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乙酸盐作为乙醇的一种活性代谢产物:对啮齿动物运动、翻正反射丧失及焦虑的研究

Acetate as an active metabolite of ethanol: studies of locomotion, loss of righting reflex, and anxiety in rodents.

作者信息

Pardo Marta, Betz Adrienne J, San Miguel Noemí, López-Cruz Laura, Salamone John D, Correa Mercè

机构信息

Àrea de Psicobiologia, Campus Riu Sec, Universitat Jaume I Castelló, Spain.

出版信息

Front Behav Neurosci. 2013 Jul 10;7:81. doi: 10.3389/fnbeh.2013.00081. eCollection 2013.

Abstract

IT HAS BEEN POSTULATED THAT A NUMBER OF THE CENTRAL EFFECTS OF ETHANOL ARE MEDIATED VIA ETHANOL METABOLITES

acetaldehyde and acetate. Ethanol is known to produce a large variety of behavioral actions such anxiolysis, narcosis, and modulation of locomotion. Acetaldehyde contributes to some of those effects although the contribution of acetate is less known. In the present studies, rats and mice were used to assess the acute and chronic effects of acetate after central or peripheral administration. Male Sprague-Dawley rats were used for the comparison between central (intraventricular, ICV) and peripheral (intraperitoneal, IP) administration of acute doses of acetate on locomotion. CD1 male mice were used to study acute IP effects of acetate on locomotion, and also the effects of chronic oral consumption of acetate (0, 500, or 1000 mg/l, during 7, 15, 30, or 60 days) on ethanol- (1.0, 2.0, 4.0, or 4.5 g/kg, IP) induced locomotion, anxiolysis, and loss of righting reflex (LORR). In rats, ICV acetate (0.7-2.8 μmoles) reduced spontaneous locomotion at doses that, in the case of ethanol and acetaldehyde, had previously been shown to stimulate locomotion. Peripheral acute administration of acetate also suppressed locomotion in rats (25-100 mg/kg), but not in mice. In addition, although chronic administration of acetate during 15 days did not have an effect on spontaneous locomotion in an open field, it blocked ethanol-induced locomotion. However, ethanol-induced anxiolysis was not affected by chronic administration of acetate. Chronic consumption of acetate (up to 60 days) did not have an effect on latency to, or duration of LORR induced by ethanol, but significantly increased the number of mice that did not achieve LORR. The present work provides new evidence supporting the hypothesis that acetate should be considered a centrally-active metabolite of ethanol that contributes to some behavioral effects of this alcohol, such as motor suppression.

摘要

据推测,乙醇的许多中枢效应是通过乙醇代谢产物介导的:乙醛和乙酸盐。已知乙醇会产生多种行为作用,如抗焦虑、麻醉和对运动的调节。乙醛对其中一些效应有作用,尽管乙酸盐的作用鲜为人知。在本研究中,使用大鼠和小鼠来评估中枢或外周给予乙酸盐后的急性和慢性效应。雄性Sprague-Dawley大鼠用于比较中枢(脑室内,ICV)和外周(腹腔内,IP)给予急性剂量乙酸盐对运动的影响。CD1雄性小鼠用于研究乙酸盐腹腔内急性给药对运动的影响,以及慢性口服乙酸盐(0、500或1000mg/l,持续7、15、30或60天)对乙醇(1.0、2.0、4.0或4.5g/kg,腹腔内注射)诱导的运动、抗焦虑和翻正反射消失(LORR)的影响。在大鼠中,脑室内注射乙酸盐(0.7 - 2.8微摩尔)在先前已显示能刺激运动的剂量下会降低自发运动。外周急性给予乙酸盐也会抑制大鼠(25 - 100mg/kg)的运动,但对小鼠无此作用。此外,虽然连续15天给予乙酸盐对旷场中的自发运动没有影响,但它会阻断乙醇诱导的运动。然而,乙醇诱导的抗焦虑作用不受乙酸盐慢性给药的影响。慢性摄入乙酸盐(长达60天)对乙醇诱导的LORR的潜伏期或持续时间没有影响,但显著增加了未达到LORR的小鼠数量。本研究提供了新的证据支持这一假设,即乙酸盐应被视为乙醇的一种具有中枢活性的代谢产物,它对这种酒精的一些行为效应有作用,如运动抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a47/3706982/ab8e751dfa2e/fnbeh-07-00081-g0001.jpg

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