Differential pharmacological properties of GABA A receptors in axon terminals and soma of dentate gyrus granule cells

• Published in: Journal of neurochemistry Vol. 109; no. 4; pp. 995 - 1007
• Main Authors: Han, Jin‐Wuk, Nakamura, Michiko, Choi, In‐Sun, Cho, Jin‐Hwa, Park, Hye‐Mi, Lee, Maan‐Gee, Choi, Byung‐Ju, Jang, Hyun‐Jung, Jang, Il‐Sung
• Format: Journal Article
• Language: English
• Published: 01.05.2009
• ISSN: 0022-3042; 1471-4159
• DOI: 10.1111/j.1471-4159.2009.06018.x

Abstract Although it has been well established that GABA A receptors are molecular targets of a variety of allosteric modulators, such as benzodiazepines, the pharmacological properties of presynaptic GABA A receptors are poorly understood. In this study, the effects of diazepam and Zn 2+ on presynaptic GABA A receptors have been investigated by measuring the GABA A receptor‐mediated facilitation of spontaneous glutamate release in mechanically dissociated rat CA3 pyramidal neurons. Diazepam significantly enhanced the muscimol‐induced facilitation (particularly at submicromolar concentrations) of spontaneous glutamate release and shifted the concentration–response relationship for muscimol toward the left, whereas Zn 2+ (≤ 100 μM) had little effect on the muscimol‐induced facilitation of spontaneous glutamate release. In contrast, Zn 2+ significantly suppressed the muscimol‐induced currents mediated by GABA A receptors expressed on dentate gyrus granule cells, which are parent neurons of mossy fibers, whereas the effect of diazepam on GABA A receptors expressed on dentate gyrus granule cells was lesser than that on presynaptic GABA A receptors. The results suggest that the pharmacological properties of GABA A receptors differ considerably between presynaptic (axon terminals) and somatic regions in the same granule cell and that presynaptic GABA A receptors should be considered as one of the important pharmacological targets of many drugs affecting GABA A receptors.