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Impulsivity in rodents with a genetic predisposition for excessive alcohol consumption is associated with a lack of a prospective strategy.具有过量饮酒遗传易感性的啮齿动物的冲动性与缺乏前瞻性策略有关。
Cogn Affect Behav Neurosci. 2017 Apr;17(2):235-251. doi: 10.3758/s13415-016-0475-7.
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Elimination of extracellular dopamine in the medial prefrontal cortex of conscious mice analysed using selective enzyme and uptake inhibitors.使用选择性酶和摄取抑制剂分析清醒小鼠内侧前额叶皮质细胞外多巴胺的清除情况。
J Physiol Pharmacol. 2016 Apr;67(2):301-9.
3
Alcohol-Preferring P Rats Exhibit Elevated Motor Impulsivity Concomitant with Operant Responding and Self-Administration of Alcohol.偏好酒精的P大鼠在酒精操作性反应和自我给药时表现出运动冲动性增强。
Alcohol Clin Exp Res. 2016 May;40(5):1100-10. doi: 10.1111/acer.13044. Epub 2016 Mar 29.
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Alcohol preferring (P) rats as a model for examining sex differences in alcohol use disorder and its treatment.偏好酒精的(P)大鼠作为研究酒精使用障碍及其治疗中性别差异的模型。
Pharmacol Biochem Behav. 2015 May;132:1-9. doi: 10.1016/j.pbb.2015.02.014. Epub 2015 Feb 21.
5
Regional variation in phasic dopamine release during alcohol and sucrose self-administration in rats.大鼠酒精和蔗糖自我给药过程中阶段性多巴胺释放的区域差异。
ACS Chem Neurosci. 2015 Jan 21;6(1):147-54. doi: 10.1021/cn500251j. Epub 2014 Dec 22.
6
Increased delay discounting tracks with a high ethanol-seeking phenotype and subsequent ethanol seeking but not consumption.更高的延迟折扣与高乙醇寻求表型及随后的乙醇寻求相关,但与乙醇消费无关。
Alcohol Clin Exp Res. 2014 Oct;38(10):2607-14. doi: 10.1111/acer.12523. Epub 2014 Oct 21.
7
Tolcapone suppresses ethanol intake in alcohol-preferring rats performing a novel cued access protocol.托卡朋抑制偏好酒精的大鼠在执行一种新型线索引导获取方案时的乙醇摄入量。
Alcohol Clin Exp Res. 2014 Sep;38(9):2468-78. doi: 10.1111/acer.12515.
8
Polymorphisms of COMT Val158Met and DAT1 3'-UTR VNTR in illicit drug use and drug-related psychiatric disorders.儿茶酚-O-甲基转移酶(COMT)Val158Met多态性和多巴胺转运体1(DAT1)3'-非翻译区可变数目串联重复序列(VNTR)与非法药物使用及药物相关精神障碍的关系
Subst Use Misuse. 2014 Sep;49(11):1385-91. doi: 10.3109/10826084.2014.901391. Epub 2014 Apr 7.
9
Genetic variation in COMT activity impacts learning and dopamine release capacity in the striatum.COMT 活性的遗传变异会影响纹状体的学习能力和多巴胺释放能力。
Learn Mem. 2014 Mar 17;21(4):205-14. doi: 10.1101/lm.032094.113.
10
Generation and characterization of humanized mice carrying COMT158 Met/Val alleles.携带COMT158 Met/Val等位基因的人源化小鼠的产生与表征
Neuropsychopharmacology. 2014 Jul;39(8):1823-32. doi: 10.1038/npp.2014.29. Epub 2014 Feb 10.

雄性和雌性Wistar大鼠及嗜酒大鼠中儿茶酚-O-甲基转移酶(COMT)的差异表达及COMT抑制的行为效应

Differential COMT expression and behavioral effects of COMT inhibition in male and female Wistar and alcohol preferring rats.

作者信息

McCane Aqilah M, DeLory Michael J, Timm Maureen M, Janetsian-Fritz Sarine S, Lapish Christopher C, Czachowski Cristine L

机构信息

Department of Psychology, Indiana University Purdue University Indianapolis, Indianapolis, IN 46202, USA.

Department of Psychology, Indiana University Purdue University Indianapolis, Indianapolis, IN 46202, USA.

出版信息

Alcohol. 2018 Mar;67:15-22. doi: 10.1016/j.alcohol.2017.08.007. Epub 2017 Aug 19.

DOI:10.1016/j.alcohol.2017.08.007
PMID:29310047
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5818329/
Abstract

Polymorphisms of the catechol-O-methyl transferase (COMT) gene have been associated with alcoholism, suggesting that alterations in the metabolism of catecholamines may be a critical component of the neuropathology of alcoholism. In the current experiments, the COMT inhibitor tolcapone was utilized in an operant behavioral model of reinforcer-seeking and drinking to determine if this compound was capable of remediating the excessive seeking and drinking phenotype of the alcohol-preferring P rat. Tolcapone was administered to male and female alcohol-reinforced P and Wistar rats. Additionally, tolcapone was administered to male sucrose-reinforced P and Wistar rats to determine if its effects also extended to a natural reinforcer. Animals were trained to make an operant response that resulted in 20 min uninterrupted access to the reinforcer solutions. Tolcapone had no effect in female rats on either seeking or consumption of ethanol. However, reductions of both reinforcer seeking and consumption were observed in male P rats, but only of seeking in Wistars. In separate experiments, using reinforcer naïve male and female animals, COMT expression was assessed via Western Blot analysis. Sex differences in COMT expression were also observed, where male P rats exhibited a marked reduction in protein expression relative to females in the PFC. Sex differences were not observed for Wistars or in the striatum and hippocampus. These data complement our previous findings in which tolcapone reduced cue-evoked responses in P rats and further suggest clinical utility of COMT inhibitors in the treatment of addiction disorders, specifically in male high drinkers.

摘要

儿茶酚-O-甲基转移酶(COMT)基因的多态性与酒精中毒有关,这表明儿茶酚胺代谢的改变可能是酒精中毒神经病理学的关键组成部分。在当前实验中,COMT抑制剂托卡朋被用于一种寻求强化物和饮酒的操作性行为模型,以确定该化合物是否能够纠正酒精偏好型P大鼠过度寻求和饮酒的表型。将托卡朋给予雄性和雌性酒精强化的P大鼠和Wistar大鼠。此外,将托卡朋给予雄性蔗糖强化的P大鼠和Wistar大鼠,以确定其作用是否也扩展到天然强化物。训练动物做出操作性反应,从而能够不间断地获取强化物溶液20分钟。托卡朋对雌性大鼠的乙醇寻求或消耗均无影响。然而,在雄性P大鼠中观察到强化物寻求和消耗均减少,但在Wistar大鼠中仅观察到寻求减少。在单独的实验中,使用对强化物无经验的雄性和雌性动物,通过蛋白质印迹分析评估COMT表达。还观察到COMT表达的性别差异,其中雄性P大鼠相对于雌性在额叶前皮质中的蛋白质表达显著降低。Wistar大鼠以及纹状体和海马体中未观察到性别差异。这些数据补充了我们之前的研究结果,即托卡朋可减少P大鼠的线索诱发反应,并进一步表明COMT抑制剂在成瘾性疾病治疗中的临床效用,特别是在男性酗酒者中。