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脑室注射山奈酚对大鼠被动回避学习记忆保留的影响:胆碱能机制的参与。

Intracerebroventricular microinjection of kaempferol on memory retention of passive avoidance learning in rats: involvement of cholinergic mechanism(s).

机构信息

Neurophysiology Research Center, Hamadan University of Medical Sciences , Hamadan , Iran.

Department of Biology, Science and Research Branch, Islamic Azad University , Tehran , Iran.

出版信息

Int J Neurosci. 2019 Dec;129(12):1203-1212. doi: 10.1080/00207454.2019.1653867. Epub 2019 Aug 26.

Abstract

Kaempferol (KM) is a flavonoid found in plant-derived foods and medicinal plants. Recently, it is well established that KM plays a protective role to develop Alzheimer's disease. The current study aimed at evaluating the effect of intracerebroventricular micro-injection of KM on memory retention of passive avoidance learning (MRPAM) and identifying the potentially related cholinergic mechanisms (ChMs) in rats. In the current study, male Wistar rats randomly divided into control, vehicle and KM (10, 20 and 40 μg/rat) groups. Moreover, MRPAM was evaluated by shuttle box test. The role of ChM was studied using non-selective and selective acetylcholine antagonists (scopolamine [SCN], 4-DAMP and methoctramine [MN], respectively) as well as pirenzepine (PZ) in combination with KM. The employment of KM (40 μg/rat) improved the SCN-induced memory impairment in MRPAM. Co-treatment with KM (40 μg/rat) plus 4-DAMP significantly increased the step-through latency (STL,  < 0.05; 167 ± 28 s) and decreased the total dark chamber (TDC,  < 0.05; 121 ± 31 s) compared with those of the 4-DAMP group (STL: 75 ± 13 s; TDC: 178 ± 46 s). Co-treatment with KM (40 μg/rat) plus PZ attenuated STL, and also increased TDC ( < 0.01; 220 ± 28 s) compared with those of the PZ group. Co-treatment with KM (10 and 20 μg/rat) and MN increased STL ( < 0.05), and deceased TDC compared with those of the MN group ( < 0.01). Totally, the results of the present study showed that cholinergic system may be involved in improving effect of KM on SCN-induced memory impairment.

摘要

山奈酚 (KM) 是一种存在于植物源性食物和药用植物中的类黄酮。最近的研究证实,KM 在预防阿尔茨海默病方面发挥着保护作用。本研究旨在评估脑室微量注射 KM 对被动回避学习记忆保留 (MRPAM) 的影响,并确定大鼠潜在的相关胆碱能机制 (ChMs)。在本研究中,雄性 Wistar 大鼠随机分为对照组、载体组和 KM (10、20 和 40μg/大鼠) 组。此外,通过穿梭箱测试评估 MRPAM。使用非选择性和选择性乙酰胆碱拮抗剂 (东莨菪碱 [SCN]、4-DAMP 和甲氧基胺 [MN],分别) 以及与 KM 联合使用的匹鲁卡品 (PZ) 研究 ChM 的作用。KM (40μg/大鼠) 的使用改善了 SCN 诱导的 MRPAM 记忆障碍。KM (40μg/大鼠) 与 4-DAMP 联合治疗可显著增加穿通潜伏期 (STL,  < 0.05;167 ± 28 s) 和减少总暗室时间 (TDC,  < 0.05;121 ± 31 s),与 4-DAMP 组相比 (STL:75 ± 13 s;TDC:178 ± 46 s)。KM (40μg/大鼠) 与 PZ 联合治疗可减轻 STL,同时增加 TDC (  < 0.01;220 ± 28 s),与 PZ 组相比。KM (10 和 20μg/大鼠) 与 MN 联合治疗可增加 STL (  < 0.05),并减少 TDC 与 MN 组相比 (  < 0.01)。总之,本研究结果表明,胆碱能系统可能参与了 KM 改善 SCN 诱导记忆障碍的作用。

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