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L-3-正丁基苯酞对慢性癫痫小鼠认知功能和心境恶劣障碍的保护作用

Protective Role of L-3--Butylphthalide in Cognitive Function and Dysthymic Disorders in Mouse With Chronic Epilepsy.

作者信息

Ye Xiaowen, Rong Zhouyi, Li Yanfang, Wang Xintian, Cheng Baoying, Cheng Yiyun, Luo Haijuan, Ti Yue, Huang Xiaohua, Liu Zhaoji, Zhang Yun-Wu, Zheng Weihong, Zheng Honghua

机构信息

Department of Neurology, Affiliated Zhongshan Hospital, Xiamen University, Xiamen, China.

Fujian Provincial Key Laboratory of Neurodegenerative Disease and Aging Research, Institute of Neuroscience, College of Medicine, Xiamen University, Xiamen, China.

出版信息

Front Pharmacol. 2018 Jul 11;9:734. doi: 10.3389/fphar.2018.00734. eCollection 2018.

Abstract

Epilepsy is a common neurological disease with recurrent seizures and neurobehavioral comorbidities, including cognitive impairment and psychiatric disorders. Recent studies suggest that L-3--butylphthalide (NBP), an extract from the seeds of Linn. (Chinese celery), ameliorates cognitive dysfunction in ischemia and/or Alzheimer's disease animal models. However, little is known about the role of NBP in epilepsy and the associated comorbidities. Here, using a pilocarpine-induced chronic epileptic mouse model, we found that NBP supplement not only alleviated seizure severity and abnormal electroencephalogram, but also rescued cognitive and emotional impairments in these epileptic mice. The possible underlying mechanisms may be associated with the protective role of NBP in reducing neuronal loss and in restoring the expression of neural synaptic proteins such as postsynaptic density protein 95 (PSD95) and glutamic acid decarboxylase 65/67 (GAD65/67). In addition, NBP treatment increased the transcription of neuroprotective factors, brain-derived neurotrophic factor and Klotho. These findings suggest that NBP treatment may be a potential strategy for ameliorating epileptogenesis and the comorbidities of cognitive and psychological impairments.

摘要

癫痫是一种常见的神经系统疾病,伴有反复发作的癫痫发作以及神经行为共病,包括认知障碍和精神疾病。最近的研究表明,L-3-正丁基苯酞(NBP),一种从芹菜籽中提取的物质,可改善缺血和/或阿尔茨海默病动物模型中的认知功能障碍。然而,关于NBP在癫痫及其相关共病中的作用知之甚少。在此,我们使用毛果芸香碱诱导的慢性癫痫小鼠模型,发现补充NBP不仅减轻了癫痫发作的严重程度和异常脑电图,还挽救了这些癫痫小鼠的认知和情感障碍。可能的潜在机制可能与NBP在减少神经元丢失以及恢复神经突触蛋白如突触后致密蛋白95(PSD95)和谷氨酸脱羧酶65/67(GAD65/67)表达方面的保护作用有关。此外,NBP治疗增加了神经保护因子脑源性神经营养因子和Klotho的转录。这些发现表明,NBP治疗可能是改善癫痫发生以及认知和心理障碍共病的一种潜在策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9d1/6051017/416203bf82be/fphar-09-00734-g001.jpg

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