Dingxian pill alleviates hippocampal neuronal apoptosis in epileptic mice through TNF-α/TNFR1 signaling pathway inhibition

被引:2
|
作者
Wang, Qin [1 ,2 ]
Qin, Baijun [3 ]
Yu, Han [4 ]
Yu, Haichun [5 ]
Zhang, Xian [6 ]
Li, Mingfen [7 ]
Zhou, Yanying [2 ]
Diao, Limei [1 ,2 ]
Liu, Huihua [6 ]
机构
[1] Guangxi Univ Chinese Med, Clin Sch Med 1, 179 Mingxiu East Rd, Nanning 530001, Guangxi, Peoples R China
[2] Guangxi Univ Chinese Med, Dept Neurol, Affiliated Hosp 1, 89-9 Dongge Rd, Nanning 530023, Guangxi, Peoples R China
[3] Chongqing City Hosp Tradit Chinese Med, Dept Gastroenterol, 6 Panxi Seventh Branch Rd, Chongqing 400021, Peoples R China
[4] Harbin Med Univ, 157 Baojian Rd, Harbin 150081, Heilongjiang, Peoples R China
[5] Guangxi Technol Coll Machinery & Elect, Nanning 530007, Guangxi, Peoples R China
[6] Guangxi Zhuang Autonomous Reg Brain Hosp, Liuzhou 545005, Guangxi, Peoples R China
[7] Guangxi Univ Chinese Med, Dept Clin Lab, Affiliated Hosp 1, Nanning 530023, Guangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Dingxian pill; Epilepsy; Hippocampal neurons; Apoptosis; TNF-alpha/TNFR1 signaling pathway; NECROSIS-FACTOR RECEPTOR-1; PROTEIN-KINASE; CELL-DEATH; TNF-ALPHA; EXPRESSION; DEPRESSION; INDUCTION; SURVIVAL; SEIZURES;
D O I
10.1016/j.jep.2024.118579
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Dingxian Pill (DXP), a famous traditional Chinese medicine prescription, and has been widely proven to have positive therapeutic effects on "Xianzheng" (the name of epilepsy in ancient China). However, the anti-epileptic molecular mechanisms of DXP are not yet fully understood and remain to be further investigated. Aim of the study: To elucidate the molecular mechanism of DXP's improvement in epileptic neuronal loss, damage and apoptosis by regulating TNF-alpha/TNFR1 signaling pathway. Materials and methods: Sixty Kunming mice were randomly divided in 6 groups: control group (equal volume of normal saline), model group (180 mg kg-1 pilocarpine hydrochloride - used to establish the epilepsy animal model), carbamazepine group (30 mg kg- 1), and low, medium, and high-dose Dingxian Pill groups (4.08, 8.16, and 16.32 g kg-1, respectively - oral administration once daily for 2 weeks). Successful establishment of the epileptic mouse model was monitored with electroencephalography. Pathological changes in hippocampal tissue were analyzed with hematoxylin-eosin staining. Hippocampal neuronal apoptosis was analyzed with TUNEL staining. TNF-alpha, TNFR1, TRADD, FADD, and caspase-8 mRNA and protein expression levels in hippocampal tissue were analyzed with real-time quantitative polymerase chain reaction, immunohistochemistry, and Western blot, respectively. Cleaved caspase-8 protein levels in hippocampal tissue were measured with immunohistochemistry and Western blot. Results: Compared to control, the model group showed an increase in continuous epileptic discharge waves on EEG, a damaged hippocampal neuron morphological structure, increased hippocampal neuronal apoptosis, and significantly increased TNF-alpha, TNFR1, TRADD, FADD, and caspase-8 mRNA and protein levels, and increased caspase-8 cleavage (P < 0.05). Compared to the model group, the carbamazepine group as well as the low-, medium-, and high-dose Dingxian Pill groups showed decreased epileptic discharges on EEG, an obvious hippocampal neuron morphological structure restoration, varying degrees of attenuated hippocampal neuronal apoptosis, and significantly decreased TNF-alpha, TNFR1, TRADD, FADD, and caspase-8 mRNA and protein levels as well as decreased caspase-8 cleavage (P < 0.05). Conclusions: Dingxian Pill exerts an anti-epileptic effect through inhibition of TNF-alpha/TNFR1 signaling pathwaymediated apoptosis in hippocampal neurons.
引用
收藏
页数:11
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