Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation Research
Search: search_blue_button Advanced Search
Circulation Research. 2007
Published online before print January 4, 2007, doi: 10.1161/01.RES.0000257370.63694.73
A more recent version of this article appeared on February 2, 2007
This Article
Right arrow Full Text (PDF)
Right arrow Data Supplement
Right arrow All Versions of this Article:
100/2/284    most recent
01.RES.0000257370.63694.73v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Padley, J. R.
Right arrow Articles by Goodchild, A. K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Padley, J. R.
Right arrow Articles by Goodchild, A. K.
Related Collections
Right arrow Cardiovascular Pharmacology
Right arrow Gene expression
Right arrow Autonomic, reflex, and neurohumoral control of circulation

Submitted on October 13, 2006
Revised on November 29, 2006
Accepted on December 20, 2006

Central Command Regulation of Circulatory Function Mediated by Descending Pontine Cholinergic Inputs to Sympathoexcitatory Rostral Ventrolateral Medulla Neurons

James R. Padley ; Natasha N. Kumar ; Qun Li ; Thomas B.V. Nguyen ; Paul M. Pilowsky ; and Ann K. Goodchild *

From the Hypertension and Stroke Research Laboratories, Kolling Institute of Medical Research, Royal North Shore Hospital and School of Medical Sciences, University of Sydney, Australia.

* To whom correspondence should be addressed. E-mail: anng{at}physiol.usyd.edu.au.

Central command is a feedforward neural mechanism that evokes parallel modifications of motor and cardiovascular function during arousal and exercise. The neural circuitry involved has not been elucidated. We have identified a cholinergic neural circuit that, when activated, mimics effects on tonic and reflex control of circulation similar to those evoked at the onset of and during exercise. Central muscarinic cholinergic receptor (mAChR) activation increased splanchnic sympathetic nerve activity (SNA) as well as the range and gain of the sympathetic baroreflex via activation of mAChR in the rostral ventrolateral medulla (RVLM) in anesthetized artificially ventilated Sprague-Dawley rats. RVLM mAChR activation also attenuated and inhibited the peripheral chemoreflex and somatosympathetic reflex, respectively. Cholinergic terminals made close appositions with a subpopulation of sympathoexcitatory RVLM neurons containing either preproenkephalin mRNA or tyrosine hydroxylase immunoreactivity. M2 and M3 receptor mRNA was present postsynaptically in only non-tyrosine hydroxylase neurons. Cholinergic inputs to the RVLM arise only from the pedunculopontine tegmental nucleus. Chemical activation of this region produced increases in muscle activity, SNA, and blood pressure and enhanced the SNA baroreflex; the latter effect was attenuated by mAChR blockade. These findings indicate a novel role for cholinergic input from the pedunculopontine tegmental nucleus to the RVLM in central cardiovascular command. This pathway is likely to be important during exercise where a centrally evoked facilitation of baroreflex control of the circulation is required to maintain blood flow to active muscle.


Key words: baroreflex • exercise • chemoreflex • somatosympathetic




This article has been cited by other articles:


Home page
HypertensionHome page
P. G.R. Burke, Q. Li, M. L. Costin, S. McMullan, P. M. Pilowsky, and A. K. Goodchild
Somatostatin 2A Receptor-Expressing Presympathetic Neurons in the Rostral Ventrolateral Medulla Maintain Blood Pressure
Hypertension, December 1, 2008; 52(6): 1127 - 1133.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
M. M. J. Farnham, Q. Li, A. K. Goodchild, and P. M. Pilowsky
PACAP is expressed in sympathoexcitatory bulbospinal C1 neurons of the brain stem and increases sympathetic nerve activity in vivo
Am J Physiol Regulatory Integrative Comp Physiol, April 1, 2008; 294(4): R1304 - R1311.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
S. Ogoh, J. P. Fisher, P. B. Raven, and P. J. Fadel
Arterial baroreflex control of muscle sympathetic nerve activity in the transition from rest to steady-state dynamic exercise in humans
Am J Physiol Heart Circ Physiol, October 1, 2007; 293(4): H2202 - H2209.
[Abstract] [Full Text] [PDF]