• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

Cyclic GTP imitates the potentiating effect of the nootrope vinpocetine on the high-threshold A-current in mollusk neurons.

作者信息

Solntseva E I

机构信息

Science Research Institute of the Brain, Russian Academy of Medical Sciences, Moscow.

出版信息

Neurosci Behav Physiol. 1999 Nov-Dec;29(6):671-5. doi: 10.1007/BF02462482.

DOI:10.1007/BF02462482
PMID:10651324
Abstract

Isolated common snail neurons were studied using two-microelectrode potential clamping to record high-threshold (threshold = 10 mV) rapidly-inactivating potassium current (I(Aht)); the effects of the nootrope vinpocetine on this current were studied and were compared with the effects of cyclic nucleotides. Intracellular application of dibutyryl derivatives of cyclic adenosine monophosphate (dcAMP) and guanosine monophosphate (dcGMP) was used. The results showed that vinpocetine potentiates or fails to alter I(Aht) in different cells, while dcGMP imitates the effect of vinpocetine. Simultaneous application of vinpocetine and dcGMP did not result in additive effects. Unlike dcGMP, dcAMP did not imitate the effects of vinpocetine, and decreased I(Aht) in most cells. These data suggest that cGMP mediates the potentiating effect of vinpocetine on I(Aht).

摘要

相似文献

1
Cyclic GTP imitates the potentiating effect of the nootrope vinpocetine on the high-threshold A-current in mollusk neurons.
Neurosci Behav Physiol. 1999 Nov-Dec;29(6):671-5. doi: 10.1007/BF02462482.
2
[Cyclic GMP mimicks potentiation effect of the nootropic agent vinpocetine on the high threshold A-current in the mollusk neurons].
Ross Fiziol Zh Im I M Sechenova. 1998 Aug;84(8):741-6.
3
The nootropic drug vinpocetine modulates different types of potassium currents in molluscan neurons.
Comp Biochem Physiol C Toxicol Pharmacol. 2001 Feb;128(2):275-80. doi: 10.1016/s1532-0456(01)00202-2.
4
[Effect of vinpocetine on various high threshold potassium currents in the mollusk neurons].
Biull Eksp Biol Med. 1998 Oct;126(10):408-11.
5
[The nootropic agent vinpocetine blocks the delayed rectifier potassium channel more strongly than the high-conductance calcium channel].
Zh Vyssh Nerv Deiat Im I P Pavlova. 1996 Sep-Oct;46(5):911-6.
6
Enhancement of low-threshold A-current of the neuronal membrane by vinpocetine.
Membr Cell Biol. 2000;14(2):181-8.
7
Nootropic agent vinpocetine blocks delayed rectified potassium currents more strongly than high-threshold calcium currents.益智药长春西汀对延迟整流钾电流的阻断作用比对高阈值钙电流的阻断作用更强。
Neurosci Behav Physiol. 1998 Mar-Apr;28(2):116-20. doi: 10.1007/BF02461956.
8
Selective suppression of the slow-inactivating potassium currents by nootropics in molluscan neurons.
Int J Neuropsychopharmacol. 2002 Sep;5(3):229-37. doi: 10.1017/S1461145702002997.
9
Vinpocetine-induced stimulation of calcium-activated potassium currents in rat pituitary GH3 cells.长春西汀对大鼠垂体GH3细胞钙激活钾电流的刺激作用。
Biochem Pharmacol. 2001 Apr 1;61(7):877-92. doi: 10.1016/s0006-2952(01)00553-6.
10
Decreases in Ca2+-dependent K+-currents due to cyclic guanosine monophosphate are not dependent on phosphorylation.由环磷酸鸟苷引起的钙离子依赖性钾电流的降低不依赖于磷酸化作用。
Neurosci Behav Physiol. 2002 May-Jun;32(3):317-22. doi: 10.1023/a:1015022609906.

本文引用的文献

1
[Effect of vinpocetine on various high threshold potassium currents in the mollusk neurons].
Biull Eksp Biol Med. 1998 Oct;126(10):408-11.
2
Mechanism of activation by cGMP-dependent protein kinase of large Ca(2+)-activated K+ channels in mesangial cells.系膜细胞中cGMP依赖性蛋白激酶对大电导钙激活钾通道的激活机制
Am J Physiol. 1996 Nov;271(5 Pt 1):C1669-77. doi: 10.1152/ajpcell.1996.271.5.C1669.
3
Molecular and functional diversity of K+ channels.钾离子通道的分子与功能多样性
Clin Exp Pharmacol Physiol. 1995 Dec;22(12):944-51. doi: 10.1111/j.1440-1681.1995.tb02331.x.
4
Activation of K+ channels and suppression of neuronal activity by secreted beta-amyloid-precursor protein.分泌型β淀粉样前体蛋白对钾离子通道的激活及神经元活动的抑制作用
Nature. 1996 Jan 4;379(6560):74-8. doi: 10.1038/379074a0.
5
Effects of VA-045, a novel apovincaminic acid derivative, on isolated blood vessels: cerebroarterial selectivity.新型阿朴长春胺酸衍生物VA-045对离体血管的作用:脑动脉选择性
Life Sci. 1993;52(18):PL181-6. doi: 10.1016/0024-3205(93)90115-j.
6
Enhancement of neuronal calcium channel currents by the nootropic agent, nefiracetam (DM-9384), in NG108-15 cells.
Brain Res. 1994 Apr 11;642(1-2):123-31. doi: 10.1016/0006-8993(94)90913-x.
7
Neuropathobiology of senile dementia and mechanism of action of nootropic drugs.老年痴呆的神经病理生物学及促智药的作用机制
Drugs Aging. 1994 Apr;4(4):285-303. doi: 10.2165/00002512-199404040-00002.
8
Influence of nootropic and antidepressive drugs on open field and running wheel behavior in spontaneously high and low active mice.益智药和抗抑郁药对自发高活动和低活动小鼠旷场及转轮行为的影响。
Pharmacol Biochem Behav. 1994 Oct;49(2):263-9. doi: 10.1016/0091-3057(94)90419-7.
9
Vinpocetine is a highly potent neuroprotectant against veratridine-induced cell death in primary cultures of rat cerebral cortex.
Neurosci Lett. 1995 Feb 9;185(2):127-30. doi: 10.1016/0304-3940(94)11241-a.
10
Vinpocetine is as potent as phenytoin to block voltage-gated Na+ channels in rat cortical neurons.长春西汀在阻断大鼠皮层神经元电压门控性钠离子通道方面与苯妥英钠效力相当。
Eur J Pharmacol. 1995 Feb 6;273(3):303-6. doi: 10.1016/0014-2999(94)00755-v.