Suppr超能文献

佛波醇二丁酸酯对牛蛙交感神经元M电流及M电流抑制的影响。

Effects of phorbol dibutyrate on M currents and M current inhibition in bullfrog sympathetic neurons.

作者信息

Brown D A, Adams P R

机构信息

Department of Pharmacology, School of Pharmacy, University of London, U.K.

出版信息

Cell Mol Neurobiol. 1987 Sep;7(3):255-69. doi: 10.1007/BF00711303.

Abstract
  1. Effects of bath-applied phorbol dibutyrate (PDBu) on M currents (IM) and on the inhibition of IM by muscarine and luteinizing hormone-releasing hormone (LHRH) were recorded in voltage-clamped bullfrog lumbar sympathetic ganglion cells. 2. PDBu (0.1-30 microM) produced a slowly developing, irreversible and partial (less than or equal to 60%) inhibition of IM. This effect was not replicated by 4-alpha-phorbol or by vehicle. 3. After treatment with PDBu, residual IM showed a reduced sensitivity to inhibition by muscarine or LHRH but not by Ba2+. The reduced response to muscarine appeared to result from a 10-fold shift in the concentration dependence for inhibition. 4. PDBu did not clearly reproduce the ability of muscarine to inhibit the slow, Ca-activated K current IAHP or to increase the leak conductance at hyperpolarized potentials. The latter effect of muscarine was enhanced, rather than inhibited, by PDBu. 5. IM and IAHP were not inhibited by 1 mM dibutyryl cyclic AMP or by 20 microM forskolin. 6. It is concluded that activation of protein kinase C, but not protein kinase A, partly replicates the effect of muscarine on frog sympathetic neurons.
摘要
  1. 在电压钳制的牛蛙腰交感神经节细胞中,记录了浴加佛波酯(PDBu)对M电流(IM)以及对毒蕈碱和促黄体生成素释放激素(LHRH)对IM的抑制作用的影响。2. PDBu(0.1 - 30微摩尔)对IM产生缓慢发展、不可逆且部分(小于或等于60%)的抑制作用。4-α-佛波醇或溶剂未重复此效应。3. 用PDBu处理后,残余的IM对毒蕈碱或LHRH的抑制敏感性降低,但对Ba2+的抑制敏感性未降低。对毒蕈碱反应的降低似乎是由于抑制的浓度依赖性发生了10倍的偏移。4. PDBu未明显重现毒蕈碱抑制缓慢的钙激活钾电流IAHP或增加超极化电位下漏电导的能力。毒蕈碱的后一种效应被PDBu增强而非抑制。5. 1毫摩尔二丁酰环磷酸腺苷或20微摩尔福斯高林未抑制IM和IAHP。6. 得出结论,蛋白激酶C而非蛋白激酶A的激活部分重现了毒蕈碱对蛙交感神经元的作用。

相似文献

2
M-current suppression by agonist and phorbol ester in bullfrog sympathetic neurons.
Pflugers Arch. 1994 Feb;426(3-4):296-303. doi: 10.1007/BF00374785.
5
Pharmacological inhibition of the M-current.M电流的药理学抑制
J Physiol. 1982 Nov;332:223-62. doi: 10.1113/jphysiol.1982.sp014411.
7
A muscarine-resistant M-current in C cells of bullfrog sympathetic ganglia.
Neurosci Lett. 1987 Mar 9;74(3):309-14. doi: 10.1016/0304-3940(87)90315-6.

引用本文的文献

1
Does diacylglycerol regulate KCNQ channels?二酰基甘油是否调节钾离子通道亚型KCNQ?
Pflugers Arch. 2006 Dec;453(3):293-301. doi: 10.1007/s00424-006-0092-3. Epub 2006 May 24.
3
Protein kinase C as mediator of arachidonic acid-induced decrease of neuronal M current.
Pflugers Arch. 1993 Oct;425(1-2):134-9. doi: 10.1007/BF00374513.
4
M-current suppression by agonist and phorbol ester in bullfrog sympathetic neurons.
Pflugers Arch. 1994 Feb;426(3-4):296-303. doi: 10.1007/BF00374785.

本文引用的文献

2
Who do barium ions imitate acetylcholine?钡离子为何会模拟乙酰胆碱?
Brain Res. 1981 Feb 9;206(1):244-50. doi: 10.1016/0006-8993(81)90125-6.
6
Pharmacological inhibition of the M-current.M电流的药理学抑制
J Physiol. 1982 Nov;332:223-62. doi: 10.1113/jphysiol.1982.sp014411.

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