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Betahistine is effective in combatting spasms in NMDA-inducing infantile spasms rat model

机译:甲板驱子是有效地对抗NMDA诱导婴儿痉挛大鼠模型的痉挛

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Infantile spasms (IS) is an age-related epileptic disorder characterized by specific spasms, hypsarrhythmia and mental retardation. Most of IS patients can not get spasm free under the available treatment and prognosis is poor. It is crucial to develop new effective drugs the treatment of IS. Histamine H3 receptor antagonist seems to be effective in some epilepsy models. Betahistine is one of H3 antagonists. For this purpose, we tested the effecacy of betahistine in a NMDA-induced IS model. The results showed that betahistine prolonged the latencies to tail-flicking and emprothonus and decreased the incidence of stereotypic behaviors in IS rats. Betahistine has increased histamine content and H3 receptor expression in the brain in a dosage-dependent manner. Then, betahistine exerts it anti-spasms effect through increaing histamine content and H3 expression. It is promising for H3 antagonists use in IS in clinic to control spasms and improve the poor prognosis.
机译:婴儿痉挛(IS)是一种与年龄相关的癫痫症,其特征是特异性痉挛,低血肿和术迟缓。大多数是患者不能在可用的治疗和预后脱脂,预后差。开发新的有效药物治疗是至关重要的。组胺H3受体拮抗剂似乎在一些癫痫模型中有效。 Betahistine是H3拮抗剂之一。为此目的,我们测试了符合NMDA诱导的β发球子的血糖。结果表明,甲板驱动率延长了尾部闪烁和eMPRICHONUS的延迟,并降低了大鼠的陈规定型行为的发病率。甲板驱动素以剂量依赖性方式增加了大脑中的组胺含量和H3受体表达。然后,甲板驱子通过增强组胺含量和H 3表达来施加抗痉挛效应。它很有希望在临床中使用H3拮抗剂来控制痉挛,提高预后差。

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