Floran B, Silva I, Nava C, Aceves J
Department of Physiology, Biophysics and Neurosciences, Centro de Investigacíon del IPN, México, D.F.
Eur J Pharmacol. 1988 Jun 10;150(3):277-86. doi: 10.1016/0014-2999(88)90008-8.
The effect of GABA agonists and antagonists on K+-stimulated [3H]GABA release was studied to assess how presynaptic GABA receptors modulate GABA release. The release was affected in a quite different manner in the pars compacta and in the pars reticulata. Muscimol markedly inhibited the release from the pars compacta but had no effect on the release from the pars reticulata. Baclofen inhibited the release from the pars reticulata without affecting the release from the pars compacta. Bicuculline itself facilitated the release from the pars compacta but inhibited the release from the pars reticulata. Picrotoxin facilitated the release from the pars compacta and had no effect in the pars reticulata. The results suggest that the release of GABA from GABAergic terminals in the substantia nigra of the rat brain is modulated by GABAA autoreceptors in the pars compacta and by GABAB receptors in the pars reticulata.
研究了γ-氨基丁酸(GABA)激动剂和拮抗剂对钾离子刺激的[3H]GABA释放的影响,以评估突触前GABA受体如何调节GABA释放。黑质致密部和网状部的释放受到的影响方式截然不同。蝇蕈醇显著抑制致密部的释放,但对网状部的释放没有影响。巴氯芬抑制网状部的释放,而不影响致密部的释放。荷包牡丹碱本身促进致密部的释放,但抑制网状部的释放。印防己毒素促进致密部的释放,对网状部没有影响。结果表明,大鼠脑黑质中GABA能终末的GABA释放受致密部的GABAA自身受体和网状部的GABAB受体调节。