• 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

γ-氨基丁酸A型受体激动剂THIP对实验大鼠自愿乙醇摄入量影响的微观结构分析

Microstructural analysis of the effects of THIP, a GABAA agonist, on voluntary ethanol intake in laboratory rats.

作者信息

Boyle A E, Smith B R, Amit Z

机构信息

Center for Studies in Behavioral Neurobiology, Concordia University, Montreal, Quebec, Canada.

出版信息

Pharmacol Biochem Behav. 1992 Dec;43(4):1121-7. doi: 10.1016/0091-3057(92)90491-w.

DOI:10.1016/0091-3057(92)90491-w
PMID:1335577
Abstract

The effects of GABAA agonist THIP on the acquisition of voluntary ethanol intake and the pattern of food and water consumption were examined through the use of a computer-controlled data acquisition system. Twenty male Long-Evans rats were randomly assigned to two groups, one of which received THIP (16 mg/kg, IP) and the other an equal volume of saline. Subjects were presented with a free choice of ethanol and water immediately following drug injections, which occurred every other day. The initial concentration of ethanol presented was 2% and was increased by increments of 2% following the second presentation of each concentration, up to a maximum concentration of 10%. Subjects treated with THIP consumed significantly greater amounts of ethanol than did saline controls. A microstructural analysis of bout patterns suggested that the increased consumption of ethanol was a function of an increase in the size, duration, and frequency of ethanol drinking bouts. Food intake was also attenuated by THIP treatment. The results indicated that the decrease in total food intake was a function of a decrease in the frequency of the food bouts. However, in contrast to that observed for ethanol intake, the size and duration of the food bouts were unchanged. The qualitatively different patterns in the microstructure of consummatory behavior for ethanol and food following THIP treatment would suggest that differential mechanisms may mediate the food and ethanol effects observed in the present study. In addition, the differential effects of THIP on ethanol consumption relative to water would suggest that GABAA manipulations may play a role in influencing the acquisition of voluntary ethanol drinking.

摘要

通过使用计算机控制的数据采集系统,研究了GABAA激动剂THIP对自愿乙醇摄入量的获取以及食物和水消耗模式的影响。将20只雄性Long-Evans大鼠随机分为两组,一组接受THIP(16毫克/千克,腹腔注射),另一组接受等体积的生理盐水。在每隔一天进行的药物注射后,让实验对象自由选择乙醇和水。最初提供的乙醇浓度为2%,在每次浓度的第二次呈现后,每次以2%的增量增加,直至最大浓度10%。接受THIP治疗的实验对象比生理盐水对照组消耗的乙醇量显著更多。对饮酒发作模式的微观结构分析表明,乙醇消耗量的增加是乙醇饮酒发作的大小、持续时间和频率增加的结果。THIP治疗也使食物摄入量减少。结果表明,总食物摄入量的减少是食物发作频率降低的结果。然而,与乙醇摄入量的情况不同,食物发作的大小和持续时间没有变化。THIP治疗后,乙醇和食物的消费行为微观结构中质的不同模式表明,不同的机制可能介导了本研究中观察到的食物和乙醇效应。此外,THIP对乙醇相对于水消耗的不同影响表明,GABAA的调节可能在影响自愿乙醇饮用的获取中起作用。

