• 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

MK 801对N-甲基-D-天冬氨酸传递的立体特异性阻断可防止SKF 38393诱导的旋转启动。

Stereospecific blockade of N-methyl-D-aspartate transmission by MK 801 prevents priming of SKF 38393-induced turning.

作者信息

Morelli M, Di Chiara G

机构信息

Institute of Experimental Pharmacology and Toxicology, University of Cagliari, Italy.

出版信息

Psychopharmacology (Berl). 1990;101(2):287-8. doi: 10.1007/BF02244143.

DOI:10.1007/BF02244143
PMID:2161552
Abstract

In rats unilaterally lesioned with 6-hydroxydopamine, the D-1 agonist SKF 38393 (3 mg/kg SC) induced contralateral turning only after priming with a dopaminergic agonist such as apomorphine. Administration of the N-methyl-D-aspartate receptor antagonist (+) MK 801 (0.1 mg/kg IP) 15 min before apomorphine (0.1 mg/kg SC) prevented the ability of apomorphine to act as a primer while potentiating its acute contralateral turning effects. The inactive isomer (-) MK 801 was without effect. The results indicate that the N-methyl-D-aspartate receptor exerts a permissive role on priming.

摘要

在单侧用6-羟基多巴胺损伤的大鼠中,D-1激动剂SKF 38393(3毫克/千克,皮下注射)仅在先用多巴胺能激动剂如阿扑吗啡引发后才诱导对侧旋转。在阿扑吗啡(0.1毫克/千克,皮下注射)前15分钟给予N-甲基-D-天冬氨酸受体拮抗剂(+)MK 801(0.1毫克/千克,腹腔注射)可阻止阿扑吗啡作为引发剂的能力,同时增强其急性对侧旋转作用。无活性异构体(-)MK 801则无作用。结果表明,N-甲基-D-天冬氨酸受体在引发过程中发挥允许作用。

相似文献

1
Stereospecific blockade of N-methyl-D-aspartate transmission by MK 801 prevents priming of SKF 38393-induced turning.MK 801对N-甲基-D-天冬氨酸传递的立体特异性阻断可防止SKF 38393诱导的旋转启动。
Psychopharmacology (Berl). 1990;101(2):287-8. doi: 10.1007/BF02244143.
2
Effect of MK 801 on priming of D1-dependent contralateral turning and its relationship to c-fos expression in the rat caudate-putamen.MK801对D1依赖性对侧旋转启动的影响及其与大鼠尾状核-壳核中c-fos表达的关系。
Behav Brain Res. 1996 Sep;79(1-2):93-100. doi: 10.1016/0166-4328(96)00002-2.
3
Sensitization to apomorphine-induced rotational behavior in 6-OHDA-lesioned rats: effects of NMDA antagonists on drug response.6-羟基多巴胺损伤大鼠对阿扑吗啡诱导的旋转行为的敏化作用:NMDA拮抗剂对药物反应的影响。
Brain Res. 1995 Jun 5;682(1-2):63-8. doi: 10.1016/0006-8993(95)00322-h.
4
Time and dose dependence of the 'priming' of the expression of dopamine receptor supersensitivity.多巴胺受体超敏反应表达“启动”的时间和剂量依赖性。
Eur J Pharmacol. 1989 Mar 21;162(2):329-35. doi: 10.1016/0014-2999(89)90296-3.
5
N-methyl-D-aspartate receptor blockade differentially modifies regional cerebral metabolic responses to D1 and D2 dopamine agonists in rats with a unilateral 6-hydroxydopamine lesion.在单侧6-羟基多巴胺损伤的大鼠中,N-甲基-D-天冬氨酸受体阻断对D1和D2多巴胺激动剂引起的局部脑代谢反应有不同的影响。
Neuroscience. 1993 Jun;54(4):1051-61. doi: 10.1016/0306-4522(93)90595-7.
6
Subchronic intermittent caffeine administration to unilaterally 6-hydroxydopamine-lesioned rats sensitizes turning behaviour in response to dopamine D(1) but not D(2) receptor agonists.对单侧6-羟基多巴胺损伤的大鼠进行亚慢性间歇性咖啡因给药,可使它们对多巴胺D(1)受体激动剂而非D(2)受体激动剂产生的旋转行为敏感化。
Behav Pharmacol. 2005 Dec;16(8):621-6. doi: 10.1097/00008877-200512000-00004.
7
Blockade of MK-801 induced ipsiversive turning in 6-OHDA lesioned rats by alpha 1-adrenoceptor antagonists.α1肾上腺素能受体拮抗剂对MK-801诱导的6-羟基多巴胺损伤大鼠向患侧旋转的阻断作用。
Pharmacol Biochem Behav. 1984 Jun;20(6):893-7. doi: 10.1016/0091-3057(84)90014-5.
8
Long-term D1-dopamine receptor sensitization in neonatal 6-OHDA-lesioned rats is blocked by an NMDA antagonist.新生6-羟基多巴胺损伤大鼠中多巴胺D1受体的长期致敏作用被NMDA拮抗剂阻断。
Brain Res. 1990 Apr 2;512(2):284-90. doi: 10.1016/0006-8993(90)90638-R.
9
Agonist-induced homologous and heterologous sensitization to D-1- and D-2-dependent contraversive turning.激动剂诱导的对 D-1 和 D-2 依赖性反向旋转的同源和异源致敏作用。
Eur J Pharmacol. 1987 Sep 2;141(1):101-7. doi: 10.1016/0014-2999(87)90415-8.
10
Priming of a D1 dopamine receptor behavioural response is dissociated from striatal immediate-early gene activity.D1多巴胺受体行为反应的启动与纹状体即刻早期基因活性相分离。
Neuroscience. 1995 May;66(2):347-59. doi: 10.1016/0306-4522(94)00582-p.

