Literature DB >> 3116216

Responses to circulatory pressures, and conduction velocity, of pulmocutaneous baroreceptors in Bufo marinus.

B N Van Vliet1, N H West.   

Abstract

1. Baroreceptor activity was recorded within the recurrent laryngeal branch of the toad vagus in forty-four preparations. The receptive fields of the receptors were located in the pulmocutaneous artery (p.c.a.), generally within 5 mm of its separation from the truncus. However, the most easily recorded afferents in this nerve were mechanoreceptors which responded to punctate stimulation of the lip of the glottis. 2. The conduction velocities of p.c.a. baroreceptor and mechanoreceptive glottal afferents recorded in the recurrent laryngeal nerve ranged from 0.3-0.7 (0.5 +/- 0.1) m s-1 and 2.2-14.0 (6.8 +/- 0.8) m s-1 respectively, which suggests that baroreceptor afferent fibres are non-myelinated and that glottal afferent fibres are myelinated. 3. The p.c.a. baroreceptor discharge was largely confined to a period of systole in which systemic and p.c.a. arterial pressure profiles were identical. The maximum discharge frequency, number of spikes per cycle, and the duration of discharge increased, and the discharge latency decreased, as p.c.a. pressures were elevated. The latency of the discharge was pronounced at low p.c.a. pressures, and could be partially accounted for by the conduction time of the baroreceptor afferents to the electrodes (up to 100 ms). 4. Carotid and aortic arterial baroreceptor and pharyngeal afferents were recorded in two pharyngeal branches of the vagus nerve which were closely associated with the carotid and aortic arterial arches. 5. It is suggested that baroreceptor populations with their receptive fields in the third- (carotid) and sixth- (p.c.a. or pulmonary) arch arteries should be considered homologous in anurans and mammals, but that those of the fourth- (aorta) arch artery should not, since the vagal branches in which their afferents are carried do not appear to be equivalent in anurans and mammals.

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Year:  1987        PMID: 3116216      PMCID: PMC1192534          DOI: 10.1113/jphysiol.1987.sp016600

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


  17 in total

1.  POSSIBLE BAROCEPTOR NERVE ENDINGS IN THE VICINITY OF THE AMPHIBIAN CAROTID LABYRINTH.

Authors:  D C ROGERS
Journal:  Acta Anat (Basel)       Date:  1964

2.  The histology of the common carotid baroceptor areas of the cat.

Authors:  J BOSS; J H GREEN
Journal:  Circ Res       Date:  1956-01       Impact factor: 17.367

3.  A Description of the Cerebral and Spinal Nerves of Rana Esculenta.

Authors:  A de Watteville
Journal:  J Anat Physiol       Date:  1874-11

Review 4.  Systemic arterial baroreceptor reflexes.

Authors:  H R Kirchheim
Journal:  Physiol Rev       Date:  1976-01       Impact factor: 37.312

5.  A laryngeal pathway for aortic baroceptor impulses.

Authors:  B L ANDREW
Journal:  J Physiol       Date:  1954-08-27       Impact factor: 5.182

6.  Afferent neural activity from pseudobranch of teleosts. Effects of P 02 , pH, osmotic pressure and Na + ions.

Authors:  P Laurent; J D Rouzeau
Journal:  Respir Physiol       Date:  1972-04

7.  Cardiovascular reflexes in conscious toads.

Authors:  A Hoffmann; M B de Souza
Journal:  J Auton Nerv Syst       Date:  1982-05

8.  The function of the carotid labyrinth in the toad.

Authors:  K Ishii; K Honda; K Ishii
Journal:  Tohoku J Exp Med       Date:  1966-02-25       Impact factor: 1.848

9.  Dynamics of blood flow through the hearts and arterial systems of anuran amphibia.

Authors:  B L Langille; D R Jones
Journal:  J Exp Biol       Date:  1977-06       Impact factor: 3.312

10.  Characteristics of rat aortic baroreceptors with nonmedullated afferent nerve fibers.

Authors:  P Thorén; W R Saum; A M Brown
Journal:  Circ Res       Date:  1977-03       Impact factor: 17.367

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