Review of pulmonary physiology Flashcards

1
Q

Main function of Lungs

A

continuous gas exchange

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2
Q

Metabolic function of Lungs

A

Angiotensis I -> Angiotensin II

Removal of amines, arachidonic acid metabolites

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3
Q

Metabolic function (PEPTIDES)

A

Angiotensin I - converted
Angiotensin II
Vasopressin
Bradykinin - 80% inactivated

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4
Q

Metabolic function (Amines)

A

Serotonin - completely removed
Norepinephrine - 30% removed
Histamine
Dopamine

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5
Q

Metabolic function (Arachidonic acid metabolites)

A

PG E2 and F2 - almost completely removed
PG A2
Prostacyclin
Leukotrienes - almost completely removed

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6
Q

start of lung development

A

5th week AOG (Arise from ventral wall of the foregut)

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7
Q

Level of Carina

A

T5 at expiration and T6 in inspiration

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8
Q

Main bronchus that is prone to aspiration

A

RIGHT

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9
Q

Boundary of Upper and Lower

A

Adults - vocal cords

pediatrics - cricoid cartilage

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10
Q

T or F, Lower respiratory tract is sterile

A

False

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11
Q

Boundaries of pleura and lungs ANTERIORLY

A

clavicle to 8th rib

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12
Q

Boundaries of pleura and lungs LATERALLY

A

10th rib l

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13
Q

Boundaries of pleura and lungs Posteriorly

A

level of T12

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14
Q

ANTERIOR CHEST WALL (PE)

