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龙生蛭胶囊通过减轻神经元氧化应激和炎症来减轻APP/PS1双转基因小鼠的阿尔茨海默样病理变化。

LongShengZhi Capsule Attenuates Alzheimer-Like Pathology in APP/PS1 Double Transgenic Mice by Reducing Neuronal Oxidative Stress and Inflammation.

作者信息

Yin Zequn, Wang Xuerui, Zheng Shihong, Cao Peichang, Chen Yuanli, Yu Maoyun, Liao Chenzhong, Zhang Zhongyuan, Han Jihong, Duan Yajun, Yang Xiaoxiao, Zhang Shuang

机构信息

Key Laboratory of Metabolism and Regulation for Major Diseases of Anhui Higher Education Institutes, College of Food and Biological Engineering, Hefei University of Technology, Hefei, China.

School of Biological and Pharmaceutical Engineering, West Anhui University, Lu'an, China.

出版信息

Front Aging Neurosci. 2020 Nov 23;12:582455. doi: 10.3389/fnagi.2020.582455. eCollection 2020.

Abstract

Alzheimer's disease (AD) is the most common form of dementia in the elderly. It may be caused by oxidative stress, inflammation, and cerebrovascular dysfunctions in the brain. LongShengZhi Capsule (LSZ), a traditional Chinese medicine, has been approved by the China Food and Drug Administration for treatment of patients with cardiovascular/cerebrovascular disease. LSZ contains several neuroprotective ingredients, including , and . In this study, we aimed to determine the effect of LSZ on the AD process. Double transgenic mice expressing the amyloid-β precursor protein and mutant human presenilin 1 (APP/PS1) to model AD were treated with LSZ for 7 months starting at 2 months of age. LSZ significantly improved the cognition of the mice without adverse effects, indicating its high degree of safety and efficacy after a long-term treatment. LSZ reduced AD biomarker Aβ plaque accumulation by inhibiting β-secretase and γ-secretase gene expression. LSZ also reduced p-Tau expression, cell death, and inflammation in the brain. Consistently, , LSZ ethanol extract enhanced neuronal viability by reducing L-glutamic acid-induced oxidative stress and inflammation in HT-22 cells. LSZ exerted antioxidative effects by enhancing superoxide dismutase and glutathione peroxidase expression, reduced Aβ accumulation by inhibiting β-secretase and γ-secretase mRNA expression, and decreased p-Tau level by inhibiting NF-κB-mediated inflammation. It also demonstrated neuroprotective effects by regulating the Fas cell surface death receptor/B-cell lymphoma 2/p53 pathway. Taken together, our study demonstrates the antioxidative stress, anti-inflammatory, and neuroprotective effects of LSZ in the AD-like pathological process and suggests it could be a potential medicine for AD treatment.

摘要

阿尔茨海默病(AD)是老年人中最常见的痴呆形式。它可能由大脑中的氧化应激、炎症和脑血管功能障碍引起。中药龙生蛭胶囊(LSZ)已获中国食品药品监督管理总局批准用于治疗心血管/脑血管疾病患者。LSZ含有多种神经保护成分,包括 ,以及 。在本研究中,我们旨在确定LSZ对AD进程的影响。从2月龄开始,对表达淀粉样前体蛋白和突变型人类早老素1(APP/PS1)以模拟AD的双转基因小鼠进行为期7个月的LSZ治疗。LSZ显著改善了小鼠的认知能力且无不良反应,表明其在长期治疗后具有高度的安全性和有效性。LSZ通过抑制β-分泌酶和γ-分泌酶基因表达减少了AD生物标志物Aβ斑块的积累。LSZ还降低了大脑中的p-Tau表达、细胞死亡和炎症。同样, ,LSZ乙醇提取物通过减轻L-谷氨酸诱导的HT-22细胞氧化应激和炎症增强了神经元活力。LSZ通过增强超氧化物歧化酶和谷胱甘肽过氧化物酶的表达发挥抗氧化作用,通过抑制β-分泌酶和γ-分泌酶mRNA表达减少Aβ积累,并通过抑制NF-κB介导的炎症降低p-Tau水平。它还通过调节Fas细胞表面死亡受体/B细胞淋巴瘤2/p53途径显示出神经保护作用。综上所述,我们的研究证明了LSZ在AD样病理过程中的抗氧化应激、抗炎和神经保护作用,并表明它可能是一种治疗AD的潜在药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afe2/7719723/b8076e14b27e/fnagi-12-582455-g001.jpg

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