Respiratory Microanatomy Flashcards

(32 cards)

1
Q

What do the upper and lower airways consist of?

A

Upper: nasal cavity, pharynx, larynx
Lower: trachea, bronchi, bronchioles, respiratory bronchioles, alveolar ducts, alveolar sacs, alveoli

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2
Q

What do the conducting zone and respiratory zone consist?

A

Conducting: nasal cavity, pharynx, larynx, trachea, bronchi, bronchioles, terminal bronchioles
Respiratory zone: respiratory bronchioles, alveolar ducts, alveolar sacs, alveoli

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3
Q

Where are [pseudostratified columnar ciliated epithelium, goblet cells, club cells, Type I pneumocytes, Type II pneumocytes and macrophages] found in the airway and their functions?

A

P/s col. cil. epithelium + goblet cells: most of CZ- nasal cavity, nasopharynx, trachea, bronchi(large). Cilia–> move mucus, Goblet –> secrete mucus
Club cells (cuboidal): bronchioles. secrete watery substance with antimicrobial properties
Type I, II pneumocytes and macrophages: respiratory zone. I–> squamous, thin air-blood barrier, II- secrete surfactant

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4
Q

Where are [cartilage, elastic fibres, collagen and smooth muscles] found in the airways and their functions?

A

Cartilage: trachea, bronchi. –> keep airways open
Elastic fibres + collagen: EVERYWHERE –> ventilation
Smooth muscles: trachea- alveolar ducts –> control airflow through bronchioles

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5
Q

What are the two layers of the mucociliary escalator?

A

Gel layer on top and sol layer below

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6
Q

What does the respiratory epithelium consist of?

A

Pseudostratified columnar ciliated epithelium + goblet cells

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7
Q

Describe the features of pulmonary arteries and veins (size, pressure, location).

A

Pulmonary arteries are large vessels to conduct entire CO, they are low pressure (too high damage the lung?) vessels that run with the airway [ 30-10mmHg]
Pulmonary veins carry oxygenated blood, they have very low pressure (pressure gradient for blood flow) with no more than 3 layers of sm muscles, also they are loners that run with CT septa. [10-0mmHg]

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8
Q

How many generations of dichromatous branching are there in the lungs?

A

23 generations

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9
Q

What are the pores of Kohn?

A

Pores found in alveoli that connect alveoli

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10
Q

What are the embryological origin of lung airways, parenchyma and pleura?

A

Airways- endoderm

Parenchyma and pleura- mesoderm

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11
Q

What are the 5 stages of lung development and their time periods?

A
Embryonic  - 26 days- 7 weeks
Pseudoglandular - 5-17 weeks
canalicular - 16-26 weeks
saccular - 24 weeks to after birth
alveolar - late foetal to 21 years
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12
Q

What happens during embryonic stage?

A

The lung bud arises as a ventral outpouching of the foregut endoderm (from the primitive oesophagus). It grows downwards and undergoes three initial rounds of branching – producing the primordia of the two lungs (primary bronchi), the lung lobes (lobar bronchi) and the bronchopulmonary segments (segmental bronchi).

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13
Q

What happens during pseudoglandular stage?

A

The respiratory tree undergoes more generations of branching, with the formation of branches including more bronchi, bronchioles all the way down to the terminal bronchiole.

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14
Q

What happens during canalicular stage?

A

Each terminal bronchiole gives rise to two or more respiratory bronchioles. Each of these divides into 3-6 alveolar ducts, which are lined by cuboidal cells. These cells then start to become attenuated. This means they begin to flatten and become more squamous, as this is necessary for gas exchange. It is possible for some babies to survive at about 22-23 weeks if this attenuation is extensive enough.

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15
Q

What happens during saccular stage?

A

he alveolar ducts give rise to clusters of thin-walled terminal air sacs (primitive alveoli). The type I alveolar cells become intimately associated with blood (and lymph) capillaries. This means there is increasing contact between capillaries and alveoli. This connection is necessary for air to be able to move through into the capillaries and for exchange to occur. The type II alveolar cells also develop and begin to produce surfactant (but this is not at significant levels to reduce the work of breathing until around 32 weeks).

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16
Q

What happens during alveolar stage?

