Journal of Neurophysiology, Vol 61, Issue 5 892-899, Copyright © 1989 by APS

ARTICLES

Voltage-clamp characterization of Cl- conductance gated by GABA and L-glutamate in single neurons of Aplysia

W. M. King and D. O. Carpenter
Wadsworth Center for Laboratories and Research, New York State Department of Health, Albany.

1. Cl- conductance gated by gamma-aminobutyric acid (GABA) and L-glutamate in the medial pleural neurons of Aplysia was studied using conventional two-electrode voltage-clamp techniques and a continuous microperfusion system that allowed rapid and uniform agonist application. 2. Both GABA and glutamate elicited current responses that rapidly activated and then decayed (desensitized) during maintained presence of agonist. 3. Recovery from desensitization was rapid for both agonists. For intermediate concentrations of each agonist, recovery was approximately 90% complete within 1 min. 4. Dose-response experiments at a holding potential of -45 mV showed that 1) maximal peak responses to glutamate were on the average approximately 40% of those to GABA, 2) the dose-peak response curve for glutamate was steeper than that for GABA, and 3) time-to-peak (risetime) and desensitization half-time decreased monotonically with dose for GABA but were relatively insensitive to dose and more variable for glutamate. 5. Peak conductances elicited by GABA were voltage dependent, increasing with depolarization, whereas the Cl- conductance elicited by glutamate was voltage independent. Risetime and desensitization kinetics were insensitive to voltage for both agonists. 6. Lowering the temperature of the perfusion medium by 10 degrees C slowed activation and desensitization for both 0.1 mM GABA and 2 mM glutamate. The responses to the two agonists differed, however, in that the peak response to glutamate increased, whereas that to GABA decreased in amplitude.(ABSTRACT TRUNCATED AT 250 WORDS)

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