Respiratory Learning Objectives- big list Flashcards

1
Q

relate form to function in describing the physiologic roles of the nasal cavities

A

turbinates/conchas and sinuses allow air to swirl around and filter and warm and also the olfactory nerves are right there

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2
Q

describe the movements of the epiglottis, the body of the larynx, and the vocal folds that protect from aspiration

A

during breathing:
soft palate ventral
epiglottis folded over soft palate to direct air into larynx
arytenoids open to decrease air resistance

during swallowing:
soft palate dorsal
epiglottis rotates up to cover airway/arytenoids
arytenoids rotate down to open esophagus for snacks

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3
Q

compare the differences in function between the oronasal, conducting, and respiratory zones

A

oronasal: olfaction, humidify and warm air, thermoregulation, filter air, slow airflow (50-70% of resistance), phonation, protection from aspiration during swallowing

conducting: further slow airflow (provides the rest of resistance), also filter air via mucociliary apparatus

respiratory: gas exchange!!

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4
Q

identify the components of the immune system active in the oronasal, conducting, and respiratory zones and describe their roles

A

in blood and tissues: PRRs, antimicrobial peptides, alveolar macrophages, monocytes, dendritic cells, neutrophils, lymphocytes, antibodies (produced by BALTs)

BALTs for immunity in the conducting zone; mucociliary apparatus

also lumen gets smaller as move down the tract, physically filtering foreign particles

respiratory zone: alveolar macrophages phagoctyose particles and send to conducting zone; type I alveolar cells can also endocytose and process through lymphatics or make them enter circulation and leave

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5
Q

moving from the trachea to the terminal airways, contrast length, total cross-sectional area, resistance to air flow, and air velocity

A

length: decreases
total/cumulative cross-sectional area: increases (so many fucking capillaries)
resistance to airflow: decreases (parallel series)
air velocity: decreases

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6
Q

name the components of the mucociliary apparatus and describe how each contributes to clearing particles from the airways

A
  1. fluid layer:
    a. gel layer, very viscous, traps particles, dilutes toxins, has antibodies
    b. sol layer: less viscous
  2. ciliated epithelium: beat constantly to clear mucus from tract
  3. goblet cells and mucous glands: secrete mucous for gel layer
  4. BALT: secretes antibody
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7
Q

define ventilation and distinguish between inspiration, passive expiration, and active expiration

A

ventilation: physically moving air in and out of lungs
inspiration: inhale air into lungs, an active process
passive expiration: due to recoil
active expiration: actively forcing air out of lungs

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8
Q

identify the muscles actively involved versus passively involved with each phase and how each muscle group contributes to air movement

A

inspiration:
1. external intercostals contract to elevate ribs
2. diaphragm contracts to pull down

also outward recoil of chest wall

quiet/passive exhalation: due to inward recoil of
1. lungs
2. rib cage
3. diaphragm

active expiration:
1. internal intercostals actively contract to pull ribs down
2. abdominal muscles actively contract to pull ribs down and compress abdominal contents

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9
Q

on a normal spirogram, distinguish between tidal volume, inspiratory reserve volume, expiratory reserve volume, and residual volume

A

tidal volume: inspiration + passive exhale
inspiratory reserve volume: biggest breath in after regular inhale
expiratory reserve volume: active expiration after passive expiration
residual volume: air left in lungs after active exhale

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10
Q

on a normal spirogram, distinguish between total lung capacity, inspiratory capacity, vital capacity, and functional residual capacity and ID which of the lung volumes comprise each

A

total lung capacity: all air in and out of lungs
inspiratory capacity: all air that can be inhaled (regular + inspiratory reserve volume)
vital capacity: TV + IRV + ERV
functional capacity: ERV + RV

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11
Q

define and contrast minute ventilation and alveolar ventilation

A

minute ventilation is all air that enters the lungs per minute (VD + VA)
alveolar ventilation: the air that enters the lungs AND participates in gas exchange, subtracting all dead space air

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12
Q

define and contrast anatomic and physiologic dead space and how each relatively compares to tidal volume

A

anatomic: air in oronasal and conducting zones
physiologic: air in alveoli that are not well perfused with blood

tidal volume is volume of dead space plus volume of air actually participating in gas exchange

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13
Q

describe how the parietal and visceral pleurae in the thorax interact to create the negative space within the intrapleural space and how air or fluid accumulating in the intrapleural space affects inspiration and that negative pressure

