Kainic acid-induced seizures in the common marmoset

被引:1
|
作者
Ishikawa, Akiyoshi [1 ]
Mizuno, Yuri [1 ]
Sakai, Keita [1 ]
Maki, Takehiro [1 ]
Tanaka, Ryo [1 ]
Oda, Yasuhiro [1 ]
Niimi, Kimie [2 ]
Takahashi, Eiki [2 ]
机构
[1] HAMRI Co Ltd, Sleep Sci Labs, Ibaraki 3060128, Japan
[2] RIKEN Ctr Brain Sci, Res Resources Div, Hirosawa 2-1, Wako, Saitama 3510198, Japan
关键词
Animal model; Common marmoset; Diazepam; Epilepsy; Kainic acid; Seizure; ANIMAL-MODELS; ANTICONVULSANT; ANTAGONISTS; EPILEPSY; ANXIETY; DRUGS;
D O I
10.1016/j.bbrc.2020.02.121
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Treatment of epilepsy remains difficult because patients suffer from pharmacoresistant forms of the disease and drug side-effects. Thus, there is an urgent need to identify not only new antiepileptic drug candidates but also novel epileptic animal models. Here, we characterize seizures induced with kainic acid (1(A) in the common marmoset (Callithrix jacchus). Adult marmosets received 0.1, 1, or 10 mg/kg of KA subcutaneously. All animals exhibited early convulsive behavior (seizure scores of I and II on the Racine scale). Seizure scores were low at lower KA doses, but the highest dose of KA tested triggered generalized seizures (scores IV and Von the Racine scale). We next performed preliminary evaluation of the efficacy of the antiepileptic drug diazepam. This drug at 1 mg/kg (delivered subcutaneously) prevented 10 mg/kg [KA-induced stage V seizures. KA administration to marmosets reliably triggers generalized seizures; therefore, the marmoset is a useful animal model in which to analyze the seizures of a nonhuman primate brain and to develop new treatments for epilepsy.(C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:595 / 599
页数:5
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