Curcuma longa L. extract and residue prevent Alzheimer's disease in mice by regulating microglia and TLR4/NF-κB signaling pathway.

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Zhihui Xu, Jianlin Li, Xiaotong Liu, Liaoyuan Liu, Weixiong Lin, Dongmei Sun, Yu Zeng
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Abstract

Background: Curcuma longa L. (CL) is renowned for its various health benefits and has shown potential in alleviating Alzheimer's disease (AD). The post-aqueous extraction residues (CLR) may retain valuable nutritional components. The research aimed to explore their chemical composition and neuroprotective mechanism against Aβ1-42-induced AD mice.

Methods: We employed UPLC-Q-Exactive/MS to characterize the chemical constituents of CL and CLR. An HPLC method was developed to quantify three predominant curcuminoids. To investigate their neuroprotective effects against Aβ1-42-induced AD mice, we assessed cognitive function using the Morris water maze and evaluated neuronal damage through histopathological examination. Molecular mechanisms were explored using immunofluorescence, ELISA, and qRT-PCR assays.

Results: The study unveiled 47 and 36 compounds in CL and CLR, respectively, and eight significant differential components. HPLC analysis revealed that CLR contained substantial curcuminoids. In Aβ1-42-induced AD mice, CL and CLR improved spatial learning and memory ability, ameliorated pathological alterations in the hippocampal region, and regulated overactivated microglia. Moreover, CL and CLR inhibited the TLR4/NF-κB inflammatory pathway.

Conclusion: CL and CLR exhibit the anti-AD effect by regulating microglia and suppressing the TLR4/NF-κB signaling pathway, which provides a scientific basis for future nutraceutical and pharmaceutical development.

姜黄提取物和残渣通过调节小胶质细胞和TLR4/NF-κB信号通路预防小鼠阿尔茨海默病。
背景:姜黄(Curcuma longa L., CL)因其多种健康益处而闻名,并已显示出缓解阿尔茨海默病(AD)的潜力。水后萃取残留物(CLR)可能保留有价值的营养成分。本研究旨在探讨其化学成分及对a β1-42诱导的AD小鼠的神经保护机制。方法:采用UPLC-Q-Exactive/MS方法对复方白藜芦醇和复方白藜芦醇进行化学成分表征。建立了高效液相色谱法测定三种主要姜黄素的含量。为了研究它们对a β1-42诱导的AD小鼠的神经保护作用,我们使用Morris水迷宫评估认知功能,并通过组织病理学检查评估神经元损伤。利用免疫荧光、ELISA和qRT-PCR分析探讨了分子机制。结果:研究发现CL和CLR中分别有47种和36种化合物,并有8种显著差异成分。高效液相色谱分析显示,姜黄素中含有大量姜黄素。在a β1-42诱导的AD小鼠中,CL和CLR可改善空间学习记忆能力,改善海马区病理改变,调节过度激活的小胶质细胞。此外,CL和CLR抑制TLR4/NF-κB炎症通路。结论:CLR和CLR通过调节小胶质细胞,抑制TLR4/NF-κB信号通路发挥抗ad作用,为今后营养品和药物开发提供科学依据。
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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
91
审稿时长
3 months
期刊介绍: JPP keeps pace with new research on how drug action may be optimized by new technologies, and attention is given to understanding and improving drug interactions in the body. At the same time, the journal maintains its established and well-respected core strengths in areas such as pharmaceutics and drug delivery, experimental and clinical pharmacology, biopharmaceutics and drug disposition, and drugs from natural sources. JPP publishes at least one special issue on a topical theme each year.
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