• 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

乙醇戒断增强大鼠伏隔核中前强啡肽系统的活性。

Ethanol withdrawal enhances the prodynorphin system activity in the rat nucleus accumbens.

作者信息

Przewłocka B, Turchan J, Lasoń W, Przewłocki R

机构信息

Department of Molecular Neuropharmacology, Institute of Pharmacology, Polish Academy of Sciences, Krakow.

出版信息

Neurosci Lett. 1997 Nov 28;238(1-2):13-6. doi: 10.1016/s0304-3940(97)00829-x.

DOI:10.1016/s0304-3940(97)00829-x
PMID:9464643
Abstract

The present study investigated the effects of ethanol withdrawal after its chronic administration on endogenous opioid systems in the nucleus accumbens of rats. An in situ hybridization study showed an increase in the prodynorphin mRNA level at 24 and 48 h (by 189 and 146%, respectively) after ethanol withdrawal, whereas the proenkephalin mRNA level remained unchanged. Furthermore, after a 48 h withdrawal period, the level of alpha-neoendorphin (alphaNEO), a prodynorphin-derived peptide, was significantly decreased (by 48%), that effect being associated with the enhancement of the K+-stimulated release of that peptide from nucleus accumbens slices. At 96 h after ethanol withdrawal, only the basal release of alphaNEO was elevated, while other parameters returned to the control level. Our data indicate that after 48 h of ethanol withdrawal, prodynorphin neurons are highly activated. The increased supply of endogenous kappa opioid receptor agonists in the nucleus accumbens at that time may promote aversive states during ethanol withdrawal.

摘要

本研究调查了长期给予乙醇后戒断对大鼠伏隔核内源性阿片系统的影响。原位杂交研究显示,乙醇戒断后24小时和48小时,前强啡肽原mRNA水平升高(分别升高189%和146%),而前脑啡肽原mRNA水平保持不变。此外,在戒断48小时后,强啡肽原衍生肽α-新内啡肽(αNEO)的水平显著降低(降低48%),该效应与伏隔核切片中该肽的钾离子刺激释放增强有关。乙醇戒断96小时后,仅αNEO的基础释放升高,而其他参数恢复到对照水平。我们的数据表明,乙醇戒断48小时后,前强啡肽原神经元被高度激活。此时伏隔核内源性κ阿片受体激动剂供应增加可能会在乙醇戒断期间促进厌恶状态。

相似文献

1
Ethanol withdrawal enhances the prodynorphin system activity in the rat nucleus accumbens.乙醇戒断增强大鼠伏隔核中前强啡肽系统的活性。
Neurosci Lett. 1997 Nov 28;238(1-2):13-6. doi: 10.1016/s0304-3940(97)00829-x.
2
The effect of single and repeated morphine administration on the prodynorphin system activity in the nucleus accumbens and striatum of the rat.单次及重复给予吗啡对大鼠伏隔核和纹状体中前强啡肽系统活性的影响。
Neuroscience. 1996 Feb;70(3):749-54. doi: 10.1016/s0306-4522(96)83012-0.
3
Effects of repeated psychostimulant administration on the prodynorphin system activity and kappa opioid receptor density in the rat brain.重复给予精神兴奋剂对大鼠脑内前强啡肽系统活性及κ阿片受体密度的影响。
Neuroscience. 1998 Aug;85(4):1051-9. doi: 10.1016/s0306-4522(97)00639-8.
4
Alteration of kappa-opioid receptor system expression in distinct brain regions of a genetic model of enhanced ethanol withdrawal severity.乙醇戒断严重程度增强的遗传模型中不同脑区κ-阿片受体系统表达的改变。
Brain Res. 2005 Jun 7;1046(1-2):77-89. doi: 10.1016/j.brainres.2005.03.043.
5
Supersensitive Kappa Opioid Receptors Promotes Ethanol Withdrawal-Related Behaviors and Reduce Dopamine Signaling in the Nucleus Accumbens.超敏κ阿片受体促进乙醇戒断相关行为并降低伏隔核中的多巴胺信号传导。
Int J Neuropsychopharmacol. 2016 Apr 29;19(5). doi: 10.1093/ijnp/pyv127. Print 2016 May.
6
Antagonism of κ opioid receptor in the nucleus accumbens prevents the depressive-like behaviors following prolonged morphine abstinence.伏隔核中κ阿片受体的拮抗作用可预防长期吗啡戒断后的抑郁样行为。
Behav Brain Res. 2015 Sep 15;291:334-341. doi: 10.1016/j.bbr.2015.05.053. Epub 2015 Jun 3.
7
Imipramine induces alterations in proenkephalin and prodynorphin mRNAs level in the nucleus accumbens and striatum in the rat.丙咪嗪可诱导大鼠伏隔核和纹状体中脑啡肽原和强啡肽原mRNA水平发生改变。
Pol J Pharmacol. 1997 Sep-Oct;49(5):351-5.
8
Dopamine receptor mRNA expression patterns by opioid peptide cells in the nucleus accumbens of the rat: a double in situ hybridization study.大鼠伏隔核中阿片肽细胞的多巴胺受体mRNA表达模式:一项双重原位杂交研究。
J Comp Neurol. 1995 Oct 9;361(1):57-76. doi: 10.1002/cne.903610106.
9
Elevated prodynorphin expression associated with ethanol withdrawal convulsions.前强啡肽原表达升高与乙醇戒断惊厥相关。
Neurochem Int. 2000 Nov-Dec;37(5-6):463-72. doi: 10.1016/s0197-0186(00)00056-5.
10
Short-term withdrawal from repeated exposure to cocaine during adolescence modulates dynorphin mRNA levels and BDNF signaling in the rat nucleus accumbens.青春期反复接触可卡因后短期戒断可调节大鼠伏隔核内强啡肽 mRNA 水平和 BDNF 信号。
Drug Alcohol Depend. 2019 Apr 1;197:127-133. doi: 10.1016/j.drugalcdep.2019.01.006. Epub 2019 Feb 13.

