Jackson 1 Flashcards
Lungs Regulate
blood pH
ventilation rate affects amount of CO2 in plasma
Lungs Provide microbial defense by means of
epithelial secretions –
lymphoid tissue in tract –
coughing and sneezing reflexes –
Lungs
6. Activate (or inactivate)
chemical messengers in blood –
e.g. convert angiotensin I to angiotensin II
Lungs 7. Defend against
blood clots – small blood clots get trapped in narrow vessels in lungs and are dissolved
Components and zones of the respiratory system
airways – series of tubes needed to exchange air between lungs and environment
lungs – site of gas exchange between air and blood
mechanical aids – skeletal muscles used to vary the volume of the thoracic cavity
upper airway – structures are
outside of the thoracic cavity
mouth/nose → pharynx → larynx → top of trachea
- conducting zone –
in thoracic cavity, but no gas exchange occurs
trachea → primary bronchi → secondary bronchi → tertiary bronchioles → bronchioles → terminal bronchioles
trachea and bronchi include cartilaginous rings and mucous glands –
bronchioles lose cartilage and glands, but add smooth muscle
respiratory zone – structures where
gas exchange can occur
respiratory bronchioles → alveolar ducts → alveolar sacs
respiratory bronchioles very
thin-walled; have alveoli in walls
Branching creates
parallel airways to maintain airflow and minimize increasing resistance to airflow. Compare this set-up to one in which multiple tubes simply become narrower.
Air is warmed and moistened – heat and water vapor are
exchanged with the blood in airway walls
Conducting zone protects against
microbes
goblet cells secrete mucus which can
trap airborne particles and pathogens;
cilia on epithelial cells move
mucus upwards to pharynx where it can be swallowed or expelled
Closed pneumothorax:
Pleural cavity pressure less than ATM
Open pneumothorax:
pleural cavity pressure = atm
tension pneumothorax:
pleural cavity pressure > ATM
Cystic fibrosis is a disease that
impairs the normal function of the conducting zone
Cystic fibrosis: mutation in genetic code for
Cl- channel reduces the amount of Na+ and Cl- secreted across the epithelium into mucus. This leads to there being less water in the mucus (due to osmosis)→ mucus is thick and dry
Cystic fibrosis: consequences of abnormal mucus -
infectious agents are trapped, but not expelled; airways are obstructed