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核黄素强化豆浆可缓解 B 族维生素耗竭-补充小鼠的氧化应激介导的肝损伤、肠道炎症和肠道微生物群改变。

Riboflavin Bioenriched Soymilk Alleviates Oxidative Stress Mediated Liver Injury, Intestinal Inflammation, and Gut Microbiota Modification in B Depletion-Repletion Mice.

机构信息

School of Food and Biological Engineering, Hefei University of Technology, Hefei 230009, People's Republic of China.

School of Biological Science and Engineering, Collaborative Innovation Center for Food Production and Safety, North Minzu University, Yinchuan 750021, People's Republic of China.

出版信息

J Agric Food Chem. 2022 Mar 30;70(12):3818-3831. doi: 10.1021/acs.jafc.2c00117. Epub 2022 Mar 18.

Abstract

Epidemiological evidence emphasizes that ariboflavinosis can lead to oxidative stress, which in turn may mediate the initiation and progression of liver injury and intestinal inflammation. Although vitamin B has gained worldwide attention for its antioxidant defense, the relationship between B status, oxidative stress, inflammatory response, and intestinal homeostasis remains indistinct. Herein, we developed a B depletion-repletion BALB/c mice model to investigate the ameliorative effects of B bioenriched fermented soymilk (BFS) on ariboflavinosis, accompanied by oxidative stress, inflammation, and gut microbiota modulation in response to B deficiency. results revealed that the phenotypic ariboflavinosis symptoms, growth rate, EGRAC status, and hepatic function reverted to normal after BFS supplementation. BFS significantly elevated CAT, SOD, T-AOC, and compromised MDA levels in the serum, simultaneously up-regulated Nrf2, CAT, and SOD2, and down-regulated Keap1 gene in the colon. The histopathological characteristics revealed significant alleviation in the liver and intestinal inflammation, confirmed by the downregulation of inflammatory (IL-1β and IL-6) and nuclear transcription (NF-κB) factors after BFS supplementation. BFS also increased the abundance and diversity of gut microbiota, increased the relative abundance of and , as well as decreased , , , and in strong conjunction with antioxidant, anti-inflammatory properties, and gut homeostasis along with the remarkable increase in cecal SCFAs content. We hereby reveal that BFS can effectively alleviate deleterious ariboflavinosis associated with oxidative stress mediated liver injury, chronic intestinal inflammation, and gut dysbiosis in the B depletion-repletion mice model activation of the Nrf2 signaling pathway.

摘要

流行病学证据强调,核黄素缺乏症可导致氧化应激,而氧化应激反过来可能介导肝损伤和肠道炎症的发生和进展。尽管维生素 B 因其抗氧化防御作用而受到全球关注,但 B 状态、氧化应激、炎症反应和肠道内稳态之间的关系仍不清楚。在此,我们构建了 BALB/c 小鼠的 B 耗竭-补充模型,以研究 B 生物强化发酵豆浆(BFS)对核黄素缺乏症的改善作用,同时还研究了 B 缺乏对氧化应激、炎症和肠道微生物群调节的影响。结果表明,补充 BFS 可使核黄素缺乏症的表型症状、生长速度、EGRAC 状态和肝功能恢复正常。BFS 显著提高了血清中的 CAT、SOD、T-AOC 水平,并降低了 MDA 水平,同时上调了结肠中的 Nrf2、CAT 和 SOD2,下调了 Keap1 基因。组织病理学特征显示,肝脏和肠道炎症明显缓解,补充 BFS 后炎症(IL-1β 和 IL-6)和核转录(NF-κB)因子下调证实了这一点。BFS 还增加了肠道微生物群的丰富度和多样性,增加了 的相对丰度,并降低了 、 、 、 和 的相对丰度,这与抗氧化、抗炎特性以及肠道内稳态有关,同时还显著增加了盲肠中的 SCFAs 含量。我们揭示了 BFS 可以有效缓解 B 耗竭-补充小鼠模型中与氧化应激介导的肝损伤、慢性肠道炎症和肠道菌群失调相关的有害核黄素缺乏症,其作用机制可能与 Nrf2 信号通路的激活有关。

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