Suppr超能文献

在新斯的明处理过的青蛙肌肉中,终板电流的衰减被乙酰胆碱或筒箭毒碱所阻断。

The decay of end-plate currents in neostigmine-treated frog muscle blocked by acetylcholine or tubocurarine.

作者信息

Guinan J J

出版信息

J Physiol. 1980 Aug;305:345-55. doi: 10.1113/jphysiol.1980.sp013368.

Abstract
  1. The decay times of e.p.c.s. (with acetylcholinesterase inhibited by neostigmine) were measured with a view to inferring the extent of acetylcholine (ACh) binding. 2. E.p.c.s from muscles blocked by ACh decayed at less than half the rate of e.p.c.s. from muscles blocked by tubocurarine, and slightly more slowly than m.e.p.c.s. from unblocked muscles. 3. ACh prolonged e.p.c.s and reduced their amplitudes when added to muscles blocked by tubocurarine. 4. After treatment with alpha-bungarotoxin, some e.p.c.s. from muscles blocked by ACh were prolonged relative to e.p.c.s from muscles blocked by tubocurarine. 5. These phenomena are interpreted as indicating that either (a) desensitized receptors bind ACh and prolong e.p.c.s by buffered diffusion or (b) in highly desensitized muscles there is a population of active receptors which bind ACh for many milliseconds.
摘要
  1. 测量了新斯的明抑制乙酰胆碱酯酶时终板电流(e.p.c.s.)的衰减时间,以推断乙酰胆碱(ACh)的结合程度。2. 由乙酰胆碱阻断的肌肉产生的终板电流衰减速度不到由筒箭毒碱阻断的肌肉产生的终板电流衰减速度的一半,且比未阻断肌肉产生的微小终板电流(m.e.p.c.s.)衰减速度稍慢。3. 当将乙酰胆碱添加到由筒箭毒碱阻断的肌肉中时,它会延长终板电流并降低其幅度。4. 用α-银环蛇毒素处理后,相对于由筒箭毒碱阻断的肌肉产生的终板电流,由乙酰胆碱阻断的肌肉产生的一些终板电流会延长。5. 这些现象被解释为表明:要么(a)脱敏受体结合乙酰胆碱并通过缓冲扩散延长终板电流;要么(b)在高度脱敏的肌肉中存在一群活性受体,它们能结合乙酰胆碱达数毫秒之久。

相似文献

8
Effects of strontium ions on end-plate channel properties.锶离子对终板通道特性的影响。
J Physiol. 1980 Sep;306:567-77. doi: 10.1113/jphysiol.1980.sp013415.

引用本文的文献

本文引用的文献

2
Active phase of frog's end-plate potential.青蛙终板电位的活动期
J Neurophysiol. 1959 Jul;22(4):395-411. doi: 10.1152/jn.1959.22.4.395.
5
A lesion of the transverse tubules of skeletal muscle.骨骼肌横小管的损伤。
J Physiol. 1969 May;201(3):515-33. doi: 10.1113/jphysiol.1969.sp008770.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验