Respiratory System Study Guide - TBL #2 Practice Flashcards

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These flashcards cover the key concepts of the respiratory system including anatomy, mechanics, gas exchange, and pathology as outlined in the TBL #2 Study Guide.

Last updated 5:22 AM on 6/18/26
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307 Terms

1
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What generations of the airway tree constitute the conducting zone?

Generations 0160-16

2
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Which structures are included in the conducting zone?

Trachea, bronchi, bronchioles, and terminal bronchioles

3
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What are the primary functions of the conducting zone?

Warms, humidifies, and filters air, but does not participate in gas exchange

4
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What is the typical volume of the anatomic dead space?

About 150mL150\,mL

5
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What generations of the airway tree constitute the respiratory zone?

Generations 172317-23

6
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Which structures make up the respiratory zone (acinus)?

Respiratory bronchioles, alveolar ducts, and alveoli

7
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Which structure marks the end of the conducting zone?

Terminal bronchioles

8
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Which structure marks the start of the respiratory zone?

Respiratory bronchioles

9
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What type of epithelium is found in the conducting zone?

Pseudostratified ciliated columnar epithelium, which becomes cuboidal near terminal bronchioles

10
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What type of epithelium is found in the alveoli?

Simple squamous epithelium

11
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Where does smooth muscle end in the airway tree?

At the terminal bronchioles

12
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Up to which point is cartilage present in the airway tree?

Through the bronchi

13
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What are the stem cells of the conducting zone?

Basal cells and club (Clara) cells

14
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Which cells in the conducting zone secrete mucus?

Goblet cells

15
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What percentage of the alveolar surface is covered by Type I pneumocytes?

97%97\%

16
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What are the functions of Type II pneumocytes?

Produce surfactant and act as stem cells

17
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What is the role of alveolar macrophages?

Phagocytosis of debris in the alveoli

18
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What is the mucociliary escalator?

The process of filtration via mucus and cilia to clear the airways

19
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What genetic mutation causes cystic fibrosis?

Mutation in the CFTRCFTR (cystic fibrosis transmembrane conductance regulator) gene

20
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What is the inheritance pattern of cystic fibrosis?

Autosomal recessive

21
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What electrolyte imbalance occurs in the mucus of CF patients?

Chloride cannot exit cells, pulling sodium and water in and thickening the mucus

22
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Which drug is mentioned as a treatment for CF that reopens chloride channels?

IvacaftorIvacaftor

23
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What is the underlying defect in Kartagener syndrome?

A dynein arm defect causing immotile cilia

24
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What are the clinical signs of Kartagener syndrome?

Chronic sinusitis, bronchiectasis, infertility, and situs inversus

25
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Why does Kartagener syndrome cause situs inversus?

Cilia normally direct organ lateralization in the embryo

26
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Is inspiration active or passive at rest?

Active (requires ATPATP)

27
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Is expiration active or passive at rest?

Passive (driven by elastic recoil)

28
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What is the primary muscle of inspiration, and what is its nerve supply?

The diaphragm, supplied by phrenic nerve roots C3C5C3-C5

29
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Which muscles are involved in primary inspiration?

Diaphragm and external intercostals

30
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Which muscles are used for forced or labored inspiration?

Sternocleidomastoid and scalenes

31
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Which muscles are used for forced expiration?

Internal intercostals, rectus abdominis, and transverse abdominis

32
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What is the mnemonic for the phrenic nerve roots?

C3,4,5 keep the diaphragm aliveC3, 4, 5\text{ keep the diaphragm alive}

33
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What do atmospheric, alveolar, and intrapleural pressures represent?

Atmospheric = zero reference; Alveolar = inside alveoli; Intrapleural = in pleural space (normally negative)

34
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What is the formula for transpulmonary pressure (TPP)?

TPP=Alveolar pressureIntrapleural pressureTPP = \text{Alveolar pressure} - \text{Intrapleural pressure}

35
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What happens if the transpulmonary pressure becomes zero or negative?

The lung collapses (atelectasis)

36
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According to Boyle's law, what is the relationship between pressure and volume?

P1×V1=P2×V2P_1 \times V_1 = P_2 \times V_2

37
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What happens to intrapleural pressure during inspiration?

