• 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

苯二氮䓬类镇静剂美达西泮与促智药甲氯芬酯联合使用对大鼠脑毒蕈碱受体活性的影响。

Effect of the combination of the benzodiazepine tranquilizer medazepam and the nootropic agent meclofenoxate on the activity of rat brain muscarinic receptors.

作者信息

Popova J S, Petkov V D

机构信息

Institute of Physiology, Bulgarian Academy of Sciences, Sofia.

出版信息

Gen Pharmacol. 1990;21(6):927-30. doi: 10.1016/0306-3623(90)90456-v.

DOI:10.1016/0306-3623(90)90456-v
PMID:2279692
Abstract
  1. The effect of 7-day treatment with the benzodiazepine tranquilizer medazepam (5 mg/kg), the nootropic agent meclofenoxate (100 mg/kg) and their combination in the same doses on the binding activity of muscarinic receptors in four rat brain structures (cerebral cortex, striatum, hippocampus and hypothalamus) were studied using the antagonist [3H]-1-quinuclidinyl benzylate [( 3H]-QNB) as radio-ligand. 2. Medazepam treatment caused significant decrease of muscarinic receptor binding affinity (Kd) and of the receptor binding capacity (Bmax) in the brain structures studied. The number of muscarinic binding sites was unsignificantly decreased only in the hippocampus. 3. Meclofenoxate treatment caused an increase of muscarinic receptor affinity and a decrease of the binding capacity in the cerebral cortex and hypothalamus and an increase of the binding affinity in the striatum and hippocampus. 4. The combination of medazepam and meclofenoxate caused no significant changes of both muscarinic receptor characteristics in the hippocampus and of the receptor affinity in the striatum and hypothalamus in comparison with control rats. The Bmax values were decreased in the cerebral cortex, striatum and hypothalamus when compared with control animals. The differences observed were slighter than those determined after the comparison of medazepam treated rats with control rats. 5. The results obtained afford an opportunity to suggest that the nootropic agent meclofenoxate acts to moderate the effect of the benzodiazepine tranquilizer medazepam on the activity of rat brain muscarinic receptors.
摘要
  1. 研究了苯二氮䓬类镇静剂美达西泮(5毫克/千克)、促智药甲氯芬酯(100毫克/千克)及其相同剂量组合对大鼠四个脑区(大脑皮层、纹状体、海马体和下丘脑)毒蕈碱受体结合活性的7天治疗效果,使用拮抗剂[3H]-1-喹核醇苄酯[(3H]-QNB)作为放射性配体。2. 美达西泮治疗导致所研究脑区中毒蕈碱受体结合亲和力(Kd)和受体结合容量(Bmax)显著降低。仅海马体中毒蕈碱结合位点数量无显著减少。3. 甲氯芬酯治疗导致大脑皮层和下丘脑中毒蕈碱受体亲和力增加、结合容量降低,纹状体和海马体中结合亲和力增加。4. 与对照大鼠相比,美达西泮和甲氯芬酯的组合导致海马体中毒蕈碱受体特征以及纹状体和下丘脑受体亲和力均无显著变化。与对照动物相比,大脑皮层、纹状体和下丘脑的Bmax值降低。观察到的差异比美达西泮治疗大鼠与对照大鼠比较后确定的差异更小。5. 所得结果表明,促智药甲氯芬酯可调节苯二氮䓬类镇静剂美达西泮对大鼠脑毒蕈碱受体活性的影响。

相似文献

1
Effect of the combination of the benzodiazepine tranquilizer medazepam and the nootropic agent meclofenoxate on the activity of rat brain muscarinic receptors.苯二氮䓬类镇静剂美达西泮与促智药甲氯芬酯联合使用对大鼠脑毒蕈碱受体活性的影响。
Gen Pharmacol. 1990;21(6):927-30. doi: 10.1016/0306-3623(90)90456-v.
2
The effect of chronic diazepam and medazepam treatment on the number and affinity of muscarinic receptors in different rat brain structures.
Gen Pharmacol. 1988;19(2):227-31. doi: 10.1016/0306-3623(88)90066-3.
3
Effects of the nootropic agents adafenoxate, meclofenoxate and the acetylcholine precursor citicholine on the brain muscarinic receptors (experiments on rats).促智药阿屈非尼、氯酯醒及乙酰胆碱前体胞磷胆碱对脑毒蕈碱受体的影响(大鼠实验)
Acta Physiol Pharmacol Bulg. 1987;13(2):3-10.
4
Age-related changes in rat brain muscarinic receptors and beta-adrenoreceptors.
Gen Pharmacol. 1989;20(5):581-4. doi: 10.1016/0306-3623(89)90089-x.
5
Effects of in vivo and in vitro treatments with N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline on putative muscarinic receptor subtypes in rat brain.N-乙氧羰基-2-乙氧基-1,2-二氢喹啉体内和体外处理对大鼠脑内假定毒蕈碱受体亚型的影响。
Mol Pharmacol. 1986 Aug;30(2):96-103.
6
Effects of meclofenoxate on the level and turnover of biogenic monoamines in the rat brain.甲氯芬酯对大鼠脑内生物源性单胺水平及更新率的影响。
Arzneimittelforschung. 1985;35(12):1778-81.
7
Development of muscarinic cholinergic receptors in inbred strains of mice: identification of receptor heterogeneity and relation to audiogenic seizure susceptibility.近交系小鼠毒蕈碱胆碱能受体的发育:受体异质性的鉴定及其与听源性癫痫易感性的关系。
Brain Res. 1979 Feb 23;162(2):231-41. doi: 10.1016/0006-8993(79)90286-5.
8
Changes in brain biogenic monoamines induced by the nootropic drugs adafenoxate and meclofenoxate and by citicholine (experiments on rats).益智药阿屈非尼和氯酯醒以及胞磷胆碱对大鼠脑生物源性单胺的影响(实验研究)
Gen Pharmacol. 1990;21(1):71-5. doi: 10.1016/0306-3623(90)90598-g.
9
Gallamine binding to muscarinic M1 and M2 receptors, studied by inhibition of [3H]pirenzepine and [3H]quinuclidinylbenzilate binding to rat brain membranes.通过抑制[3H]哌仑西平和[3H]喹核醇基苯甲酸酯与大鼠脑膜的结合来研究加拉明与毒蕈碱M1和M2受体的结合。
Mol Pharmacol. 1986 Jul;30(1):58-68.
10
[Effects of midazolam on muscarinic receptor of brain in healthy and scopolamine-treated rats].[咪达唑仑对健康及东莨菪碱处理大鼠脑内毒蕈碱受体的影响]
Beijing Da Xue Xue Bao Yi Xue Ban. 2006 Jun 18;38(3):284-8.

引用本文的文献

1
Cholinergic mechanisms in physical dependence on barbiturates, ethanol and benzodiazepines.巴比妥类、乙醇和苯二氮䓬类药物身体依赖中的胆碱能机制。
J Neural Transm Gen Sect. 1992;88(3):199-221. doi: 10.1007/BF01244733.