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α-酮戊二酸通过增加乳杆菌丰度和通过 Wnt-Hippo 信号调节干细胞增殖来减轻小鼠结肠炎。

Alpha-Ketoglutarate Attenuates Colitis in Mice by Increasing Lactobacillus Abundance and Regulating Stem Cell Proliferation via Wnt-Hippo Signaling.

机构信息

State Key Laboratory of Animal Nutrition, China Agricultural University, Beijing, 100193, China.

Beijing Advanced Innovation Center for Food Nutrition and Human Health, China Agricultural University, Beijing, 100193, China.

出版信息

Mol Nutr Food Res. 2022 May;66(10):e2100955. doi: 10.1002/mnfr.202100955. Epub 2022 Mar 20.

DOI:10.1002/mnfr.202100955
PMID:35220672
Abstract

SCOPE

Inflammatory bowel disease is an inflammatory gastrointestinal disorder associated with intestinal barrier damage, cell proliferation disorder, and dysbiosis of the intestinal microbiota. It remains unknown whether alpha-ketoglutarate (α-KG) can alleviate colitis in mice.

METHODS AND RESULTS

Six-week-old male C57BL/6 mice supplemented with or without 0.5% α-KG (delivered in the form of sodium salt) are subjected to drinking water or 2.5% DSS to induce colitis. The results show that α-KG administration is attenuated the severity of colitis, as is indicated by reduced body-weight loss, colon shortening and colonic hyperplasia, and repressed proinflammatory cytokine secretion in DSS-challenged mice. Additionally, DSS-induced increases in malondialdehyde (MDA) and hydrogen peroxide (H O ), and decreases in glutathione (GSH) levels are attenuated by α-KG administration. Further study shows that the protective effect of α-KG is associated with restoring gut barrier integrity by enhancing the expression of tight junction proteins, increasing Lactobacillus levels, and regulating gut hyperplasia by the Wnt-Hippo signaling pathway in DSS-induced colitis.

CONCLUSION

Collectively, the data provided herein demonstrate that α-KG administration is attenuated mucosal inflammation, barrier dysfunction, and gut microflora dysbiosis. This beneficial effect is associated with increased Lactobacillus levels and regulated colon hyperplasia by the Wnt-Hippo signaling pathway.

摘要

范围

炎症性肠病是一种与肠道屏障损伤、细胞增殖紊乱和肠道微生物群落失调相关的炎症性胃肠道疾病。目前尚不清楚α-酮戊二酸(α-KG)是否可以缓解小鼠的结肠炎。

方法和结果

给 6 周龄雄性 C57BL/6 小鼠补充或不补充 0.5%α-KG(以钠盐的形式提供),并让其饮用或摄入 2.5% DSS 以诱导结肠炎。结果表明,α-KG 给药可减轻结肠炎的严重程度,表现在体重减轻、结肠缩短和结肠增生减轻,以及抑制 DSS 挑战小鼠的促炎细胞因子分泌减少。此外,α-KG 给药可减轻 DSS 诱导的丙二醛(MDA)和过氧化氢(H2O2)增加以及谷胱甘肽(GSH)水平降低。进一步的研究表明,α-KG 的保护作用与通过增强紧密连接蛋白的表达、增加乳杆菌水平以及通过 Wnt-Hippo 信号通路调节肠道增生来恢复肠道屏障完整性有关。

结论

总之,本文提供的数据表明,α-KG 给药可减轻黏膜炎症、屏障功能障碍和肠道微生物群落失调。这种有益作用与乳杆菌水平的增加以及 Wnt-Hippo 信号通路调节结肠增生有关。

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