• 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

多巴胺 D1 受体激动剂对松鼠猴和大鼠腺苷酸环化酶刺激作用的差异疗效。

Differential efficacies of dopamine D1 receptor agonists for stimulating adenylyl cyclase in squirrel monkey and rat.

作者信息

Izenwasser S, Katz J L

机构信息

Psychobiology Section, NIDA Addiction Research Center, Baltimore, MD.

出版信息

Eur J Pharmacol. 1993 Jun 15;246(1):39-44. doi: 10.1016/0922-4106(93)90007-v.

DOI:10.1016/0922-4106(93)90007-v
PMID:8102607
Abstract

Adenylyl cyclase activity was stimulated by dopamine to approximately 200% over basal activity in both squirrel monkey caudate and rat caudate-putamen. The selective dopamine D1 receptor agonists SKF 82958, A68930, dihydrexidine, CY 208-243, and SKF 75670 each produced similar maximal stimulation across the two species. SKF 38393, SKF 81297, and 6-Br-APB, however, each had higher efficacy in rat than in monkey. These results suggest differences in dopamine D1 receptors in the two species.

摘要

在松鼠猴尾状核和大鼠尾状核-壳核中,多巴胺可将腺苷酸环化酶活性刺激至比基础活性高约200%。选择性多巴胺D1受体激动剂SKF 82958、A68930、二氢麦角隐亭、CY 208-243和SKF 75670在这两个物种中均产生了相似的最大刺激作用。然而,SKF 38393、SKF 81297和6-溴-APB在大鼠中的效力均高于猴子。这些结果表明这两个物种的多巴胺D1受体存在差异。

相似文献

1
Differential efficacies of dopamine D1 receptor agonists for stimulating adenylyl cyclase in squirrel monkey and rat.多巴胺 D1 受体激动剂对松鼠猴和大鼠腺苷酸环化酶刺激作用的差异疗效。
Eur J Pharmacol. 1993 Jun 15;246(1):39-44. doi: 10.1016/0922-4106(93)90007-v.
2
Lower efficacy of the dopamine D1 agonist, SKF 38393, to stimulate adenylyl cyclase activity in primate than in rodent striatum.多巴胺D1激动剂SKF 38393在灵长类动物中刺激腺苷酸环化酶活性的效力低于在啮齿动物纹状体中的效力。
Eur J Pharmacol. 1991 Sep 17;202(2):273-6. doi: 10.1016/0014-2999(91)90304-9.
3
Dopamine D1 receptors: efficacy of full (dihydrexidine) vs. partial (SKF38393) agonists in primates vs. rodents.多巴胺D1受体:在灵长类动物与啮齿动物中,完全激动剂(二氢麦角隐亭)与部分激动剂(SKF38393)的功效比较
Eur J Pharmacol. 1993 Sep 28;242(2):165-72. doi: 10.1016/0014-2999(93)90076-t.
4
Differential regulation of D1 dopamine receptor- and of A2a adenosine receptor-stimulated adenylyl cyclase by mu-, delta 1-, and delta 2-opioid agonists in rat caudate putamen.大鼠尾状核壳核中μ-、δ1-和δ2-阿片样激动剂对D1多巴胺受体和A2a腺苷受体刺激的腺苷酸环化酶的差异调节
J Neurochem. 1995 Jul;65(1):125-33. doi: 10.1046/j.1471-4159.1995.65010125.x.
5
Evidence for a distinct D1-like dopamine receptor that couples to activation of phosphoinositide metabolism in brain.大脑中存在一种与磷酸肌醇代谢激活偶联的独特D1样多巴胺受体的证据。
J Neurochem. 1994 May;62(5):2045-8. doi: 10.1046/j.1471-4159.1994.62052045.x.
6
Decreased striatal dopamine D1 receptor-stimulated adenylyl cyclase activity in human methamphetamine users.人类甲基苯丙胺使用者纹状体多巴胺D1受体刺激的腺苷酸环化酶活性降低。
Am J Psychiatry. 2003 May;160(5):896-903. doi: 10.1176/appi.ajp.160.5.896.
7
Dopamine D1 receptor involvement in the discriminative-stimulus effects of SKF 81297 in squirrel monkeys.多巴胺D1受体参与SKF 81297对松鼠猴的辨别刺激效应。
J Pharmacol Exp Ther. 1993 Nov;267(2):765-75.
8
"Full" dopamine D1 agonists in human caudate: biochemical properties and therapeutic implications.人类尾状核中的“完全”多巴胺D1激动剂:生化特性及治疗意义
Neuropharmacology. 1995 May;34(5):481-8. doi: 10.1016/0028-3908(95)00014-w.
9
A68930: a potent agonist specific for the dopamine D1 receptor.
Neurochem Int. 1992 Mar;20 Suppl:157S-160S. doi: 10.1016/0197-0186(92)90230-o.
10
Dopamine receptor agonists: selectivity and dopamine D1 receptor efficacy.
Eur J Pharmacol. 1990 Jun 12;188(6):335-47. doi: 10.1016/0922-4106(90)90194-3.

