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Evidence that hemorrhagic hypotension is mediated by the ventrolateral periaqueductal gray region.

Abstract
Severe hemorrhage lowers arterial pressure by suppressing sympathetic activity. This study tested the hypothesis that the decompensatory phase of hemorrhage is mediated by the ventrolateral periaqueductal gray (vlPAG), a region importantly involved in the autonomic and behavioral responses to stress and trauma. Neuronal activity in the vlPAG was inhibited with either lidocaine or cobalt chloride 5 min before hemorrhage (2.5 ml/100 g body wt) was initiated in conscious, unrestrained rats. Bilateral injection of lidocaine (0.5 microl of a 2% or 1 microl of a 5% solution) into the caudal vlPAG delayed the onset and reduced the magnitude of the hypotension produced by hemorrhage significantly. In contrast, inactivation of the dorsolateral PAG with lidocaine was ineffective. Cobalt chloride (5 mM; 0.5 microl), which inhibits synaptic transmission but not axonal conductance, also attenuated hemorrhagic hypotension significantly. Microinjection of lidocaine or cobalt chloride into the vlPAG of normotensive, nonhemorrhaged rats did not influence cardiovascular function. These data indicate that the vlPAG plays an important role in the response to hemorrhage.
AuthorsS Cavun, W R Millington
JournalAmerican journal of physiology. Regulatory, integrative and comparative physiology (Am J Physiol Regul Integr Comp Physiol) Vol. 281 Issue 3 Pg. R747-52 (Sep 2001) ISSN: 0363-6119 [Print] United States
PMID11506988 (Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • Cobalt
  • Lidocaine
  • cobaltous chloride
Topics
  • Animals
  • Blood Pressure (drug effects, physiology)
  • Cobalt (administration & dosage)
  • Heart Rate (drug effects, physiology)
  • Hemorrhage (complications, physiopathology)
  • Hypotension (etiology, physiopathology, prevention & control)
  • Lidocaine (administration & dosage)
  • Male
  • Microinjections
  • Periaqueductal Gray (drug effects, physiopathology)
  • Rats
  • Synaptic Transmission (drug effects)
  • Wakefulness (physiology)

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