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首页> 外文期刊>International Journal of Pharmacology >Effect of Co-administration of Compound Danshen Dripping Pills and Valproic Acid on Temporal Lobe Epilepsy
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Effect of Co-administration of Compound Danshen Dripping Pills and Valproic Acid on Temporal Lobe Epilepsy

机译:复合丹参滴丸和丙戊酸对颞叶癫痫的影响

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Background and Objective: Temporal Lobe Epilepsy (TLE), accompanied by cognitive impairment, is known for its drug resistance. Compound Danshen Dripping Pills (CDDP), a widely used Chinese Traditional Medicine (TDM), is an effective complementary medicine for the clinical treatment of TLE. The present work was aimed to explore the curative effect of co-administration of CDDP and valproic acid (VPA) in the kainic acid (KA)-induced TLE rat model. Materials and Methods: Male Sprague-Dawley (SD) rats were stochastically divided into five groups (n = 60): Saline, Model, CDDP, VPA and VPA CDDP groups. TLE model was established via stereotactic injections of KA. VPA (189 mg kgG1 ), CDDP (85 mg kgG1 ) or combined VPA (189 mg kgG1 ) and CDDP (85 mg kgG1 ) were respectively administered to rats in the treatment groups via i.g. for 60 days. Cognitive function was evaluated by the radial-arm maze and surviving neuron cells were observed and counted using Nissl staining. The expression of genes and proteins of the apoptosis factors caspase-3 and caspase-8 was detected by real-time fluorescence quantitative PCR and Western Blot. Results: Compared with the Model group, memory and learning skills were improved (p0.01) and neuronal cell death in the CA3 region was alleviated (p0.01) with co-administration treatment of VPA and CDDP. The mRNA and protein expression of caspase-3 and caspase-8 in the VPA CDDP group was both attenuated. Conclusion: VPA combined with CDDP could reduce neuronal damage and cognitive impairment with the possible mechanism to inhibit apoptosis by regulating apoptosis factors like caspase-3 and caspase-8.
机译:背景和目的:伴随着认知障碍的颞叶癫痫(TLE)以其耐药性而闻名。复方丹参滴丸(CDDP)是一种广泛使用的中药(TDM),是一种有效的互补药,用于临床治疗TLE。目前的作品旨在探讨CDDP和丙戊酸(VPA)在Kinain酸(Ka)诱导的TLE大鼠模型中的疗效。材料和方法:雄性Sprague-Dawley(SD)大鼠随机分为五组(n = 60):盐水,模型,CDDP,VPA和VPA CDDP组。通过立体定向注射仪的Ka建立了TLE模型。 VPA(189mg Kgg1),CDDP(85mg Kgg1)或组合的VPA(189mg Kgg1)和CDDP(85mg Kgg1)分别通过I.G分别给予治疗组中的大鼠。 60天。通过径向臂迷宫评估认知功能,并使用NISSL染色观察并计算存活的神经元细胞。通过实时荧光定量PCR和Western印迹检测凋亡因子Caspase-3和Caspase-8的基因和蛋白质的表达。结果:与模型组相比,改善了内存和学习技巧(P <0.01),并且CA3区中的神经元细胞死亡(P <0.01),具有对VPA和CDDP的共同治疗。在VPA CDDP组中Caspase-3和Caspase-8的mRNA和蛋白表达均衰减。结论:VPA联合CDDP可以通过调节Caspase-3和Caspase-8等细胞凋亡因子来抑制细胞凋亡的可能机制,降低神经元损伤和认知障碍。

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