• 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

Evidence for genetic correlation of hypnotic effects and cerebellar Purkinje neuron depression in response to ethanol in mice.

作者信息

Spuhler K, Hoffer B, Weiner N, Palmer M

出版信息

Pharmacol Biochem Behav. 1982 Sep;17(3):569-78. doi: 10.1016/0091-3057(82)90320-3.

DOI:10.1016/0091-3057(82)90320-3
PMID:7146053
Abstract

In the present study, we compared phenotypic differences in behavioral and neurophysiological responses to acute ethanol administration among eight inbred strains of mice. Genetic variation for behavioral sedation, as measured by loss of the righting reflex (sleep time) after a hypnotic dose of ethanol, was shown to be present among the inbred strain population. In addition, a large genetic component of variation in the depressant action of ethanol on the spontaneous discharge of cerebellar Purkinje neurons was found. Results from an analysis of covariance of the behavioral and electrophysiological phenotypes, measured on each mouse among the inbred strains, provided strong evidence for a high genetic correlation between sleep time and inhibition of cerebellar Purkinje neuron discharge in response to acute ethanol administration. Taken together with our previously reported data on ethanol-induced electrophysiological changes in selectively bred lines, the results described here strongly support the hypothesis that the cerebellar Purkinje neuron is one important locus for the acute soporific effects of alcohol.

摘要

相似文献

1
Evidence for genetic correlation of hypnotic effects and cerebellar Purkinje neuron depression in response to ethanol in mice.
Pharmacol Biochem Behav. 1982 Sep;17(3):569-78. doi: 10.1016/0091-3057(82)90320-3.
2
Genetic correlation of ethanol-induced ataxia and cerebellar Purkinje neuron depression among inbred strains and selected lines of rats.
Alcohol Clin Exp Res. 1987 Oct;11(5):494-501. doi: 10.1111/j.1530-0277.1987.tb01930.x.
3
Correlation of Purkinje neuron depression and hypnotic effects of ethanol in inbred strains of rats.大鼠近交系中浦肯野神经元抑制与乙醇催眠作用的相关性。
Alcohol Clin Exp Res. 1985 Jan-Feb;9(1):56-8. doi: 10.1111/j.1530-0277.1985.tb05050.x.
4
Genetic covariation in low alcohol-sensitive and high alcohol-sensitive selected lines of rats: behavioral and electrophysiological sensitivities to the depressant effects of ethanol and the development of acute neuronal tolerance to ethanol in situ at generation eight.
J Pharmacol Exp Ther. 1992 Feb;260(2):879-86.
5
Calcium differentially alters behavioral and electrophysiological responses to ethanol in selectively bred mouse lines.
Alcohol Clin Exp Res. 1987 Oct;11(5):457-63. doi: 10.1111/j.1530-0277.1987.tb01923.x.
6
Cerebellar role in the differential ethanol sensitivity of long sleep and short sleep mice.
Pharmacol Biochem Behav. 1983;18 Suppl 1:495-9. doi: 10.1016/0091-3057(83)90224-1.
7
Ethanol-induced depressions in cerebellar and hippocampal neurons of mice selectively bred for differences in ethanol sensitivity: an electrophysiological study.
Pharmacol Biochem Behav. 1981 Feb;14(2):227-34. doi: 10.1016/0091-3057(81)90248-3.
8
Differential sensitivity of cerebellar purkinje neurons to ethanol in selectively outbred lines of mice: maintenance in vitro independent of synaptic transmission.小鼠选择性近交系中小脑浦肯野神经元对乙醇的差异敏感性:体外培养中不依赖突触传递的维持
Brain Res. 1983 Mar 28;264(1):69-78. doi: 10.1016/0006-8993(83)91121-6.
9
Electrophysiological correlates of ethanol-induced sedation in differentially sensitive lines of mice.乙醇诱导的镇静在不同敏感性小鼠品系中的电生理相关性
Science. 1980 Dec 5;210(4474):1143-5. doi: 10.1126/science.7444444.
10
Distinctions among sedative, disinhibitory, and ataxic properties of ethanol in inbred and selectively bred mice.近交系和选择性培育小鼠中乙醇的镇静、去抑制和共济失调特性之间的差异。
Psychopharmacology (Berl). 1990;101(1):93-9. doi: 10.1007/BF02253724.

引用本文的文献

1
Knock-in Mice Expressing an Ethanol-Resistant GluN2A NMDA Receptor Subunit Show Altered Responses to Ethanol.表达乙醇抗性 GluN2A NMDA 受体亚基的基因敲入小鼠对乙醇表现出不同的反应。
Alcohol Clin Exp Res. 2020 Feb;44(2):479-491. doi: 10.1111/acer.14273. Epub 2020 Jan 14.
2
Clozapine-induced locomotor suppression is mediated by 5-HT2A receptors in the forebrain.氯氮平诱导的运动抑制是由前脑的 5-HT2A 受体介导的。
Neuropsychopharmacology. 2012 Dec;37(13):2747-55. doi: 10.1038/npp.2012.139. Epub 2012 Aug 8.
3
Microarray analysis identifies cerebellar genes sensitive to chronic ethanol treatment in PKCgamma mice.
微阵列分析鉴定出PKCγ小鼠中对慢性乙醇处理敏感的小脑基因。
Alcohol. 2006 Aug;40(1):19-33. doi: 10.1016/j.alcohol.2006.09.004.
4
Confirmation of quantitative trait loci for ethanol sensitivity and neurotensin receptor density in crosses derived from the inbred high and low alcohol sensitive selectively bred rat lines.在由近交高酒精敏感性和低酒精敏感性选择性培育大鼠品系杂交产生的后代中,对乙醇敏感性和神经降压素受体密度的数量性状基因座进行确认。
Psychopharmacology (Berl). 2006 Oct;188(3):343-54. doi: 10.1007/s00213-006-0512-2. Epub 2006 Sep 5.
5
Expression profiling identifies novel candidate genes for ethanol sensitivity QTLs.表达谱分析鉴定出乙醇敏感性数量性状位点的新候选基因。
Mamm Genome. 2006 Feb;17(2):147-56. doi: 10.1007/s00335-005-0065-4. Epub 2006 Feb 7.
6
Strain distribution patterns for genetic markers in the LSXSS recombinant-inbred series.
Mamm Genome. 1996 Jun;7(6):408-12. doi: 10.1007/s003359900122.
7
Opioid operant self-administration, analgesia, stimulation and respiratory depression in mu-deficient mice.μ-阿片受体缺陷小鼠的阿片类药物操作性自我给药、镇痛、兴奋及呼吸抑制作用
Psychopharmacology (Berl). 1995 Jan;117(1):23-31. doi: 10.1007/BF02245094.
8
Selected mouse lines, alcohol and behavior.选定的小鼠品系、酒精与行为。
Experientia. 1989 Sep 15;45(9):805-27. doi: 10.1007/BF01954056.