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Respiratory Physiology Part Two

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Title: Respiratory Physiology Part Two


1
Respiratory Physiology Part Two
  • Acid-Base Balance
  • Gas Transfer in Air
  • Lung Ventilation
  • Pulmonary Circulation
  • Heat Water Loss

2
Regulation of Body pH
  • Body pH in animals is normally slightly alkaline
    i.e. fewer H than OH- ions in body e.g. human
    blood plasma at 370C pH 7.4
  • Changes in cellular pH arise as a result of
    cellular functions as a means of regulatory
    control e.g. stimulation of glycolysis in frog
    muscle by insulin
  • Cells also undergo changes in pH as a result of
    external influences e.g. cells become acidotic
    during hypoxia because of an imbalance between
    proton production resulting form hydrolysis of
    ATP to ADP proton consumption by NAD in those
    tissues subjected to anaerobic metabolism

3
Regulation of Body pH
  • 1. H Production Excretion H Distribution
  • H produced through metabolism of ingested foods
    excreted on continuous basis - the largest pool
    of H greatest flux in H traffic is associated
    with metabolic production of CO2 (which at the pH
    of the body reacts with H2O to form H HCO3-)
    fig 13-10a - at respiratory surface, HCO3- is
    converted to CO2 which is then excreted fig
    13-10b
  • If CO2 production excretion are balanced, the
    overall effect of CO2 flux on body pH will be zero

4
Regulation of Body pH
  • 1. H Production Excretion H Distribution
    cont
  • if CO2 excretion lt production CO2 accumulates
    body will be acidified if the reverse, body pH
    will rise terrestrial vertebrates can vary the
    rate of CO2 excretion to maintain body pH
  •  ingestion of meat usually results in net intake
    of acid, whereas ingestion of plant food often
    results in net intake of base overall effect of
    food ingestion metabolism is a small continual
    production of acid body pH is maintained by
    excreting this acid via the kidney in terrestrial
    vertebrates or across regions of body surface
    such as gills of fishes or skin of frogs

5
Regulation of Body pH cont
  • 1. H Production Excretion H Distribution
    cont
  • if lung ventilation is reduced so CO2 excretion
    drops below CO2 production, body CO2 levels rise
    and pH will fall decrease in body pH
    respiratory acidosis reverse effect rise in pH
    due to increased lung ventilation respiratory
    alkalosis (using respiratory to differentiate
    changes otherwise related to metabolism of kidney
    function e.g. anaerobic metabolism results in
    net acid production which reduces body pH these
    changes metabolic acidosis vs. vomiting
    chloride loss bicarbonate increase with
    increase in pH metabolic alkalosis)

6
Regulation of Body pH cont
  • 1. H Production Excretion H Distribution
    cont
  • body fluids are electroneutral I.e. sum of anions
    sum of cations normal electrolyte status of
    human plasma is depicted in fig. 13-15 p. 541
    (sum of bicarbarbonate, phosphates protein
    anions buffer base
  • most cell membranes are much more permeable to
    CO2 than H or bicarbonate cell membrane
    permeability to H (while usually low) often is gt
    permeable to K, Cl- HCO3- (notable exception
    is RBC membrane which is very permeable to HCO3-
    and Cl- but not very perm to H)

7
Regulation of Body pH cont
  • An increase in extracellular PCO2 causes an
    increase in both bicarbonate H concentration
    thus creating gradients for CO2, HCO3- H
    across the cell membrane
  • In cells that are very permeable to CO2 but not
    very permeable to H or bicarbonate, such a
    situation leads to rapid movement of CO2 into the
    cell as CO2 is converted to HCO3-, the
    intracellular pH falls sharply
  • Acidification associated with increased PCO2
    often occurs much more rapidly in intracelluar
    compartment than in the extracelluar compartment
    because carbonic anhydrase (which catalyzes the
    conversion of CO2 to HCO3-,) is present inside
    cells but not always in extracellular fluid

8
Regulation of Body pH cont
  • proton-exchange anion exchange mechanisms in
    plasma membrane play NB role in adjusting
    intracellular pH
  • An acid load in the cell is accompanied by H
    efflux coupled to Na influx by HCO3- influx
    coupled to Cl- efflux the movement of HCO3-
    into the cell is equivalent to movement of H out
    of the cell because HCO3- ions that enter the
    cell are converted to CO2, releasing OH- ions
    increasing pH the CO2 so formed leaves the cell
    is converted to HCO3-, releasing protons
  • This cycling of CO2 HCO3- (Jacobs-Stewart
    Cycle) functions to remove H ions form cell
    interior in the face of an intracellular acid
    load such as that generated by anaerobic
    metabolism

