Literature DB >> 5571915

Switching of the respiratory phases and evoked phrenic responses produced by rostral pontine electrical stimulation.

M I Cohen.   

Abstract

1. In midcollicular-decerebrate, gallamine-paralysed, vagotomized cats, efferent phrenic discharge was recorded as an indicator of the central respiratory cycle. Electrical stimulation (50-250/sec) delivered in the rostral lateral pontine ;pneumotaxic centre' region (in and near nucleus parabrachialis), and set to occur at specified times in the cycle, produced powerful respiratory effects: (a) at dorsolateral points, inspiratory-facilitatory effects (increase of phrenic discharge, shortening of the expiratory phase); (b) at ventrolateral points, expiratory-facilitatory effects (decrease of phrenic discharge, shortening of the inspiratory phase, lengthening of the expiratory phase).2. At both inspiratory-facilitatory and expiratory-facilitatory points, a single stimulus delivered during the inspiratory phase produced a short-latency (4-7 msec) reduction of phrenic discharge, followed by a wave of increased activity. The short latency of the response indicates the existence of paucisynaptic descending inhibitory pathways. Succeeding stimuli in a high-frequency train produced alternating waves of evoked activity and depression; the form of the responses depended on stimulus frequency and on locus of stimulation.3. At inspiratory-facilitatory points, short stimulus trains (10-30 stimuli) of adequate strength delivered in the middle and late expiratory phase caused early termination of the phase (latency 100-300 msec) and switching to a complete inspiratory phase, in which the phrenic discharge pattern resembled that in a normal inspiratory phase. Similarly, adequate stimulus trains applied at expiratory-facilitatory points during the middle and late inspiratory phase caused early termination of the phase and switching to a complete expiratory phase.4. The threshold for occurrence of each type of phase-switching response depended on stimulus current, frequency, number of stimuli, and time of stimulus delivery. As stimulus trains were delivered later in the phase, the threshold for switching to the succeeding phase was progressively reduced. Moreover, the nature of the evoked effects was a non-linear function of stimulus characteristics: a small increase of stimulus efficacy changed the system's response from (a) moderate shortening of the phase or transient change in phrenic discharge, to (b) complete termination of the phase.5. These results indicate that, as each respiratory phase progresses, there is a steady increase of excitability in systems which promote the onset of the succeeding phase. Further, the existence of a relatively sharp threshold for switching of the respiratory phases suggests that the phase transitions occur when critical levels of excitation and inhibition are reached synchronously in populations of respiratory neurones.

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Mesh:

Year:  1971        PMID: 5571915      PMCID: PMC1331548          DOI: 10.1113/jphysiol.1971.sp009563

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  20 in total

1.  [Phrenic response evoked by stimulation of the parabrachial nucleus in cats].

Authors:  F Bertrand
Journal:  J Physiol (Paris)       Date:  1969

2.  Discharge patterns of brain-stem respiratory neurons during Hering-Breuer reflex evoked by lung inflation.

Authors:  M I Cohen
Journal:  J Neurophysiol       Date:  1969-05       Impact factor: 2.714

3.  Spontaneous and evoked oscillations in respiratory and sympathetic discharge.

Authors:  M I Cohen; P M Gootman
Journal:  Brain Res       Date:  1969-11       Impact factor: 3.252

4.  [Stimulatory physiologic demonstration of inspiratory and expiratory reactive territories at the pontine level of the rabbit brain stem. A contribution to the problem of the pneumotactic mechanism].

Authors:  P Polz; R W Hunsperger
Journal:  Helv Physiol Pharmacol Acta       Date:  1968

5.  Discharge patterns of brain-stem respiratory neurons in relation to carbon dioxide tension.

Authors:  M I Cohen
Journal:  J Neurophysiol       Date:  1968-03       Impact factor: 2.714

6.  Respiratory synchronizing function of nucleus parabrachialis medialis: pneumotaxic mechanisms.

Authors:  F Bertrand; A Hugelin
Journal:  J Neurophysiol       Date:  1971-03       Impact factor: 2.714

7.  [Tonic unitary activity with respiratory periodic modulation in the region of the cat parabrachialis nucleus].

