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大剂量的Omega-3多不饱和脂肪酸可减轻幼龄点燃大鼠的癫痫发作、认知障碍和海马体氧化性DNA损伤。

Omega-3 polyunsaturated fatty acids in large doses attenuate seizures, cognitive impairment, and hippocampal oxidative DNA damage in young kindled rats.

作者信息

Abdel-Wahab Basel A, Al-Qahtani Jobran M, El-Safty Samy A

机构信息

Department of Pharmacology, College of Medicine, Assiut University, Assiut, Egypt.

Department of Pediatrics, College of Medicine, Najran University, Najran, Saudi Arabia.

出版信息

Neurosci Lett. 2015 Jan 1;584:173-7. doi: 10.1016/j.neulet.2014.10.003. Epub 2014 Oct 12.

Abstract

Omega-3 (OM3) dietary polyunsaturated fatty acids have promising seizure-protective effects, as well as enhancing effects of cognitive development and memory-related learning. This study aimed to explore the effect of large doses of OM3 on cognitive impairment and hippocampal oxidative DNA damage produced by seizures in epileptic children using a PTZ-kindled young rat model. Cognitive functions, biomarkers of oxidative stress, and DNA damage were assessed in PTZ-kindled young rats (30 mg/kg, i.p. once every other day for 13 injections) pretreated with OM3 (200-500 mg/kg, p.o.). Pretreatment with OM3 at the tested doses significantly attenuated PTZ-induced seizures and decreased cognitive impairment in both passive avoidance and elevated plus maze tests in the PTZ-kindled rats. Moreover, OM3 significantly attenuated the increase in hippocampal malondialdehyde and 8-hydroxy-2'-deoxyguanosine (8-OHdG) levels, as well as the decrease in reduced glutathione (GSH) levels and GSH-peroxidase activity induced by PTZ kindling, in a dose-related manner. Relatively large dose levels of OM3 (200-500 mg/kg) effectively attenuated seizures and their associated cognitive deficits, and reduced oxidative stress and hippocampal DNA damage in PTZ-kindled young rats.

摘要

ω-3(OM3)膳食多不饱和脂肪酸具有显著的抗癫痫作用,以及促进认知发育和与记忆相关学习的作用。本研究旨在利用戊四氮点燃幼鼠模型,探讨大剂量OM3对癫痫患儿癫痫发作所致认知障碍和海马氧化DNA损伤的影响。对经OM3(200 - 500 mg/kg,口服)预处理的戊四氮点燃幼鼠(30 mg/kg,腹腔注射,隔日1次,共注射13次)的认知功能、氧化应激生物标志物和DNA损伤进行评估。在测试剂量下,OM3预处理显著减轻了戊四氮诱导的癫痫发作,并降低了戊四氮点燃大鼠在被动回避和高架十字迷宫试验中的认知障碍。此外,OM3以剂量相关的方式显著减轻了戊四氮点燃诱导的海马丙二醛和8-羟基-2'-脱氧鸟苷(8-OHdG)水平的升高,以及还原型谷胱甘肽(GSH)水平的降低和GSH-过氧化物酶活性的降低。相对大剂量水平的OM3(200 - 500 mg/kg)有效减轻了戊四氮点燃幼鼠的癫痫发作及其相关的认知缺陷,并减少了氧化应激和海马DNA损伤。

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