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通过对单个谷氨酸受体进行膜片钳分析来确定激动剂效力

Agonist potency determination by patch clamp analysis of single glutamate receptors.

作者信息

Gration K A, Lambert J J, Ramsey R L, Rand R P, Usherwood P N

出版信息

Brain Res. 1981 Dec 28;230(1-2):400-5. doi: 10.1016/0006-8993(81)90423-6.

Abstract

Agonists (L-quisqualate, L-glutamate and L-cysteine sulphinate) of the locust muscle glutamate receptor differ in potency. Patch clamp analysis of single glutamate receptors reveals that the relative potencies of agonists are determined both by the life-times of the channels that they gate and their probability of activating the glutamate receptor-ionophore complex. Furthermore, agonists which most readily activate the receptor channel complex gate channels with longer life-times than agonists which are less efficient in this respect.

摘要

蝗虫肌肉谷氨酸受体的激动剂(L-喹啉酸、L-谷氨酸和L-半胱氨酸亚磺酸盐)在效力上存在差异。对单个谷氨酸受体进行膜片钳分析表明,激动剂的相对效力既取决于它们所开启通道的寿命,也取决于它们激活谷氨酸受体-离子载体复合物的概率。此外,与在这方面效率较低的激动剂相比,最容易激活受体通道复合物的激动剂所开启的通道寿命更长。

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