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吡啶斯的明与烟碱型乙酰胆碱受体 - 离子通道复合物的相互作用性质。II. 膜片钳研究。

The nature of the interactions of pyridostigmine with the nicotinic acetylcholine receptor-ionic channel complex. II. Patch clamp studies.

作者信息

Akaike A, Ikeda S R, Brookes N, Pascuzzo G J, Rickett D L, Albuquerque E X

出版信息

Mol Pharmacol. 1984 Jan;25(1):102-12.

PMID:6323946
Abstract

Patch clamping of myoballs to record single channels was performed to examine the interaction of the anticholinesterase agent pyridostigmine (Pyr) with the acetylcholine (ACh) receptor-ion channel complex. Single ACh channel currents were recorded from tissue-cultured muscle cells of neonatal rats (myoballs). Pyr (50-100 microM) decreased the frequency of channel-opening events activated by ACh, and induced a modified form of the ACh channel currents. Channel conductance was lower in the presence of Pyr, and channel lifetime remained unaltered or only slightly prolonged. In addition, channel openings were frequently interrupted by fast flickers in the presence of Pyr. Higher concentrations (200 microM-1 mM) of the drug induced irregular waves of bursting activity during the initial phase of the application, and, subsequently, significantly reduced the frequency of channel openings. Infrequent channel openings with low conductance were observed in the patch when the micropipette was filled with Pyr alone. These results suggest that, in addition to its anticholinesterase activity, Pyr reacts with the ACh receptor, and both alone or in combination with ACh induces an altered, desensitized species of the nicotinic receptor-ion channel complex.

摘要

通过对肌球进行膜片钳记录单通道电流,以研究抗胆碱酯酶药物吡啶斯的明(Pyr)与乙酰胆碱(ACh)受体 - 离子通道复合物之间的相互作用。从新生大鼠的组织培养肌细胞(肌球)记录单个ACh通道电流。Pyr(50 - 100微摩尔)降低了由ACh激活的通道开放事件的频率,并诱导了ACh通道电流的一种改变形式。在有Pyr存在时,通道电导较低,通道寿命保持不变或仅略有延长。此外,在有Pyr存在时,通道开放经常被快速闪烁中断。更高浓度(200微摩尔 - 1毫摩尔)的该药物在应用初始阶段诱导爆发性活动的不规则波,随后显著降低通道开放频率。当微电极仅填充有Pyr时,在膜片中观察到低电导的不频繁通道开放。这些结果表明,除了其抗胆碱酯酶活性外,Pyr还与ACh受体反应,单独或与ACh联合诱导烟碱型受体 - 离子通道复合物的一种改变的、脱敏的形式。

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