Authors:  F Bertrand; A Hugelin
Journal:  J Physiol (Paris)       Date:  1968

8.  Suprapontine reticular control of intrinsic respiratory mechanisms.

Authors:  M I Cohen; A Hugelin
Journal:  Arch Ital Biol       Date:  1965-06-10       Impact factor: 1.000

9.  Brain-stem regions for stimulus-bound and stimulus-related respiration.

Authors:  E S Tan
Journal:  Exp Neurol       Date:  1967-04       Impact factor: 5.330

10.  Medullary activation of intercostal fusimotor and alpha motoneurones.

Authors:  P Andersen; T A Sears
Journal:  J Physiol       Date:  1970-08       Impact factor: 5.182

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  54 in total

1.  Interrelationships of the volume and time components of individual breaths in resting man.

Authors:  J N Davis; D Stagg
Journal:  J Physiol       Date:  1975-02       Impact factor: 5.182

2.  Site-specific effects on respiratory rhythm and pattern of ibotenic acid injections in the pontine respiratory group of goats.

Authors:  J M Bonis; S E Neumueller; K L Krause; T Kiner; A Smith; B D Marshall; B Qian; L G Pan; H V Forster
Journal:  J Appl Physiol (1985)       Date:  2010-04-29

3.  A role for the Kolliker-Fuse nucleus in cholinergic modulation of breathing at night during wakefulness and NREM sleep.

Authors:  J M Bonis; S E Neumueller; K L Krause; T Kiner; A Smith; B D Marshall; B Qian; L G Pan; H V Forster
Journal:  J Appl Physiol (1985)       Date:  2010-04-29

4.  Projections of preBötzinger complex neurons in adult rats.

Authors:  Wenbin Tan; Silvia Pagliardini; Paul Yang; Wiktor A Janczewski; Jack L Feldman
Journal:  J Comp Neurol       Date:  2010-05-15       Impact factor: 3.215

5.  Differing control of neural activities during various portions of expiration in the cat.

Authors:  W M St John; D Zhou
Journal:  J Physiol       Date:  1989-11       Impact factor: 5.182

6.  Large-scale activity in neural nets II: A model for the brainstem respiratory oscillator.

Authors:  J L Feldman; J D Cowan
Journal:  Biol Cybern       Date:  1975       Impact factor: 2.086

7.  Kölliker–Fuse neurons send collateral projections to multiple hypoxia-activated and nonactivated structures in rat brainstem and spinal cord.

Authors:  Gang Song; Hui Wang; Hui Xu; Chi-Sang Poon
Journal:  Brain Struct Funct       Date:  2012-01-28       Impact factor: 3.270

8.  Respiratory depression caused by either morphine microinjection or repetitive electrical stimulation in the region of the nucleus parabrachialis of cats.

Authors:  K Eguchi; E Tadaki; D Simbulan; T Kumazawa
Journal:  Pflugers Arch       Date:  1987-08       Impact factor: 3.657

9.  Lateral parabrachial nucleus mediates shortening of expiration during hypoxia.

Authors:  Gang Song; Chi-Sang Poon
Journal:  Respir Physiol Neurobiol       Date:  2008-10-17       Impact factor: 1.931

10.  Clinically relevant infusion rates of mu-opioid agonist remifentanil cause bradypnea in decerebrate dogs but not via direct effects in the pre-Bötzinger complex region.

Authors:  Sanda Mustapic; Tomislav Radocaj; Antonio Sanchez; Zoran Dogas; Astrid G Stucke; Francis A Hopp; Eckehard A E Stuth; Edward J Zuperku
Journal:  J Neurophysiol       Date:  2009-11-11       Impact factor: 2.714

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