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N-乙基马来酰亚胺使苯二氮䓬结合位点失活。

Inactivation of benzodiazepine binding sites by N-ethylmaleimide.

作者信息

Martini C, Lucacchini A

出版信息

J Neurochem. 1982 Jun;38(6):1768-70. doi: 10.1111/j.1471-4159.1982.tb06661.x.

Abstract

The benzodiazepine receptors of bovine brain membranes have been identified by the specific binding of radiolabeled [3H]diazepam. Pretreatment of membranes with N-ethylmaleimide causes a dose- and time-dependent decrease of 45 to 60% in the number of binding sites. No decrease occurs when membranes are pretreated with N-ethylmaleimide before administration, or in the presence, of diazepam. Binding of [3H]diazepam to the remaining sites occurs with the same characteristics as binding to the untreated receptor population.

摘要

通过放射性标记的[3H]地西泮的特异性结合,已鉴定出牛脑膜中的苯二氮䓬受体。用N-乙基马来酰亚胺预处理膜会导致结合位点数量呈剂量和时间依赖性减少45%至60%。在给予地西泮之前或存在地西泮的情况下用N-乙基马来酰亚胺预处理膜时,结合位点数量不会减少。[3H]地西泮与剩余位点的结合与与未处理的受体群体的结合具有相同的特征。

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