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在不同脂肪酸和镁饮食条件下给予慢性卡马西平的小鼠的脑抗惊厥保护。

Brain anticonvulsant protection of mice given chronic carbamazepine under various fatty acid and magnesium diet conditions.

机构信息

NMPA, CNPS, Paris XI University, Orsay, France.

出版信息

Prostaglandins Leukot Essent Fatty Acids. 2012 Aug-Sep;87(2-3):63-70. doi: 10.1016/j.plefa.2012.06.002. Epub 2012 Jun 30.

DOI:10.1016/j.plefa.2012.06.002
PMID:22749692
Abstract

The anticonvulsant and mood stabilizer drug carbamazepine (CBZ) was evaluated for anti-seizure activity after drug pretreatment of young weaning mice given various oil-based diets. These diets had various mono-(MUFA) and poly-(PUFA) unsaturated fatty acid contents, were associated or not with magnesium deprivation, and were given over the entire experimental period (34 days). The diets included a commercial and three purified synthetic diets (n-6 PUFA, n-3 PUFA and MUFA-based chows containing 5% corn/sunflower oils 1:3, 5% rapeseed oil and 5% high oleic acid sunflower oil/sunflower oil 7:3, respectively). A 10-days CBZ treatment (50 mg/kg/day fragmented in two daily intraperitoneal injections of 25 mg/kg) was given 20 days after initiating diet administration and evaluations of mice was performed 4 days after arrest of CBZ in various seizure tests. In these conditions, CBZ pretreatment still exhibited anticonvulsant protection especially in magnesium-deficient animals. Ethosuximide (ESM)-like profiles under MUFA and n-3 PUFA diets and unusual GABA(A)ergic profile under n-6 PUFA diet in magnesium-deficiency dependent audiogenic seizures (MDDAS) test as well as protection against NMDA-induced seizures in all lipid (n-3 PUFA>MUFA and n-6 PUFA) diet conditions were observed in CBZ-pretreated mice. By highlighting ESM-like and anti-NMDA mechanisms previously induced by an n-3 PUFA diet, present CBZ anticonvulsant properties suggest brain protective targets common to CBZ and n-3 PUFAs.

摘要

抗惊厥和情绪稳定剂药物卡马西平(CBZ)在给予不同油基饮食的年轻断奶小鼠药物预处理后,用于评估其抗惊厥活性。这些饮食具有不同的单(MUFA)和多(PUFA)不饱和脂肪酸含量,与镁缺乏有关或无关,并在整个实验期间(34 天)给予。饮食包括一种商业和三种纯化的合成饮食(n-6 PUFA、n-3 PUFA 和 MUFA 基础的饲料,分别含有 5%玉米/葵花籽油 1:3、5%菜籽油和 5%高油酸葵花籽油/葵花籽油 7:3)。在开始饮食管理后 20 天给予 10 天的 CBZ 治疗(50mg/kg/天,分为每日两次腹腔内注射 25mg/kg),并在各种惊厥试验中 CBZ 停止后 4 天对小鼠进行评估。在这些条件下,CBZ 预处理仍表现出抗惊厥保护作用,特别是在镁缺乏的动物中。在镁缺乏依赖性听觉性惊厥(MDDAS)试验中,MUFA 和 n-3 PUFA 饮食下表现出类似于乙琥胺(ESM)的特征,n-6 PUFA 饮食下表现出异常的 GABA(A)能特征,以及在所有脂质(n-3 PUFA>MUFA 和 n-6 PUFA)饮食条件下对 NMDA 诱导的惊厥的保护作用,在 CBZ 预处理的小鼠中观察到。通过强调先前由 n-3 PUFA 饮食诱导的 ESM 样和抗 NMDA 机制,目前 CBZ 的抗惊厥特性表明 CBZ 和 n-3 PUFAs 具有共同的脑保护靶标。

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