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(桑植)生物碱通过肠道微生物群和胰岛内2-甲氧基雌二醇生物合成改善胰腺β细胞功能。

(Sangzhi) Alkaloids Improve Pancreatic β-Cell Function Through Gut Microbial and Intra-Islet 2-Methoxyestradiol Biosynthesis.

作者信息

Wu Nan, Lu Lusi, Liu Yiming, He Sunyue, Xu Chunyi, Wu Ying, Zhao Yuchen, Lin Xihua, Zhang Wenjing, Zhou Jiaqiang

机构信息

Department of Endocrinology and Metabolism, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou 310058, China.

出版信息

Biomedicines. 2025 Aug 19;13(8):2013. doi: 10.3390/biomedicines13082013.

Abstract

: (Sangzhi) Alkaloids (SZ-A) are natural hypoglycemic compounds known to enhance insulin secretion. Given the emerging role of the gut microbiota in regulating β-cell function, in this study, we aimed to investigate whether SZ-A exert their beneficial effects through modulating the gut microbiota and its metabolites. : A diabetic mouse model was established using a high-fat diet and streptozotocin, followed by 20 weeks of SZ-A treatment. Gut microbiota and metabolites were profiled via 16S rRNA sequencing and liquid chromatography-mass spectrometry, respectively. Spearman's correlation analysis was used to explore associations between gut microbiota and metabolites. Single-cell RNA sequencing (scRNA-seq) was used to assess gene expression and signaling pathway changes in β cells. : Our results demonstrate that SZ-A alleviated hyperglycemia and increased islet numbers in T2DM mice. SZ-A treatment also reshaped the gut microbiota, notably enriching quantities of and , which may contribute to increasing levels of 2-methoxyestradiol (2-ME), a bioactive metabolite. Moreover, scRNA-seq revealed an increased proportion of COMT cells in the islets, suggesting that 2-ME may also be synthesized within the islets. In vitro, 2-ME suppressed HIF-1α signaling and promoted insulin secretion, indicating that 2-ME may act as a crucial mediator of the beneficial effects of SZ-A. : SZ-A improve β-cell function by increasing 2-ME levels via gut microbiota modulation and islet production, ultimately suppressing HIF-1α signaling and restoring β-cell homeostasis.

摘要

(桑植)生物碱(SZ-A)是已知的可增强胰岛素分泌的天然降血糖化合物。鉴于肠道微生物群在调节β细胞功能中日益重要的作用,在本研究中,我们旨在探究SZ-A是否通过调节肠道微生物群及其代谢产物发挥其有益作用。:使用高脂饮食和链脲佐菌素建立糖尿病小鼠模型,随后进行20周的SZ-A治疗。分别通过16S rRNA测序和液相色谱-质谱对肠道微生物群和代谢产物进行分析。采用Spearman相关性分析来探究肠道微生物群与代谢产物之间的关联。使用单细胞RNA测序(scRNA-seq)来评估β细胞中的基因表达和信号通路变化。:我们的结果表明,SZ-A可减轻2型糖尿病小鼠的高血糖并增加胰岛数量。SZ-A治疗还重塑了肠道微生物群,显著增加了[具体微生物名称1]和[具体微生物名称2]的数量,这可能有助于提高生物活性代谢产物2-甲氧基雌二醇(2-ME)的水平。此外,scRNA-seq显示胰岛中COMT细胞的比例增加,表明2-ME也可能在胰岛内合成。在体外,2-ME抑制HIF-1α信号传导并促进胰岛素分泌,表明2-ME可能是SZ-A有益作用的关键介质。:SZ-A通过调节肠道微生物群和胰岛生成来提高2-ME水平,最终抑制HIF-1α信号传导并恢复β细胞稳态,从而改善β细胞功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84e4/12383358/2daf35408055/biomedicines-13-02013-g001.jpg

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