Inhibition of RAGE-mediated inflammatory signaling by Boletus edulis Bull: Fr. Polysaccharide alleviates lipotoxicity-induced metabolic dysfunction.

IF 5.6 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Meimei Zhao, Ziteng Yu, Xinyi Zhao, Ruijiao Zhu, Mengcong Li, Lu Yu, Ziwei Song, Jiangwei Lv
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引用次数: 0

Abstract

Lipotoxicity is increasingly recognized as a potential cause of metabolic syndrome, yet effective treatments are still lacking. Boletus edulis (B. edulis) Bull: Fr., is a classical mushroom used in traditional Chinese medicine. Polysaccharides, its primary pharmacological components, are widely known to offer various health benefits, but their anti-lipotoxicity properties remain poorly understood. This study aimed to investigate a natural B. edulis Bull: Fr. polysaccharide (BP) for its effectiveness and underlying molecular mechanisms in mitigating hepatic lipotoxicity. In vitro, BP enhanced glucose uptake and reduced lipid accumulation and oxidative stress in Oleic acid (OA)-treated LO2 cells. It downregulated receptor for advanced glycation end-products (RAGE) expression, inhibited mitogen-activated protein kinase (MAPK) activation, and normalized key proteins involved in glucose and lipid metabolism, thereby alleviating OA-induced lipotoxicity. In vivo, high-fat diet-fed mice injected with BP exhibited similar metabolic improvements, with the reversal of RAGE/reactive oxygen species (ROS)/MAPK signaling in liver tissue, further supporting the molecular mechanisms observed in vitro in modulating lipotoxicity. Collectively, these findings underscore BP as a potent bioactive preparation with significant pharmacological potential in alleviating hepatic lipotoxicity.

牛肉芽孢杆菌多糖抑制rage介导的炎症信号通路减轻脂毒诱导的代谢功能障碍。
脂肪毒性越来越被认为是代谢综合征的潜在原因,但仍然缺乏有效的治疗方法。肉芽孢杆菌(Boletus edulis)牛:属,是一种经典的中药食用菌。多糖,其主要药理成分,众所周知,提供各种健康益处,但其抗脂肪毒性仍知之甚少。本研究旨在探讨天然牛蒡多糖(BP)减轻肝脏脂肪毒性的有效性及其潜在的分子机制。在体外,BP增加了油酸(OA)处理的LO2细胞的葡萄糖摄取,减少了脂质积累和氧化应激。下调晚期糖基化终产物受体(RAGE)表达,抑制丝裂原活化蛋白激酶(MAPK)活化,使参与糖脂代谢的关键蛋白正常化,从而减轻oa诱导的脂肪毒性。在体内,注射BP的高脂饮食小鼠表现出类似的代谢改善,肝脏组织中RAGE/活性氧(ROS)/MAPK信号的逆转,进一步支持了体外观察到的调节脂肪毒性的分子机制。总的来说,这些发现强调了BP作为一种有效的生物活性制剂,在减轻肝脏脂肪毒性方面具有显著的药理潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biochemical pharmacology
Biochemical pharmacology 医学-药学
CiteScore
10.30
自引率
1.70%
发文量
420
审稿时长
17 days
期刊介绍: Biochemical Pharmacology publishes original research findings, Commentaries and review articles related to the elucidation of cellular and tissue function(s) at the biochemical and molecular levels, the modification of cellular phenotype(s) by genetic, transcriptional/translational or drug/compound-induced modifications, as well as the pharmacodynamics and pharmacokinetics of xenobiotics and drugs, the latter including both small molecules and biologics. The journal''s target audience includes scientists engaged in the identification and study of the mechanisms of action of xenobiotics, biologics and drugs and in the drug discovery and development process. All areas of cellular biology and cellular, tissue/organ and whole animal pharmacology fall within the scope of the journal. Drug classes covered include anti-infectives, anti-inflammatory agents, chemotherapeutics, cardiovascular, endocrinological, immunological, metabolic, neurological and psychiatric drugs, as well as research on drug metabolism and kinetics. While medicinal chemistry is a topic of complimentary interest, manuscripts in this area must contain sufficient biological data to characterize pharmacologically the compounds reported. Submissions describing work focused predominately on chemical synthesis and molecular modeling will not be considered for review. While particular emphasis is placed on reporting the results of molecular and biochemical studies, research involving the use of tissue and animal models of human pathophysiology and toxicology is of interest to the extent that it helps define drug mechanisms of action, safety and efficacy.
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