引用本文的文献

1
Gs- versus Golf-dependent functional selectivity mediated by the dopamine D receptor.由多巴胺D受体介导的Gs与高尔夫球依赖性功能选择性
Nat Commun. 2018 Feb 5;9(1):486. doi: 10.1038/s41467-017-02606-w.
2
Dopamine D receptor activation maintains motor coordination and balance in rats.多巴胺 D 受体激活可维持大鼠的运动协调性和平衡。
Metab Brain Dis. 2018 Feb;33(1):99-105. doi: 10.1007/s11011-017-0126-x. Epub 2017 Oct 19.
3
Dopamine D1 receptors, regulation of gene expression in the brain, and neurodegeneration.多巴胺 D1 受体、大脑基因表达的调控与神经退行性变。
CNS Neurol Disord Drug Targets. 2010 Nov;9(5):526-38. doi: 10.2174/187152710793361496.
4
Fluoxetine does not alter the ability of dopamine D(1)- and D(2)-like agonists to substitute for cocaine in squirrel monkeys.氟西汀不会改变多巴胺 D(1) 和 D(2) 样激动剂替代松鼠猴体内可卡因的能力。
Pharmacol Biochem Behav. 2009 Apr;92(2):219-23. doi: 10.1016/j.pbb.2008.11.013. Epub 2008 Dec 7.
5
Pharmacological analysis of human D1 AND D2 dopamine receptor missense variants.人类D1和D2多巴胺受体错义变体的药理学分析
J Mol Neurosci. 2008 Mar;34(3):211-23. doi: 10.1007/s12031-007-9030-x. Epub 2008 Jan 18.
6
Evidence for the sensitivity of operant timing behaviour to stimulation of D1 dopamine receptors.操作性定时行为对D1多巴胺受体刺激敏感性的证据。
Psychopharmacology (Berl). 2007 Dec;195(2):213-22. doi: 10.1007/s00213-007-0892-y. Epub 2007 Aug 1.
7
Prenatal exposure to cocaine increases the rewarding potency of cocaine and selective dopaminergic agonists in adult mice.产前接触可卡因会增加成年小鼠对可卡因和选择性多巴胺能激动剂的奖赏效力。
Biol Psychiatry. 2008 Jan 15;63(2):214-21. doi: 10.1016/j.biopsych.2007.01.014. Epub 2007 Jun 13.
8
Effects of dopamine D1 receptor agonists in rats trained to discriminate dihydrexidine.多巴胺D1受体激动剂对经训练辨别二氢麦角汀的大鼠的影响。
Psychopharmacology (Berl). 2006 May;186(1):25-31. doi: 10.1007/s00213-006-0342-2. Epub 2006 Mar 31.
9
Attenuation of relapse to cocaine seeking by dopamine D1 receptor agonists and antagonists in non-human primates.多巴胺D1受体激动剂和拮抗剂对非人灵长类动物可卡因觅求复发的抑制作用
Psychopharmacology (Berl). 2003 Jul;168(1-2):124-131. doi: 10.1007/s00213-002-1365-y. Epub 2003 Feb 27.
10
Self-administration of D1 receptor agonists by squirrel monkeys.松鼠猴对D1受体激动剂的自我给药
Psychopharmacology (Berl). 1996 May;125(2):97-104. doi: 10.1007/BF02249407.