4-Pulmonary System Overview Flashcards
important elements of respir sys
full list
- mechanism for centrally regulating ventilation
- air pump
- surface for gas exchange
- mechanism for gas transport
- circulatory system
- mechanism for reg distribution of blood
important functions
condensed
- gas exchange/metabolism
- acid base balance
- phonation
- defense mech/handle bioactive materials
upper airway structures
- nasal cavity
- paranasal sinuses
- pharynx
- larynx
upper airways function
- air conditioning for respir sys
- source of resistance to airflow
- warm inspired air to body temp
- humidify/saturate with water inspired air for gas exchange
- filter/entrap/clear particulates
- defense by nasal epithelium secretions
inc secretions = inc resistance
airway generations
0 = trachea
1-10 = bronchi (with cartilage)
11-16 = bronchioles (no cart)
17-19 = respiratory bronchioles
20-22 = alveolar ducts
23 = alveolar sacs
16 terminal bronchioles
bronchus characteristics
- mucus blanket
- goblet cells
- smooth muscle
- mucus glands
- cartilage
G1-10
bronchioles characteristics
- ciliated epithelium
- thin smooth muscle
- elastic tissue
- NO cartilage
- goblet cells (up to terminal bronchioles then no)
G11-19
alveolus characteristics
- NO smooth muslce
- NO cart
- just elastic tissue
non adrenergic non cholinergic nerves
NANC
when activate = relaxation of bronchiolar smooth muscle via NO and vasoactive intestinal peptide
adrenergic activation
abundant B2 adrenoreceptors to relax/bronchodilate
muscarinic acetylcholine receptors
parasymps stim to contract bronchiolar smooth muscle and inc glandular secretions
irritant receptors
activation in trachea and bronchi = reflex contraction of smooth muscle + stim mucosal glands in resp to irritant
mucus production system
- gel layer
- sol layer
- goblet cells (prod mucus esp inc when smoke or pollutants)
- submucosal glands (mucus and serous cells, present where cartilage at, controlled by ANS)
periciliary fluid
makes up sol layer of mucus blanket
-made by ciliated epi cells
-maintained by chloride secretion and sodium absorption
transports mucus with pollutants out of respir system after gets trapped in gel layer
cystic fibrosis
mutation in CFTR
-abnormal Cl secretion = disinhibit Na channel so sol layer becomes dehydrated (water move out of periciliary mucus)
freq lung infection and damage, xs thick mucus, salty skin/sweat, poor growth
survival age 40
treating cystic fibrosis
goal to prevent/control infections + remove mucus from lungs
-use meds to target mutations or infection or bronchodilators
-PT to improve mucus clearance and fix posture, percussion
respiratory unit consists of
- bronchiole
- alveolar ducts
- atria
- alveoli
site of gas exchange
pores of kohn
pores b/t adjacent alveoli so collateral ventilation occurs if lung partially deflated
-bad though for passage of fluid and bacteria
cell types on alveolar surface
- type I = make up the wall/surface area, flat cells with large cytoplasmic extensions, fewer than II
- type II = larger/thicker cells, produce surfactant
- macrophages = engulf and destroy foreign material
respiratory membrane
fused basement membranes of capillary and alveolaus but leaky
-site of gas exchange
respiratory membrane made of
- layer of fluid lining the alveolus with surfactant
- alveolar epithelium
- epithelial basement membrane
- interstitial space
- capillary basement membrane
- capillary endothelial membrane
lung interstitium composition
- lymphatics
- capillaries
- immune cells
- fibroblasts
- connective tissue (collagen/elastin)
interstitial lung disease
interstitium enlarged with inflamm cells and edema fluid or increased extracellular matrix
-will interfere with gas exchange
pleural membranes
single continous membrane that folds back on itself
-lines lungs with visceral pleura and chest cavity with parietal