• 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

Interactions between serotonin and cisapride on myenteric neurons.

作者信息

Nemeth P R, Ort C A, Zafirov D H, Wood J D

出版信息

Eur J Pharmacol. 1985 Jan 15;108(1):77-83. doi: 10.1016/0014-2999(85)90285-7.

DOI:10.1016/0014-2999(85)90285-7
PMID:3979436
Abstract

Intracellular recording methods were used to investigate the interactions between serotonin (5-HT) and cisapride on myenteric neurons of guinea-pig small intestine. Serotonin had three actions on the neurons. One was a slowly rising depolarization associated with increased input resistance and discharge of spikes that lasted six or more times longer than the duration of the 5-HT application. The second action was a transient depolarization associated with decreased input resistance and brief discharge of spikes. This response desensitized quickly and could be evoked only at intervals of 2 to 3 min. The third action of 5-HT was presynaptic inhibition of acetylcholine release at nicotinic synapses. Cisapride reduced or abolished both the prolonged and transient responses to 5-HT. The threshold concentration for reduction of the responses was 0.1 microM and the responses were abolished at 1.0 to 10 microM. Cisapride suppressed stimulus-evoked slow excitatory postsynaptic potentials (EPSPs) in the same cells for which cisapride blocked the prolonged responses to 5-HT. There were no effects of cisapride on resting electrical behavior or spike generation. Cisapride reduced the amplitude of fast cholinergic EPSPs, suggesting that it behaved as an agonist at the presynaptic serotonergic receptors.

摘要

相似文献

1
Interactions between serotonin and cisapride on myenteric neurons.
Eur J Pharmacol. 1985 Jan 15;108(1):77-83. doi: 10.1016/0014-2999(85)90285-7.
2
Effects of 5-HT1A and 5-HT4 receptor agonists on slow synaptic potentials in enteric neurons.5-羟色胺1A和5-羟色胺4受体激动剂对肠神经元慢突触电位的影响。
Eur J Pharmacol. 1995 May 4;278(1):67-74. doi: 10.1016/0014-2999(95)00101-p.
3
Actions of 5-hydroxytryptamine on myenteric neurons in guinea pig gastric antrum.5-羟色胺对豚鼠胃窦部肌间神经元的作用。
Am J Physiol. 1992 Dec;263(6 Pt 1):G838-46. doi: 10.1152/ajpgi.1992.263.6.G838.
4
Synaptic activation and properties of 5-hydroxytryptamine(3) receptors in myenteric neurons of guinea pig intestine.豚鼠肠道肌间神经元中5-羟色胺(3)受体的突触激活及特性
J Pharmacol Exp Ther. 1999 Aug;290(2):803-10.
5
Effects of cisapride on cholinergic neurotransmission and propulsive motility in the guinea pig ileum.
Gastroenterology. 1989 May;96(5 Pt 1):1257-64. doi: 10.1016/s0016-5085(89)80012-5.
6
Synaptic behaviour in the myenteric plexus of the guinea-pig gastric antrum.豚鼠胃窦肌间神经丛中的突触行为。
J Physiol. 1992 Jan;445:389-406. doi: 10.1113/jphysiol.1992.sp018930.
7
Stimulation of formation of cAMP by 5-hydroxytryptamine in myenteric ganglia isolated from guinea pig small intestine.5-羟色胺对从豚鼠小肠分离出的肠肌间神经节中环磷酸腺苷形成的刺激作用。
Life Sci. 1994;55(9):685-92. doi: 10.1016/0024-3205(94)00675-x.
8
Cisapride potentiates fast nicotinic synaptic potentials in the myenteric plexus of the guinea pig ileum.西沙必利增强豚鼠回肠肌间神经丛中快速烟碱型突触电位。
Proc West Pharmacol Soc. 1988;31:9-11.
9
Slow excitatory post-synaptic potentials in myenteric AH neurons of the guinea-pig ileum are reduced by the 5-hydroxytryptamine7 receptor antagonist SB 269970.豚鼠回肠肌间神经丛AH神经元中的慢兴奋性突触后电位可被5-羟色胺7受体拮抗剂SB 269970降低。
Neuroscience. 2005;134(3):975-86. doi: 10.1016/j.neuroscience.2005.05.006.
10
Actions of nitric oxide-generating sodium nitroprusside in myenteric plexus of guinea pig small intestine.一氧化氮供体硝普钠对豚鼠小肠肌间神经丛的作用。
Am J Physiol. 1993 Nov;265(5 Pt 1):G887-93. doi: 10.1152/ajpgi.1993.265.5.G887.

引用本文的文献

1
Prokinetic actions of luminally acting 5-HT receptor agonists.腔内在作用的 5-HT 受体激动剂的促动力作用。
Neurogastroenterol Motil. 2021 Apr;33(4):e14026. doi: 10.1111/nmo.14026. Epub 2020 Nov 12.
2
Gastroprokinetic agent, mosapride inhibits 5-HT receptor currents in NCB-20 cells.促胃肠动力药莫沙必利可抑制NCB - 20细胞中的5 - HT受体电流。
Korean J Physiol Pharmacol. 2019 Sep;23(5):419-426. doi: 10.4196/kjpp.2019.23.5.419. Epub 2019 Aug 26.
3
Influence of sumatriptan on gastric fundus tone and on the perception of gastric distension in man.
舒马曲坦对人体胃底张力及胃扩张感知的影响。
Gut. 2000 Apr;46(4):468-73. doi: 10.1136/gut.46.4.468.
4
A risk-benefit assessment of cisapride in the treatment of gastrointestinal disorders.西沙必利治疗胃肠道疾病的风险效益评估。
Drug Saf. 1995 Jun;12(6):384-92. doi: 10.2165/00002018-199512060-00004.
5
5-Hydroxytryptamine2 and 5-hydroxytryptamine3 receptors mediate serotonin-induced short-circuit current in pig jejunum.5-羟色胺2和5-羟色胺3受体介导5-羟色胺诱导的猪空肠短路电流。
J Comp Physiol B. 1994;164(5):343-8. doi: 10.1007/BF00302548.
6
Neuronal involvement in type 1 hypersensitivity reactions in gut epithelia.肠道上皮中神经元参与1型超敏反应。
Br J Pharmacol. 1987 Nov;92(3):647-55. doi: 10.1111/j.1476-5381.1987.tb11368.x.
7
Cisapride. A preliminary review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use as a prokinetic agent in gastrointestinal motility disorders.西沙必利。对其药效学和药代动力学特性以及作为胃肠动力障碍促动力剂的治疗用途的初步综述。
Drugs. 1988 Dec;36(6):652-81. doi: 10.2165/00003495-198836060-00002.
8
Cisapride inhibits motility of the sphincter of Oddi in the Australian possum.西沙必利可抑制澳大利亚负鼠奥狄氏括约肌的运动。
Dig Dis Sci. 1990 Jun;35(6):711-5. doi: 10.1007/BF01540172.