Dual GABAA receptor-mediated inhibition in rat presympathetic paraventricular nucleus neurons

Jin Bong Park, Silvia Skalska, Sookjin Son, Javier E. Stern

Research output: Contribution to journalArticle

51 Scopus citations

Abstract

The inhibitory neurotransmitter GABA plays a key role in the modulation of paraventricular nucleus (PVN) neuronal excitability and sympathoexcitatory outflow, under both physiological and pathological conditions. In addition to mediating conventional synaptic transmission (phasic inhibition), GABAA receptors of distinct biophysical, molecular and pharmacological properties have been recently found to underlie a slower, persistent form of inhibition (tonic inhibition). Whether the 'tonic' inhibitory modality is present in presympathetic PVN neurons, and what its role is in modulating their activity is at present unknown. Here, we combined tract-tracing techniques with patch-clamp electrophysiology to address these questions. Recordings obtained from PVN-RVLM (rostral ventrolateral medulla) projecting neurons show that besides blocking GABAA-mediated inhibitory postsynaptic currents (IPSCs, Iphasic), the GABAA receptor blockers bicuculline and picrotoxin caused an outward shift in the holding current (Itonic). Conversely, the high affinity GABAA blocker gabazine blocked Iphasic without affecting Itonic. THIP, a GABAA receptor agonist that preferentially activates δ- over γ-containing receptors, enhanced the magnitude of Itonic. Our results also indicate that during conditions of strong and/or synchronous synaptic activity, Itonic may be activated by spillover of synaptically released GABA. Blockade of Itonic induced membrane depolarization, increased firing activity, and enhanced the input-output function of PVN-RVLM neurons. Altogether, our results support the presence of a persistent GABAA-mediated inhibitory modality in presympathetic PVN neurons, which plays a major role in modulating their excitability and firing activity.

Original languageEnglish (US)
Pages (from-to)539-551
Number of pages13
JournalJournal of Physiology
Volume582
Issue number2
DOIs
StatePublished - Jul 2007

ASJC Scopus subject areas

  • Physiology

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