Beneficial Effects of Silibinin Against Kainic Acid-induced Neurotoxicity in the Hippocampus in vivo

被引:25
作者
Kim, Sehwan [1 ]
Jung, Un Ju [2 ]
Oh, Yong-Seok [3 ]
Jeon, Min-Tae [1 ]
Kim, Hyung-Jun [4 ]
Shin, Won-Ho [5 ]
Hong, Jungwan [6 ]
Kim, Sang Ryong [1 ,6 ]
机构
[1] Kyungpook Natl Univ, Plus KNU Creat BioRes Grp BK21, Sch Life Sci, Daegu 41566, South Korea
[2] Pukyong Natl Univ, Dept Food Sci & Nutr, Busan 48513, South Korea
[3] Daegu Gyeongbuk Inst Sci & Technol, Dept Brain Cognit Sci, Daegu 42988, South Korea
[4] Korea Brain Res Inst, Dept Neural Dev & Dis, Dept Struct & Funct Neural Network, Daegu 41062, South Korea
[5] Korea Inst Toxicol, Predict Model Res Ctr, Daejeon 34114, South Korea
[6] Kyungpook Natl Univ, Brain Sci & Engn Inst, Daegu 41944, South Korea
基金
新加坡国家研究基金会;
关键词
Silibinin; Epilepsy; Granule cell dispersion; Kainic acid; Neuroprotection; GRANULE CELL DISPERSION; TEMPORAL-LOBE EPILEPSY; INDUCED HYPERSENSITIVITY REACTIONS; DENTATE GYRUS; SIGNALING PATHWAY; INFLAMMATORY CYTOKINES; OXIDATIVE STRESS; CANCER-CELLS; MOUSE MODEL; INHIBITION;
D O I
10.5607/en.2017.26.5.266
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Silibinin, an active constituent of silymarin extracted from milk thistle, has been previously reported to confer protection to the adult brain against neurodegeneration. However, its effects against epileptic seizures have not been examined yet. In order to investigate the effects of silibinin against epileptic seizures, we used a relevant mouse model in which seizures are manifested as status epilepticus, induced by kainic acid (KA) treatment. Silibinin was injected intraperitoneally, starting 1 day before an intrahippocampal KA injection and continued daily until analysis of each experiment. Our results indicated that silibinin-treatment could reduce seizure susceptibility and frequency of spontaneous recurrent seizures (SRS) induced by KA administration, and attenuate granule cell dispersion (GCD), a morphological alteration characteristic of the dentate gyrus (DG) in temporal lobe epilepsy (TLE). Moreover, its treatment significantly reduced the aberrant levels of apoptotic, autophagic and pro-inflammatory molecules induced by KA administration, resulting in neuroprotection in the hippocampus. Thus, these results suggest that silibinin may be a beneficial natural compound for preventing epileptic events.
引用
收藏
页码:266 / 277
页数:12
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