引用本文的文献

1
Involvement of Glutamate NMDA Receptors in the Acute, Long-Term, and Conditioned Effects of Amphetamine on Rat 50 kHz Ultrasonic Vocalizations.谷氨酸N-甲基-D-天冬氨酸受体在苯丙胺对大鼠50千赫兹超声波发声的急性、长期及条件性效应中的作用。
Int J Neuropsychopharmacol. 2015 May 19;18(11):pyv057. doi: 10.1093/ijnp/pyv057.
2
Blockade ofNMDA receptors differentially affectsD-1 andD-2 mediated turning behavior in the 6-hydroxydopamine model of Parkinson.阻断 NMDA 受体在 6-羟多巴胺帕金森模型中对 D-1 和 D-2 介导的转向行为的影响不同。
Amino Acids. 1991 Jun;1(2):205-13. doi: 10.1007/BF00806918.
3
The 6-hydroxydopamine model of Parkinson's disease.

本文引用的文献

1
Agonist-induced homologous and heterologous sensitization to D-1- and D-2-dependent contraversive turning.激动剂诱导的对 D-1 和 D-2 依赖性反向旋转的同源和异源致敏作用。
Eur J Pharmacol. 1987 Sep 2;141(1):101-7. doi: 10.1016/0014-2999(87)90415-8.
2
Selective impairment of learning and blockade of long-term potentiation by an N-methyl-D-aspartate receptor antagonist, AP5.N-甲基-D-天冬氨酸受体拮抗剂AP5对学习的选择性损害及对长时程增强的阻断作用
Nature. 1986;319(6056):774-6. doi: 10.1038/319774a0.
3
[3H]MK-801 labels a site on the N-methyl-D-aspartate receptor channel complex in rat brain membranes.
帕金森病的6-羟基多巴胺模型。
Neurotox Res. 2007 Apr;11(3-4):151-67. doi: 10.1007/BF03033565.
4
Development of both conditioning and sensitization of the behavioral activating effects of amphetamine is blocked by the non-competitive NMDA receptor antagonist, MK-801.苯丙胺行为激活作用的条件反射和敏化作用的发展均被非竞争性NMDA受体拮抗剂MK-801阻断。
Psychopharmacology (Berl). 1993;110(1-2):125-32. doi: 10.1007/BF02246961.
5
Effects of MK-801 stereoisomers on schedule-controlled behavior in rats.MK-801 立体异构体对大鼠定时控制行为的影响。
Psychopharmacology (Berl). 1991;105(4):477-80. doi: 10.1007/BF02244366.
6
MK801 attenuates behavioural adaptation to chronic nicotine administration in rats.MK801减弱大鼠对慢性尼古丁给药的行为适应性。
Br J Pharmacol. 1992 Mar;105(3):514-5. doi: 10.1111/j.1476-5381.1992.tb09010.x.
[3H]MK - 801标记大鼠脑膜中N - 甲基 - D - 天冬氨酸受体通道复合物上的一个位点。
J Neurochem. 1988 Jan;50(1):274-81. doi: 10.1111/j.1471-4159.1988.tb13260.x.
4
Time and dose dependence of the 'priming' of the expression of dopamine receptor supersensitivity.多巴胺受体超敏反应表达“启动”的时间和剂量依赖性。
Eur J Pharmacol. 1989 Mar 21;162(2):329-35. doi: 10.1016/0014-2999(89)90296-3.