• 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

对氟哌啶醇诱导的僵住症的敏感化与耐受性:多种决定因素

Sensitization versus tolerance to haloperidol-induced catalepsy: multiple determinants.

作者信息

Barnes D E, Robinson B, Csernansky J G, Bellows E P

机构信息

Department of Veterans Affairs, Laboratory of Clinical Psychopharmacology, Palo Alto, CA 94304.

出版信息

Pharmacol Biochem Behav. 1990 Aug;36(4):883-7. doi: 10.1016/0091-3057(90)90094-x.

DOI:10.1016/0091-3057(90)90094-x
PMID:2217518
Abstract

The effects of dose, administration frequency, and behavioral testing conditions on the development of tolerance versus sensitization to haloperidol-induced catalepsy were tested in rats. Animals received daily or weekly injections of haloperidol (0.05-5.00 mg/kg SC) for up to 22 days. Catalepsy assessments were made either once or repeatedly using two tests: the horizontal bar and the inclined screen. Tolerance was found only in animals treated daily with haloperidol (1.5 mg/kg) and tested repeatedly on the horizontal bar. In contrast, sensitization was observed with various haloperidol doses, daily or weekly administration schedules (for most doses), either horizontal bar or inclined screen catalepsy tests, and repeated or single testing. Sensitization developed most strongly following weekly drug administration and repeated testing on the horizontal bar. No single experimental variable produced a definitive pattern of change in catalepsy over time. Dose, drug administration schedule, and behavioral test conditions all influenced the evolution of catalepsy during chronic haloperidol treatment.

摘要

在大鼠中测试了剂量、给药频率和行为测试条件对氟哌啶醇诱导的僵住症耐受性与敏化作用发展的影响。动物每天或每周接受氟哌啶醇(0.05 - 5.00 mg/kg皮下注射)注射,持续22天。使用横杆和倾斜屏幕两种测试方法,对僵住症进行单次或重复评估。仅在每天接受氟哌啶醇(1.5 mg/kg)治疗并在横杆上重复测试的动物中发现了耐受性。相比之下,在各种氟哌啶醇剂量、每日或每周给药方案(大多数剂量)、横杆或倾斜屏幕僵住症测试以及重复或单次测试中均观察到了敏化作用。在每周给药并在横杆上重复测试后,敏化作用最为强烈。没有单一的实验变量能产生随时间变化的僵住症明确变化模式。剂量、给药方案和行为测试条件均影响慢性氟哌啶醇治疗期间僵住症的演变。

相似文献

1
Sensitization versus tolerance to haloperidol-induced catalepsy: multiple determinants.对氟哌啶醇诱导的僵住症的敏感化与耐受性:多种决定因素
Pharmacol Biochem Behav. 1990 Aug;36(4):883-7. doi: 10.1016/0091-3057(90)90094-x.
2
Haloperidol conditioned catalepsy in rats: a possible role for D1-like receptors.氟哌啶醇诱导的大鼠僵住症:D1 样受体的可能作用。
Int J Neuropsychopharmacol. 2012 Nov;15(10):1525-34. doi: 10.1017/S1461145711001696. Epub 2011 Nov 18.
3
Effects of age and isolation on the evolution of catalepsy during chronic haloperidol treatment.
Braz J Med Biol Res. 1992;25(9):925-8.
4
Differential tolerance to cataleptic effects of SCH 23390 and haloperidol after repeated administration.重复给药后对 SCH 23390 和氟哌啶醇僵住效应的差异耐受性。
Psychopharmacology (Berl). 1989;98(4):472-5. doi: 10.1007/BF00441944.
5
Repeated testing of rats markedly enhances the duration of effects induced by haloperidol on treadmill locomotion, catalepsy, and a conditioned avoidance response.对大鼠进行反复测试可显著延长氟哌啶醇对跑步机运动、僵住症和条件性回避反应所诱导效应的持续时间。
Pharmacol Biochem Behav. 1987 May;27(1):159-64. doi: 10.1016/0091-3057(87)90490-4.
6
Tolerance of haloperidol catalepsy.
Eur J Pharmacol. 1977 Feb 7;41(3):321-7. doi: 10.1016/0014-2999(77)90325-9.
7
Increase of spiny I activity in striatum after development of context-dependent sensitization of catalepsy in rats.大鼠僵住症的情境依赖性致敏形成后纹状体中棘状I活性的增加。
Neurosci Lett. 2004 Jan 2;354(1):10-3. doi: 10.1016/j.neulet.2003.09.020.
8
Conditioned tolerance to haloperidol- and droperidol-induced catalepsy.
Naunyn Schmiedebergs Arch Pharmacol. 1988 Apr;337(4):385-91. doi: 10.1007/BF00169528.
9
Reduced expression of haloperidol conditioned catalepsy in rats by the dopamine D3 receptor antagonists nafadotride and NGB 2904.纳曲酮和 NGB 2904 降低了多巴胺 D3 受体拮抗剂引起的氟哌啶醇条件性僵住反应。
Eur Neuropsychopharmacol. 2012 Oct;22(10):761-8. doi: 10.1016/j.euroneuro.2012.02.004. Epub 2012 Mar 10.
10
Haloperidol-induced within-session response decrement patterns and catalepsy in rats: behavioural dissociation.氟哌啶醇诱导大鼠在实验过程中的反应递减模式及僵住症:行为解离
Behav Pharmacol. 1999 Feb;10(1):105-11. doi: 10.1097/00008877-199902000-00010.