9
Regulation of Body pH
  • Factors influencing intracellular pH cont -
    Intracellular pH remains stable if rate of acid
    loading (from metabolism or from influx into the
    cell) is equal to rate of acid removal any
    sudden increase in cell acidity will be countered
    by factors influencing intracellular pH
  • a. buffering by physical buffers (e.g proteins
    phosphates) located within the cell
  • b. reaction of HCO3 with H ions, forming CO2,
    which then diffuses out of cell
  • c. passive diffusion or active transport of H
    ions from the cell
  • d. cation-exchange mechanisms (Na/H
    Na/NH4), anion-exchange mechanisms (HCO3-/Cl-)
    or both in plasma membrane

10
Regulation of Body pH cont
  •  2. Factors influencing intracellular pH cont
  • pH influences many cellular activities some
    positively, some negatively e.g. many enzymes are
    inhibited by low pH such as those involved with
    glycolysis
  • 3. Factors influencing body pH stable body pH
    requires that acid production be matched to acid
    excretion in mammals, this is achieved b
    adjusting the excretion of CO2 via the lungs
    excretion of acid or bicarbonate via the kidneys
    (remember the A-type acid-excreting B-type
    cells base-excreting in aquatic animals,
    external body surfaces have the capacity to
    extrude acid in ways similar to that of
    collecting duct of mammalian kidney (e.g. skin of
    frogs gills of freshwater fishes have an ATPase
    on apical surface of epithelium that excretes
    protons fish gills also have apical HCO3-/Cl-
    exchanger)

11
Regulation of Body pH cont
  • Factors influencing body pH cont - Temperature
    can have a marked effect on body pH because the
    dissociation of water varies with temperature
    the pH of neutrality is 7.00 only at 250C
  • ability of body to redistribute acid between body
    compartments has functional significance because
    some tissues are more adversely affected by
    changes in pH than others e.g. brain is
    particularly sensitive whereas muscles tolerate
    much larger oscillations in pH

12
Gas Transfer in Air Lungs
  • Remember lungs gills are quite different are
    ventilated indifferent ways (the dissimilarities
    exist because the density viscosity of H2O are
    both approximately 1000 times greater than those
    of air and water contains only 1/30 as much
    molecular O2 PLUS gas molecules diffuse 10,000
    times more rapidly in air than in H2O PLUS air
    breathing consists of the reciprocal movement of
    air into out of lungs whereas water breathing
    consists of a unidirectional flow of H20 over
    gills

13
Functional Anatomy of the Lung
  • complex network of tubes sacs with the actual
    structure varying among species fig. 13-21 p. 546
  • sizes of terminal air spaces in lungs becomes
    progressively smaller from amphibians to reptiles
    to mammals while total number of air spaces per
    unit volume become greater
  • focus on mammalian lung consists of millions of
    blind-ended interconnected spaces (alveoli)
    main airway (trachea) subdivides to form bronchi
    bronchioles which branch repeatedly leading to
    terminal bronchioles respiratory bronchioles
    each of which is connected to terminal alveolar
    ducts alveoli
  • Total cross-sectional area of airway increases
    rapidly as a result of extensive branching
    (although the diameter of individual air ducts
    decreases from trachea to terminal bronchioles)

14
Gas Transfer in Air Lungs cont
  • gases are transferred across thin-walled alveoli
    airways leading to terminal bronchioles
    constitute nonrespiratory portion (i.e. no gas
    transfer) of lung alveoli are interconnected by
    series of holes (pores of Kohn) which allow
    collateral movement of air significant factor
    in gas distribution during lung ventilation
  • air ducts leading to respiratory portion of lung
    contain cartilage a little smooth muscle
    lined with cilia epithelium of ducts secretes
    mucus, which is moved toward the mouth by cilia
    (mucus escalator) keeps lungs clean in
    respiratory portions of lung, smooth muscle
    replaces cartilage contraction of this smooth
    muscle can have a marked effect on the dimensions
    of the airways in the lungs

15
Gas Transfer in Air Lungs cont
  • Diffusion Barrier crossed by O2 moving from air
    to blood is made up of
  • 1. an aqueous surface film
  • 2. epithelial cells of alveolus
  • 3. interstitial layer
  • 4. endothelial cells of capillaries
  • 5. blood plasma
  • 6. membrane of RBCs Fig. 13-22b p. 547

16
Gas Transfer in Air Lungs cont
  • 3 types of lung epithelial cells
  • 1. Type I (most abundant) squamous cells with
    thin plate-like structure extends between 2
    adjacent alveoli
  • 2. Type II laminated body within cells with
    surface villi they produce surfactant (more
    later)
  • 3. Type III rich in mitochondria numerous
    microvilli (NaCl uptake from lung fluid?)
    number of alveolar macrophages wander over
    surface of respiratory epithelium

