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44 Cards in this Set

  • Front
  • Back
List the layers of the generic respiratory tract from inside to outside:
"E-L-M_S-C-A; epithelium, lamina propria, muscularis, submucosa, cartilage, adventitia
vibrissae
nasal cavity vestibule; short hairs that filter out large particles
the nasal cavity is lined by _____ epithelium that transitions to
______ epithelium.
non-keratinized stratified squamous, respiratory
Most of the nasal cavity, the air sinuses, and the nasopharynx, are covered by _____ epithelium. Immediately deep to the epithelium is a _____ that connects to the bone and contains distended veins (swell bodies), arteries and mucoserous glands.
respiratory, lamina propria
The upper third of the nasal cavity is lined _____ epithelium, a variation on the typical respiratory epithelium where the sense of smell is located.
olfactory
olfactory epihelium
Extremely thick layer of pseudostratified ciliated columnar epithelium
Olfactory (Bowman’s) glands
glands in the lamina propria that releases a serous fluid to dissolve and bind oderant molecules.
olfactory cells
bipolar sensory nerve cells with an apical *olfactory vessicle* projection sprouting modified cilia
olfactory cilia
non-motile, fnx as odor receptors
Olfactory epithelial Brush Cells are ____ cells.
sensory
Basal cells compirse the ____ cell population.
stem
The epiglottis is at the junction between the oral cavity and the ______.
larynx
The epiglottis has both _____ (oral) and _____ (larynx) epithelium covering a core of _____ cartilage with many muco-serous glands in the _____.
stratified squamous, respiratory, elastic, lamina propria
The ____ vocal fold is the more inferior of the two and a space between the true and false folds, the ventricle, helps create resonance.
true
The false fold has _____ epithelium covering somewhat loose connective tissue with adipocytes.
respiratory
The true fold has______ epithelium covering a core of dense connective tissue
stratified squamous
Prolonged, violent coughing and irritation can cause the respiratory epithelium to undergo *Metaplasia into _____ epithelium.
stratified squamous; If prolonged, permanent dysplasia can occur, potentially leading to squamous cell lung carcinoma.
C-shaped _____ cartilages hold the airway open. Their open end is bridged by a sheet of smooth muscle and ______ connective tissue.
hyaline, fibroelastic
_____ cells and the ______ glands release mucous into the airway where it traps small particulate matter.
goblet, mucosal; chronic irritation of the airways causes the goblet cell number to increase
_____ cells sweep the mucous towards the oropharynx to be swallowed or expectorated.
ciliated
All bronchi are lined by _____ epithelium with ____ cells and seromucous glands
respiratory, goblet
asthma
Excessive constriction of bronchiolar smooth muscle. Associated with difficult air expiration, mucus accumulation in airways, & inflammatory cell infiltration. Often progressive & associated with allergic reactions since allergens can cause mast cell release of histamine & heparin.
asthma is treated with______
bronchiolar smooth muscle relaxants such as epinephrine & isoproterenol
A primary bronchus delivers air to each _____ and then splits into a secondary (to each _____) and tertiary (to each _____) bronchi.
lung, lobe, bronchopulmonary segment
The walls of the bronchi have a substantial amount of _____ that regulates the diameter of the airway.
smooth muscle; as the bronchi progress into the lungs the cartilage rings become irregular cartilage plates.
Bronchioles are lined by _____ epithelium, but as the passageways get smaller, the epithelium becomes more ____.
respiratory, cuboidal; Goblet cells gradually disappear & bronchiolar exocrine cells start appearing in the smaller passages until there are no more goblet cells.
do bronchioles have cartilage plates?
nope
bronchiolar exocrine cells (Clara cells)
Non-ciliated, domed, cuboidal cells that line the bronchioles.
Secrete glycosaminoglycans that prevent collapse of the smaller airways and release ions into the lumen.
cystic fibrosis
disease in which the mucous in the airways (and other organs) is abnormally thick and viscous. Caused by a mutation in the CTFR gene that encodes a Cl- pump. The lack of chloride ions in the airway also creates a lack of H20, which normally follows the ions osmotically which makes the mucous thick
terminal bronchioles
simple cuboidal epithelium; contain smooth muscle; no cartilage; no goblet cells; contain bronchiolar exocrine cells; no pneumocytes
Why are they called "terminal" bronchioles?
end of the conducting airway
Gas exchange occurs in _____ bronchioles, alveolar _____, alveolar______ and _____.
respiratory, ducts, sacs and aveoli
respiratory bronchioles
simple cuboidal lining of ciliated and bronchiolar exocrine cells. smooth muscle and elastic fibers in mucosa, which are interrupted by alveoli; no goblet cells; have pneumocytes
alveolar ducts
simple squamous epithelium consisting of type I & II pneumocytes; contain smooth muscle in mucosa; no ciliated or bronchiolar exocrine cells; **last portion of respiratory system containing smooth muscle
alveoli
Terminal air spaces where gas exchange occurs btw air and blood; walls that contain elastic and reticular fibers. Lined by type I and type II pneumocytes
type I pneumocytes
40% of pneumocyte population but they cover ~ 95% of alveolar surface; simple squamous cells that are very flat and allow gas diffusion to occur through their cytoplasm.
**Not able to divide.
type II pneumocytes
cuboidal cells; 60% of pneumocyte population but only 5% of alveolar surface area. **Can divide & regenerate BOTH types of pneumocytes.
pulmonary surfactant
type II pneumocytes contain lamellar bodies which are released as pulmonary surfactant. Surfactant reduces surface tension to facilitate expansion during inspiration and prevent collapse in expiration.
interalveolar septa
Contain continuous capillaries that exchange O2 from the alveoli for CO2 from the blood.
blood gas barrier
Thinnest regions are 0.2 µm or less in thickness.
Three layers:
-type I pneumocyte and surfactant layer
-basal lamina of pneumocytes & capillary endothelial cells fuse
-capillary endothelium
Neonatal Respiratory Distress Syndrome
premature infants who lack adequate amounts of surfactant. Type II pneumocytes do not produce it until the 35th week of gestation.
In Neonatal Respiratory Distress Syndrome, ______ can be administered before birth to induce surfactant synthesis.
glucocorticoids
What are the two forms of emphysema?
-Genetic deficiency in the enzyme α1 antitrypsin, which protects elastic tissue from macrophage activity.
-Acquired from smoking or other inhaled substances that inhibit α1 antitrypsin.
alveolar macrophages (dust cells)
phagocytic; clean up ultra-fine debris from the alveolar spaces and elsewhere in the airway.
Full alveolar macrophages migrate into the lumen and are transported up the “mucociliary escalator” to the pharynx.
Inflammatory conditions and different heart conditions can cause an increase in macrophage number and activity