分裂藻微藻脂肪酸对酒精性肝病的保护作用:网络药理学和体内研究

IF 1.6 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS Assay and drug development technologies Pub Date : 2025-01-16 DOI:10.1089/adt.2024.106
Cailin Luo, Li Tian, Yangmin Wen, Zhihua Zheng
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引用次数: 0

摘要

本研究旨在通过网络药理学和体内分析,阐明分裂藻微藻脂肪酸(MFA)抗酒精性肝病(ALD)的保肝机制。采用网络药理学和分子对接方法预测MFA治疗ALD的潜在机制。为了证实这些预测,使用急性酒精性肝损伤小鼠模型来评估MFA对血清丙氨酸转氨酶(ALT)、碱性磷酸酶(ALP)、天冬氨酸转氨酶(AST)、总蛋白(TP)和白蛋白(ALB)水平的影响。此外,观察肝组织病理学及磷脂酰肌醇3激酶(PI3K)和蛋白激酶B (AKT)蛋白的表达水平。在MFA中发现了7种有效成分和53个潜在靶点(包括7个核心靶点)。京都基因和基因组百科全书通路分析表明,这7个核心靶点涉及多种生物学通路,特别是与癌症、病毒感染和PI3K/AKT信号通路相关的生物学通路。此外,分子对接研究表明,MFA中的二十二碳六烯酸和二十二碳五烯酸对这7个关键靶点具有很强的结合亲和力。动物实验表明,MFA可显著降低急性酒精性肝损伤小鼠的AST、ALT和ALP水平,同时升高ALB和TP水平。此外,MFA改善肝脏组织病理,显著下调肝脏中PI3K和AKT蛋白的表达。这些结果表明MFA可能通过靶向多种途径具有治疗ALD的潜力,其机制可能涉及抑制PI3K/AKT信号通路。
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Protective Effects of Schizochytrium Microalgal Fatty Acids on Alcoholic Liver Disease: A Network Pharmacology and In Vivo Study.

This study aimed to elucidate the hepatoprotective mechanisms of microalgal fatty acids (MFA) from Schizochytrium against alcoholic liver disease (ALD) through network pharmacology and in vivo analysis. Network pharmacology and molecular docking methodologies were employed to predict the potential mechanisms of MFA against ALD. To substantiate these predictions, an acute alcoholic liver injury mouse model was utilized to assess the impact of MFA on serum levels of alanine aminotransferase (ALT), alkaline phosphatase (ALP), aspartate aminotransferase (AST), total protein (TP), and albumin (ALB). Additionally, liver histopathology and the expression levels of phosphatidylinositol 3 kinase (PI3K) and protein kinase B (AKT) protein were evaluated. Seven active ingredients and 53 potential targets (including 7 core targets) for ALD treatment were identified in MFA. Kyoto Encyclopedia of Genes and Genomes pathway analyses indicated that these seven core targets are implicated in various biological pathways, notably those associated with cancer, viral infections, and the PI3K/AKT signaling pathway. Furthermore, molecular docking studies demonstrated that docosahexaenoic acid and docosapentaenoic acid in MFA exhibited strong binding affinity for these seven crucial targets. Animal experiments demonstrated that administration of MFA significantly decreased the levels of AST, ALT, and ALP, while increasing the levels of ALB and TP in mice with acute alcoholic liver injury. Moreover, MFA ameliorated liver tissue pathology and markedly down-regulated the expression of PI3K and AKT proteins in the liver. These results suggest that MFA may possess therapeutic potential for ALD by targeting multiple pathways, with its mechanisms likely involving the inhibition of the PI3K/AKT signaling pathway.

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来源期刊
Assay and drug development technologies
Assay and drug development technologies 医学-生化研究方法
CiteScore
3.60
自引率
0.00%
发文量
33
审稿时长
>12 weeks
期刊介绍: ASSAY and Drug Development Technologies provides access to novel techniques and robust tools that enable critical advances in early-stage screening. This research published in the Journal leads to important therapeutics and platforms for drug discovery and development. This reputable peer-reviewed journal features original papers application-oriented technology reviews, topical issues on novel and burgeoning areas of research, and reports in methodology and technology application. ASSAY and Drug Development Technologies coverage includes: -Assay design, target development, and high-throughput technologies- Hit to Lead optimization and medicinal chemistry through preclinical candidate selection- Lab automation, sample management, bioinformatics, data mining, virtual screening, and data analysis- Approaches to assays configured for gene families, inherited, and infectious diseases- Assays and strategies for adapting model organisms to drug discovery- The use of stem cells as models of disease- Translation of phenotypic outputs to target identification- Exploration and mechanistic studies of the technical basis for assay and screening artifacts
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