引用本文的文献

1
The Dynorphin/-Opioid Receptor System at the Interface of Hyperalgesia/Hyperkatifeia and Addiction.痛觉过敏/痛觉亢进与成瘾界面的强啡肽/-阿片受体系统
Curr Addict Rep. 2025;12(1):11. doi: 10.1007/s40429-025-00618-x. Epub 2025 Feb 4.
2
Systemic kappa opioid receptor antagonism accelerates reinforcement learning via augmentation of novelty processing in male mice.系统 κ 阿片受体拮抗作用通过增强雄性小鼠新奇处理来加速强化学习。
Neuropsychopharmacology. 2023 May;48(6):857-868. doi: 10.1038/s41386-023-01547-x. Epub 2023 Feb 17.
3
Recapitulating phenotypes of alcohol dependence via overexpression of Oprk1 in the ventral tegmental area of non-dependent TH::Cre rats.
通过在非依赖的 TH::Cre 大鼠腹侧被盖区过表达 Oprk1 来重现酒精依赖的表型。
Neuropharmacology. 2023 May 1;228:109457. doi: 10.1016/j.neuropharm.2023.109457. Epub 2023 Feb 9.
4
Drug Addiction: Hyperkatifeia/Negative Reinforcement as a Framework for Medications Development.药物成瘾:Hyperkatifeia/负性强化作为药物开发的框架。
Pharmacol Rev. 2021 Jan;73(1):163-201. doi: 10.1124/pharmrev.120.000083.
5
Behavioral, neurobiological, and neurochemical mechanisms of ethanol self-administration: A translational review.乙醇自我给药的行为、神经生物学和神经化学机制:转化综述。
Pharmacol Ther. 2020 Aug;212:107573. doi: 10.1016/j.pharmthera.2020.107573. Epub 2020 May 11.
6
Dynorphin and its role in alcohol use disorder.内啡肽及其在酒精使用障碍中的作用。
Brain Res. 2020 May 15;1735:146742. doi: 10.1016/j.brainres.2020.146742. Epub 2020 Feb 28.
7
Exploring Sex Differences in the Attenuation of Ethanol Drinking by Naltrexone in Dependent Rats During Early and Protracted Abstinence.探究纳曲酮在依赖大鼠早期和长期戒断期间对乙醇饮用量的抑制作用中的性别差异。
Alcohol Clin Exp Res. 2018 Dec;42(12):2466-2478. doi: 10.1111/acer.13898. Epub 2018 Oct 28.
8
In vivo detection of optically-evoked opioid peptide release.体内检测光激发阿片肽释放。
Elife. 2018 Sep 3;7:e36520. doi: 10.7554/eLife.36520.
9
Contribution of Dynorphin and Orexin Neuropeptide Systems to the Motivational Effects of Alcohol.强啡肽和食欲素神经肽系统对酒精动机效应的作用。
Handb Exp Pharmacol. 2018;248:473-503. doi: 10.1007/164_2018_100.
10
The κ-opioid receptor antagonist JDTic decreases ethanol intake in alcohol-preferring AA rats.κ 阿片受体拮抗剂 JDTic 可减少酒精偏爱 AA 大鼠的乙醇摄入量。
Psychopharmacology (Berl). 2018 May;235(5):1581-1591. doi: 10.1007/s00213-018-4868-x. Epub 2018 Feb 28.