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迷迭香酸可预防大鼠慢性乙醇诱导的学习记忆损伤。

Rosmarinic acid protects against chronic ethanol-induced learning and memory deficits in rats.

机构信息

a Department of Biology , School of Basic Sciences, Bu-Ali Sina University , Hamedan , Iran.

b Department of Basic Veterinary Science , Faculty of Veterinary Medicine, University of Zabol , Iran.

出版信息

Nutr Neurosci. 2017 Nov;20(9):547-554. doi: 10.1080/1028415X.2016.1203125. Epub 2016 Jul 1.

Abstract

OBJECTIVES

Ethanol consumption induces neurological disorders including cognitive dysfunction. Oxidative damage is considered a likely cause of cognitive deficits. We aimed to investigate the effects of rosmarinic acid (RA) in different doses for 30 days on chronic ethanol-induced cognitive dysfunction using the passive avoidance learning (PAL) and memory task in comparison with donepezil, a reference drug. We also evaluated the levels of superoxide dismutase (SOD), catalase (CAT), and lipid peroxidation in hippocampus as possible mechanisms.

METHODS

Memory impairment was induced by 15% w/v ethanol (2 g/kg, i.g.) administration for 30 days. RA (8, 16, and 32 mg/kg, i.g.) or donepezil (2 mg/kg, i.g.) was administered 30 minutes before ethanol. The acquisition trial was done 1 hour after the last administration of RA and donepezil. At the end, animals were weighed and hippocami were isolated for analyzing of oxidant/antioxidant markers.

RESULTS

Ethanol caused cognition deficits in the PAL and memory task. While RA 16 and 32 mg/kg improved cognition in control rats, it prevented learning and memory deficits of alcoholic groups. RA 8 mg/kg did not influence cognitive function in both control and alcoholic rats. RA 32 mg/kg had comparable effects with donepezil in prevention of acquisition and retention memory impairment. The higher doses of RA not only prevented increased lipid peroxidation and nitrite content but also decreased SOD, CAT, GSH, and FRAP levels in alcoholic groups and exerted antioxidant effects in non-alcoholic rats.

DISCUSSION

We showed that RA administration dose-dependently prevented cognitive impairment induced by chronic ethanol in PAL and memory and disturbed oxidant/antioxidant status as a possible mechanism. The antioxidant, anticholinesterase, and neuroprotective properties of RA may be involved in the observed effects. Therefore, RA represents a potential therapeutic option against chronic ethanol-induced amnesia which deserves consideration and further examination.

摘要

目的

乙醇摄入可引起神经紊乱,包括认知功能障碍。氧化损伤被认为是认知缺陷的一个可能原因。我们旨在通过比较阳性回避学习(PAL)和记忆任务,研究不同剂量迷迭香酸(RA)在 30 天内对慢性乙醇诱导的认知功能障碍的影响,RA 与参考药物多奈哌齐作比较。我们还评估了海马中超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和脂质过氧化水平,以作为可能的机制。

方法

通过给予 15%(w/v)乙醇(2g/kg,ig)30 天来诱导记忆损伤。RA(8、16 和 32mg/kg,ig)或多奈哌齐(2mg/kg,ig)在最后一次给予 RA 和多奈哌齐 30 分钟前给药。在最后一次给药 1 小时后进行获得性试验。最后,称重动物并分离海马以分析氧化应激/抗氧化标志物。

结果

乙醇导致 PAL 和记忆任务中的认知障碍。虽然 RA 16 和 32mg/kg 改善了对照组大鼠的认知功能,但它可预防酒精组的学习和记忆障碍。RA 8mg/kg 对对照组和酒精组大鼠的认知功能均无影响。RA 32mg/kg 与多奈哌齐在预防获得性和保留性记忆损伤方面具有相当的效果。较高剂量的 RA 不仅防止了脂质过氧化和亚硝酸盐含量的增加,而且降低了酒精组的 SOD、CAT、GSH 和 FRAP 水平,并在非酒精性大鼠中发挥了抗氧化作用。

讨论

我们表明,RA 给药剂量依赖性地预防了 PAL 和记忆中的慢性乙醇诱导的认知障碍,并干扰了氧化应激/抗氧化状态,这可能是一种机制。RA 的抗氧化、抗胆碱酯酶和神经保护特性可能与观察到的作用有关。因此,RA 代表了一种治疗慢性乙醇诱导的健忘症的潜在选择,值得考虑和进一步研究。

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