Whole cell and single channel properties of a new GABA receptor transiently expressed in the hippocampus

M. Martina*, F. Strata, E. Cherubini

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

30 Scopus citations

Abstract

1. The patch-clamp technique was used to characterize, in acutely dissociated CA3 rat hippocampal neurons, the whole cell and single channel properties of a novel response to γ-aminobutyric acid (GABA) present only during a restricted period of postnatal development. 2. At postnatal days 0- 10 (P0-P10), both GABA (100 μM) and isoguvacine (50 μM) evoked at a holding potential of -50 mV, in symmetrical chloride solution, whole cell inward currents. Bicuculline blocked the response to isoguvacine but only reduced the response to GABA (from 512 ± 137 pA to 60 ± 13 pA, mean ± SE). After P12, bicuculline abolished the response to GABA. 3. The bicuculline- insensitive GABA currents were Cl- mediated and antagonized by picrotoxin. The desensitization rate was slower than the conventional bicuculline- sensitive response. The peak to plateau ratio induced by 0.1 or 1 mM of GABA shifted from 4.6 ± 0.4 and 17.7 ± 2.6 to 1.5 ± 0.1 and 3.1 ± 0.5 in the absence or in the presence of bicuculline, respectively. The recovery from desensitization was significantly faster for the bicuculline-insensitive responses. 4. In excised outside-out patches, GABA (20 μM) activated, in the presence of bicuculline (100 μM), single channel currents having conductances of 14, 22, and 31 pS. These values were similar to those obtained in the same preparation, in the absence of bicuculline. 5. These findings suggest that this new receptor type, which mediates bicuculline- insensitive responses with slow kinetics, may potentiate the depolarizing action of GABA during a critical period of postnatal development and therefore play a crucial role in synaptogenesis.

Original languageEnglish (US)
Pages (from-to)902-906
Number of pages5
JournalJournal of Neurophysiology
Volume73
Issue number2
DOIs
StatePublished - Jan 1 1995

ASJC Scopus subject areas

  • Neuroscience(all)
  • Physiology

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