A

the potential space (don’t want it to be an actual huge space) between the visceral and parietal pleura is filled with a tiny volume of parietal fluid (serous-like) that not only reduced friction but also generates its own force, where the polarity of water attracts the west surfaces of the membranes together, keeping the two pleura stuck together as lungs try to pull inward from chest wall and chest wall tries to pull outward by generating negative pressure between them

this suction aids the outward elasticity of the thoracic wall (ribcage/muscles) which tends to pull the lungs outward

if air or fluid accumulates, destroys this negative pressure and makes breathing hard

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14
Q

relate Boyle’s law to the sequential changes in volumes and pressures that occur during inspiration and expiration

A

Boyle’s is P1V1=P2V2 so as the thoracic cavity expands during inhalation and pressure drops as volume increases, air will flow from high to low and flow in to try to establish equilibrium with the atmosphere, and save into alveoli, and then back out again

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15
Q

define compliance, elastance, surface tension, and airway resistance and explain how each is related to the others and affects inhalation and deflation of the lungs

A

elastance: recoil force
compliance: how responsive the object is to force
surface tension: reduced by surfactant, but must be overcome to inflate alveoli
airway resistance: directly proportional to length, inversely proportional to radius to the 4th power

compliance is how easy it is to stretch the rubber band of the lungs, elastance takes care of passive exhalation and airway resistance is how easy air can get through system during inhalation

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16
Q

describe how pulmonary surfactant facilitates alveolar expansion and affects alveolar surface tension

A

surface tension makes water molecules want to clump together, making alveoli want to deflate but surfactant reduces that surface tension just enough so that alveoli are open

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17
Q

describe how the pressure gradient in the airways and airway resistance affect the rate or velocity of air flow in and out of the lungs moving from the trachea to the terminal airways

A

PO2:
pulmonary
inspired air: 160
alveoli: 100
O2 flows into alveoli
systemic:
arteries: 95
tissue capillaries: 40
O2 flows into tissue capillaries

PCO2:
pulmonary:
inspired air: 27
alveoli: 40
CO2 flows out of alveoli
systemic:
tissue capillaries: 45
systemic arteries: 40
CO2 flows out of capillaries into venous blood

bulk flow drives gases down to alveolar level, diffusion takes care of alveolar level gas exchange

18
Q

compare the relative levels of O2 and CO2 in the arterial and venous sides of the pulmonary, systemic, and bronchial circuits

A

pulmonary:
arterial: deoxygenated
venous: oxygenated

systemic and bronchial:
arterial: oxygenated
venous: deoxygenated

19
Q

compare flow, pressure, resistance, and response to hypoxemia in the pulmonary vascular circuit versus the systemic circuit

A

systemic: vasodilation to increase blood delivering oxygen to starved tissues

pulmonary: vasoconstriction to decrease blood flow to give alveoli more time for gas exchange

20
Q

describe where the bronchial circulation can enter and leave both pulmonary and systemic circuits

A

bronchial artery: branches from aorta
bronchial postcapillary venules merge with pulmonary venules, then pulmonary veins and azygous veins, then back to left atrium

21
Q

describe the mechanisms by which pulmonary vasculature accommodates increased cardiac output

A

pulmonary veins can expand to accommodate the increased flow (delta P = Q x R)

22
Q

describe the effects of inspiration and expiration on blood flow in pulmonary capillaries and extra-alveolar vessels (arterioles and veins) in the lungs

A

inspiration: thoracic cavity volume increases, extra-alveolar vessels expand, intra-alveolar vessels are compressed (increased vascular resistance)

expiration: thoracic cavity volume decreases, extra-alveolar vessels are compressed, intra-alveolar vessels expand

23
Q

describe how starling’s forces impact the movement of fluid between the pulmonary capillaries, the interstitial space, and alveolar lumen; compare the relative differences of these forces to those in systemic vasculature

A

hydrostatic pressure is lower than systemic (blood pressure);m because don’t want a bunch of fluid exiting the pulmonary capillaries because that would overwhelm the pump that removes fluid from alveoli and lead to pulmonary edema

24
Q

explain what happens to partial pressures for a total gaseous mixture and for individual gases if one gas is added or subtracted

A

add: decrease partial pressure of all other gases in the mixture
subtract: increase partial pressure of all other gases in the mixture

25
Q

describe how humidification with water vapor affects partial pressures of gases of inspired air

A

adding H2O is gas form, so decreases the partial pressures of all other gases in the mixture

