Exam #3: Respiratory Physiology Flashcards

1
Q

What does the brain sense in controlling respiratory drive?

A
The respiratory centers in the medulla sense the arterial partial pressure of: 
- O2 
- CO2 
and 
- pH

Note that these gases must be DISSOLVED to exert partial pressure & not conjugated

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2
Q

What are the functions of the respiratory system?

A
  • Gas exchange
  • Acid-Base Balance
  • Phonation
  • Defense mechanisms (alveolar macrophages)
  • Metabolism & handling of bioactive materails
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3
Q

What structures are included in the upper airway? What is the major function of the upper airway?

A

Everything from the nose to the vocal cords, including the sinuses

Conditioning of inspired air i.e.

  • Warm
  • Humidify
  • Filter (larger than 10um)
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4
Q

What provides the majority of resistance in the upper airway? What happens when there is a URI?

A
  • The nose provides 50% of the resistance to air coming into the body
  • In URI, further increases in nasal resistance lead to mouth breathing when resistance is too high
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5
Q

Describe the branching of the airway from the trachea to the alveoli.

A
Trachea
Main stem bronchi 
Segmental bronchi 
Bronchioles 
Terminal Bronchioles 
Respiratory Bronchioles 
Alevolar ducts 
Alveolar sacs
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6
Q

Where do the alveoli start to appear?

A

After 16th generation; the terminal bronchioles are the smallest airways without alveoli

(Respiratory bronchioles DO have alveoli)

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7
Q

What is considered the conuducting portion of the airway? What is the respiratory portion of the airway?

A

The first 16 generations of the lung, including the terminal bronchioles; this is the portion of the airway that brings gas in but does NOT function in respiration

The last 7 generations of the lung that are directly involved in gas exchange are considered the respiratory portion

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8
Q

Which portions of the airway contain cartilage and which do not?

A
Cartilage= trachea & bronchi 
Non-cartilage= bronchioles & alveolar ducts
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9
Q

What is the main source of airway resistance in the lower respiratory tract? Why?

A

Bronchioles

NO cartilage

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10
Q

When does bronchiole constriction occur? How is it treated?

A

Asthma, COPD

B2 agonist (albuterol)

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11
Q

What are the structural properties of the alveoli?

A

NO cartilage
NO smooth muscle

Thin membrane that is involved in gas exchange

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12
Q

How is mucous production & clearance balanced?

A
  • Goblet cells & submucosal tracheobronchial glands produce mucous (PNS innervation mostly)
  • Ciliated epithelial cells push mucous upward
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13
Q

What is the function of mucous?

A

Smoother air inflow

Humidifation

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14
Q

What is the effect of PNS stimulation in the lung?

A

Mucous secretion

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15
Q

What enviornmental factors increase mucous production?

A

Smoke

Pollutants

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16
Q

What is periciliary fluid? What is the function of perciliary fluid?

A

Perciliary fluid is the fluid produced by ciliated epithelial cells, which is involved in:

1) Cl- secretion
2) Na+ absorption

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17
Q

Describe the pathophysiology of Cystic Fibrosis.

A

CFTR mutations lead to:

1) Abnormal Cl- secretion
2) Inability to absorb Na+

Net= Thick mucous

18
Q

What is the difference between Type 1 & 2 pneumocytes in the alveoli?

A

Type-1= structural “squamous lining cells”

  • Fewer in number
  • Account for 95% of the alveolar surface area

Type-2= surfactant producing or “granular pneumocytes”

19
Q

What is surfactant? What is the function of surfactant?

A

Surfactant= a protein & phospholipid substance that decreases surface tension to prevent alveoli collapse

20
Q

What is the respiratory unit? What is the function of the respiratory unit?

A

Terminal bronchiole
Alveolar ducts
Atria
Alveoli

This is the site of gas exchange

21
Q

What are pores of Kohn? What is the function of the pores of Kohn?