It becomes more negative

38
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During inspiration, how does alveolar pressure change before air flows in?

Alveolar volume rises, causing alveolar pressure to drop below atmospheric pressure

39
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During what activities can intrapleural pressure become positive?

Coughing, sneezing, vomiting, and straining

40
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What is Functional Residual Capacity (FRC)?

The resting end-expiratory point where inward lung elastic recoil balances outward chest wall spring

41
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At what point is pulmonary vascular resistance (PVR) at its minimum?

At functional residual capacity (FRC)

42
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What is the equation for Minute Ventilation (V˙E\dot{V}_E)?

V˙E=VT×RR\dot{V}_E = VT \times RR

43
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What is the equation for Alveolar Ventilation (V˙A\dot{V}_A)?

V˙A=(VTVD)×RR\dot{V}_A = (VT - VD) \times RR

44
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What are the normal values for Respiratory Rate (RR) and Tidal Volume (VT)?

RR=1220 breaths/minRR = 12-20\text{ breaths/min}; VT500mL/breathVT \approx 500\,mL/breath (or 68mL/kg6-8\,mL/kg)

45
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What is the difference between minute ventilation and alveolar ventilation?

Minute ventilation includes dead space air, while alveolar ventilation only counts air contributing to gas exchange

46
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What is the definition of Compliance (C)?

C=ΔVΔPC = \frac{\Delta V}{\Delta P}

47
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How does surfactant affect lung compliance?

Surfactant increases compliance by reducing surface tension

48
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What is the normal compliance value for the combined lung and chest wall system?

0.13L/cmH2O0.13\,L/cmH_2O

49
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What is the normal compliance value for the lungs alone?

0.22L/cmH2O0.22\,L/cmH_2O

50
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Conditions like emphysema and normal aging cause what change in compliance?

Increased compliance (easier to fill, less elastic recoil)

51
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Conditions like pulmonary fibrosis, pneumonia, and ARDS cause what change in compliance?

Decreased compliance (stiffer lung, harder to fill)

52
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What is hysteresis in respiratory physiology?

The difference in the pressure-volume curve between inflation and deflation of the same breath

53
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Why is inflating the lung harder than deflating it?

More pressure is needed to overcome alveolar surface tension at the start of inspiration

54
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In an obstructive disease like emphysema, what happens to the slope of the compliance curve?

The slope becomes steeper (abnormally high compliance)

55
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In a restrictive disease like fibrosis, what happens to the slope of the compliance curve?

The slope becomes flatter (abnormally low compliance)

56
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What is the primary component of surfactant?

Dipalmitoylphosphatidylcholine (DPPCDPPC)

57
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When do Type II pneumocytes begin secreting surfactant, and when are mature levels reached?

Starting around 2022 weeks20-22\text{ weeks}; mature levels by 35 weeks\approx 35\text{ weeks} gestation

58
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Which hormones stimulate surfactant synthesis?

Cortisol, thyroxine, and prolactin

59
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Which hormone inhibits surfactant synthesis?

Insulin

60
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What is the Law of Laplace for a sphere (alveolus)?

Collapsing pressure=2×Surface tensionRadius\text{Collapsing pressure} = \frac{2 \times \text{Surface tension}}{\text{Radius}}

61
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Why do smaller alveoli have a higher tendency to collapse?

Smaller radius leads to a higher collapsing pressure for a given surface tension

62
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What causes Neonatal Respiratory Distress Syndrome (NRDS)?

Surfactant deficiency leading to high surface tension and alveolar collapse

63
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What is the classic finding on a chest X-ray for NRDS?

Ground-glass appearance

64
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Why are infants of diabetic mothers at higher risk for NRDS?

High fetal insulin suppresses surfactant production

65
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What amiotic fluid screening test predicts NRDS?

Lecithin/sphingomyelinLecithin/sphingomyelin (L/SL/S) ratio; <1.5<1.5 predicts NRDS (2\ge 2 is reassuring)

66
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What is the prenatal treatment to prevent NRDS?

Maternal glucocorticoids (e.g., betamethasone, dexamethasone)

67
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What are the complications of high supplemental oxygen in newborns (RIB mnemonic)?

Retinopathy of prematurity, Intraventricular hemorrhage, and Bronchopulmonary dysplasia

68
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What is the basic equation for Airflow (Q˙\dot{Q})?

