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