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飞蝗(沙漠蝗)中对使君子氨酸敏感的谷氨酸受体可被细胞内注射的 philanthotoxin 和精胺所拮抗。

Quisqualate-sensitive glutamate receptors of the locust Schistocerca gregaria are antagonised by intracellularly applied philanthotoxin and spermine.

作者信息

Brundell P, Goodnow R, Kerry C J, Nakanishi K, Sudan H L, Usherwood P N

机构信息

Department of Life Science, University of Nottingham, U.K.

出版信息

Neurosci Lett. 1991 Oct 14;131(2):196-200. doi: 10.1016/0304-3940(91)90612-w.

Abstract

The effects of intracellularly and extracellularly applied synthetic analogues of delta-philanthotoxin (PhTX-433) and the polyamine spermine on the excitatory postsynaptic current (EPSC) of glutamatergic synapses and single channel currents gated by quisqualate-sensitive glutamate receptors (QUIS-R) on locust leg muscle have been compared. When applied extracellularly all 3 compounds reversibly antagonised the EPSC and the single channel currents. Antagonism was voltage independent, but use (agonist) dependent. Antagonism also occurred when they were injected into muscle fibres, but in this case it was not use dependent. It is proposed that spermine and the two toxins bind to the closed and open channel conformations of QUIS-R at a site near the intracellular opening of the channel gated by this receptor.

摘要

已比较了细胞内和细胞外应用的δ- philanthotoxin(PhTX - 433)合成类似物以及多胺精胺对蝗虫腿部肌肉谷氨酸能突触的兴奋性突触后电流(EPSC)和由quisqualate敏感型谷氨酸受体(QUIS - R)门控的单通道电流的影响。当细胞外应用时,所有这3种化合物均可逆性拮抗EPSC和单通道电流。拮抗作用与电压无关,但与使用(激动剂)有关。当将它们注射到肌纤维中时也会发生拮抗作用,但在这种情况下与使用无关。有人提出,精胺和这两种毒素在由该受体门控的通道的细胞内开口附近的位点与QUIS - R的关闭和开放通道构象结合。

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