• 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

Antinociceptive and antiamnesic properties of the presynaptic cholinergic amplifier PG-9.

作者信息

Ghelardini C, Galeotti N, Gualtieri F, Marchese V, Bellucci C, Bartolini A

机构信息

Department of Pharmacology, University of Florence, Italy.

出版信息

J Pharmacol Exp Ther. 1998 Mar;284(3):806-16.

PMID:9495837
Abstract

The antinociceptive effect of 3 alpha-tropyl 2-(p-bromophenyl)propionate [(+/-)-PG-9] (10-40 mg kg-1 s.c.; 30-60 mg kg-1 p.o.; 10-30 mg kg-1 i.v.; 10-30 micrograms/mouse i.c.v.) was examined in mice, rats and guinea pigs by use of the hot-plate, abdominal-constriction, tail-flick and paw-pressure tests. (+/-)-PG-9 antinociception peaked 15 min after injection and then slowly diminished. The antinociception produced by (+/-)-PG-9 was prevented by the unselective muscarinic antagonist atropine, the M1-selective antagonists pirenzepine and dicyclomine and the acetylcholine depletor hemicholinium-3, but not by the opioid antagonist naloxone, the gamma-aminobutyric acidB antagonist 3-aminopropyl-diethoxy-methyl-phosphinic acid, the H3 agonist R-(alpha)-methylhistamine, the D2 antagonist quinpirole, the 5-hydroxytryptamine4 antagonist 2-methoxy-4-amino-5-chlorobenzoic acid 2-(diethylamino)ethyl ester hydrochloride, the 5-hydroxytryptamin1A antagonist 1-(2-methoxyphenyl)-4-[4-(2-phthalimido)butyl]piperazine hydrobromide and the polyamines depletor reserpine. Based on these data, it can be postulated that (+/-)-PG-9 exerted an antinociceptive effect mediated by a central potentiation of cholinergic transmission. (+/-)-PG-9 (10-40 mg kg-1 i.p.) was able to prevent amnesia induced by scopolamine (1 mg kg-1 i.p.) and dicyclomine (2 mg kg-1 i.p.) in the mouse passive-avoidance test. Affinity profiles of (+/-)-PG-9 for muscarinic receptor subtypes, determined by functional studies (rabbit vas deferens for M1, guinea pig atrium for M2, guinea pig ileum for M3 and immature guinea pig uterus for putative M4), have shown an M4/M1 selectivity ratio of 10.2 that might be responsible for the antinociception and the anti-amnesic effect induced by (+/-)-PG-9 through an increase in acetylcholine extracellular levels. In the antinociceptive and antiamnesic dose range, (+/-)-PG-9 did not impair mouse performance evaluated by the rota-rod test and Animex apparatus.

摘要

相似文献

1
Antinociceptive and antiamnesic properties of the presynaptic cholinergic amplifier PG-9.
J Pharmacol Exp Ther. 1998 Mar;284(3):806-16.
2
Antinociceptive profile of 3-alpha-tropanyl 2-(4-Cl-phenoxy)butyrate (SM-21) [corrected]: a novel analgesic with a presynaptic cholinergic mechanism of action.
J Pharmacol Exp Ther. 1997 Jul;282(1):430-9.
3
The central cholinergic system has a role in the antinociception induced in rodents and guinea pigs by the antimigraine drug sumatriptan.中枢胆碱能系统在抗偏头痛药物舒马曲坦诱导啮齿动物和豚鼠产生抗伤害感受中发挥作用。
J Pharmacol Exp Ther. 1996 Nov;279(2):884-90.
4
Antinociception induced by SM 32 depends on a central cholinergic mechanism.
Pharmacol Res. 1997 Feb;35(2):141-7. doi: 10.1006/phrs.1996.0110.
5
Investigation into atropine-induced antinociception.阿托品诱导的抗伤害感受研究。
Br J Pharmacol. 1990 Sep;101(1):49-54. doi: 10.1111/j.1476-5381.1990.tb12087.x.
6
M1 receptor agonist activity is not a requirement for muscarinic antinociception.毒蕈碱抗伤害感受并不需要M1受体激动剂活性。
J Pharmacol Exp Ther. 1997 May;281(2):868-75.
7
Binding profiles of a series of 2-arylpropionic acid esters on cloned human muscarinic receptor subtypes (m1-m5) and their relationship to nootropic activity.一系列2-芳基丙酸酯对克隆的人毒蕈碱受体亚型(m1 - m5)的结合特征及其与促智活性的关系。
Arzneimittelforschung. 1999 Jun;49(6):483-8. doi: 10.1055/s-0031-1300447.
8
Antinociceptive effects of the novel spirocyclopiperazinium salt compound LXM-10 in mice.新型螺环哌嗪鎓盐化合物LXM-10对小鼠的抗伤害感受作用
Pharmacol Biochem Behav. 2007 Apr;86(4):643-50. doi: 10.1016/j.pbb.2007.02.009. Epub 2007 Feb 16.
9
Memory facilitation and stimulation of endogenous nerve growth factor synthesis by the acetylcholine releaser PG-9.乙酰胆碱释放剂PG-9对记忆的促进作用及内源性神经生长因子合成的刺激作用。
Jpn J Pharmacol. 1998 Nov;78(3):245-51. doi: 10.1254/jjp.78.245.
10
Prochlorperazine induces central antinociception mediated by the muscarinic system.
Pharmacol Res. 2004 Sep;50(3):351-8. doi: 10.1016/j.phrs.2004.02.005.

引用本文的文献

1
DMSO Delays Alzheimer Disease Causing Aβ-induced Paralysis in Through Modulation of Glutamate/Acetylcholine Neurotransmission.二甲基亚砜通过调节谷氨酸/乙酰胆碱神经传递延缓阿尔茨海默病导致的Aβ诱导的麻痹。
Ann Neurosci. 2021 Jan;28(1-2):55-64. doi: 10.1177/09727531211046369. Epub 2021 Oct 5.
2
The modulation of fragile X behaviors by the muscarinic M4 antagonist, tropicamide.毒蕈碱M4拮抗剂托吡卡胺对脆性X行为的调节作用。
Behav Neurosci. 2011 Oct;125(5):783-90. doi: 10.1037/a0025202.
3
Modulation of behavioral phenotypes by a muscarinic M1 antagonist in a mouse model of fragile X syndrome.
M1 型毒蕈碱受体拮抗剂调制脆性 X 综合征小鼠模型的行为表型。
Psychopharmacology (Berl). 2011 Sep;217(1):143-51. doi: 10.1007/s00213-011-2276-6. Epub 2011 Apr 13.
4
Effects of the selective M1 muscarinic receptor antagonist dicyclomine on emotional memory.选择性M1毒蕈碱受体拮抗剂双环维林对情绪记忆的影响。
Learn Mem. 2000 Sep-Oct;7(5):287-92. doi: 10.1101/lm.34900.