Negishi M, Ito S
Department of Cell Biology, Osaka Bioscience Institute, Japan.
Biochem Pharmacol. 1990 Dec 15;40(12):2719-25. doi: 10.1016/0006-2952(90)90593-a.
The effects of GABA on catecholamine release and phosphoinositide metabolism were studied in cultured bovine adrenal chromaffin cells. GABA and muscimol, a specific agonist for the GABAA receptor, each evoked a gradual secretion of catecholamines from the cells in the presence of ouabain, an inhibitor of Na+, K(+)-ATPase. This release was inhibited by bicuculline, a specific antagonist for the GABAA receptor, or by picrotoxin, a blocker of GABA-gated Cl- channels, and was potentiated by diazepam or pentobarbital. GABA or muscimol induced a concentration-dependent formation of inositol phosphates. This accumulation of inositol phosphates was also inhibited by bicuculline, picrotoxin or removal of extracellular Ca2+, and also potentiated by diazepam and pentobarbital. Nicardipine suppressed GABA-induced catecholamine release in the presence of ouabain and accumulation of inositol phosphates, while verapamil, diltiazem, and omega-conotoxin failed to inhibit these responses to GABA. The phosphoinositide-specific phospholipase C inhibitor neomycin also inhibited both GABA-induced accumulation of inositol phosphates and stimulation of catecholamine release in the presence of ouabain. These results taken together indicate that GABA evoked catecholamine release from the chromaffin cells in the presence of ouabain by stimulation of phosphoinositide metabolism in a Ca2(+)-sensitive manner via activation of GABAA receptor-coupled Cl- channels.
在培养的牛肾上腺嗜铬细胞中研究了γ-氨基丁酸(GABA)对儿茶酚胺释放和磷酸肌醇代谢的影响。GABA和GABAA受体的特异性激动剂蝇蕈醇,在钠钾ATP酶抑制剂哇巴因存在的情况下,均可引起细胞中儿茶酚胺的逐渐分泌。这种释放受到GABAA受体的特异性拮抗剂荷包牡丹碱或GABA门控氯离子通道阻滞剂印防己毒素的抑制,并被地西泮或戊巴比妥增强。GABA或蝇蕈醇诱导了磷酸肌醇的浓度依赖性形成。磷酸肌醇的这种积累也受到荷包牡丹碱、印防己毒素或细胞外钙离子去除的抑制,并且也被地西泮和戊巴比妥增强。硝苯地平在哇巴因存在的情况下抑制了GABA诱导的儿茶酚胺释放和磷酸肌醇的积累,而维拉帕米、地尔硫卓和ω-芋螺毒素未能抑制对GABA的这些反应。磷酸肌醇特异性磷脂酶C抑制剂新霉素也抑制了在哇巴因存在的情况下GABA诱导的磷酸肌醇积累和儿茶酚胺释放的刺激。这些结果综合表明,在哇巴因存在的情况下,GABA通过激活GABAA受体偶联的氯离子通道以钙敏感的方式刺激磷酸肌醇代谢,从而引起嗜铬细胞释放儿茶酚胺。