Antiepileptic and Neuroprotective Effects of Rheum tanguticum Root Extract on Trimethyltin-Induced Epilepsy and Neurodegeneration: In Vivo and in Silico Analyses.

IF 2.5 4区 医学 Q3 NEUROSCIENCES Journal of integrative neuroscience Pub Date : 2024-06-21 DOI:10.31083/j.jin2306122
Jae-Young Choi, Sohi Kang, Minh Nhat Tran, Sanghun Lee, Seung Mok Ryu, Sung-Wook Chae, Do-Hyun Kim, Ye Eun Lee, Sohee Jeong, Changjong Moon, Joong Sun Kim, Soong-In Lee
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Abstract

Background: Rheum tanguticum root, cataloged as "Daehwang" in the Korean Pharmacopeia, is rich in various anthraquinones known for their anti-inflammatory and antioxidant properties. Formulations containing Daehwang are traditionally employed for treating neurological conditions. This study aimed to substantiate the antiepileptic and neuroprotective efficacy of R. tanguticum root extract (RTE) against trimethyltin (TMT)-induced epileptic seizures and hippocampal neurodegeneration.

Methods: The constituents of RTE were identified by ultra-performance liquid chromatography (UPLC). Experimental animals were grouped into the following five categories: control, TMT, and three TMT+RTE groups with dosages of 10, 30, and 100 mg/kg. Seizure severity was assessed daily for comparison between the groups. Brain tissue samples were examined to determine the extent of neurodegeneration and neuroinflammation using histological and molecular biology techniques. Network pharmacology analysis involved extracting herbal targets for Daehwang and disease targets for epilepsy from multiple databases. A protein-protein interaction network was built using the Search Tool for the Retrieval of Interacting Genes/Proteins (STRING) database, and pivotal targets were determined by topological analysis. Enrichment analysis was performed using the Database for Annotation, Visualization, and Integrated Discovery (DAVID) tool to elucidate the underlying mechanisms.

Results: The RTE formulation was found to contain sennoside A, sennoside B, chrysophanol, emodin, physcion, (+)-catechin, and quercetin-3-O-glucuronoid. RTE effectively inhibited TMT-induced seizures at 10, 30, and 100 mg/kg dosages and attenuated hippocampal neuronal decay and neuroinflammation at 30 and 100 mg/kg dosages. Furthermore, RTE significantly reduced mRNA levels of tumor necrosis factor (TNF-α), glial fibrillary acidic protein (GFAP), and c-fos in hippocampal tissues. Network analysis revealed TNF, Interleukin-1 beta (IL-1β), Interleukin-6 (IL-6), Protein c-fos (FOS), RAC-alpha serine/threonine-protein kinase (AKT1), and Mammalian target of rapamycin (mTOR) as the core targets. Enrichment analysis demonstrated significant involvement of R. tanguticum components in neurodegeneration (p = 4.35 × 10-5) and TNF signaling pathway (p = 9.94 × 10-5).

Conclusions: The in vivo and in silico analyses performed in this study suggests that RTE can potentially modulate TMT-induced epileptic seizures and neurodegeneration. Therefore, R. tanguticum root is a promising herbal treatment option for antiepileptic and neuroprotective applications.

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大黄根提取物对三甲基锡诱导的癫痫和神经变性的抗癫痫和神经保护作用:体内和硅学分析。
背景:大黄(Rheum tanguticum)根在韩国药典中被收录为 "Daehwang",富含各种蒽醌类物质,具有抗炎和抗氧化特性。含有大黄的制剂传统上用于治疗神经系统疾病。本研究旨在证实大黄根提取物(RTE)对三甲基锡(TMT)诱导的癫痫发作和海马神经变性具有抗癫痫和神经保护作用:方法:采用超高效液相色谱法(UPLC)鉴定根提取物的成分。实验动物分为以下五组:对照组、TMT 组和三个 TMT+RTE 组,剂量分别为 10、30 和 100 毫克/千克。每天评估癫痫发作的严重程度,以便在各组之间进行比较。采用组织学和分子生物学技术对脑组织样本进行检查,以确定神经变性和神经炎症的程度。网络药理学分析包括从多个数据库中提取大黄的中药靶点和癫痫的疾病靶点。使用检索基因/蛋白质相互作用的搜索工具(STRING)数据库建立了蛋白质-蛋白质相互作用网络,并通过拓扑分析确定了关键靶点。使用注释、可视化和综合发现数据库(DAVID)工具进行了富集分析,以阐明其潜在机制:结果表明:RTE制剂中含有番泻苷A、番泻苷B、菊花酚、大黄素、大黄素、(+)-儿茶素和槲皮素-3-O-葡萄糖醛酸。10、30和100毫克/千克剂量的RTE可有效抑制TMT诱导的癫痫发作,30和100毫克/千克剂量的RTE可减轻海马神经元衰退和神经炎症。此外,RTE 还能明显降低海马组织中肿瘤坏死因子(TNF-α)、神经胶质纤维酸性蛋白(GFAP)和 c-fos 的 mRNA 水平。网络分析显示 TNF、白细胞介素-1 beta (IL-1β)、白细胞介素-6 (IL-6)、c-fos 蛋白 (FOS)、RAC-α 丝氨酸/苏氨酸蛋白激酶 (AKT1) 和哺乳动物雷帕霉素靶标 (mTOR) 是核心靶标。富集分析表明,R. tanguticum 成分在神经变性(p = 4.35 × 10-5)和 TNF 信号通路(p = 9.94 × 10-5)中有重要参与:本研究中进行的体内和硅学分析表明,RTE 有可能调节 TMT 诱导的癫痫发作和神经变性。因此,R. tanguticum 根是一种很有前景的抗癫痫和神经保护草药。
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来源期刊
CiteScore
2.80
自引率
5.60%
发文量
173
审稿时长
2 months
期刊介绍: JIN is an international peer-reviewed, open access journal. JIN publishes leading-edge research at the interface of theoretical and experimental neuroscience, focusing across hierarchical levels of brain organization to better understand how diverse functions are integrated. We encourage submissions from scientists of all specialties that relate to brain functioning.
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