• 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

茴拉西坦增强,而咪达唑仑抑制豚鼠海马切片中的长时程增强。

Aniracetam augments, and midazolam inhibits, the long-term potentiation in guinea-pig hippocampal slices.

作者信息

Satoh M, Ishihara K, Iwama T, Takagi H

出版信息

Neurosci Lett. 1986 Jul 24;68(2):216-20. doi: 10.1016/0304-3940(86)90145-x.

DOI:10.1016/0304-3940(86)90145-x
PMID:3018633
Abstract

The effects of aniracetam, a nootropic drug, and midazolam, which produces amnesia, on the long-term potentiation (LTP) of population spikes was investigated using hippocampal slices (CA3 area) from the guinea pig. Aniracetam at concentrations of 10(-7) and 10(-8) M, but not at 10(-6) M, significantly augmented LTP. On the other hand, midazolam (10(-9) M) significantly suppressed LTP. The suppressive effect was antagonized by Ro 15-1788 (10(-8) M). Both drugs did not affect the population spikes in the absence of tetanic stimulation at those concentrations. It was suggested that in vitro application of LTP is a feasible model system for evaluating the nootropic activity of drugs.

摘要

使用豚鼠海马切片(CA3区)研究了促智药阿尼西坦和产生失忆作用的咪达唑仑对群体峰电位长时程增强(LTP)的影响。浓度为10^(-7) M和10^(-8) M的阿尼西坦可显著增强LTP,但10^(-6) M时则无此作用。另一方面,咪达唑仑(10^(-9) M)可显著抑制LTP。Ro 15-1788(10^(-8) M)可拮抗这种抑制作用。在这些浓度下,两种药物在无强直刺激时均不影响群体峰电位。提示LTP的体外应用是评估药物促智活性的一种可行的模型系统。

相似文献

1
Aniracetam augments, and midazolam inhibits, the long-term potentiation in guinea-pig hippocampal slices.茴拉西坦增强,而咪达唑仑抑制豚鼠海马切片中的长时程增强。
Neurosci Lett. 1986 Jul 24;68(2):216-20. doi: 10.1016/0304-3940(86)90145-x.
2
Different susceptibilities of long-term potentiations in CA3 and CA1 regions of guinea pig hippocampal slices to nootropic drugs.豚鼠海马脑片CA3区和CA1区长时程增强对益智药物的不同敏感性。
Neurosci Lett. 1988 Nov 11;93(2-3):236-41. doi: 10.1016/0304-3940(88)90088-2.
3
Midazolam inhibits long-term potentiation through modulation of GABAA receptors.
Neuropharmacology. 1996 Mar;35(3):347-57. doi: 10.1016/0028-3908(95)00182-4.
4
Somatostatin augments long-term potentiation of the mossy fiber-CA3 system in guinea-pig hippocampal slices.生长抑素增强豚鼠海马切片中苔藓纤维 - CA3 系统的长时程增强效应。
Brain Res. 1991 Jul 12;553(2):188-94. doi: 10.1016/0006-8993(91)90823-e.
5
FK960, a novel potential anti-dementia drug, augments long-term potentiation in mossy fiber-CA3 pathway of guinea-pig hippocampal slices.新型潜在抗痴呆药物FK960增强豚鼠海马切片苔藓纤维-CA3通路中的长时程增强。
Brain Res. 1998 Jun 1;794(2):248-54. doi: 10.1016/s0006-8993(98)00232-7.
6
Propentofylline enhances the formation of long-term potentiation in guinea pig hippocampal slices.丙戊茶碱增强豚鼠海马切片中长时程增强的形成。
Neurosci Lett. 1994 Aug 1;176(2):189-92. doi: 10.1016/0304-3940(94)90079-5.
7
Benzodiazepine inverse agonists augment long-term potentiation in CA1 and CA3 of guinea pig hippocampal slices.苯二氮䓬反向激动剂增强豚鼠海马切片CA1和CA3区的长时程增强效应。
Neuropharmacology. 1993 Feb;32(2):127-31. doi: 10.1016/0028-3908(93)90092-h.
8
Indeloxazine augments long-term potentiation in the mossy fiber-CA3 system of guinea pig hippocampal slices.茚达品增强豚鼠海马脑片苔藓纤维-CA3系统中的长时程增强效应。
J Pharmacobiodyn. 1989 Dec;12(12):771-4. doi: 10.1248/bpb1978.12.771.
9
Effects of aniracetam after LTP induction are suggestive of interactions on the kinetics of the AMPA receptor channel.
Brain Res. 1998 Mar 30;788(1-2):269-86. doi: 10.1016/s0006-8993(97)01444-3.
10
A 'long-term-potentiation-like' facilitation of hippocampal synaptic transmission induced by the nootropic nefiracetam.益智药奈非西坦诱导的海马突触传递的“类长时程增强”易化作用。
Brain Res. 1999 May 1;826(2):281-8. doi: 10.1016/s0006-8993(99)01312-8.

