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芦丁水合物通过提高乙酰胆碱水平、抑制 JNK 和 ERK1/2 的激活以及激活 mTOR 信号通路来改善氯化镉诱导的大鼠空间记忆丧失和神经细胞凋亡。

Rutin hydrate ameliorates cadmium chloride-induced spatial memory loss and neural apoptosis in rats by enhancing levels of acetylcholine, inhibiting JNK and ERK1/2 activation and activating mTOR signalling.

机构信息

a Department of Medical Biochemistry, College of Medicine , King Khalid University , Abha , Saudi Arabia.

b Department of Medical Biochemistry, Faculty of Medicine , Tanta University , Tanta , Egypt.

出版信息

Arch Physiol Biochem. 2018 Oct;124(4):367-377. doi: 10.1080/13813455.2017.1411370. Epub 2017 Dec 7.

Abstract

This study aimed at studying the potential neuroprotective effect of Rutin hydrate (RH) alone or in conjugation with α-tocopherol against cadmium chloride (CdCl)-induced neurotoxicity and cognitive impairment in rats and to investigate the mechanisms of action. Rats intoxicated with CdCl were treated with the vehicle, RH, α-tocopherol or combined treatment were examined, and compared to control rats received vehicle or individual doses of either drug. Data confirmed that RH improves spatial memory function by increasing acetylcholine availability, boosting endogenous antioxidant potential, activating cell survival and inhibiting apoptotic pathways, an effect that is more effective when RH was conjugated with α-tocopherol. Mechanism of RH action includes activation of PP2A mediated inhibiting of ERK1/2 and JNK apoptotic pathways and inhibition of PTEN mediated activation of mTOR survival pathway. In conclusion, RH affords a potent neuroprotection against CdCl-induced brain damage and memory dysfunction and co-administration of α-tocopherol enhances its activity.

摘要

本研究旨在研究芦丁水合物(RH)单独或与α-生育酚联合使用对氯化镉(CdCl)诱导的大鼠神经毒性和认知障碍的潜在神经保护作用,并探讨其作用机制。用 CdCl 使大鼠中毒,然后用载体、RH、α-生育酚或联合治疗进行处理,并与接受载体或两种药物单独剂量的对照大鼠进行比较。数据证实,RH 通过增加乙酰胆碱的可用性、增强内源性抗氧化潜力、激活细胞存活和抑制细胞凋亡途径来改善空间记忆功能,当 RH 与α-生育酚结合使用时,效果更为明显。RH 的作用机制包括激活 PP2A 介导的抑制 ERK1/2 和 JNK 凋亡途径以及抑制 PTEN 介导的 mTOR 存活途径的激活。总之,RH 对 CdCl 诱导的脑损伤和记忆功能障碍具有强大的神经保护作用,而α-生育酚的联合给药增强了其活性。

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