Q˙=ΔPR\dot{Q} = \frac{\Delta P}{R}

69
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What is Poiseuille's Law for airway resistance (R)?

R=8×η×lπ×r4R = \frac{8 \times \eta \times l}{\pi \times r^4}

70
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By what factor does resistance drop if the airway radius doubles?

A factor of 1616 (242^4)

71
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Where in the airway tree is resistance highest?

In the medium-sized bronchi

72
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Why is resistance low in the terminal bronchioles?

Because they are arranged in parallel, which lowers total combined resistance

73
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How does mean arterial pressure compare between the pulmonary and systemic circulations?

Pulmonary is low pressure (15mmHg\approx 15\,mmHg); systemic is high pressure (90100mmHg\approx 90-100\,mmHg)

74
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What is the pulmonary vascular response to hypoxia?

Vasoconstriction (hypoxic pulmonary vasoconstriction)

75
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What is the systemic vascular response to hypoxia?

Vasodilation

76
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What is the adaptive purpose of hypoxic pulmonary vasoconstriction?

It redirects blood away from poorly ventilated alveoli toward better-ventilated ones to optimize V/Q matching

77
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What can chronic hypoxic vasoconstriction lead to?

Pulmonary hypertension and right heart strain (cor pulmonale)

78
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Where in the brainstem is the automatic breathing rhythm generated?

Medulla oblongata

79
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What is the function of the dorsal respiratory group (DRG)?

Sets the basic inspiratory rhythm and receives sensory input via CN IX and CN X

80
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When is the ventral respiratory group (VRG) activated?

During forced inspiration and forced (active) expiration

81
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What is the role of the pneumotaxic center in the pons?

Inhibits inspiration and limits tidal volume, speeding the rate

82
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What is the role of the apneustic center in the pons?

Promotes inspiration and prolongs inspiratory bursts

83
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Where are central chemoreceptors located, and what is their primary stimulus?

Ventral surface of the medulla; stimulated by H+H^+ in the CSF (driven by CO2CO_2)

84
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Where are peripheral chemoreceptors located?

Carotid bodies (carotid bifurcation) and aortic bodies (aortic arch)

85
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What is the primary stimulus for peripheral chemoreceptors?

Decreased PaO2PaO_2 (especially below 60mmHg60\,mmHg)

86
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Which nerves carry afferent signals from the carotid and aortic bodies?

CNIXCN\,IX (carotid bodies) and CNXCN\,X (aortic bodies)

87
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Why should you be cautious giving high supplemental oxygen to chronic CO2CO_2 retainers?

It can blunt their hypoxic drive, which has become their dominant stimulus for breathing

88
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What is the Hering-Breuer reflex?

A protective stretch reflex where airway receptors inhibit inspiration to prevent over-distension

89
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Describe Kussmaul breathing and its typical cause.

Deep, rapid, labored breathing; caused by severe metabolic acidosis (e.g., DKA)

90
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Describe Cheyne-Stokes breathing.

Cyclic crescendo-decrescendo pattern alternating with apnea

91
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What are typical causes of Cheyne-Stokes breathing?

Central sleep apnea, congestive heart failure, and CNS injury

92
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Describe Biot (ataxic) breathing and its significance.

Irregular, unpredictable breaths with apnea; indicates severe brainstem/medullary damage

93
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Which lung volume cannot be measured by spirometry?

Residual Volume (RVRV)

94
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What is Inspiratory Capacity (IC) composed of?

IC=IRV+VTIC = IRV + VT

95
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What is Functional Residual Capacity (FRC) composed of?

FRC=RV+ERVFRC = RV + ERV

96
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What is Vital Capacity (VC) composed of?

VC=IRV+VT+ERVVC = IRV + VT + ERV

97
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What is the formula for Total Lung Capacity (TLC)?

TLC=VC+RVTLC = VC + RV (or IRV+VT+ERV+RVIRV + VT + ERV + RV)

98
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What is a normal FEV1/FVC ratio?

7080%70-80\%

99
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In obstructive disease, what happens to the FEV1/FVC ratio?

It decreases (<70%<70\%)

100
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In restrictive disease, what happens to the FEV1/FVC ratio?

It is normal or increased (70%\ge 70\%)