A

The number of terminal sacs increases. The alveoli mature through continued thinning of the squamous epithelial lining and establishment of more intimate contacts with the surrounding capillaries. So, development of the lungs continues after birth, with development occurring at the alveolar level. There are no new alveoli produced after about 3 years old, but the surface area may increase. There is secondary septation which occurs. This involves adding additional septa to the alveoli (increasing the number of walls) which greatly increases the surface area available for gas exchange. The alveoli also mature through continued thinning of the squamous epithelial lining and establishment of more intimate contacts with surrounding capillaries (through increased number of walls).

17
Q

What are the breathing characteristics of neonatal respiratory distress syndrome?

A
  • sucking in between the ribcage due very negative intrapleural pressure required to inflate the lungs.
  • increased work of breathing (breathing faster and harder) due to stiff lungs
  • rapid breathing due to thickened gas transfer tissue
  • less surfactant causing collapse of airways and further contribute to sitffness of lungs
    need intubation, ventilation and exogenous surfactant therapy
18
Q

What is chronic lung disease of prematurity/ bronchopulmonary dysplasia and their symptoms?

A

Abnormal development of airways - must breath harder and faster. Alveoli appear different due to inflammation adn scarring.
Symptoms: persistent increased work of breathing- indrawing of tissue between ribs and increased resp rate
abnormal cxr
requiring oxygen ventilation until 36 weeks for those under 32

19
Q

What are the autonomic control of pulmonary arterioles?

A

SNS- a-adrenoreceptors- vasoconstriction

PSNS- muscarinic- vasodilation

20
Q

what are the 5 factors that regulate diffusion of gas across tissue?

A
  • thickiness of tissue
  • solubility of gas
  • molecular weight of gas
  • partial pressure across tissue
  • area
21
Q

What factors create the Bohr’s shift? and which direction is the Bohr’s shift

A

shift the oxygen dissociation curve to the right (for a given PO2, lower affinity of Hb for O2 so more O2 released)
increased CO2, [H+}, temperature, DPG

22
Q

why do we need RBC rather than just Hb?

A
  • decrease blood viscosity
  • provide environment for DPG (helps unload O2)
  • encapsulate and concentrate carbonic anhydrase (for CO2 transport)
  • prevent Hb loss through filtration via kidney
  • concave shape helps pass through tight spaces
23
Q

What are the 4 ways CO2 are transported in blood?

A
  1. dissolved in solution
  2. exist as HCO3- (60% in plasma)
  3. combined to amine group (esp Hg)
  4. As H2CO3 and CO32-
24
Q

What is the Haldene effect for CO2 dissociation curve?

A

The Haldene effect is about how the affinity for CO2 by venous blood is greater than arterial. THis is because at lungs, reduced affinity so CO2 release. At low PO2 (tissues), greater affinity for CO2 uptake. THis enhances unloading of CO2 from tissue to blood

25
Where are the peripheral chemoreceptors located?
1) sinus + glossopharyngeal nerve down the nucleus solitarii tractus (part of drg in medulla) to carotid bodies at the top of carotid arteries 2) aortic + vagus nerve down the nucleus tractus solitarii('') to aortic bodies (positioned between the subclavian artery and CCA for right and aorta and CA for left)
26
What are teh two cell types in carotid body
``` glomus cells (sensory) support cells ```
27
Which chemoreceptor are the main role in regulating hypercapnia ventilatory response?
Chemoreceptors (80%)
28
What are the roles o fthe 4 surfactant proteins?
A+D- regulation of surfactant synthesis, host defense A- ST reduction B+C- formation and stabilisation of phospholipid monolayer, B- formation of tubular myelin
29
How are surfactant degraded and catabolised?
- taken up by type 2 cells - eaten by macrophage - move upwards carried by cilia due to ST grad - degraded by extracellular enz act - epithelial reabsorption into lymph or blood
30
What are the functions of surfactant?
- improves pulmonary compliance - aids fluid balance (reducing tendency for fluid to be sucked into airspaces) - host defense (SP-A and D binds to pathogens) - also reduce formation and maintenance of liq plugs, reduce adhesion primarily in upper airways aids hydration and rheology mucus
31
What does COPD-X stand for?
``` C- confirm diagnosis O- optimise function P- prevent deterioration D- develop self management plan X- manage exacerbations ```
32
What are the paraneoplastic syndrome?
SMall cell lung cancer- e.g. cushing syndrome secondary to ACTHm inappropriate ADH secretion Non small cel- hypercalcemia secondary to secretion of PTH-rp finger clubbing