Affiliation:
1. Department of Pharmacology and Therapeutics, McGill University, Montreal, Quebec H3G 1Y6, Canada; and
2. Departments of Neurology and Physiology, UCLA School of Medicine, Los Angeles, California 90095
Abstract
De Koninck, Yves and Istvan Mody. Endogenous GABA activates small-conductance K+ channels underlying slow IPSCs in rat hippocampal neurons. J. Neurophysiol. 77: 2202–2208, 1997. The objective of this study was to determine the properties of K+ channels activated by endogenously released trasmitter under synaptic conditions. First, the levels of γ-aminobutyric acid (GABA) were depleted in hippocampal nerve endings to establish the relative contribution of endogenously released GABA to the activation of GABAB receptors mediating slow inhibitory postsynaptic currents (IPSCs). Inhibition of glutamic acid decarboxylase and GABA reuptake effectively depleted >85% of the releasable GABA pool, producing parallel reductions of GABAA and GABAB receptor-mediated IPSCs, indicating that both classes of receptors are activated synaptically by endogenously released GABA. Whole cell patch-clamp recordings of stimulus-evoked slow IPSCs at potentials hyperpolarized from the potassium reversal potential were consistent with the activation of a nonrectifying ( n = 3) or slightly outwardly rectifying ( n = 4) K+ conductance by the endogenously released GABA. Spectral analysis of the decay phase of GABAB IPSCs revealed several time constants indicating complex underlying channel kinetics. Nonstationary variance analysis yielded a small unitary conductance in the range of 5–13 pS, consistent with a large number of channels activated during evoked currents. These results indicate that in granule cells of the dentate gyrus, GABA released synaptically from interneuron terminals activates an unusually small K+ conductance, with no or slight outward rectification. This conductance is therefore unlike those typically reported for neuronal G protein-coupled K+ channels or those activated by exogenously applied baclofen with larger, inwardly rectifying conductances.
Publisher
American Physiological Society
Subject
Physiology,General Neuroscience
Cited by
23 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献