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辛烯基琥珀酸酐淀粉通过调节肠道微生物群和代谢减轻酒精性肝病

Octenyl Succinic Anhydride Starch Alleviates Alcoholic Liver Disease by Modulating Gut Microbiota and Metabolism.

作者信息

Liu Chang, Liu Tangqian, Ma Rongrong, Pan Xiaohua, Tian Yaoqi

机构信息

State Key Laboratory of Food Science and Resources, Jiangnan University, Wuxi 214122, China.

School of Food Science and Technology, Jiangnan University, Wuxi 214122, China.

出版信息

Nutrients. 2025 Aug 27;17(17):2779. doi: 10.3390/nu17172779.

Abstract

: Alcoholic liver disease (ALD) is intricately linked to gut microbiota dysbiosis and metabolic disturbances along the gut-liver axis. Octenyl succinic anhydride (OSA) starch escapes digestion in the small intestine and ferments in the colon, modulating gut microbiota and metabolism. This study explored the protective effects of OSA starch against ALD and elucidated the underlying gut microbiota-metabolite interactions. A chronic ethanol-fed mouse model was conducted to evaluate the protective effects of OSA starch against ALD, and multi-omics analyses integrating 16S rRNA sequencing, PICRUSt2 functional predictions, and metabolomics were used to reveal potential mechanism. : OSA starch supplementation in ALD mice significantly reduced liver fat accumulation, lowered the liver index to 4.11%, and restored serum transaminase levels closer to normal. Multi-omics analyses revealed that OSA starch enriched beneficial gut bacteria such as and . OSA starch also enhanced microbial metabolic functions, including pyruvate, butanoate, and propanoate metabolism. These shifts were accompanied by regulation of fecal and serum metabolites, including pyruvate, 2-hydroxybutanoic acid, and lactic acid. Structural equation modeling further confirmed that OSA starch ameliorates ALD via coordinated modulation of gut microbiota, microbial functions, metabolites, and serum markers. : OSA starch protects against alcoholic liver injury by remodeling the gut-liver metabolic network, presenting a promising dietary strategy for ALD.

摘要

酒精性肝病(ALD)与肠道微生物群失调以及沿肠-肝轴的代谢紊乱密切相关。辛烯基琥珀酸酐(OSA)淀粉在小肠中不被消化,在结肠中发酵,调节肠道微生物群和代谢。本研究探讨了OSA淀粉对ALD的保护作用,并阐明了潜在的肠道微生物群-代谢物相互作用。建立了慢性乙醇喂养小鼠模型来评估OSA淀粉对ALD的保护作用,并使用整合16S rRNA测序、PICRUSt2功能预测和代谢组学的多组学分析来揭示潜在机制。在ALD小鼠中补充OSA淀粉可显著减少肝脏脂肪堆积,将肝脏指数降至4.11%,并使血清转氨酶水平恢复到更接近正常的水平。多组学分析表明,OSA淀粉丰富了有益的肠道细菌,如 和 。OSA淀粉还增强了微生物代谢功能,包括丙酮酸、丁酸和丙酸代谢。这些变化伴随着粪便和血清代谢物的调节,包括丙酮酸、2-羟基丁酸和乳酸。结构方程模型进一步证实,OSA淀粉通过协调调节肠道微生物群、微生物功能、代谢物和血清标志物来改善ALD。OSA淀粉通过重塑肠-肝代谢网络来预防酒精性肝损伤,为ALD提供了一种有前景的饮食策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0962/12430434/086574a1a2e5/nutrients-17-02779-g001.jpg

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