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黄酒中高度支化的 α-D-葡聚糖的结构解析及其通过调节肠道微生物群和修复肠道屏障发挥的保肝活性。

Structural elucidation of a highly branched α-D-glucan from Huangjiu and its hepatoprotective activity via gut microbiome regulation and intestinal barrier repairment.

机构信息

National Engineering Research Center of Cereal Fermentation and Food Biomanufacturing, School of Food Science and Technology, Jiangnan University, Wuxi 214122, Jiangsu, China.

National Engineering Research Center of Cereal Fermentation and Food Biomanufacturing, School of Food Science and Technology, Jiangnan University, Wuxi 214122, Jiangsu, China; Jiangnan University (Shaoxing) Industrial Technology Research Institute, Shaoxing 312000, Zhejiang, China; Jiangsu Provincial Engineering Research Center for Bioactive Product Processing, Jiangnan University, Wuxi 214122, Jiangsu, China.

出版信息

Carbohydr Polym. 2024 Jan 15;324:121423. doi: 10.1016/j.carbpol.2023.121423. Epub 2023 Sep 21.

DOI:10.1016/j.carbpol.2023.121423
PMID:37985032
Abstract

Polysaccharides in Huangjiu, a traditional fermented food, are expected to be potentially effective ingredients in protecting against alcoholic liver disease (ALD). Elucidating their precise structural and functional characteristics is essential for in-depth understanding of structure-activity relationships of hepatoprotective polysaccharides. Herein, a major polysaccharide component HJPS1-2 was purified from Huangjiu with an average molecular weight of 3.49 kDa. Structural analyses inferred that HJPS1-2 backbone was composed of (1 → 4)-linked α-D-Glcp and a single α(1 → 6)-D-Glcp-α(1 → 6)-D-Glcp branched unit for every three α(1 → 4)-D-Glcp. An ALD mouse model was further established to clarify the underlying effect of HJPS1-2 on ALD alleviation. Biochemical detection and histopathological assessment revealed that HJPS1-2 intervention remarkably improved ethanol-induced hepatic dysfunction and steatosis. HJPS1-2 treatment ameliorated gut microbiota dysbiosis of ALD mice in a dose-dependent manner, mainly manifested as restoration of microbial diversities, community structure and bacterial interaction patterns. Compared with ethanol group, the strikingly elevated intestinal short-chain fatty acids' levels and enhanced intestinal barrier function after HJPS1-2 intake might contribute to reduced serum and liver lipopolysaccharide levels and subsequently suppressed release of hepatic inflammatory cytokines, thus mitigating ALD. Collectively, this research supports the potential of food-derived polysaccharides to hinder the early formation and progression of ALD through maintaining intestinal homeostasis.

摘要

黄酒中的多糖有望成为预防酒精性肝病 (ALD) 的潜在有效成分。阐明其确切的结构和功能特征对于深入了解具有保肝作用的多糖的结构-活性关系至关重要。在此,从黄酒中分离得到一种主要的多糖成分 HJPS1-2,其平均分子量为 3.49 kDa。结构分析推断,HJPS1-2 骨架由(1→4)-连接的 α-D-Glcp 和单一的 α(1→6)-D-Glcp-α(1→6)-D-Glcp 分支单元组成,每三个 α(1→4)-D-Glcp 就有一个。进一步建立了 ALD 小鼠模型,以阐明 HJPS1-2 对 ALD 缓解的潜在作用。生化检测和组织病理学评估表明,HJPS1-2 干预可显著改善乙醇诱导的肝功能障碍和脂肪变性。HJPS1-2 处理以剂量依赖的方式改善了 ALD 小鼠的肠道微生物失调,主要表现为微生物多样性、群落结构和细菌相互作用模式的恢复。与乙醇组相比,HJPS1-2 摄入后肠道短链脂肪酸水平显著升高,肠道屏障功能增强,可能导致血清和肝脏内毒素水平降低,随后抑制肝脏炎症细胞因子的释放,从而减轻 ALD。总之,这项研究支持了通过维持肠道内环境稳态,从食物中提取的多糖可以抑制 ALD 的早期形成和进展。

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