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. 1995 Jul;115(6):953–960. doi: 10.1111/j.1476-5381.1995.tb15903.x

Potentiation, activation and blockade of GABAA receptors of clonal murine hypothalamic GT1-7 neurones by propofol.

S Adodra 1, T G Hales 1
PMCID: PMC1909023  PMID: 7582526

Abstract

1. The actions of GABA and the intravenous general anaesthetic propofol (2,6-diisopropylphenol) on GABAA receptors of self-replicating GT1-7 hypothalamic neurones were investigated by the patch clamp technique. 2. GABA (1 microM-1 mM) dose-dependently activated inward currents with an EC50 of 27 microM, recorded from whole cells voltage-clamped at -60 mV. GABA (100 microM)-activated currents reversed at the Cl-equilibrium potential. 3. Propofol (0.1-100 microM) dose-dependently potentiated GABA (100 microM)-evoked currents with an EC50 of 5 microM. 4. In the absence of GABA, propofol (10 microM-1 mM) activated small inward currents with a reversal potential similar to the Cl- equilibrium potential. The peak current amplitudes activated by propofol were only 31% of those activated by GABA in the same cells. 5. Like GABA (100 microM)-activated currents, propofol (100 microM)-activated currents were inhibited by the GABAA receptor antagonist, bicuculline (10 microM) and were abolished by Zn2+ (100 microM). 6. Propofol (10, 30 and 100 microM) dose-dependently activated currents in the absence of GABA. However, the peak amplitude of currents activated by propofol declined with concentrations > 100 microM. The cessation of application of a high dose of propofol (1 mM) was associated with a current 'surge'. 7. The surge current, seen after application of propofol (1 mM), had a reversal potential similar to the Cl- equilibrium potential. The ratio between peak current amplitude in the presence of propofol (1 mM) and surge current amplitude after propofol application, were not dependent on holding potential.(ABSTRACT TRUNCATED AT 250 WORDS)

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Selected References

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