17
Lung Ventilation - Terminology
  • 1. Eupnea normal, quite breathing at rest
  • 2. Hyperventilation/Hypoventilation increase
    (or decrease) in amount of air moved into or out
    of lungs by changes in rate/depth of breathing
    such that ventilation no longer matches CO2
    production blood CO2 levels changes
  • 3. Hyperpnea increase lung ventilation due to
    increased breathing in response to elevated CO2
    production (e.g. during exercise)
  • 4. Apnea absence of breathing
  • 5. Dyspnea laboured breathing
  • 6. Polypnea increased in breathing rate
    without increase in depth of breathing

18
Lung Ventilation cont
  • amount of air moved into or out of lungs with
    each breath tidal volume
  • air exchanged between alveoli environment
    passes through nonrespiratory sections i.e. at
    end of exhalation (expiration) air in
    nonrespriatory sections is high in CO2/low in O2
    is first to be inhaled with next breath at
    end of inhalation (inspiration) air in
    nonrespiratory sections is high in O2 low in
    CO2 is first exhaled volume of air not
    involved in gas transfer anatomic dead-space
    volume (some air may be supplied to nonfunctional
    alveoli or some alveoli may be ventilated at too
    high a rate, increasing volume of air not
    direclty involved in gas exchange physiological
    dead-space volume which includes the anatomic
    dead-space)

19
Lung Ventilation cont
  • amount of fresh air moving into/out of alveolar
    air sacs TV minus anatomic dead-space volume
    referred to as alveolar ventilation volume only
    this air is involved in gas exchange
  • maximum amount of air moved into or out of lungs
    vital capacity of lungs
  • O2 content is lower CO2 content is higher in
    alveolar gas than in ambient air because only a
    portion of the lungs gas volume is changed with
    each breath
  • O2 CO2 levels in alveolar gas are determined by
    both rate of gas transfer across respiratory
    epithelium rate of alveolar ventilation
    (alveolar ventilation depends on breathing rate,
    tidal volume anatomic dead-space volume)

20
Lung Ventilation cont
  • Artificial increases in anatomic dead space (such
    as those produced in humans breathing through a
    length of hose) result in a rise in CO2 a fall
    in O2 in the lungs these activates
    chemoreceptors, leading to an increase in TV
  • Animals with long necks (giraffe trumpeter
    swan) tracheal length therefore anatomic
    dead-space volume, is greater than those with
    short necks in order to maintain adequate gas
    partial pressures in lungs, long-necked animals
    have high tidal volumes
  • RR TV vary considerably among animals e.g.
    humans 12/min TV at rest 10 of total lung
    volume

21
Lung Ventilation cont
  • In summary, O2 CO2 levels in alveolar gas are
    determined by ventilation rate of gas transfer
  • Ventilation of respiratory epithelium is
    determined by RR, TV anatomic dead-space volume

22
Pulmonary Circulation
  • 1. pulmonary circulation deoxygenated blood
    from pulmonary artery from heart (taking up O2
    giving up CO2)
  • 2. bronchial circulation smaller supply
    comes from systemic (body) circulation supplies
    lung tissues themselves with O2 other
    substrates fro growth maintenance

23
Pulmonary Circulation cont
  • birds mammals BPs in pulmonary circulation lt
    those in systemic circulation this lower BP
    reduces filtration of fluid into lung extensive
    lymph drainage of lung tissues also helps ensure
    that no fluid collects in lung NB features
    because any fluid collecting in lung increases
    diffusion distance between blood air reduces
    gas transfer
  • Pulmonary vessels are very distensible subject
    to distortion by breathing movements
  • Arterial BP (also therefore blood flow) increases
    with distance form the apex of the lung in
    bottom half of vertical lung, where venous
    pressure exceeds alveolar pressure, blood flow is
    determined by the difference between arterial
    venous BPs

24
Pulmonary Circulation cont
  • mammalian pulmonary circulation lacks
    well-defined arterioles, both sympathetic
    adrenergic parasympathetic cholinergic fibers
    innervate smooth muscle around pulmonary blood
    vessels bronchioles
  • reduction in either O2 levels or pH cause local
    vasoconstriction of pulmonary blood vessels
  • CO in pulmonary circuit is equal to CO to
    systemic circuit in mammals birds (vs.
    amphibians reptiles which have a single or
    partially divided ventricle that ejects blood
    into both the pulmonary systemic circulation,
    the ratio of pulmonary to systemic blood flow can
    be altered