A

R Lung - UPPER and MIDDLE LOBE

L Lung - UPPER LOBE

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15
Q

Type of airflow in conducting zone

A

bulk flow

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16
Q

Type of airflow in respiratory zone

A

diffusion

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17
Q

volume of anatomic dead space

A

150 ml

no gas exchange

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18
Q

ADS + alveolar dead space

A

Physiologic dead space

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19
Q

Overall volume that do not participate in ventilation

A

Physiologic dead Space

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20
Q

Areas with ventilation but poor perfusion

A

alveolar dead space

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21
Q

Chief sites of greatest resistance

A

Medium sized bronchi

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22
Q

Part of the conducting zone where glands and cartilage first disappear

A

bronchioles

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23
Q

cuboidal, non ciliated, secrete surfactants and GAGs

A

Clara cells

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24
Q

site of gas exchange due to the presence of alveoli

A

RESPIRATORY ZONE

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25
Most of the lung volume is in the?
Respiratory zone - 3 L
26
volume that is inhaled and then exhaled with each normal breathing
Tidal volume -500ml
27
The maximum volume that can be exhaled from the resting end-expiratory level
ERV- 1100ml
28
The maximum volume that can beinhaled above a normal tidal inspiration
IRV - 3000ml
29
Volume remaining in lungs after maximum expiration (cannot be measured by spirometry)
RV - 1200ml
30
Maximum volume that can be inhaled from normal resting end-expiratory level
Inspiratory capacity - 3500ml
31
Volume remaining in lungs during regular breathing
Functional residual capacity
32
Maximum volume that may be exhaled following a maximum insiration or inhaled following a maximum expiration
Vital Capacity
33
Formula for Vital capacity
TLC - RV
34
Volume contained within the lungs following maximum inspiration
5800ml
35
Normal pulmonary capillary blood flow
70ml
36
Histology of bronchi
ciliated pseudostratfied columnar
37
Histology of bronchioles
cuboidal
38
Histology of alveoli
squamous
39
Ratio between thickness of submucosal mucus glands and wall thickness between epithelium and cartilage that covers the bronchi
REID index Normal : <0.4 Chronic bronchitis >0.4
40
Innervation of smooth muscle in the airway
parasympathetic
41
Type of receptor predominantly found in the airway
beta 2
42
Primary determinant of resting bronchomotor tone
cholinergic system
43
Decreases vagal tone
M1 and M3
44
autoinhibitory effect on acetylcholine release and have negative inhibitory effect
M2 receptor
45
Normal ciliary beating
12-15/sec
46
Bronchial glands
terminal bronchioles Parasympathetic control
47
Gel layer
Mucin +lipids
48
Sol layer
water + electrolytes
49
Liquid in Sol layer Regulation
Na channel cAMP mediated Cl channel cystic fibrosis transmembrane conductance regulator Ca activated CL channel
50
Cystic fibrosis
defective CFTR sweat gland test
51
Secretes glycosaminoglycans to protect bronchial lining
clara cells
52
Blood gas barrier
0.3-0.4 micron
53
Type I cells
flattend; forms 95% of alveolar wall
54
Type II cells
cuboidal, secretes surfactants (cytosomes) moremetabolically active
55
SUrfactants
Phospholipid Dipalmitoyl Phosphatidyl Choline
56
multilamellar bodies, precursors to pulmonary surfactants
cytosomes
57
Laplace Law
lager SA, smaller surface tension
58
Compliance
P/V
59
normal lung compliance =
0.15/L cm H2O
60
Compliance differ on inspiration and expiration for identical volumes
Hysteresis
61
Keeps airsacs open even in maximum exhalation
hysteresis
62
Lung is stiffer during?
inflation
63
Emphysema = high or Low compliance
High (decreased elastic recoil)
64
Fibrosis = high or Low compliance
LOW
65
point where pressure outside the airways and pressure inside the airways are equal
Equal pressure point
66
formula for Alveolar Pressure (Palv)
Pleural Pressure (Ppl) + Elastic Pressure (Pel)
67
When you inhale = more positive or negative?
more negative
68
Exhalation is an active or a passive process?
Passive
69
FEV1/FVC ratio of restrictive pathology
PRESERVED
70
FEV1/FVC ratio of Obstructive pathology
LOWE
71
Physiological attributes of COPD
airway obstruction + low elastic recoil
72
Trapped air due to inability to expel right amount
HYPERINFLATION
73
Dynamic hyperinflation
Unmasked during exercise Increased RR More aair trapped
74
SPace that lies between the epithelial basement membrane and the vascular basement membrane
Interstitium
75
Architectural framework of the lung
Interstitium
76
Cellular components of interstitium
Macrophages Mesenchymal cells Lympocytes
77
Major component of the EC matrix of interstitium
Collagen IV
78
Controls porosity of interstitium
Perlecan
79
Controls rigidity of interstitium
Hyaluronan
80
Diameter of alveolo-capillary membrane
10 um
81
time for oxgenation of each RBC
0.75 secs
82
Law governing diffusion of oxygen and carbon dioxide
Fick's law
83
Solubillity of CO2
20x than oxygen
84
Blood supply
Pulmonary arteries and veins
85
Flow of blood to thelungs/pulmonary capillaries
Perfusion (Q)
86
Flow of air into alveolar spaces
Ventilation (V)
87
More perfusion more ventilation (lobe of lung)
Lower lungs
88
Ventilation is greater where?
base due to lower interpleural pressure
89
At the upper lungs (Ventilation is __ compared to perfusion)
HIGHER
90
Bad ventilation, good perfusion
SHUNT
91
good ventilation, bad perfusion
Dead space
92
PULMONARY VS SYSTEMIC
Lower pressure in pulmonary Higher capacitance in pulmonary Less resistance in pulmonary
93
Most potent vasoconstrictor
Oxygen (hypoxemia)
94
Normal PaO2 sustainable for life?
60 mmHg
95
Increased O2 affinity, decreased O2 release
Shift to the LEft
96
Decreased O2 affinity, Increased O2 release
Shift to the right
97
Where do bleeding from hemoptysis comes from?
bronchial circulation
98
Central respiratory center
Medulla oblongata
99
Peripheral chemoreceptors
located in carotid artery and aortic arch bifurcation | Connected to the medulla via glossopharyngeal and vagus nerve
100
5 mechanisms causing hypoxemia
1. Low inspired O2 2. V/Q mismatch 3. Shunting 4. Decrease in diffusing capacity 5. Hypoventilation
101
hallmark of alveolar hypoventilation
paCO2 always increased
102
hallmark of Shunt
Hypoxemia is refractory to supplemental oxygen
103
ARDS
``` All the air sacs are filled with liquid Not able to ventilate NOT a vascular shunt No VENTILATION BUT PERFUSION CONTINUES Physiologic dead space is increased ```