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Peroxisome proliferator-activated receptor (PPAR) agonists as promising new medications for drug addiction: preclinical evidence.过氧化物酶体增殖物激活受体(PPAR)激动剂作为治疗药物成瘾的有前途的新药:临床前证据。
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本文引用的文献

1
Activation of PPARγ by pioglitazone potentiates the effects of naltrexone on alcohol drinking and relapse in msP rats.吡格列酮激活 PPARγ 增强纳曲酮对 msP 大鼠饮酒和复饮的作用。
Alcohol Clin Exp Res. 2013 Aug;37(8):1351-60. doi: 10.1111/acer.12091. Epub 2013 Mar 29.
2
Novel use of a lipid-lowering fibrate medication to prevent nicotine reward and relapse: preclinical findings.新型降脂纤维酸类药物预防尼古丁奖赏和复吸的作用:临床前研究结果。
Neuropsychopharmacology. 2012 Jul;37(8):1838-47. doi: 10.1038/npp.2012.31. Epub 2012 Mar 28.
3
Effects of a selective cannabinoid CB2 agonist and antagonist on intravenous nicotine self administration and reinstatement of nicotine seeking.选择性大麻素 CB2 激动剂和拮抗剂对静脉注射尼古丁自我给药和尼古丁觅药行为复吸的影响。
PLoS One. 2012;7(1):e29900. doi: 10.1371/journal.pone.0029900. Epub 2012 Jan 26.
4
Endocannabinoid regulation of acute and protracted nicotine withdrawal: effect of FAAH inhibition.内源性大麻素系统对急性和慢性尼古丁戒断的调节:脂肪酸酰胺水解酶抑制的作用。
PLoS One. 2011;6(11):e28142. doi: 10.1371/journal.pone.0028142. Epub 2011 Nov 30.
5
Blockade of dopamine d4 receptors attenuates reinstatement of extinguished nicotine-seeking behavior in rats.阻断多巴胺 D4 受体可减弱大鼠已消除的尼古丁觅药行为的复燃。
Neuropsychopharmacology. 2012 Feb;37(3):685-96. doi: 10.1038/npp.2011.245. Epub 2011 Oct 26.
6
Varenicline decreases nicotine self-administration and cue-induced reinstatement of nicotine-seeking behaviour in rats when a long pretreatment time is used.文拉法辛在使用较长的预处理时间时,可减少大鼠的尼古丁自主给药和线索诱导的觅药行为复吸。
Int J Neuropsychopharmacol. 2012 Oct;15(9):1265-74. doi: 10.1017/S1461145711001398. Epub 2011 Sep 23.
7
Cannabinoid receptor stimulation increases motivation for nicotine and nicotine seeking.大麻素受体刺激增加了对尼古丁和尼古丁寻找的动机。
Addict Biol. 2012 Jan;17(1):47-61. doi: 10.1111/j.1369-1600.2011.00314.x. Epub 2011 Apr 26.
8
Pharmacologically induced alcohol craving in treatment seeking alcoholics correlates with alcoholism severity, but is insensitive to acamprosate.在寻求治疗的酗酒者中,药物引起的酒精渴求与酒精中毒严重程度相关,但对安非他酮不敏感。
Neuropsychopharmacology. 2011 May;36(6):1178-86. doi: 10.1038/npp.2010.253. Epub 2011 Feb 2.
9
Activation of nuclear PPARγ receptors by the antidiabetic agent pioglitazone suppresses alcohol drinking and relapse to alcohol seeking.糖尿病治疗药物吡格列酮通过激活核受体 PPARγ,抑制酒精摄入和觅酒行为复发。
Biol Psychiatry. 2011 Apr 1;69(7):642-9. doi: 10.1016/j.biopsych.2010.12.010. Epub 2011 Jan 31.
10
Blockade of nicotine reward and reinstatement by activation of alpha-type peroxisome proliferator-activated receptors.通过激活α型过氧化物酶体增殖物激活受体阻断尼古丁奖赏和复吸。
Biol Psychiatry. 2011 Apr 1;69(7):633-41. doi: 10.1016/j.biopsych.2010.07.009.

过氧化物酶体增殖物激活受体(PPAR)激动剂作为治疗药物成瘾的有前途的新药:临床前证据。

Peroxisome proliferator-activated receptor (PPAR) agonists as promising new medications for drug addiction: preclinical evidence.

机构信息

Translational Addiction Research Laboratory, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.

出版信息

Curr Drug Targets. 2013 Jun;14(7):768-76. doi: 10.2174/1389450111314070006.

DOI:10.2174/1389450111314070006
PMID:23614675
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3826450/
Abstract

This review examines the growing literature on the role of peroxisome proliferator-activated receptors (PPARs) in addiction. There are two subtypes of PPAR receptors that have been studied in addiction: PPAR-α and PPAR-γ. The role of each PPAR subtype in common models of addictive behavior, mainly pre-clinical models, is summarized. In particular, studies are reviewed that investigated the effects of PPAR-α agonists on relapse, sensitization, conditioned place preference, withdrawal and drug intake, and effects of PPAR-γ agonists on relapse, withdrawal and drug intake. Finally, studies that investigated the effects of PPAR agonists on neural pathways of addiction are reviewed. Taken together these preclinical data indicate that PPAR agonists are promising new medications for drug addiction treatment.

摘要

这篇综述考察了关于过氧化物酶体增殖物激活受体(PPARs)在成瘾中的作用的不断增长的文献。有两种亚型的 PPAR 受体已在成瘾中进行了研究:PPAR-α和 PPAR-γ。总结了每种 PPAR 亚型在常见成瘾行为模型中的作用,主要是临床前模型。特别回顾了研究 PPAR-α激动剂对复发、敏化、条件性位置偏爱、戒断和药物摄入的影响,以及 PPAR-γ激动剂对复发、戒断和药物摄入的影响。最后,综述了研究 PPAR 激动剂对成瘾神经通路影响的研究。这些临床前数据表明,PPAR 激动剂是治疗药物成瘾的有前途的新药。