引用本文的文献

1
Antipsychotic Behavioral Phenotypes in the Mouse Collaborative Cross Recombinant Inbred Inter-Crosses (RIX).小鼠协作杂交重组近交系间杂交(RIX)中的抗精神病行为表型
G3 (Bethesda). 2020 Sep 2;10(9):3165-3177. doi: 10.1534/g3.120.400975.
2
Gnal haploinsufficiency causes genomic instability and increased sensitivity to haloperidol.Gnal 杂合不足导致基因组不稳定和对氟哌啶醇的敏感性增加。
Exp Neurol. 2019 Aug;318:61-70. doi: 10.1016/j.expneurol.2019.04.014. Epub 2019 Apr 26.
3
Histone deacetylase inhibitors reverse age-related increases in side effects of haloperidol in mice.
组蛋白去乙酰化酶抑制剂可逆转小鼠中与年龄相关的氟哌啶醇副作用增加的现象。
Psychopharmacology (Berl). 2017 Aug;234(16):2385-2398. doi: 10.1007/s00213-017-4629-2. Epub 2017 Apr 18.
4
Antipsychotic-induced sensitization and tolerance: Behavioral characteristics, developmental impacts, and neurobiological mechanisms.抗精神病药物诱导的敏化和耐受:行为特征、发育影响及神经生物学机制。
J Psychopharmacol. 2016 Aug;30(8):749-70. doi: 10.1177/0269881116654697. Epub 2016 Jul 1.
5
Repeated administration of aripiprazole produces a sensitization effect in the suppression of avoidance responding and phencyclidine-induced hyperlocomotion and increases D2 receptor-mediated behavioral function.重复给予阿立哌唑会在抑制回避反应和苯环利定诱导的运动亢进方面产生敏化作用,并增强D2受体介导的行为功能。
J Psychopharmacol. 2015 Apr;29(4):390-400. doi: 10.1177/0269881114565937. Epub 2015 Jan 13.
6
Genetics of adverse reactions to haloperidol in a mouse diallel: a drug-placebo experiment and Bayesian causal analysis.小鼠双列杂交中氟哌啶醇不良反应的遗传学:一项药物-安慰剂实验及贝叶斯因果分析
Genetics. 2014 Jan;196(1):321-47. doi: 10.1534/genetics.113.156901. Epub 2013 Nov 15.
7
Olanzapine sensitization and clozapine tolerance: from adolescence to adulthood in the conditioned avoidance response model.奥氮平敏化和氯氮平耐受:在条件性回避反应模型中从青春期到成年。
Neuropsychopharmacology. 2013 Feb;38(3):513-24. doi: 10.1038/npp.2012.213. Epub 2012 Nov 7.
8
Parametric studies of antipsychotic-induced sensitization in the conditioned avoidance response model: roles of number of drug exposure, drug dose, and test-retest interval.抗精神病药物诱导的条件性回避反应模型致敏作用的参数研究:药物暴露次数、药物剂量和重测间隔的作用
Behav Pharmacol. 2012 Aug;23(4):380-91. doi: 10.1097/FBP.0b013e32835651ea.
9
Genome-wide association mapping of loci for antipsychotic-induced extrapyramidal symptoms in mice.全基因组关联分析发现与抗精神病药引起的小鼠锥体外系症状相关的基因座。
Mamm Genome. 2012 Jun;23(5-6):322-35. doi: 10.1007/s00335-011-9385-8. Epub 2011 Dec 30.
10
Antipsychotic-induced vacuous chewing movements and extrapyramidal side effects are highly heritable in mice.抗精神病药引起的空嚼运动和锥体外系副作用在小鼠中具有高度遗传性。
Pharmacogenomics J. 2012 Apr;12(2):147-55. doi: 10.1038/tpj.2010.82. Epub 2010 Nov 16.