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姜黄素改善衰老加速小鼠记忆表现的神经生物学和药理学有效性。

Neurobiological and pharmacological validity of curcumin in ameliorating memory performance of senescence-accelerated mice.

机构信息

Dept. of Anatomy, Wenzhou Medical College, Wenzhou 325035, Zhejiang Province, China.

出版信息

Pharmacol Biochem Behav. 2013 Apr;105:76-82. doi: 10.1016/j.pbb.2013.02.002. Epub 2013 Feb 8.

Abstract

The senescence-accelerated mouse prone 8 (SAMP8 mice) is known as a neurodegenerative model and may show age-related deficits of cognition. Curcumin, a major active component of spic turmeric, could increase the capacity of learning and memory in the aged rat. However, it is not known whether curcumin could improve cognitive deficits in SAMP8 mice. The present study was undertaken to evaluate the effect of curcumin on the learning and memory of SAMP8 mice and its possible mechanisms. Subjects were randomly divided into four groups: SAMR1 mice, SAMP8 mice and two SAMP8 mice groups treated, intragastrically, with curcumin at the dose of 20 and 50mg/kg per day, respectively. After 25days, spatial memory, superoxide dismutase (SOD) activity, malondialdehyde (MDA) content, p-calcium/calmodulin-dependent kinase II (p-CaMKII) and p-N-methyl-d-aspartate receptor subunit 1 (p-NMDAR1) expression in the hippocampus of mice were examined by using the Morris water maze, biochemical analysis, immunohistochemistry and Western blot. Compared with SAMR1 mice, SAMP8 mice had longer escape latency, higher MDA content, lower SOD activity in the hippocampus, and lower intensity of p-CaMKII in the stratum lucidum of hippocampal CA3 and p-NMDAR1 expression in the hippocampal membrane fraction. Both 20 and 50mg/kg curcumin administration significantly shortened the escape latencies and decreased the hippocampal MDA content in the SAMP8 mice. 50mg/kg curcumin administration significantly ameliorated the hippocampal SOD activity, and increased the intensity of p-CaMKII in the stratum lucidum of hippocampal CA3 and p-NMDAR1 expression in the hippocampal membrane fraction of the SAMP8 mice. The present study demonstrated that curcumin treatment could attenuate cognitive deficits of SAMP8 mice in a dose-dependent manner by decreasing the oxidative stress and improving the expression of p-CaMKII and p-NMDAR1 in the hippocampus. Thus treatment with curcumin may have a potential therapeutic agent for aging-related cognitive dysfunctions.

摘要

衰老大鼠快速老化模型 8 号(SAMP8 小鼠)被认为是一种神经退行性疾病模型,可能表现出与年龄相关的认知缺陷。姜黄素是姜黄的主要活性成分之一,可提高老年大鼠的学习和记忆能力。然而,姜黄素是否能改善 SAMP8 小鼠的认知缺陷尚不清楚。本研究旨在评估姜黄素对 SAMP8 小鼠学习和记忆的影响及其可能的机制。实验动物随机分为 4 组:SAMR1 小鼠、SAMP8 小鼠及 SAMP8 小鼠经灌胃给予姜黄素 20mg/kg 和 50mg/kg 治疗组。25 天后,通过 Morris 水迷宫、生化分析、免疫组化和 Western blot 检测各组小鼠的空间记忆、超氧化物歧化酶(SOD)活性、丙二醛(MDA)含量、海马 CA3 区锥体细胞层 p-钙调蛋白依赖性激酶 II(p-CaMKII)和 p-N-甲基-D-天冬氨酸受体 1 亚基(p-NMDAR1)的表达。与 SAMR1 小鼠相比,SAMP8 小鼠逃避潜伏期较长,海马 MDA 含量较高,SOD 活性较低,海马 CA3 区锥体细胞层 p-CaMKII 表达强度较低,海马膜 p-NMDAR1 表达水平较低。20mg/kg 和 50mg/kg 姜黄素均可显著缩短 SAMP8 小鼠的逃避潜伏期,降低海马 MDA 含量。50mg/kg 姜黄素可显著改善 SAMP8 小鼠的海马 SOD 活性,增加海马 CA3 区锥体细胞层 p-CaMKII 表达强度和海马膜 p-NMDAR1 表达水平。本研究表明,姜黄素治疗可通过降低氧化应激和改善海马 p-CaMKII 和 p-NMDAR1 的表达来改善 SAMP8 小鼠的认知缺陷,且呈剂量依赖性。因此,姜黄素可能是一种有潜力的治疗与衰老相关认知功能障碍的药物。

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