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Costanzo-Respiratory Physiology

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Question
Answer
conducting zone subdivisions   nose, nasopharynx, larynx, trachea, bronchi, bronchioles, terminal bronchioles  
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conducting zone structure & fxn   bring air into and out of lungs lined with mucus-secreting ciliated cells contain smooth m. and innervated by SNS & PNS SNS activate B2 receptors and relax/dilate PNS activate muscarinic receptors and constrict/contract  
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albuterol   B2-adrenergic agonist used to dilate airways to treat athsma  
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respiratory zone subdivisions   respiratory bronchioles, alveolar ducts, alveolar sacs  
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respiratory zone structure & fxn   participates in gas exchange-->thin walls & large surface area lined with alveoli walls lined with elastic fibers & epithelial cells contain type I & II pneumocytes and alveolar macrophages  
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type II pneumocyte   synthesizes pulmonary surfactant necessary to reduce alveoli surface tension has regenerative capacity for type I and II pneumocytes  
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alveolar macrophages   phagocytic cells fill with debri then migrate to bronchioles-->keeps alveoli free of dust & debri imp. bc respiratory zone has no cilia  
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gravitational effect on pulmonary blood flow   blood flow not evenly distributed in lungs when standing blood flow lowest at apex and highest at base  
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spirometer   measures static lung volume  
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tidal volume   normal quiet breathing approx. 500 mL = air in alveoli + air in airways  
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inspiratory reserve volume   additional volume inspired above tidal volume approx. 3000 mL  
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expiratory reserve volume   additional volume expired below tidal volume approx. 1200 mL  
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residual volume   volume of gas remaining in lungs after maximal forced expiration approx. 1200 mL  
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dead space   volume of airways and lungs that don't participate in gas exchange -anatomic dead space -physiologic dead space both values should be nearly equal in normal persons-->functional dead space should be small  
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anatomic dead space   volume of air in conducting airways 1/3 of each tidal volume fills anatomic dead space  
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physiologic dead space   total volume of lung that doesn't participate in gas exchange = anatomic dead space + functional dead space in alveoli  
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type of air in alveoli at end-inspiration   1) alveolar air from previous breath 2)inspired air that participates in gas exchange  
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inspiratory capacity (IC)   tidal volume + inspiratory volume approx. 3500 mL  
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functional residual capacity (FRC)   expiratory reserve + residual volume approx. 2400 mL also known as equilibrium volume: volume remaining in lungs after normal tidal volume expired  
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vital capacity (VC)   inspiratory volume + expiratory reserve volume approx. 4700 mL; value increases with body size, M gender, physical conditioning; value decreases with age volume expired after maximal inspiration  
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forced vital capacity   total volume of air that can be forcibly expired after maximal inspiration FEV1/FVC useful in differentiating between lung disease; normally 0.8 -obstructive lung disease (athsma) ratio decreases -restrictive lung disease (fibrosis) ratio increas  
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muscles of inspiration   *diaphragm during exercise also use external intercostal muscles and accessory muscles  
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muscles of expiration   *normally passive process during exercise/disease use abdominal muscles and internal intercostal muscles  
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lung compliance   describes change in lung volume for given change in pressure higher during expiration than inspiration due to surface tension between liquid-air interface inversely correlated with elastic properties ex) thick and thin rubber band  
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negative intrapleural pressure   created by opposing forces between collapsing lung and chest wall that springs out  
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pneumothorax   when air introduced into intrapleural space and leads to 1) collapsed lung 2) chest wall springs out  
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emphysema   increased lung compliance due to loss of elastic fibers leading to decreased elastic recoil pt needs to breathe at higher lung volumes to increase elastic recoil class symptom: barrel-shaped chest  
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fibrosis   decrease lung compliance due to stiffening of lung tissue AKA restrictive disease  
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alveolar surface tension   created by attractive forces between adjacent liquid molecules lining alveoli creates high collapsing pressure in small alveoli  
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surfactant   produced by type II alveolar cells mixture of phospholipids-->most imp. constituent dipalmitoyl phophotidylcholine reduces surface tension & collapsing press by breaking up forces between liquid molecules  
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neonatal respiratory distress syndrome   neonates lacking surfactant-->imp. because increases lung compliance and reduces work of expanding lungs surfactant synthesis produced early as gestational WK24-almost always present by WK35 atelectasis and hypoxemia develops  
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transmural pressure in lungs   transpulmonary press. = alveolar pressure - intrapleural pressure (+) value is expanding pressure on lungs (-) value is collapsing pressure on lungs  
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physiologic shunt   2% CO normally bypasses alveoli two sources: 1) bronchial blood flow and 2) coronary venous blood why Pao2<PAo2  
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diffusion-limited gas exchange   gas exchange limited by diffusion process diffusion will continue as long as partial pressure for gas maintained  
