• 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

在动物模型中,暴露治疗线索的行为和药物联合治疗策略对可卡因复发预防的影响存在性别差异。

Sex differences in the effects of a combined behavioral and pharmacological treatment strategy for cocaine relapse prevention in an animal model of cue exposure therapy.

机构信息

Department of Psychological and Brain Sciences, Boston University, Boston, USA; Center for Systems Neuroscience, Boston University, Boston, USA.

Department of Psychological and Brain Sciences, Boston University, Boston, USA.

出版信息

Behav Brain Res. 2020 Oct 1;395:112839. doi: 10.1016/j.bbr.2020.112839. Epub 2020 Aug 2.

DOI:10.1016/j.bbr.2020.112839
PMID:32750464
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7492466/
Abstract

Brief interventions of environmental enrichment (EE) or the glycine transporter-1 inhibitor Org24598 administered with cocaine-cue extinction training were shown previously to inhibit reacquisition of cocaine self-administration in male rats trained to self-administer a moderate 0.3 mg/kg dose of cocaine. Determining how EE and Org24598 synergize in combination in an animal model of cue exposure therapy is novel. Important changes made in this investigation were increasing the cocaine training dose to 1.0 mg/kg and determining sex differences. Adult male and female rats self-administering 1.0 mg/kg cocaine for 35-40 daily sessions exhibited an addiction-like phenotype under a second-order schedule of cocaine delivery and cue presentation. Rats next underwent 6 weekly extinction training sessions for which treatments consisted of EE or NoEE and Vehicle or Org24598 (3.0 mg/kg in males; 3.0 or 7.5 mg/kg in females). Rats then were tested for reacquisition of cocaine self-administration for 15 daily sessions. In males, the combined EE +3.0 mg/kg Org24598 treatment facilitated extinction learning and inhibited reacquisition of cocaine self-administration to a greater extent than no treatment and to individual EE or 3.0 mg/kg Org24598 treatments. In females, EE +7.5 mg/kg Org24598 facilitated extinction learning, but did not inhibit reacquisition of cocaine self-administration. Thus, there were sex differences in the ability of EE + Org24598 administered in conjunction with extinction training to inhibit cocaine relapse in rats exhibiting an addiction-like phenotype. These findings suggest that this multimodal treatment approach might be a feasible option during cue exposure therapy in cocaine-dependent men, but not women.

摘要

以前的研究表明,环境富集(EE)或甘氨酸转运体-1 抑制剂 Org24598 的简短干预措施,与可卡因线索消退训练一起使用,可以抑制在接受中等剂量 0.3 毫克/千克可卡因自我给药训练的雄性大鼠中可卡因自我给药的重新获得。在暴露于线索的动物模型中,确定 EE 和 Org24598 如何协同作用是新颖的。在这项研究中,进行了重要的改变,将可卡因训练剂量增加到 1.0 毫克/千克,并确定了性别差异。接受 1.0 毫克/千克可卡因 35-40 天的成年雄性和雌性大鼠,在可卡因给予和线索呈现的二阶时间表下表现出类似成瘾的表型。然后,大鼠接受了 6 周的消退训练,治疗方法包括 EE 或无 EE 和载体或 Org24598(雄性 3.0 毫克/千克;雌性 3.0 或 7.5 毫克/千克)。然后,大鼠进行了 15 天的可卡因自我给药重新获得测试。在雄性中,联合 EE +3.0 毫克/千克 Org24598 治疗促进了消退学习,并比不治疗和单独 EE 或 3.0 毫克/千克 Org24598 治疗更能抑制可卡因自我给药的重新获得。在雌性中,EE +7.5 毫克/千克 Org24598 促进了消退学习,但没有抑制可卡因自我给药的重新获得。因此,在表现出类似成瘾的表型的大鼠中,EE +Org24598 与消退训练联合给药抑制可卡因复吸的能力存在性别差异。这些发现表明,这种多模式治疗方法可能是可卡因依赖男性在暴露于线索治疗期间的可行选择,但不是女性。

