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灵龟护肝汤通过 AMPK 通路在阿尔茨海默病神经保护中的潜在作用。

Linggui Zhugan decoction as a potential medicine for neuroprotection in Alzheimer's Disease via AMPK pathway.

机构信息

School of Traditional Chinese Medicine, Nanjing University of Traditional Chinese Medicine, Nanjing, Jiangsu 210046, China.

Zhang Zhongjing Key Laboratory of Prescriptions and Immunomodulation, Zhang Zhongjing Traditional Chinese Medicine College, Nanyang Institute of Technology, Nanyang, Henan 473306, China.

出版信息

Cell Mol Biol (Noisy-le-grand). 2024 Jul 28;70(7):161-167. doi: 10.14715/cmb/2024.70.7.23.

Abstract

Alzheimer's disease (AD) is a degenerative dementia illness that causes atrophy of the temporal and frontal lobes of the cerebral cortex. Linggui Zhugan (LGZG), a classic Chinese herbal formula, was initially recognized as a safe and effective treatment of cardiovascular diseases for long history. This study intended to assess the effects and the molecular mechanism of LGZG on AD progress. C57BL/6 mice were divided into six groups: normal mice, amyloid precursor protein/presenilin 1 (APP/PS1) mice (model group), positive control group (model mice treated with donepezil), high, medium and low LGZG group (model mice treated with 7g/kg/d, 3.5g/kg/d or 1.75g/kg/d LGZG respectively). Water maze results showed that the escape latency and path length of high and medium LGZG groups declined compared to the model mice, the decline degree was dose-dependent. The hippocampal slices of six groups were analyzed by Nissl-staining, Perls' iron staining and immunofluorescence assay. The results indicated LGZG could restore morphological anomalies and alleviate iron deposition of AD mice, and the GXP4 positive cells increased significantly. The MDA, Fe2+ and GSH were measured by biochemical testing, whose results illustrated that LGZG could normalize MDA, Fe2+ and GSH levels in AD model compared to un-treated APP/PS1 model. The higher dose of LGZG the mice received, the more intensive effects on those levels of molecules. Western blot results showed that LGZG could affect NeuN, AMPK, p53, SLC7A11 and GPX4 levels in the hippocampus of AD model, which was all proteins related to AMPK pathway. In conclusion, LGZG has a neuroprotective effect on AD through AMPK pathway by alleviating oxidative stress and ferroptosis.

摘要

阿尔茨海默病(AD)是一种退行性痴呆疾病,可导致大脑皮层颞叶和额叶萎缩。灵龟柱骨丹(LGZG)是一种经典的中药方剂,长期以来被认为是治疗心血管疾病的安全有效药物。本研究旨在评估 LGZG 对 AD 进展的影响及其分子机制。将 C57BL/6 小鼠分为六组:正常小鼠、淀粉样前体蛋白/早老素 1(APP/PS1)小鼠(模型组)、阳性对照组(模型小鼠用多奈哌齐治疗)、高、中、低 LGZG 组(模型小鼠用 7g/kg/d、3.5g/kg/d 或 1.75g/kg/d LGZG 治疗)。水迷宫结果表明,与模型组相比,高、中 LGZG 组的逃避潜伏期和路径长度缩短,下降程度呈剂量依赖性。通过尼氏染色、普鲁士蓝染色和免疫荧光法分析六组海马切片。结果表明,LGZG 可恢复 AD 小鼠的形态异常,减轻铁沉积,GXP4 阳性细胞显著增加。通过生化试验测量 MDA、Fe2+和 GSH,结果表明与未经处理的 APP/PS1 模型相比,LGZG 可使 AD 模型中的 MDA、Fe2+和 GSH 水平正常化。小鼠接受的 LGZG 剂量越高,对这些分子水平的影响越强烈。Western blot 结果表明,LGZG 可影响 AD 模型海马中的 NeuN、AMPK、p53、SLC7A11 和 GPX4 水平,这些都是与 AMPK 通路相关的蛋白质。总之,LGZG 通过减轻氧化应激和铁死亡对 AD 具有神经保护作用,其作用机制与 AMPK 通路有关。

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