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perfusion-limited gas exchange   gas exchange limited by blood flow partial pressure gradient not maintained-->blood flow must increase to increase gas exchange  
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perfusion-limited O2 transport   O2 transport during normal conditions; alveolar air and capillary blood equilibrate 1/3 way down capillary  
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diffusion-limited O2 transport   occurs during pathological conditions and strenuous exercise total O2 transfer is greatly reduced  
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O2 transport at high altitude   Po2 in alveolar gas decreases because barometric pressure decreases; partial pressure gradient greatly reduced along with O2 diffusion equilibration is slower  
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dissolved O2 in blood   approx. 2% of total O2 in blood-->insufficient meet demands of tissue  
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O2 bound to hemoglobin   approx. 98% of total O2 in blood hemoglobin contains four subunits (2 alpha chains and 2 beta chains); each subunit binds one O2 molecule hemoglobin heme moiety must be in Fe2+ state to bind O2  
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methemoglobin   heme moiety contains Fe3+ and does not bind O2 deficiency of methemoglobin reductase is a congenital variant of the disease  
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fetal hemoglobin   beta chains are replaced by gamma chains modification results in higher O2 affinity-->facilitates O2 movement from mother to fetus  
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hemoglobin S   abnormal variant that causes sickle cell disease beta subunits are abnormal and distorts RBC in the deoxygenated form-->can occlude small blood vessels O2 affinity is low  
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O2-hemoglobin dissociation curve   sigmoidal shape-->affinity increases with each successive O2 molecule bound-->phenomenon called positive cooperativity  
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P50 on O2-hemoglobin dissociation curve   point used as indicator for change in hemoglobin affinity for O2 -increase reflects decreased affinity -decrease reflects increased affinity  
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O2-hemoglobin dissociation curve shift to the right   reflects decreased O2 affinity-->increased P50-->facilitates O2 unloading result of increased Pco2, temperature, 2,3-DPG and decreased pH  
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2,3-diphosphoglycerate   byproduct of glycolysis in RBC binds to beta chains of deoxyhemoglobin-->reduces O2 affinity  
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O2-hemoglobin dissociation curve shift to the left   reflects increased O2 affinity-->decreased P50-->makes O2 unloading harder result of decreased Pco2, temperature, 2,3-DPG/hemoglobin F and increased pH  
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carbon monoxide   decreases O2 bound to hemoglobin-->has 250x higher affinity to hemoglobin than O2 shifts O2-hemoglobin dissociation curve to left-->unbound heme groups have increased affinity for O2  
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oxygen transport in blood   2% dissolved O2 98% O2 bound to hemoglobin  
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carbon dioxide transport in blood   5% dissolved CO2 3% carbaminohemoglobin-->binds to terminal amino groups on proteins 90% bicarbonate  
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hypoxic vasoconstriction   decrease in PAO2 produces pulmonary vasoconstriction adaptive mechanism-->reduces pulmonary blood flow to poorly ventilated areas where it would be "wasted"  
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thromboxane A2   powerful vascoconstrictor of arterioles and veins product of arachidonic acid metabolism via cyclooxygenase pathway produced in response to lung injury in macrophages, leukocytes, and endothelial cells  
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prostacyclin (prostaglandin I2)   potent local vasodilator product of arachidonic acid metabolism via cyclooxygenase pathway produced by lung endothelial cells  
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leukotrienes   causes airway constriction product of arachidonic acid metabolism via lipoxygenase pathway  
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blood flow distribution in lung   zone 1-low blood flow; PA>Pa>Pv zone 2-med blood flow; Pa>PA>Pv zone 3-high blood flow; Pa>Pv>PA  
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right-to-left-shunt   septal defect between right and left ventricle portion of CO not oxygenated-->hypoxemia always occurs due to dilutional effect cannot be corrected by breathing high O2 gas  
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left-to-right shunt   common and doesn't cause hypoxemia result of: 1) patent ductus arteriosus 2) traumatic injury right heart CO > left heart CO Po2 in right heart blood is elevated  
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V/Q distribution in lungs   zone 1-highest V/Q; highest Pao2; lowest Paco2 zone 3-lowest V/Q; lowest Pao2; highest Paco2  
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V/Q mismatches   dead space- V/Q=infinity; no perfusion; alveolar gas same comp as humidified inspired air high V/Q low V/Q- ventilation decreased shunt- V/Q=0; no ventilation; airway obstruction; right-to-left shunt; blood same comp as mixed venous blood  
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medullary respiratory center   1)inspiratory center: controls basic breathing rhythm; input from CNIX and X; output via phrenic n. 2)expiratory center: inactive during quiet breathing because expiration passive process; active during exercise located in reticular formation  
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apneustic center   produces abnormal breathing pattern with prolonged inspiratory gasps due to prolonged contraction of diaphragm located in lower pons  
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pneumotaxic center   turns off inspiration;limits tidal volume located in upper pons  
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hypoxemia vs hypoxia   hypoxemia-->decrease in arterial Po2 hypoxia-->decrease in O2 delivery  
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causes of hypoxia   1)decreased CO 2)anemia 3)carbon monoxide poisoning 4)cyanide poisoning  
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causes of hypoxemia   1)high altitude 2)hypoventilation 3)diffusion defects-->alleviated by supplemental O2 4)V/Q defects 5)right-to-left shunts-->not alleviated by supplemental O2  
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