引用本文的文献

1
Effects of Smart Drugs on Cholinergic System and Non-Neuronal Acetylcholine in the Mouse Hippocampus: Histopathological Approach.智能药物对小鼠海马体胆碱能系统和非神经元乙酰胆碱的影响:组织病理学方法
J Clin Med. 2022 Jun 9;11(12):3310. doi: 10.3390/jcm11123310.
2
Interleukin-1β in Central Nervous System Injury and Repair.中枢神经系统损伤与修复中的白细胞介素-1β
Eur J Neurodegener Dis. 2012 Aug;1(2):195-211.
3
Therapeutic potential of positive AMPA modulators and their relationship to AMPA receptor subunits. A review of preclinical data.
阳性AMPA调节剂的治疗潜力及其与AMPA受体亚基的关系。临床前数据综述。
Psychopharmacology (Berl). 2005 Apr;179(1):154-63. doi: 10.1007/s00213-004-2065-6. Epub 2005 Jan 26.
4
Mechanisms of deafferentation-induced plasticity in human motor cortex.人类运动皮层去传入诱导可塑性的机制
J Neurosci. 1998 Sep 1;18(17):7000-7. doi: 10.1523/JNEUROSCI.18-17-07000.1998.
5
Modulating effect of the nootropic drug, piracetam on stress- and subsequent morphine-induced prolactin secretion in male rats.促智药吡拉西坦对雄性大鼠应激及随后吗啡诱导的催乳素分泌的调节作用。
Br J Pharmacol. 1996 Feb;117(3):502-506. doi: 10.1111/j.1476-5381.1996.tb15218.x.
6
Pharmacology of nootropics and metabolically active compounds in relation to their use in dementia.促智药和代谢活性化合物在痴呆治疗中的药理学应用
Psychopharmacology (Berl). 1990;101(2):147-59. doi: 10.1007/BF02244119.
7
Oxiracetam and D-pyroglutamic acid antagonize a disruption of passive avoidance behaviour induced by the N-methyl-D-aspartate receptor antagonist 2-amino-5-phosphonovalerate.奥拉西坦和D-焦谷氨酸可拮抗由N-甲基-D-天冬氨酸受体拮抗剂2-氨基-5-磷酸基戊酸诱导的被动回避行为障碍。
Psychopharmacology (Berl). 1990;100(1):130-1. doi: 10.1007/BF02245803.
8
Effect of the nootropic drug oxiracetam on field potentials of rat hippocampal slices.促智药奥拉西坦对大鼠海马脑片场电位的影响。
Br J Pharmacol. 1990 Jan;99(1):189-93. doi: 10.1111/j.1476-5381.1990.tb14676.x.
9
Effects of four non-cholinergic cognitive enhancers in comparison with tacrine and galanthamine on scopolamine-induced amnesia in rats.
Psychopharmacology (Berl). 1992;106(1):26-30. doi: 10.1007/BF02253584.
10
Oxiracetam antagonizes the disruptive effects of scopolamine on memory in the radial maze.奥拉西坦可拮抗东莨菪碱对放射状迷宫中记忆的破坏作用。
Psychopharmacology (Berl). 1992;106(2):175-8. doi: 10.1007/BF02801969.