相似文献

1
Sex differences in the effects of a combined behavioral and pharmacological treatment strategy for cocaine relapse prevention in an animal model of cue exposure therapy.在动物模型中,暴露治疗线索的行为和药物联合治疗策略对可卡因复发预防的影响存在性别差异。
Behav Brain Res. 2020 Oct 1;395:112839. doi: 10.1016/j.bbr.2020.112839. Epub 2020 Aug 2.
2
Glycine transporter-1 inhibition preceding extinction training inhibits reacquisition of cocaine seeking.在消退训练之前抑制甘氨酸转运蛋白-1 可抑制可卡因觅药行为的再获得。
Neuropsychopharmacology. 2012 Dec;37(13):2837-45. doi: 10.1038/npp.2012.155. Epub 2012 Sep 5.
3
Facilitative effects of environmental enrichment for cocaine relapse prevention are dependent on extinction training context and involve increased TrkB signaling in dorsal hippocampus and ventromedial prefrontal cortex.环境丰富化对可卡因复吸预防的促进作用依赖于消褪训练背景,并涉及背侧海马体和腹内侧前额叶皮层中 TrkB 信号的增加。
Behav Brain Res. 2020 May 27;386:112596. doi: 10.1016/j.bbr.2020.112596. Epub 2020 Mar 16.
4
Environmental enrichment facilitates cocaine-cue extinction, deters reacquisition of cocaine self-administration and alters AMPAR GluA1 expression and phosphorylation.环境富集促进可卡因线索消退,抑制可卡因自我给药的重新习得,并改变α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPAR)GluA1亚基的表达和磷酸化。
Addict Biol. 2017 Jan;22(1):152-162. doi: 10.1111/adb.12313. Epub 2015 Sep 18.
5
Inhibiting glycine transporter-1 facilitates cocaine-cue extinction and attenuates reacquisition of cocaine-seeking behavior.抑制甘氨酸转运蛋白-1 可促进可卡因线索消退,并减弱可卡因觅药行为的再获得。
Drug Alcohol Depend. 2012 Apr 1;122(1-2):119-26. doi: 10.1016/j.drugalcdep.2011.09.017. Epub 2011 Oct 10.
6
Molecular mechanisms underlying sex and treatment-dependent differences in an animal model of cue-exposure therapy for cocaine relapse prevention.用于预防可卡因复吸的线索暴露疗法动物模型中,性别及治疗依赖性差异背后的分子机制。
Front Neurosci. 2024 Aug 8;18:1425447. doi: 10.3389/fnins.2024.1425447. eCollection 2024.
7
D-cycloserine deters reacquisition of cocaine self-administration by augmenting extinction learning.D-环丝氨酸通过增强消退学习来阻止可卡因自我给药的复吸。
Neuropsychopharmacology. 2010 Jan;35(2):357-67. doi: 10.1038/npp.2009.139.
8
Environmental enrichment reduces cocaine seeking and reinstatement induced by cues and stress but not by cocaine.环境丰容减少了线索和应激引起的可卡因觅药和复吸,但不能减少可卡因本身引起的觅药和复吸。
Neuropsychopharmacology. 2009 Dec;34(13):2767-78. doi: 10.1038/npp.2009.127. Epub 2009 Sep 9.
9
Changes in expression of c-Fos protein following cocaine-cue extinction learning.可卡因线索消去学习后 c-Fos 蛋白表达的变化。
Behav Brain Res. 2012 Sep 1;234(1):100-6. doi: 10.1016/j.bbr.2012.06.010. Epub 2012 Jun 18.
10
D-cycloserine reduces the context specificity of pavlovian extinction of cocaine cues through actions in the nucleus accumbens.D-环丝氨酸通过作用于伏隔核减少了可卡因线索条件性消退的情境特异性。
J Neurosci. 2010 Aug 4;30(31):10526-33. doi: 10.1523/JNEUROSCI.2523-10.2010.

引用本文的文献

1
Molecular mechanisms underlying sex and treatment-dependent differences in an animal model of cue-exposure therapy for cocaine relapse prevention.用于预防可卡因复吸的线索暴露疗法动物模型中,性别及治疗依赖性差异背后的分子机制。
Front Neurosci. 2024 Aug 8;18:1425447. doi: 10.3389/fnins.2024.1425447. eCollection 2024.