26
Q

describe the difference between bulk flow and diffusion including whether each changes the concentrations of gas particles in the air or liquid medium; indicate where each occures

A

bulk flow: requires a pressure gradient, all molecules move together, is fast, occurs everywhere above the level of alveoli
diffusion: requires a concentration gradient, molecules only move if down their concentration gradient, is slow, occurs in alveoli

27
Q

describe how changes in each of the factors in Fick’s law affect diffusion of gases across membranes

A

rate of transport across a membrane is directly related to
1. difference in partial pressures across the membrane (greater difference means faster transfer)
2. membrane’s diffusing capacity, dependent on
membrane solubility, membrane area, membrane thickness, molecular weight of the gas

28
Q

describe the 2 methods by which O2 is carried in the blood and indicate the relative importance of each

A
  1. less than 2% dissolved in plasma; this is measured when we measure PO2
  2. more than 98% is in RBCs bound to hemoglobin, participating in gas exchange
29
Q

describe how hemoglobin and iron in the heme molecule function to carry O2

A

each molecule has 4 hemes with an iron molecule in the center that reversibly binds O2; meaning 1 molecule of hemoglobin can bind up to 4 molecules of oxygen

30
Q

describe the oxygen-hemoglobin saturation curve and the relationship between partial pressure of oxygen and percent oxygen saturation

A

higher PO2 means higher percent saturation of hemoglobin with O2

31
Q

explain allosteric effect of oxygen binding hemoglobin

A

one oxygen binding to hemoglobin causes a conformational change in the molecule, making it easer for more O2 to bind

32
Q

explain how the oxygen-hemoglobin saturation curve reflects the physiologic movement of O2 between the pulmonary and systemic capillary beds

A

the curve is shifted to the left meaning that more O2 is bound when PO2 is high in pulmonary circulation and shifted to the right meaning that more O2 is dropping off (less bound) in systemic circulation

33
Q

describe the 4 factors that influence the oxygen-hemoglobin saturation curve

A
  1. temperature: higher means less O2 bound
  2. ph: more acidic means less O2 bound
  3. 2,3-DPG: more present means less O2 bound
  4. pCO2: if high means less O2 bound
34
Q

identify the respiratory centers in the brain involved in controlling breathing rate and depth; indicate the main role of each center

A

the 3 respiratory centers involved in controlling involuntary/basal breathing are:

  1. medulla oblongata
    1a. dorsal respiratory group of medulla oblongata: initiates and maintains inspiration
    1b. ventral respiratory group: inactive during normal quiet breathing, but during exercise is activated by forceful inspiration and signals to abdominal muscles to contract for expiration
  2. pons:
    2a. pneumotaxic center: inhibits medullary inspiratory center to increase respiratory rate
    2b. apneustic center: stimulates inspiratory center to prolong the inspiratory period
  3. hypothalamus and other portions of the limbic system take over in emotional states, clinically important to separate stress from an actual issue in the clinic

(basic rhythm is generated by medulla and adjusted by pons; at rest expiration is PASSIVE!)

35
Q

describe the roles of central and peripheral chemoreceptors in detecting changes in O2 and CO2 levels and blood pH

(include the relative sensitivity of each type of chemoreceptor of O2, CO2, and pH and how the chemoreceptors integrate with the respiratory centers)

A

central: detect increased CO2 and H+ but most sensitive to CO2

central chemoreceptors detect increased CO2 (can cross the blood brain barrier, H+ cannot) and create a respiratory drive to increase ventilation, but need carbonic anhydrase for this to occur

peripheral: detects decreased O2, increased CO2, and increased H+ (the only chemoreceptors sensitive to O2)

two main peripheral chemoreceptors:
1. carotid (uses CN IX)
2. aortic bodies (use CNX)
both have glomus cells that sense changes in blood, signal to medullary respiratory center to increase ventilation, have a very fast response

example is how the carotid body chemoreceptors are at an area of very high blood flow, so if detect MAJOR increases in CO2 and H+ or even minor decreases in O2, will increase ventilation

36
Q

how are the medulla and pons integrators attached to the muscles they control?

