A galactoglucomannan from Termitomyces intermedius: Structural characterization, anti-obesity and anti-inflammatory activities

IF 9.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Mengyao WU , Kunzhui CHEN , Xiyin ZHENG , Yingbin SHEN , Tak-Ho LO , Xinquan YANG
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引用次数: 0

Abstract

Termitomyces mushrooms exhibit a wide range of beneficial properties, yet detailed structural characterization and exploration of their structure-activity relationships, particularly in the anti-obesity contexts, remain limited. A novel galactoglucomannan (TIP-1–1) was isolated from Termitomyces intermedius. Structural analysis showed TIP-1–1 is a 2.7 kDa polysaccharide mainly composed of glucose, galactose and mannose (mass ratio: 75.7: 10.7: 13.6). The backbone contained linear 1,6-linked β-Glcp, 1,3-linked β-Glcp, 1,6-linked α-Galp, and 1,3,6-linked α-Manp contained a branched structure that substituted primarily with 1,3,6-linked α-Manp and 1,3-linked β-Glcp residues. Functionally, TIP-1–1 mitigated HFD-induced obesity in mice by reducing body weight, fat mass, and improving glucose homeostasis and lipid profiles, with effects comparable to GLP-1. It suppressed pro-inflammatory cytokines such as NO, TNF-α, IL-6, IL-1β, leptin and restored adiponectin and IL-10 levels both in vivo and in vitro, suggesting anti-inflammatory mechanisms underlying its anti-obesity effects. In lipid metabolism studies, TIP-1–1 inhibited adipocyte lipogenesis by activating AMPK, suppressing the expression of ACC and FASN, and reducing triglyceride accumulation. Mechanistically, AMPK siRNA knockdown abolished these effects, confirming its central role in TIP-1–1-mediated suppression of de novo fatty acid synthesis. These findings established TIP-1–1 as a dual-acting anti-obesity agent with therapeutic potential via anti-inflammatory and AMPK/ACC/FASN lipogenic inhibition.
来自中间白蚁菌的半乳糖葡甘露聚糖:结构表征、抗肥胖和抗炎活性。
白蚁菌蘑菇具有广泛的有益特性,但详细的结构表征和对其结构-活性关系的探索,特别是在抗肥胖方面,仍然有限。从中间白蚁中分离到一种新的半乳糖葡甘露聚糖(TIP-1-1)。结构分析表明,TIP-1-1是一种2.7kDa的多糖,主要由葡萄糖、半乳糖和甘露糖组成,质量比为75.7:10.7:13.6。主链含有线性1,6-链β-Glcp, 1,3-链β-Glcp, 1,6-链α-Galp, 1,3,6-链α-Manp含有支链结构,主要取代1,3,6-链α-Manp和1,3-链β-Glcp残基。在功能上,TIP-1-1通过降低体重、脂肪量、改善葡萄糖稳态和脂质谱,减轻了hfd诱导的小鼠肥胖,其效果与GLP-1相当。在体内和体外均可抑制NO、TNF-α、IL-6、IL-1β、瘦素等促炎细胞因子,恢复脂联素和IL-10水平,提示其抗肥胖作用的抗炎机制。在脂质代谢研究中,TIP-1-1通过激活AMPK、抑制ACC和FASN的表达、减少甘油三酯的积累来抑制脂肪细胞的脂肪生成。从机制上讲,AMPK siRNA敲低消除了这些作用,证实了其在tip -1-1介导的从头脂肪酸合成抑制中的核心作用。这些发现证实了TIP-1-1是一种双作用的抗肥胖药物,具有抗炎和抑制AMPK/ACC/FASN增脂的治疗潜力。
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来源期刊
Pharmacological research
Pharmacological research 医学-药学
CiteScore
18.70
自引率
3.20%
发文量
491
审稿时长
8 days
期刊介绍: Pharmacological Research publishes cutting-edge articles in biomedical sciences to cover a broad range of topics that move the pharmacological field forward. Pharmacological research publishes articles on molecular, biochemical, translational, and clinical research (including clinical trials); it is proud of its rapid publication of accepted papers that comprises a dedicated, fast acceptance and publication track for high profile articles.
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