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机构地区:[1]中国科学院上海生理研究所
出 处:《生理学报》1995年第1期1-10,共10页Acta Physiologica Sinica
基 金:国家科学基金;中国科学院上海生命科学研究中心;生命科学联合开放实验室资助
摘 要:两栖类卵母细胞表达系统经注射鲫鱼(Carassiuscarassius)脑mRNA后可表达多种神经递质受体和某些离子通道。本工作利用电压箝方法结合药理学手段对GABA受体和谷氨酸离子型受体作了较详细的研究。结果表明,由GABA诱发的电流反应中,约90%由GABAA受体介导,剩余约10%的成分对GABAA受体的专一性拮抗剂Bicuculline不敏感,而GABAB受体的专一性激动剂Baclofen不能引起电流反应,因此这部分受体特性与GABAC受体相似。表达的谷氨酸受体包括离子型受体和代谢型受体。离子型受体中除了少量NMDA受体,绝大部分属KA/AMPA受体亚型。在研究谷氨酸受体各种激动剂的相互作用时,发现NMDA能竞争性地压抑由KA诱发的电流,提示NMDA可能是KA/AMPA受体的弱拮抗剂。GABA receptor and inotropic glutamate receptors were expressed in amphibian oocytes and studied with the voltage-clamp technique and pharmacological method afterinjection of mRNA from carp (Carassius carassius) brains. It was found that about90% of the response to GABA was mediated by GABAA receptor, but there was alsoabout 10% of the response which was insensitive to bicuculline, a selective antagonist to GABAA receptor, baclofen, a selective agonist to GABAB receptor, had no effect on the injected oocytes. These observations suggest the existence of GABAC receptor. Subtypes of glutamate receptors, including NMDA subtype, KA/ AMPA subtype and metabotropic glutamate receptors were also expressed and the dose-response relationswere studied. Furthermore, we found that NMDA competitively suppressed the currentresponse to KA, suggesting that NMDA probably was a weak antagonist of the KA/AMPA receptor.
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