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异黄酮对大鼠酒精药代动力学及饮酒行为的影响。

Effects of isoflavones on alcohol pharmacokinetics and alcohol-drinking behavior in rats.

作者信息

Lin R C, Li T K

机构信息

Department of Medicine, Indiana University School of Medicine, and Veterans Affairs Medical Center, Indianapolis 46202-5124, USA.

出版信息

Am J Clin Nutr. 1998 Dec;68(6 Suppl):1512S-1515S. doi: 10.1093/ajcn/68.6.1512S.

Abstract

Puerarin, daidzin, and daidzein are 3 major isoflavonoid compounds isolated from Pueraria lobata, an edible vine used widely in China for various medicinal purposes. We studied the antiinebriation and the antidipsotropic effects of these antioxidants in rats. Daidzin and daidzein shortened alcohol-induced sleep time (loss of righting reflex) in rats that were given ethanol intragastrically but not in those given ethanol intraperitoneally. When daidzin was given to animals intragastrically with the ethanol solution, the blood alcohol concentration (BAC) was found to peak later and be lower than in control rats that were given only the ethanol solution. BACs also receded more slowly if daidzin was fed to the animals. None of the 3 isoflavonoid compounds administered orally affected liver alcohol dehydrogenase or aldehyde dehydrogenase activities, as was reported for intraperitoneal administration. Further experiments indicated that the suppression of the BAC by daidzin was due mainly to delay of stomach emptying. All 3 compounds suppressed voluntary alcohol consumption in alcohol-preferring rats. The decrease in alcohol consumption was accompanied by an increase in water intake, so that the total volume of liquid consumed daily remained unchanged. Daily food consumption and body weight gain were not affected. Alcohol preference returned to baseline levels after the isoflavonoids were discontinued. We postulate that the suppression of alcohol reinforcement produced by these compounds is mediated centrally in the brain reward pathway.

摘要

葛根素、大豆苷和大豆黄酮是从野葛中分离出的3种主要异黄酮化合物,野葛是一种在中国广泛用于各种药用目的的可食用藤蔓植物。我们研究了这些抗氧化剂对大鼠的解酒和抗嗜酒作用。大豆苷和大豆黄酮缩短了经胃内给予乙醇的大鼠的酒精诱导睡眠时间(翻正反射消失),但对经腹腔给予乙醇的大鼠无效。当大豆苷与乙醇溶液一起经胃内给予动物时,发现血酒精浓度(BAC)达到峰值的时间较晚,且低于仅给予乙醇溶液的对照大鼠。如果给动物喂食大豆苷,BAC的下降也更缓慢。口服给予的这3种异黄酮化合物均未影响肝脏乙醇脱氢酶或乙醛脱氢酶的活性,腹腔给药的情况已有报道。进一步的实验表明,大豆苷对BAC的抑制主要是由于胃排空延迟。所有3种化合物均抑制了嗜酒大鼠的自愿饮酒量。饮酒量的减少伴随着饮水量的增加,因此每日消耗的液体总量保持不变。每日食物消耗量和体重增加不受影响。停用异黄酮后,酒精偏好恢复到基线水平。我们推测,这些化合物对酒精强化作用的抑制是在大脑奖赏通路中由中枢介导的。

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