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戊巴比妥和(+)-依托咪酯对地西泮和蝇蕈醇结合的增强作用:通过大鼠皮质电子辐照失活估计分子排列的大小

The enhancement of diazepam and muscimol binding by pentobarbital and (+)-etomidate: size of the molecular arrangement estimated by electron irradiation inactivation of rat cortex.

作者信息

Maksay G, Nielsen M, Simonyi M

出版信息

Neurosci Lett. 1986 Sep 25;70(1):116-20. doi: 10.1016/0304-3940(86)90448-9.

Abstract

Synaptosomal membranes were prepared from frozen rat cortices irradiated by 10 MeV electrons and the enhancement of [3H]diazepam and [3H]muscimol binding by pentobarbital (PB) and (+)-etomidate was studied. The target sizes of the corresponding parts of the receptor complex were estimated from the decrease in the enhancement as a function of irradiation dose. Different radiation inactivation constants suggest different regulatory units for the enhancement by PB and (+)-etomidate. Target sizes for PB and (+)-etomidate enhancement of [3H]diazepam binding were 127 +/- 14 and 360 + 124 kDa, respectively.

摘要

从经10兆电子伏电子辐照的冷冻大鼠皮质中制备突触体膜,并研究戊巴比妥(PB)和(+)-依托咪酯对[3H]地西泮和[3H]蝇蕈醇结合的增强作用。根据增强作用随辐照剂量的降低情况,估算受体复合物相应部分的靶标大小。不同的辐射失活常数表明,PB和(+)-依托咪酯增强作用的调节单元不同。PB和(+)-依托咪酯增强[3H]地西泮结合的靶标大小分别为127±14和360 + 124 kDa。

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