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拉考酰胺和乙琥胺长期治疗对匹罗卡品诱导的小鼠癫痫持续状态后神经前体细胞和认知功能的影响

Effect of Lacosamide and Ethosuximide Chronic Treatment on Neural Precursor Cells and Cognitive Functions after Pilocarpine Induced Status Epilepticus in Mice.

作者信息

Szewczyk Aleksandra, Zagaja Mirosław, Szala-Rycaj Joanna, Maj Maciej, Andres-Mach Marta

机构信息

Isobolographic Analysis Laboratory, Institute of Rural Health, Jaczewskiego 2, 20-090 Lublin, Poland.

Department of Biopharmacy, Medical University of Lublin, Chodzki 4A, 20-093 Lublin, Poland.

出版信息

Brain Sci. 2021 Jul 30;11(8):1014. doi: 10.3390/brainsci11081014.

Abstract

Seizures in about 40% of patients with epilepsy fail to respond to anti-seizure medication (ASM) and may lead to uncontrolled and prolonged seizures often inducing status epilepticus (SE). The aim of the study was to evaluate the impact of a long-term treatment with two different generation ASMs: ethosuximide (ETS, a classic ASM) and lacosamide (LCM, a 3rd generation ASM) on neural stem cells' (NSCs') proliferation and learning and memory functions after pilocarpine (PILO)-induced SE in mice. The following drugs were used: LCM (10 mg/kg), ETS (20 mg/kg), and PILO (300 mg/kg). Cell counting was done using confocal microscope and ImageJ software. Cognitive functions were evaluated with the Morris water maze (MWM) test. The level of several selected neurometabolites was measured with magnetic resonance spectroscopy (MRS). Obtained results indicated no significant impact of ETS treatment on the neurogenesis process in PILO mice. Interestingly, LCM significantly decreased the total amount of newborn neurons. The MWM test indicated no significant changes in the time and distance traveled by the ETS and LCM groups compared to PILO control mice, although all measured parameters were more favorable for the PILO mice treated with ASM. Conclusions: The presented results show that long term treatment with LCM and ETS seems to be safe for the cognitive functions and the proper course of neurogenesis in the mouse PILO-induced SE model, although one should remember that LCM administered chronically may act to reduce new neurons' formation.

摘要

约40%的癫痫患者的癫痫发作对抗癫痫药物(ASM)无反应,可能导致癫痫发作失控且持续时间延长,常诱发癫痫持续状态(SE)。本研究的目的是评估两种不同代次的ASM长期治疗:乙琥胺(ETS,一种经典ASM)和拉科酰胺(LCM,第三代ASM)对匹罗卡品(PILO)诱导的小鼠SE后神经干细胞(NSC)增殖以及学习和记忆功能的影响。使用了以下药物:LCM(10 mg/kg)、ETS(20 mg/kg)和PILO(300 mg/kg)。使用共聚焦显微镜和ImageJ软件进行细胞计数。用莫里斯水迷宫(MWM)试验评估认知功能。用磁共振波谱(MRS)测量几种选定神经代谢物的水平。所得结果表明,ETS治疗对PILO小鼠的神经发生过程无显著影响。有趣的是,LCM显著减少了新生神经元的总数。MWM试验表明,与PILO对照小鼠相比,ETS和LCM组的游动时间和距离无显著变化,尽管所有测量参数对接受ASM治疗的PILO小鼠更为有利。结论:呈现的结果表明,在小鼠PILO诱导的SE模型中,长期用LCM和ETS治疗对认知功能和神经发生的正常进程似乎是安全的,尽管应该记住,长期给予LCM可能会减少新神经元的形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb3c/8392532/3c611bd5ccf4/brainsci-11-01014-g001.jpg

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