相似文献

1
Microstructural analysis of the effects of THIP, a GABAA agonist, on voluntary ethanol intake in laboratory rats.γ-氨基丁酸A型受体激动剂THIP对实验大鼠自愿乙醇摄入量影响的微观结构分析
Pharmacol Biochem Behav. 1992 Dec;43(4):1121-7. doi: 10.1016/0091-3057(92)90491-w.
2
Bidirectional effects of GABAergic agonists and antagonists on maintenance of voluntary ethanol intake in rats.γ-氨基丁酸能激动剂和拮抗剂对大鼠自愿乙醇摄入量维持的双向影响。
Pharmacol Biochem Behav. 1993 Sep;46(1):179-82. doi: 10.1016/0091-3057(93)90338-t.
3
GABAergic involvement in the acquisition of voluntary ethanol intake in laboratory rats.γ-氨基丁酸能系统参与实验大鼠自愿摄入乙醇的习得过程。
Alcohol Alcohol. 1992 May;27(3):227-31.
4
The effects of the GABA(B) agonist baclofen on the temporal and structural characteristics of ethanol intake.γ-氨基丁酸B(GABA(B))受体激动剂巴氯芬对乙醇摄入的时间和结构特征的影响。
Alcohol. 1999 Apr;17(3):231-40. doi: 10.1016/s0741-8329(98)00053-6.
5
Effect of ganaxolone and THIP on operant and limited-access ethanol self-administration.甘氨双唑和 THIP 对操作性和有限制接触乙醇自我给药的影响。
Neuropharmacology. 2012 Sep;63(4):555-64. doi: 10.1016/j.neuropharm.2012.05.007. Epub 2012 May 18.
6
Alteration of ethanol drinking in mice via modulation of the GABA(A) receptor with ganaxolone, finasteride, and gaboxadol.通过调节 GABA(A) 受体,利用 ganaxolone、finasteride 和 gaboxadol 改变小鼠的乙醇饮用量。
Alcohol Clin Exp Res. 2011 Nov;35(11):1994-2007. doi: 10.1111/j.1530-0277.2011.01551.x. Epub 2011 Jun 7.
7
Site-specific microinjection of Gaboxadol into the infralimbic cortex modulates ethanol intake in male C57BL/6J mice.将加波沙朵位点特异性微量注射到雄性C57BL/6J小鼠的边缘下皮质中可调节乙醇摄入量。
Behav Brain Res. 2014 Oct 15;273:8-15. doi: 10.1016/j.bbr.2014.07.020. Epub 2014 Jul 18.
8
A descriptive analysis of the structure and temporal pattern of voluntary ethanol intake within an acquisition paradigm.在习得范式内对自愿乙醇摄入量的结构和时间模式进行描述性分析。
J Stud Alcohol. 1997 Jul;58(4):382-91. doi: 10.15288/jsa.1997.58.382.
9
Alcohol as a food: a commentary on Richter.
Physiol Behav. 1996 Dec;60(6):1485-90. doi: 10.1016/s0031-9384(96)00309-5.
10
Microstructural analysis of rat ethanol and water drinking patterns using a modified operant self-administration model.使用改良的操作性自我给药模型对大鼠乙醇和水饮用模式的微观结构分析。
Physiol Behav. 2015 Oct 1;149:119-30. doi: 10.1016/j.physbeh.2015.05.034. Epub 2015 May 31.

引用本文的文献

1
Excitatory/inhibitory balance across ontogeny contributes to age-specific behavioral outcomes of ethanol-like challenge in conditioned taste aversion.发育过程中兴奋性/抑制性平衡导致条件性味觉厌恶中类似乙醇挑战的特定年龄行为结果。
Dev Psychobiol. 2019 Dec;61(8):1157-1167. doi: 10.1002/dev.21864. Epub 2019 May 13.
2
Activation of extrasynaptic δ-GABA receptors globally or within the posterior-VTA has estrous-dependent effects on consumption of alcohol and estrous-independent effects on locomotion.在突触外δ-氨基丁酸(GABA)受体在整体水平或腹侧被盖区后部内的激活,对酒精消耗具有发情周期依赖性效应,而对运动具有发情周期非依赖性效应。
Horm Behav. 2017 Sep;95:65-75. doi: 10.1016/j.yhbeh.2017.07.015. Epub 2017 Sep 20.
3
Site-specific microinjection of Gaboxadol into the infralimbic cortex modulates ethanol intake in male C57BL/6J mice.
将加波沙朵位点特异性微量注射到雄性C57BL/6J小鼠的边缘下皮质中可调节乙醇摄入量。
Behav Brain Res. 2014 Oct 15;273:8-15. doi: 10.1016/j.bbr.2014.07.020. Epub 2014 Jul 18.
4
Effect of ganaxolone and THIP on operant and limited-access ethanol self-administration.甘氨双唑和 THIP 对操作性和有限制接触乙醇自我给药的影响。
Neuropharmacology. 2012 Sep;63(4):555-64. doi: 10.1016/j.neuropharm.2012.05.007. Epub 2012 May 18.
5
Inhibition of 5alpha-reduced steroid biosynthesis impedes acquisition of ethanol drinking in male C57BL/6J mice.抑制5α-还原类固醇生物合成会阻碍雄性C57BL/6J小鼠对乙醇的摄取。
Alcohol Clin Exp Res. 2008 Aug;32(8):1408-16. doi: 10.1111/j.1530-0277.2008.00718.x. Epub 2008 Jun 28.
6
GABAergic modulation of binge-like ethanol intake in C57BL/6J mice.C57BL/6J小鼠中γ-氨基丁酸能对类似暴饮暴食的乙醇摄入的调节作用
Pharmacol Biochem Behav. 2007 Nov;88(1):105-13. doi: 10.1016/j.pbb.2007.07.011. Epub 2007 Jul 25.