A
  • Pores between alveoli that provide inter-alveolar communication
  • Collateral ventilation

Note that bacteria can transmit through these pores

22
Q

How are capillaries associated with alveoli?

A

Each alveoli is wrapped around by roughly 500 capillaries–makes a “sheet of flow”

23
Q

What is the respiratory membrane?

A

The place between the alveoli & capillary where gas exchange occurs; it includes:

  • Alveolar epithelium
  • Epithelial basement membrane
  • Interstitial space
  • Capillary basement membrane
  • Capillary endothelium
24
Q

What lines the alveolar surface of the respiratory membrane?

A

Surfactant

25
Q

What pathological change in the respiratory membrane does pneumonia cause?

A

Increases fluid & bacteria on the alveolar side of the respiratory membrane

26
Q

What is a hallmark of COPD in the respiratory membrane?

A

Thickened epithelial basement membrane (alveolar basement membrane)

27
Q

Describe the pathophysiology of CHF at the level of the respiratory membrane.

A

Increased capillary hydrostatic pressure pushes fluid into the interstitial space–> increased thickness of the respiratory membrane & limits gas exchange

28
Q

What can damage the capillary basement membrane? What happens with damage to the capillary basement membrane?

A
  • Toxins

- Fluid creep into the interstitial fluid

29
Q

How can autoimmune disease disrupt the respiratory membrane?

A

Antibody complexes on the capillary side of the respiratory membrane

30
Q

Describe the composition of the lung interstitium.

A
Connective tissue 
Smooth muscle 
Lymphatics 
Capillaries 
Variety of other cells 

*Fibroblasts

31
Q

What is the function of fibroblasts in the interstitium?

A

Production of collagen & elastin, which provides the lung with distensibility & elastic recoil

32
Q

What is the function of the plerua?

A

Transmitting the negative pressure produced by the chest wall that allows for expansion of the lungs

33
Q

What are stomata?

A

Stomata are openings in the parietal pleura that serve as the exit point for pleural fluid that drains into the lymphatic system

34
Q

What produces most of the plerual fluid?

A

Parietal pleura contains systemic capillaries that extrude fluid into the pleural space

35
Q

Pathophysiology of pleural effusion.

A

Prevents negative pressure from allowing expansion of the lungs

36
Q

When is pleural effusion most commonly seen? What is the pathophysiology?

A

CHF causes increased pulmonary venous hydrostatic pressure that exudes fluid from the VISCERAL side into the pleural cavity

(i.e. from the pulmonary capillaries that are directly connected to the pulmonary veins that drain into the left atrium)

37
Q

In cases of hypoalbuminemia (CKD) how is pleural effusion caused?

A
  • Hypoalbuminemia (from kidney disease)causes a decrease in oncotic pressure of the systemic capillaries (pleural side)
  • This increases fluid movement OUT of the capillaries & into the pleural space
38
Q

How can decreased pleural pressure (atelectasis) cause pleural effusion? What causes atelectasis?

A
  • Block of alveoli leads to lobar collapse
  • Lobar collapse decreases pleural pressure so that it is MORE NEGATIVE
  • Fluid is pulled into the pleural space

E.g. Pneumonia, cancer

39
Q

How is pleural effusion caused by blockage of the lymphatic system?

A

Stoma cannot drain
Fluid builds in the pleural space

E.g. tumor

40
Q

What is the difference between Goblet cells & Submucosal tracheobronchial glands? How are these cells clinically related?

A

Goblet= mucous secreting cells that are increased in response to cigarette smoke

Submucosal tracheobronchial= normally present where there is cartilage & secrete mucous + serous fluid
- Increased in chronic bronchitis into the bronchioles

41
Q

Compare & contrast the parietal pleura to the visceral pleura.

A

Parietal pleura=

  • Stomata
  • Microvessels closer to pleural surface, which is why most of the pleural fluid comes from the parietal pleura
  • Systemic capillaries

Visceral pleura=

  • No stomata
  • Microvessels farther
  • Pulmonary capillaries