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Effect of Co-administration of Compound Danshen Dripping Pills and Valproic Acid on Temporal Lobe Epilepsy


Article Information

Title: Effect of Co-administration of Compound Danshen Dripping Pills and Valproic Acid on Temporal Lobe Epilepsy

Authors: Xi Hua, Chunxiang Liu, Yujun Qiao, Chen Jia, Rui Zhang, Haisheng Jiao

Journal: International Journal of Pharmacology

HEC Recognition History
Category From To
Y 2021-07-01 2022-06-30
Y 2020-07-01 2021-06-30

Publisher: Asian Network for Scientific Information

Country: Pakistan

Year: 2021

Volume: 17

Issue: 4

Language: English

DOI: 10.10.3923/ijp.2021.200.207

Keywords: Cognitive impairmentValproic acidTemporal Lobe Epilepsycaspase-3danshen dripping pillneuronal apoptosisChinese traditional medicinehippocampal neuronal

Categories

Abstract

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 kg&#150;1), CDDP (85 mg kg&#150;1) or combined VPA (189 mg kg&#150;1) and CDDP (85 mg kg&#150;1) 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 (p<0.01) and neuronal cell death in the CA3 region was alleviated (p<0.01) 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.


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