Pre- and Post-Treatment with Novel Antiepileptic Drug Oxcarbazepine Exerts Neuroprotective Effect in the Hippocampus in a Gerbil Model of Transient Global Cerebral Ischemia

被引:12
作者
Ahn, Ji Hyeon [1 ]
Shin, Bich Na [2 ]
Park, Joon Ha [3 ]
Lee, Tae-Kyeong [4 ]
Park, Young Eun [4 ]
Lee, Jae-Chul [4 ]
Yang, Go Eun [5 ]
Shin, Myoung Cheol [6 ]
Cho, Jun Hwi [6 ]
Lee, Kyu Chang [7 ]
Won, Moo-Ho [4 ]
Kim, Hyeyoung [6 ,7 ]
机构
[1] Hallym Univ, Res Inst Biosci & Biotechnol, Dept Biomed Sci, Chunchon 24252, Gangwon, South Korea
[2] Hallym Univ, Sch Med, Dept Physiol, Chunchon 24252, Gangwon, South Korea
[3] Dongguk Univ, Dept Anat, Coll Korean Med, Gyeongju 38066, Gyeongbuk, South Korea
[4] Kangwon Natl Univ, Sch Med, Dept Neurobiol, Chunchon 24341, Gangwon, South Korea
[5] Kangwon Natl Univ Hosp, Dept Radiol, Chunchon 24289, Gangwon, South Korea
[6] Kangwon Natl Univ, Sch Med, Dept Emergency Med, Chunchon 24341, Gangwon, South Korea
[7] Konkuk Univ, Chungju Hosp, Dept Anesthesiol & Pain Med, Sch Med, Chungju 27376, Chungbuk, South Korea
基金
新加坡国家研究基金会;
关键词
anti-epileptic drug; transient cerebral ischemia; pyramidal neurons; neuroprotection; glial activation; DELAYED NEURONAL DEATH; CA1; REGION; CELL-DEATH; CARBAMAZEPINE; ACTIVATION; EXPRESSION; INJURY; HYPERACTIVITY; LAMOTRIGINE; INHIBITION;
D O I
10.3390/brainsci9100279
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Oxcarbazepine, an antiepileptic drug, has been reported to modulate voltage-dependent sodium channels, and it is commonly used in epilepsy treatment. In this study, we investigated the neuroprotective effect of oxcarbazepine in the hippocampus after transient ischemia in gerbils. Gerbils randomly received oxcarbazepine 100 or 200 mg/kg before and after transient ischemia. We examined its neuroprotective effect in the cornu ammonis 1 subfield of the gerbil hippocampus at 5 days after transient ischemia by using cresyl violet staining, neuronal nuclei immunohistochemistry and Fluoro-Jade B histofluorescence staining for neuroprotection, and by using glial fibrillary protein and ionized calcium-binding adapter molecule 1 immunohistochemistry for reaction of astrocytes and microglia, respectively. Pre- and post-treatment with 200 mg/kg of oxcarbazepine, but not 100 mg/kg of oxcarbazepine, protected pyramidal neurons of the cornu ammonis 1 subfield from transient ischemic damage. In addition, pre- and post-treatment with oxcarbazepine (200 mg/kg) significantly ameliorated astrocytes and microglia activation in the ischemic cornu ammonis 1 subfield. In brief, our current results indicate that post-treatment as well as pre-treatment with 200 mg/kg of oxcarbazepine can protect neurons from ischemic insults via attenuation of the glia reaction.
引用
收藏
页数:14
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