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丙戊酸盐诱导肥胖大鼠模型的评估。

Evaluation of a rat model of valproate-induced obesity.

作者信息

Wolden-Hanson T, Gidal B E, Atkinson R L

机构信息

Beers-Murphy Clinical Nutrition Center and the Department of Nutritional Sciences, University of Wisconsin-Madison, USA.

出版信息

Pharmacotherapy. 1998 Sep-Oct;18(5):1075-81.

PMID:9758318
Abstract

Long-term treatment with the anticonvulsant valproate (VPA) leads to well-documented weight gain and obesity in humans. In an attempt to develop an animal model of this condition, adult rats were given VPA 20 g/kg (high-dose) or 2 g/kg (low-dose) in their daily feeding or orally 120 mg/kg body weight/day in two divided doses, and food intake and body weight were assessed. Valproate resulted in lower body weights in all protocols. Food intake was lower (p<0.001) for rats receiving high-dose VPA than for controls. Feed efficiency (change in weight divided by cumulative food intake for that period) was lower than that of controls for both high (p<0.0001) and low doses (NS). Metabolic rate and physical activity were not different between control and VPA animals, although decreased food intake would be expected to decrease metabolic rate. Valproate failed to produce obesity in rats in any treatment period. For reasons that are unclear, rats do not appear to be suitable as a model to study this adverse side effect of VPA in humans with epilepsy.

摘要

长期使用抗惊厥药物丙戊酸盐(VPA)治疗会导致人类出现有充分文献记载的体重增加和肥胖。为了建立这种情况的动物模型,成年大鼠在每日喂食中给予20 g/kg(高剂量)或2 g/kg(低剂量)的VPA,或按体重120 mg/kg/天分两次口服给药,然后评估食物摄入量和体重。在所有实验方案中,丙戊酸盐都会导致体重降低。接受高剂量VPA的大鼠的食物摄入量低于对照组(p<0.001)。高剂量组(p<0.0001)和低剂量组(无显著性差异)的饲料效率(体重变化除以该时期的累积食物摄入量)均低于对照组。尽管预期食物摄入量减少会降低代谢率,但对照组和VPA处理组动物之间的代谢率和身体活动并无差异。在任何治疗时期,丙戊酸盐都未能使大鼠出现肥胖。由于尚不清楚的原因,大鼠似乎不适合作为研究VPA对癫痫患者这一不良副作用的模型。

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