JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 72: 2222-2236, 1994;
0022-3077/94 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Habler, H. J.
Right arrow Articles by Peters, O. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Habler, H. J.
Right arrow Articles by Peters, O. A.

Journal of Neurophysiology, Vol 72, Issue 5 2222-2236, Copyright © 1994 by APS


ARTICLES

Reflex patterns in postganglionic neurons supplying skin and skeletal muscle of the rat hindlimb

H. J. Habler, W. Janig, M. Krummel and O. A. Peters
Physiologisches Institut, Christian-Albrechts-Universitat Kiel, Germany.

1. Reflex patterns were analyzed in spontaneously active postganglionic vasoconstrictor neurons supplying skeletal muscle [muscle vasoconstrictor (MVC) neurons] and hairy skin [cutaneous vasoconstrictor (CVC) neurons] of the rat hindlimb. Postganglionic activity was recorded from single units and from filaments containing the axons of several spontaneously active neurons (multiunit preparations). The animals were freely breathing or artificially ventilated and maintained, in different experiments, under three different types of anesthesia (pentobarbital, chloralose, urethan). Reflexes were elicited by stimulation of arterial baroreceptors, chemoreceptors, cutaneous nociceptors, and cold receptors and visceral receptors from urinary bladder and colon. 2. Spontaneous activity of single postganglionic neurons ranged from 0.3 to 3.6 imp/s (median 1.15 imp/s and 1.0 imp/s in MVC and CVC neurons, respectively). Postganglionic axons conducted at 0.56 +/- 0.15 m/s (mean +/- SD, MVC neurons) and 0.53 +/- 0.11 m/s (CVC neurons). There was almost no difference in the rate of spontaneous activity under the three anesthetics used and whether the animals were artificially ventilated or breathing freely. 3. Stimulation of arterial baroreceptors by increasing arterial blood pressure by > 30 mmHg with intravenous injections of phenylephrine or angiotensin led to a depression of the activity in almost all vasoconstrictor neurons. In simultaneous recordings, with an identical increase of blood pressure, the magnitude of inhibition was greater in MVC neurons than in CVC neurons. Phasic stimulation of the arterial baroreceptors by the pulse pressure wave evoked a pronounced cardiac rhythmicity in the activity of the majority of MVC neurons (78%), but in only a small fraction of CVC neurons (18%). In most CVC neurons the cardiac rhythmicity was weak (33%) or absent (49%). When quantified the difference in the degree of cardiac rhythmicity between simultaneously recorded MVC and CVC neurons was highly significant (P < 0.001). 4. Noxious mechanical stimulation of skin of the ipsilateral hindpaw activated 20/35 MVC preparations (57%) and inhibited 25/47 CVC preparations (53%). Some CVC neurons (19%) were also activated, whereas the remainder of neurons were not affected. The quality of responses to noxious stimulation was correlated with the degree of cardiac rhythmicity that the sympathetic neurons displayed in their activity. A similar reciprocal response pattern in CVC and MVC neurons, albeit less pronounced, was observed to intense cold stimuli (chlor-ethyl spray) applied to the hindlimb. 5. This reciprocal pattern of the responses of MVC and CVC neurons was not observed when nociceptors from the contralateral hindlimb were stimulated and when cold stimuli were applied to the abdominal skin.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
R. Kanbar, B. Chapuis, V. Orea, C. Barres, and C. Julien
Baroreflex control of lumbar and renal sympathetic nerve activity in conscious rats
Am J Physiol Regulatory Integrative Comp Physiol, July 1, 2008; 295(1): R8 - R14.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
C. Johnson, S. Hudson, and J. Marshall
Responses evoked in single sympathetic nerve fibres of the rat tail artery by systemic hypoxia are dependent on core temperature
J. Physiol., October 1, 2007; 584(1): 221 - 233.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
H. Ishii, T. Niioka, H. Watanabe, and H. Izumi
Inhibitory effects of excess sympathetic activity on parasympathetic vasodilation in the rat masseter muscle
Am J Physiol Regulatory Integrative Comp Physiol, August 1, 2007; 293(2): R729 - R736.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
M. Tanaka, Y. Ootsuka, M. J. McKinley, and R. M. McAllen
Independent vasomotor control of rat tail and proximal hairy skin
J. Physiol., July 1, 2007; 582(1): 421 - 433.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
A. E. Simms, J. F. R. Paton, and A. E. Pickering
Hierarchical recruitment of the sympathetic and parasympathetic limbs of the baroreflex in normotensive and spontaneously hypertensive rats
J. Physiol., March 1, 2007; 579(2): 473 - 486.
[Abstract] [Full Text] [PDF]


Home page
Exp PhysiolHome page
J. H. Coote
Landmarks in understanding the central nervous control of the cardiovascular system
Exp Physiol, January 1, 2007; 92(1): 3 - 18.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. W. Nason Jr and P. Mason
Medullary Raphe Neurons Facilitate Brown Adipose Tissue Activation
J. Neurosci., January 25, 2006; 26(4): 1190 - 1198.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
A. M. Coney, M. Bishay, and J. M. Marshall
Influence of endogenous nitric oxide on sympathetic vasoconstriction in normoxia, acute and chronic systemic hypoxia in the rat
J. Physiol., March 15, 2004; 555(3): 793 - 804.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. Jamieson, H. D. Boyd, and E. M. McLachlan
Simulations to Derive Membrane Resistivity in Three Phenotypes of Guinea Pig Sympathetic Postganglionic Neuron
J Neurophysiol, May 1, 2003; 89(5): 2430 - 2440.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
C. D. Johnson, A. M. Coney, and J. M. Marshall
Roles of norepinephrine and ATP in sympathetically evoked vasoconstriction in rat tail and hindlimb in vivo
Am J Physiol Heart Circ Physiol, December 1, 2001; 281(6): H2432 - H2440.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
H.-J. Habler, T. Bartsch, and W. Janig
Rhythmicity in Single Fiber Postganglionic Activity Supplying the Rat Tail
J Neurophysiol, May 1, 1999; 81(5): 2026 - 2036.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
C. D. Johnson and M. P. Gilbey
Effects of aortic nerve stimulation on discharges of sympathetic neurons innervating rat tail artery and vein
Am J Physiol Regulatory Integrative Comp Physiol, October 1, 1998; 275(4): R942 - R949.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
T. J. Scislo, R. A. Augustyniak, and D. S. O'Leary
Differential arterial baroreflex regulation of renal, lumbar, and adrenal sympathetic nerve activity in the rat
Am J Physiol Regulatory Integrative Comp Physiol, October 1, 1998; 275(4): R995 - R1002.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
H.-J. Habler, G. Wasner, and W. Janig
Attenuation of Neurogenic Vasoconstriction by Nitric Oxide in Hindlimb Microvascular Beds of the Rat In Vivo
Hypertension, October 1, 1997; 30(4): 957 - 961.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online