Effects of eugenol on granule cell dispersion in a mouse model of temporal lobe epilepsy

被引:19
作者
Jeong, Kyoung Hoon [1 ,3 ]
Lee, Dong-Seok [1 ,2 ]
Kim, Sang Ryong [1 ,2 ,3 ]
机构
[1] Kyungpook Natl Univ, Sch Life Sci, Plus KNU Creat BioRes Grp BK 21, Taegu 702701, South Korea
[2] Kyungpook Natl Univ, Inst Life Sci & Biotechnol, Taegu 702701, South Korea
[3] Kyungpook Natl Univ, Brain Sci & Engn Inst, Taegu 702701, South Korea
基金
新加坡国家研究基金会;
关键词
Eugenol; Seizure; Granule cell dispersion; Mammalian target of rapamycin complex 1; Hippocampus; PROTECTS HIPPOCAMPAL-NEURONS; SIGNALING PATHWAY; MAMMALIAN TARGET; DENTATE GYRUS; ESSENTIAL OIL; CARYOPHYLLATA;
D O I
10.1016/j.eplepsyres.2015.06.001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Granule cell dispersion (GCD), a structural abnormality, is characteristic of temporal lobe epilepsy (TLE). Eugenol (EUG) is an essential component of medicinal herbs and is suggested to exert anticonvulsant activity. However, it is unclear whether EUG ameliorates the abnormal morphological changes in granule cells induced by epileptic insults. In the present study, we examined whether intraperitoneal injection of EUG attenuated increased seizure activity and GCD following intrahippocampal injection of kainic acid (KA). Our results showed that EUG significantly increased the seizure threshold, resulting in delayed seizure onset, and reduced GCD in KA-induced epilepsy. Moreover, EUG treatment significantly attenuated KA-induced activation of mammalian target of rapamycin complex 1 (mTORC1), which is involved in GCD development, in the dentate gyrus (DG). These results suggest that EUG may have beneficial effects in the treatment of epilepsy through its ability to inhibit GCD via suppression of KA-induced mTORC1 activation in the hippocampal DG in vivo. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:73 / 76
页数:4
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