• 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

多巴胺中脑边缘神经元的损伤会阻断内源性脑啡肽诱导的行为效应,但不会阻断μ阿片受体激动剂诱导的行为效应。

Lesion of dopamine mesolimbic neurons blocks behavioral effects induced by the endogenous enkephalins but not by a mu-opioid receptor agonist.

作者信息

Calenco-Choukroun G, Daugé V, Gacel G, Roques B P

机构信息

Pharmacochimie Moléculaire, INSERM U266, CNRS UA498, UFR des Sciences Pharmaceutiques et Biologiques, Paris, France.

出版信息

Eur J Pharmacol. 1991 Dec 17;209(3):267-71. doi: 10.1016/0014-2999(91)90181-o.

DOI:10.1016/0014-2999(91)90181-o
PMID:1665799
Abstract

Lesioning of dopamine neurons by injection of 6-hydroxydopamine into the nucleus accumbens blocked the increased rearing activity measured in the open-field and induced by injection into the ventral tegmental area of: [R)-3-(N-hydroxylcarboxamido-2-benzyl-propanoyl)-L-alanine), kelatorphan (complete inhibitor of enkephalin catabolism) or by (Tyr-D-Ser(OtBu)-Gly-Phe-Leu-Thr(OtBu)): BUBU (selective delta agonist) but not the hypolocomotion evoked by the mu agonist (Tyr-D-Ala-Gly-N(Me)-Phe-Glyol): DAMGO. This suggests the involvement of different neuronal pathways in mu and delta effects.

摘要

通过向伏隔核注射6-羟基多巴胺来损伤多巴胺神经元,可阻断在旷场中测量到的、由向腹侧被盖区注射[R)-3-(N-羟基羧酰胺基-2-苄基-丙酰基)-L-丙氨酸]、凯拉托品(脑啡肽分解代谢的完全抑制剂)或(Tyr-D-Ser(OtBu)-Gly-Phe-Leu-Thr(OtBu)):BUBU(选择性δ激动剂)所诱导的增强的竖毛活动,但不能阻断μ激动剂(Tyr-D-Ala-Gly-N(Me)-Phe-Glyol):DAMGO所诱发的运动减少。这表明不同的神经元通路参与了μ和δ效应。

相似文献

1
Lesion of dopamine mesolimbic neurons blocks behavioral effects induced by the endogenous enkephalins but not by a mu-opioid receptor agonist.多巴胺中脑边缘神经元的损伤会阻断内源性脑啡肽诱导的行为效应,但不会阻断μ阿片受体激动剂诱导的行为效应。
Eur J Pharmacol. 1991 Dec 17;209(3):267-71. doi: 10.1016/0014-2999(91)90181-o.
2
Blockade of dopamine receptors reverses the behavioral effects of endogenous enkephalins in the Nucleus caudatus but not in the Nucleus accumbens: differential involvement of delta and mu opioid receptors.多巴胺受体的阻断可逆转内源性脑啡肽在尾状核而非伏隔核中的行为效应:δ和μ阿片受体的不同参与情况。
Psychopharmacology (Berl). 1989;99(2):168-75. doi: 10.1007/BF00442803.
3
Differential involvement of ventral tegmental mu, delta and kappa opioid receptors in modulation of basal mesolimbic dopamine release: in vivo microdialysis studies.腹侧被盖区的μ、δ和κ阿片受体在调节中脑边缘多巴胺基础释放中的差异作用:体内微透析研究
J Pharmacol Exp Ther. 1993 Sep;266(3):1236-46.
4
Behavioral effects of endogenous or exogenous (mu, delta) opioid peptides: relation with DA mesolimbic pathways.
Prog Clin Biol Res. 1990;328:417-20.
5
Mu opioid receptor involvement in enkephalin activation of dopamine neurons in the ventral tegmental area.μ阿片受体参与腹侧被盖区多巴胺神经元的脑啡肽激活。
J Pharmacol Exp Ther. 1987 Apr;241(1):328-37.
6
Dopamine depletion produces augmented behavioral responses to a mu-, but not a delta-opioid receptor agonist in the nucleus accumbens: lack of a role for receptor upregulation.多巴胺耗竭会增强伏隔核中对μ阿片受体激动剂而非δ阿片受体激动剂的行为反应:受体上调不起作用。
Synapse. 1992 May;11(1):47-57. doi: 10.1002/syn.890110107.
7
Electrochemical evidence of increased dopamine transmission in prefrontal cortex and nucleus accumbens elicited by ventral tegmental mu-opioid receptor activation in freely behaving rats.在自由活动的大鼠中,腹侧被盖区μ-阿片受体激活引发前额叶皮质和伏隔核多巴胺传递增加的电化学证据。
Synapse. 1995 Oct;21(2):110-22. doi: 10.1002/syn.890210204.
8
Brain passage of BUBU, a highly selective and potent agonist for delta opioid receptors: in vivo binding and mu versus delta receptors occupancy.BUBU(一种对δ阿片受体具有高度选择性和强效的激动剂)在脑内的通过情况:体内结合以及μ受体与δ受体占有率
Pharmacol Biochem Behav. 1991 Jan;38(1):155-62. doi: 10.1016/0091-3057(91)90604-z.
9
Comparison of the behavioural effects induced by administration in rat nucleus accumbens or nucleus caudatus of selective mu and delta opioid peptides or kelatorphan an inhibitor of enkephalin-degrading-enzymes.选择性μ和δ阿片肽或脑啡肽降解酶抑制剂凯拉托芬在大鼠伏隔核或尾状核给药所诱导的行为效应比较。
Psychopharmacology (Berl). 1988;96(3):343-52. doi: 10.1007/BF00216060.
10
Further evidence for a role of delta-opiate receptors in the presynaptic regulation of newly synthesized dopamine release.δ-阿片受体在新合成多巴胺释放的突触前调节中作用的进一步证据。
Eur J Pharmacol. 1986 Jul 15;126(1-2):1-9. doi: 10.1016/0014-2999(86)90731-4.

引用本文的文献

1
Opposite role of CCKA and CCKB receptors in the modulation of endogenous enkephalin antidepressant-like effects.胆囊收缩素A和B受体在内源性脑啡肽抗抑郁样效应调节中的相反作用。
Psychopharmacology (Berl). 1995 Aug;120(4):400-8. doi: 10.1007/BF02245811.
2
Antidepressant-like effects of CCKB antagonists in mice: antagonism by naltrindole.CCKB拮抗剂对小鼠的抗抑郁样作用:纳曲吲哚的拮抗作用
Br J Pharmacol. 1994 Mar;111(3):956-60. doi: 10.1111/j.1476-5381.1994.tb14832.x.