A
  1. pontine respiratory group (pneumotaxic and apneustic) connect to the phrenic nerve which innervates the diaphragm
  2. the dorsal respiratory group of the medulla connects to the phrenic nerve which innervates the diaphragm
  3. the ventral respiratory group in the medulla connects to the phrenic nerve (to diaphragm) and also to intercostal nerves to both internal and external intercostal muscles
37
Q

describe the major peripheral neural sensors that monitor breathing and the changes each one affects when stimulated (5)

A
  1. stretch receptors (slowly adapting pulmonary stretch receptors/ PSRs): mechanoreceptors located in smooth muscle of bronchial and bronchiolar walls that, when the lungs are overstretched, signal the DRG via the vagus nerve and increase expiratory time
  2. pulmonary irritant receptors (PIRs): nerve endings in airway epithelium that detect irritants and initiate coughing and sneezing, as well as bronchoconstriction, mucus secretion, and hyperpnea (also called rapidly-adapting pulmonary stretch receptors that detect the rate of lung inflation, facilitating inspiration and counteracting the action of PSRs)
  3. bronchial C fibers: also sense chemical insults and inflammatory mediators; facilitate inspiration similar to PIRs
  4. J receptors in lungs (juxta-capillary receptors): in alveolar interstitium, respond to pathologic stimuli and cause shallow, rapid breathing
  5. muscle and joint proprioreceptors: increase ventilation during exercise
38
Q

explain how arterial blood gas measurements reflect oxygenation and ventilation

A

increased O2: could indicate exposure of air to the sample (air bubble if super high) or supplemental O2
decreased O2: could indicate: damage to respiratory membrane, increased tissue demand for oxygen (either from exercise, septic shock, etc.)

increased CO2: increased cell respiration, respiratory membrane unable to diffuse CO2, or decreased ventilation (could be due to anesthesia)

39
Q

understand the differences and similarities in respiratory tract anatomy in birds, reptiles, amphibians, and fish

understand the unique differences in respiratory function, control of ventilation, and gaseous exchange in birds, reptiles, amphibians, and fish

(both are in this answer but rly just look over the ppt)

A

this is a lot; summary, see ppt!

birds: have a nasal salt gland, do not have an epiglottis or a soft palate (rima glottis regulates passage of air), trachea has complete cartilaginous rings, have a syrinx, lungs have a fixed volume, have air sacs (no gas exchange at air sacs), cross current blood flow and unidirectional airflow, respiratory muscles are smooth muscles so will continue breathing when anesthetized, do not have a diaphragm

reptiles: no muscular diaphragm (cannot cough, exudate can accumulate), lower oxygen demands and reduced ventilation (NVP), lungs are more simple, sac-like, withr educed gas exchange ability, ventilation under skeletal intercostal control, hypoxia increases ventilation frequency, hypercapnia increases tidal volume

amphibians: have reduced oxygen demands, can utilize gills, lungs, cutaneous respiration (species dependent), lungs similar to lizard, no diaphragm, ventilation through gular pumping (ribbit motion), have VP and NVP, have external, simplified, feathery gills if present, cutaneous respiration is the most important in some species due to unique vasculature of skin with a thin permeable epidermis

fish: water is much denser and less oxygenated than air, so need a high throughput system with minimal resistance (uniflow), have a concurrent gas exchange system to maximize O2 extraction, gills are where gas exchange occurs, secondary lamellae in contact with countercurrent blood flow for exchange

40
Q

understand how the differences in respiratory tract anatomy and physiology can be important when investigating disease or performing anesthesia

A

birds:
1. don’t used cuffed ET tubes bc of complete tracheal rings
2. the syrinx is a common site for foreign body obstruction, granulomas, or infections
3. the lung system is so efficient that if see open-mouth breath, bird is 80-90% dead
4. since have smooth respiratory muscle, will keep ventilating under anesthesia
5. can cannulate air sacs to provide alternative airway in cases of tracheal/syringeal obstruction

reptiles:
1. chelonians have complete tracheal rings so don’t use cuffed ET tubes
2. masking down is a waste of time for anesthesia because can hold breath for hours and also cardiac shunting
3. ventilation is controlled by smooth muscle, so must ventilate for them in anesthesia
4. all should be apneic at surgical plane of anesthesia; if breathing, DONT CUT
5. when recovering from anesthesia, decrease O2 by switching to room air and increase CO2 by decreasing ventilation frequency or won’t take a breath for hours
6. lack of muscular diaphragm means any disease in coelom can affect respiration and also don’t place in lateral or sternal recumbency until in a surgical plane of anesthesia

amphibians: due to ability of cutaneous respiration, if just using intubation may not fully anesthetize; and also very sensitive to environmental toxins