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山莨菪碱对乙酰胆碱受体通道的阻断作用

[Blocking effect of anisodamine on acetylcholine receptor channels].

作者信息

Zhao C L, Ron S, Liu C G, He X P, Xie Z P

机构信息

Department of Biology, Tsinghua University, Beijing, China.

出版信息

Zhongguo Yao Li Xue Bao. 1993 Mar;14(2):190-2.

PMID:8352020
Abstract

Anisodamine, an analog of atropine, was isolated first in China. Patch-clamp technique was used to study the inhibitory effect of anisodamine (Ani) on acetylcholine receptor on the membrane of muscle innervated by neuron. Neural tube in embryo of Xenopus laevis were cultured. By whole-cell clamp and outside-out patch, we found that the inhibitory effect of Ani was obvious on both miniature end-plate currents (MEPC) and single channel. This effect was reversible and the minimal concentration for complete inhibition was 60 mumol.L-1, vs 1 and 0.5 mmol.L-1 for atropine and scopolamine, respectively. Our results indicate that Ani blocks both M-ACh and N-ACh receptors.

摘要

山莨菪碱是阿托品的类似物,最早在中国被分离出来。采用膜片钳技术研究山莨菪碱(Ani)对神经元支配肌肉膜上乙酰胆碱受体的抑制作用。培养非洲爪蟾胚胎的神经管。通过全细胞钳制和外向膜片钳技术,我们发现Ani对微小终板电流(MEPC)和单通道均有明显的抑制作用。这种作用是可逆的,完全抑制的最小浓度为60 μmol·L-1,而阿托品和东莨菪碱分别为1和0.5 mmol·L-1。我们的结果表明,Ani可阻断M型乙酰胆碱受体和N型乙酰胆碱受体。

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