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Influence of GABAergic mechanisms on baroreceptor inputs to nucleus tractus solitarii of rats

  • Piero Ruggeri
  • , Carla E. Cogo
  • , Viviana Picchio
  • , Claudio Molinari
  • , Rosa Ermirio
  • , Franco R. Calaresu

Research output: Contribution to journalArticlepeer-review

Abstract

The firing frequency of baroreceptive neurons in the nucleus tractus solitarii (NTS) during microiontophoretic application of muscimol, a γ- aminobutyric acid (GABA)(A) agonist, or baclofen, a GABA(B) agonist, was monitored in anesthetized rats. Muscimol decreased the spontaneous discharge of 69 of 73 (94.5%) NTS baroreceptive neurons without affecting the remaining four neurons (5.5%). The statistical comparison on a bin-by-bin basis of the peri-R wave interval histograms of the discharge of each NTS neuron showed that the inhibitory action of muscimol was always exerted on the whole neuronal discharge independently of its correlation to the cardiac cycle. Baclofen inhibited 60 of 73 (82.2%) NTS neurons without affecting the remaining 13 neurons (17.8%). In 31 of 60 (51.7%) neurons inhibited by baclofen, this substance significantly affected only pulse-synchronous peaks of neuronal discharge without significant inhibition of the neuronal firing between cardiac cycle-related peaks. Fifty-eight of 73 (79.5%) NTS neurons studied were inhibited by both muscimol and baclofen, 11 neurons (15%) only by muscimol, 2 neurons (2.7%) only by baclofen, and 2 neurons (2.7%) were unaffected by both substances. These results demonstrate that both GABA(A) and GABA(B) receptors mediate inhibition of the spontaneous discharge in the great majority of the NTS baroreceptive neurons studied and suggest different functions of the two types of GABA receptors in influencing baroreceptor inputs to the NTS.

Original languageEnglish
Pages (from-to)H931-H936
JournalAmerican Journal of Physiology - Heart and Circulatory Physiology
Volume271
Issue number3 40-3
DOIs
Publication statusPublished - Sept 1996

Keywords

  • brain stem
  • cardiovascular control
  • γ-aminobutyric acid
  • γ-aminobutyric acid receptors

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