection
allows identification of antigens
47
Fungal infections are controlled by
phagocytes and T lymphocytes
48
systemic fugal infections are difficult to treat because
``` similar to body cells - Rx attacks host cell as well thick, rigid cell wall composed of polysaccarides - resistant to Tx Evasion of immune system ```
49
protein C and S are
anti-thrombotic
50
synthesis of coagulation factors occures
in the liver
51
All coagulation factors with exception of factor III circulate in blood stream inactively T/F
True
52
heparin inactivates
thrombin and factor X
53
fibinolysis occurs in response to
plasmin
54
CNS symptoms in acute leukemia are due to
cerebral bleeding
55
oncogenic activation can result from a mutated gene coding for
growth factor signaling enzymes transcription factors
56
non disjuntion chromosome mutations
``` down syndrome (21) edward syndrom (18) patau (13) ```
57
sex chromosome disorders
turner (45:x) | klinefelter (XXXXY or XXY)
58
deletion of chromosomes
cri du chat (deletion of part of 5)