本文引用的文献

1
Facilitative effects of environmental enrichment for cocaine relapse prevention are dependent on extinction training context and involve increased TrkB signaling in dorsal hippocampus and ventromedial prefrontal cortex.环境丰富化对可卡因复吸预防的促进作用依赖于消褪训练背景,并涉及背侧海马体和腹内侧前额叶皮层中 TrkB 信号的增加。
Behav Brain Res. 2020 May 27;386:112596. doi: 10.1016/j.bbr.2020.112596. Epub 2020 Mar 16.
2
Comparative Pro-cognitive and Neurochemical Profiles of Glycine Modulatory Site Agonists and Glycine Reuptake Inhibitors in the Rat: Potential Relevance to Cognitive Dysfunction and Its Management.甘氨酸调节位点激动剂和甘氨酸再摄取抑制剂在大鼠中的比较前认知和神经化学特征:对认知功能障碍及其管理的潜在相关性。
Mol Neurobiol. 2020 May;57(5):2144-2166. doi: 10.1007/s12035-020-01875-9. Epub 2020 Jan 20.
3
Clinical validation of reduction in cocaine frequency level as an endpoint in clinical trials for cocaine use disorder.临床验证可卡因使用障碍临床试验中可卡因使用频率降低作为终点的有效性。
Drug Alcohol Depend. 2019 Dec 1;205:107648. doi: 10.1016/j.drugalcdep.2019.107648. Epub 2019 Oct 21.
4
Infralimbic Estradiol Enhances Neuronal Excitability and Facilitates Extinction of Cocaine Seeking in Female Rats a BDNF/TrkB Mechanism.边缘下雌二醇增强雌性大鼠神经元兴奋性并促进可卡因觅求行为消退:一种BDNF/TrkB机制
Front Behav Neurosci. 2019 Jul 31;13:168. doi: 10.3389/fnbeh.2019.00168. eCollection 2019.
5
Neuron-Derived Estrogen Regulates Synaptic Plasticity and Memory.神经元衍生的雌激素调节突触可塑性和记忆。
J Neurosci. 2019 Apr 10;39(15):2792-2809. doi: 10.1523/JNEUROSCI.1970-18.2019. Epub 2019 Feb 6.
6
Alternation in dopamine D-like and metabotropic glutamate type 5 receptor density caused by differing housing conditions during abstinence from cocaine self-administration in rats.在大鼠可卡因自我给药戒断期间,不同的饲养条件引起多巴胺 D 样和代谢型谷氨酸受体 5 密度的改变。
J Psychopharmacol. 2019 Mar;33(3):372-382. doi: 10.1177/0269881118821113. Epub 2019 Jan 15.
7
Neuroplasticity-related correlates of environmental enrichment combined with physical activity differ between the sexes.环境富集与体力活动相结合的神经可塑性相关相关性在性别之间存在差异。
Eur Neuropsychopharmacol. 2019 Jan;29(1):1-15. doi: 10.1016/j.euroneuro.2018.11.1107. Epub 2018 Nov 27.
8
Sex Differences in the Rapid Cell Signaling Mechanisms Underlying the Memory-Enhancing Effects of 17β-Estradiol.17β-雌二醇增强记忆的快速细胞信号转导机制中的性别差异。
eNeuro. 2018 Oct 30;5(5). doi: 10.1523/ENEURO.0267-18.2018. eCollection 2018 Sep-Oct.
9
A placebo-controlled randomized trial of D-cycloserine augmentation of cue exposure therapy for smoking cessation.D-环丝氨酸增强线索暴露疗法戒烟的安慰剂对照随机试验。
Cogn Behav Ther. 2019 Jan;48(1):65-76. doi: 10.1080/16506073.2018.1476908. Epub 2018 Aug 16.
10
A Protocol for Measuring Cue Reactivity in a Rat Model of Cocaine Use Disorder.一种用于测量可卡因使用障碍大鼠模型中线索反应性的方案。
J Vis Exp. 2018 Jun 18(136):55864. doi: 10.3791/55864.