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长期乙醇处理可增强乙醇诱导的大鼠伏隔核间质内源性大麻素水平的升高。

Chronic ethanol treatment potentiates ethanol-induced increases in interstitial nucleus accumbens endocannabinoid levels in rats.

作者信息

Alvarez-Jaimes Lily, Stouffer David G, Parsons Loren H

机构信息

Committee on the Neurobiology of Addictive Disorders, The Scripps Research Institute, La Jolla, California, USA.

出版信息

J Neurochem. 2009 Oct;111(1):37-48. doi: 10.1111/j.1471-4159.2009.06301.x. Epub 2009 Jul 23.

Abstract

We employed in vivo microdialysis to characterize the effect of an ethanol challenge injection on endocannabinoid levels in the nucleus accumbens of ethanol-naïve and chronic ethanol-treated rats. Ethanol (0.75 and 2 g/kg, i.p.) dose-dependently increased dialysate 2-arachidonoylglycerol (to a maximum 157 +/- 20% of baseline) and decreased anandamide (to a minimum 52 +/- 9% of baseline) in ethanol-naïve rats. The endocannabinoid clearance inhibitor N-(4-hydrophenyl) arachidonoylamide (AM404; 3 mg/kg) potentiated ethanol effects on 2-arachidonoylglycerol levels but did not alter ethanol-induced decreases in anandamide. AM404 alone did not alter dialysate levels of either endocannabinoid. Then, we characterized the effect of ethanol challenge on nucleus accumbens endocannabinoid levels in rats previously maintained on an ethanol-containing liquid diet. Ethanol challenge produced a greater and more prolonged increase in 2-arachidonoylglycerol (to a maximum 394 +/- 135% of baseline) in ethanol-experienced than in ethanol-naïve rats. The profile in ethanol-experienced rats was similar to that produced by AM404 pre-treatment in ethanol-naïve rats. AM404 in ethanol-experienced rats led to a further enhancement in the 2-arachidonoylglycerol response to ethanol challenge (to a maximum 704 +/- 174% of baseline). Our findings demonstrate that ethanol-induced increases in nucleus accumbens 2-arachidonoylglycerol are potentiated in animals with a history of ethanol consumption.

摘要

我们采用体内微透析技术,以表征乙醇激发注射对未接触过乙醇和长期接受乙醇处理的大鼠伏隔核内源性大麻素水平的影响。在未接触过乙醇的大鼠中,乙醇(0.75和2克/千克,腹腔注射)剂量依赖性地增加了透析液中2-花生四烯酸甘油酯(最高达到基线的157±20%),并降低了花生四烯酸乙醇胺(最低降至基线的52±9%)。内源性大麻素清除抑制剂N-(4-羟基苯基)花生四烯酸酰胺(AM404;3毫克/千克)增强了乙醇对2-花生四烯酸甘油酯水平的影响,但未改变乙醇引起的花生四烯酸乙醇胺的降低。单独使用AM404不会改变两种内源性大麻素的透析液水平。然后,我们表征了乙醇激发对先前维持在含乙醇液体饮食的大鼠伏隔核内源性大麻素水平的影响。与未接触过乙醇的大鼠相比,乙醇激发在有乙醇接触史的大鼠中引起2-花生四烯酸甘油酯更大且更持久的增加(最高达到基线的394±135%)。有乙醇接触史的大鼠的情况与在未接触过乙醇的大鼠中用AM404预处理所产生的情况相似。在有乙醇接触史的大鼠中使用AM404导致对乙醇激发的2-花生四烯酸甘油酯反应进一步增强(最高达到基线的704±174%)。我们的研究结果表明,在有乙醇摄入史的动物中,乙醇诱导的伏隔核2-花生四烯酸甘油酯增加会增强。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7bc/3946540/65a3d6a2e0c6/nihms523806f1.jpg

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