Respiratory System and Gas Exchange - Karius/Cole Flashcards

(50 cards)

1
Q

what comprises the conducting portion?

what is its function?

A

nasal cavity, nasopharynx, trachea, bronchi, bronchioles, and terminal bronchioles

carry air to and from gas exchange site

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2
Q

what is the fx of respiratory portion?

where is it located?

A

gas exchange occurs here

from respiratory bronchioles to alveoli

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3
Q

what is the function of the nasal cavity and paranasal sinuses?

A

warm and moisten air

filter dust particles in air

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4
Q

what kind of tissue is the respiratory portion lined with?

A

pseudostratified ciliated epithelium w/goblet cells

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5
Q

how is incoming air warmed?

A

by blood in venous plexus

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6
Q

what creates turbulence to help warm and moisten air?

A

sup., mid., and inf., conchae

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7
Q

what type of tissue are paranasal sinuses lined by?

A

thin pseudostratified columnar ciliated epithelium with few goblet cells

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8
Q

what is part of the lamina propria of the respiratory system?

A
made of loose CT
SECS Best
seromucous glands
elastic fibers
cartilage
smooth m. 
bone
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9
Q

what is the respiratory epithelium made of?

A

ciliated columnar cells

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10
Q

what special features located here?

A

mucins - hydrophobic glycoproteins that make mucus

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11
Q

what makes airway mucus?

A

goblet cells
clara cells
serous cells of submucosal glands

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12
Q

what does mucus contain?

A
mucins
antimicrobial molecules (LID - lysozyme, IgA, defensins)
immunomodulatory molecules (secretoglobin and cytokines)
protective molecules (trefoil proteins and heregulin)
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13
Q

what layers is airway mucus made of?

A

pericilliary layer

mucus gel layer atop the periciliiary layer

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14
Q

what is cystic fibrosis?

what is the defect?

A

abnormally thick mucus in respiratory and gi tracts

CFTR gene, results in defective Cl- transport and INC Na+ absorption

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15
Q

what is the clinical presentation of cystic fibrosis?

A

cough, purulent secretions, dyspnea

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16
Q

where do bronchial carcinoid tumors arise from?

A

basal and NE cells (of Kulchitsky)

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17
Q

what does the epithelium change to in smokers?

A

changes TO stratified squamous
dec. in ciliated columnar cells
INC in goblet cells

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18
Q

what does the fibroelastic ligament do?

made of what?

A

prevents overdistension of the lumen

collage and elastic fibers

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19
Q

what does the trachealis m. do?

A

smooth m. that results in narrowing during cough reflex

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20
Q

where is BALT located?

A

wall of intrapulmonary bronchus

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21
Q

what is asthma characterized by?

A

reversible bronchoconstriction of the smooth m. bundles

reduction in the lumen of the airways

22
Q

what is a pulmonary lobule?

A

terminal bronchiole and assoc. regions of pulmonary tissues that it supplies

23
Q

what are clara cells?

what do they secrete?

A

epithelial cells w/dome-shaped apical domain that lacks cilia

surfactant

24
Q

what happens after an airway injury?

via what enzymes?

A

club cells proliferate and migrate to replenish alveolar epithelial cells (alveolar bronchiolization)

cytochrome P-450 enzymes (CYP4B1)

25
what structures are examples of anatomic dead space?
trachea | bronchi
26
what is alveolar dead space?
alveoli that do not participate in gas exchange | alveoli gets air but NO BLOOD
27
what is physiological dead space?
alveolar + anatomical
28
what kind of epithelium line alveoli?
simple squamous
29
what is the normal resting V/Q ration?
0.8
30
diffusion rate equation | J= ?
J = surface area x Diffusion coeffecient x (P1 - P2) DIVIDED by distance
31
under normal resting conditions how much O2 and CO2 is exchanged every minute?
250 ml O2 200 ml CO2
32
what are alveoli separated by?
interalveolar septa w/2 simple squamous epithelial layers with an interstitium bw them
33
what are the characteristics of type I alveolar cells?
make up 90% of surface area only 40% of cell population make up the cell wall (pneumocytes)
34
what do type II alveolar cells produce? where are they located?
surfactant at the angles formed by adjacent alveolar septa
35
what are macrophages called in the alveoli?
dust cells
36
where do dust cells migrate? where are they transported to?
bronchi pharynx
37
what are dust cells called in CHF?
heart failure cells | LV fails to keep pace with venous return from lungs
38
neutrophils release elastase, what does this do?
kills elastic tissue, less elastic tissue present and thus the walls enlarge
39
what blocks the neutralizes the release of elastase?
serum alpha-1 antitrypsin
40
what is emphysema caused by?
permanent enlargement of the air spaces distal to terminal bronchioles
41
what does the blood-air barrier contain?
cytoplasm of squamous epithelial cells (type I alveolar) fused basal lamina of type I alveolar and capillary endothelial cells cytoplasm of capillary endothelial
42
what is included in the diffusion distance? what is an avg amount?
fluid layer alveolar epithelium interstitial space blood vessel wall 0.6 microns
43
what is ARDS?
form of pulmonary edema that causes respiratory failure resulting from INC. permeability of alveolocapillary membrane INC in Cp or damage to alveolar epithelial lining due to endotoxins or trauma
44
what does the diffusion coefficient depend on?
solubility of the gas in water (O2 less soluble than CO2) | molecular weight of the gas (CO2 heavier than O2)
45
what does DL O2 equal? what is normal at resting conditions?
1.23 x DL CO 21
46
what is DL CO2 at rest?
400
47
what is LaPlace's Law?
P = 2T/r
48
what is the effect of surfactant in the alveolus?
DEC T, so there is no Pressure gradient for air
49
What is neonatal respiratory distress syndrome?
baby lungs are unable to make surfactant | common in infants born before 25-26 weeks
50
What are the 3 respiratory system portions?
air-conduction respiratory mechanism of ventilation