25
Mechanisms for Ventilation of Lung
  • these vary by species reflecting functional
    anatomy of lungs associated structures
    primarily consider mammals
  • lungs elastic, multi-chambered bags suspected
    within the pleural cavity (aka thoracic cavity)
    open to exterior via single tube (trachea) fig.
    13-28 p. 552 walls formed by ribs diaphragm
    lungs fill most of thoracic cage, leaving a
    low-volume pleural space between lungs thoracic
    wall this space is sealed filled with fluid
    fig 13-28 p. 552

26
Mechanisms for Ventilation of Lung cont
  • lungs elasticity creates pressure below
    atmospheric pressure in fluid-filled pleural
    space (fluid provides flexible, lubricated
    connection between outer lung surface thoracic
    wall (thus, when thoracic cavity changes volume,
    gas-filled lungs do too)
  • pneumothorax when thoracic cage is punctured
    air is drawn into pleural cavity lungs collapse
  • during normal breathing thoracic cage is
    expanded contracted by series of skeletal
    muscles, diaphragm external internal
    intercostals muscles these muscle contractions
    are determined by activity of motor neurons
    controlled by the respiratory center within the
    medulla oblongata

27
Mechanisms for Ventilation of Lung cont
  • volume of thorax increases as ribs are raised
    moved outward by contraction of external
    intercostals by contraction (lowering) of
    diaphragm fig. 13-30 p. 552 (contraction of
    diaphragm accounts for 2/3 of increase in
    pulmonary volume increase in thoracic volume
    reduces alveolar pressure air is drawn into
    lungs relaxation of diaphragm external
    intercostals muscles reduces thoracic volume
    raises alveolar pressure forcing air out of
    lungs (generally, inhalation is controlled and
    exhalation is passive)

28
Pulmonary surfactants
  • Lung wall tension depends on properties of wall
    surface tension at the liquid-air interface
    surface tension is a force that tends to minimize
    the area of a liquid surface causing liquid
    droplets to form a sphere (makes surface film
    resistant to stretch)
  • Fluid lining is not simply water but surfactant
    lipoprotein complexes that bestow very low
    surface tension on liquid-air interface

29
Roles of Surfactants
  • 1. low surface tension of fluid lining alveoli
    allows alveoli to expand easily during breathing
    reduces effort of inflating lung (as noted
    above)
  • 2. alveoli fold as their volume decreases
    would stick/become glued together by surface
    tension if not for surfactant (reducing surface
    tension to allow easy inflation of collapsed
    alveoli) when lung volume is reduced extremely,
    the lung will collapse atelectasis however, due
    to presence of surfactant, even a collapsed lung
    can be re-inflated easily

30
Roles of Surfactants cont
  • 3. allow newborn babies to inflate their lungs
    (in mammals, surfactant appears in fetal lung
    prior to birth without surfactant babies
    cannot inflate lungs called neonatal
    respiratory distress syndrome)
  • 4.  reduce resistance to blood flow by increasing
    compliance of capillary-alveolar sheet
  • 5. increase osmotic pressure of lung fluid
    reducing water flux across lung epithelium

31
Heat Water Loss
  • increases in lung ventilation not only increase
    gas transfer but also result increased losses of
    heat water
  • cool, dry air entering lungs of mammals is
    humidified (by H2O evaporation from surface of
    respiratory epithelium) heated as air in
    contact with respiratory surface becomes
    saturated with H2O vapor comes into thermal
    equilibrium with blood exhalation of this hot,
    humid air results in considerable loss of heat
    H2O because evaporation of H2O cools nasal
    mucosa, temperature gradient exists along nasal
    passages (cool at tip of nose, warm towards
    glottis) (cooling of exhalant air in nasal
    passages results in conservation of both heat
    water) structural variety in nasal passages
    among vertebrates

32
Regulation of Gas Transfer
  • energy is expended in ventilating respiratory
    surface with air(or water) in perfusing
    respiratory epithelium with blood significant
    selective pressure in favour of evolution of
    mechanisms for close regulation of ventilation
    perfusion in order to conserve energy

33
Neuronal Regulation of Breathing
  • Medullary respiratory center respiratory
    muscles activated by spinal motor neurons which
    receive inputs from neurons that constitute
    medullary respiratory center (such control can be
    very precise allowing extremely fine control of
    air flow e.g. whistling, singing, talking)

34
Neuronal Regulation of Breathing cont
  • Inhalation of lungs stimulates pulmonary stretch
    receptors in bronchi bronchioles which have a
    reflex inhibitory effect via vagus nerve on
    medullary inspiratory center thus on
    inspiration medulla contains a central rhythm
    generator that drives pattern generator within
    medullary respiratory center to cause breathing
    movements (remember mechanorecptors
    chemoreceptors provide info to medullary
    respiratory center too fig. 13-46 p. 566)
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