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韩国红参通过调节小鼠肠道微生物群减轻葡聚糖硫酸钠诱导的结肠炎。

Korean Red Ginseng alleviates dextran sodium sulfate-induced colitis through gut microbiota modulation in mice.

作者信息

Jeong Ji-Soo, Baek Ga-Hyeon, Kim Jeong-Won, Kim Jin-Hwa, Chung Eun-Hye, Ko Je-Won, Kwon Mi-Jin, Kim Sang-Kyu, Lee Seung-Ho, Kim Jun-Seob, Kim Tae-Won

机构信息

College of Veterinary Medicine (BK21 FOUR Program), Chungnam National University, Daejeon, Republic of Korea.

Department of Nano-Bioengineering, Incheon National University, Incheon, Republic of Korea.

出版信息

J Ginseng Res. 2024 Nov;48(6):581-591. doi: 10.1016/j.jgr.2024.08.001. Epub 2024 Aug 9.

Abstract

BACKGROUND

There is a growing interest in understanding the association between the gut microbiota and inflammatory bowel disease (IBD). Natural compounds, such as Korean Red Ginseng (KRG), show promise for IBD treatment because of their ability to influence gut microbiota. This study explored the effects of KRG on gut microbiota modulation and subsequent intestinal epithelial cell regeneration in an experimental colitis model.

METHOD

Using a mouse model of colitis induced by 2 % dextran sodium sulfate, the study administered 200 or 400 mg/kg/day of KRG to evaluate its biological effects. Colitis symptoms were assessed through body weight, disease activity index, colon length, and histological analysis. The microbial composition in the fecal was determined using 16S rRNA sequencing. To evaluate regeneration signals in the colon, western blotting and immunohistochemistry assays were conducted.

RESULT

Administration of KRG effectively mitigated colitis symptoms in mice, as indicated by histological examination showing alleviated epithelial damage and inflammation, along with increased mucus production. Microbiota analysis showed that KRG significantly altered microbial diversity, favoring beneficial taxa and suppressing harmful taxa. Moreover, ameliorated β-catenin/transcription factor-4 protein expression, a key signal associated with epithelial cell regeneration, was observed in the KRG treated groups, accompanied by improved intestinal linings.

CONCLUSION

These findings suggest that KRG exerts biological effects in colitis by modulating gut microbiota and creating a favorable intestinal environment, thereby reducing regenerative signals. Further research is warranted to elucidate the cellular and molecular mechanisms underlying the interaction of KRG with gut microbiota and pave the way for effective IBD therapies.

摘要

背景

人们对了解肠道微生物群与炎症性肠病(IBD)之间的关联越来越感兴趣。天然化合物,如韩国红参(KRG),因其影响肠道微生物群的能力而显示出治疗IBD的潜力。本研究在实验性结肠炎模型中探讨了KRG对肠道微生物群调节及随后肠上皮细胞再生的影响。

方法

使用2%葡聚糖硫酸钠诱导的小鼠结肠炎模型,该研究给予200或400mg/kg/天的KRG以评估其生物学效应。通过体重、疾病活动指数、结肠长度和组织学分析评估结肠炎症状。使用16S rRNA测序确定粪便中的微生物组成。为了评估结肠中的再生信号,进行了蛋白质印迹和免疫组织化学分析。

结果

组织学检查显示上皮损伤和炎症减轻,黏液分泌增加,表明给予KRG可有效减轻小鼠的结肠炎症状。微生物群分析表明,KRG显著改变了微生物多样性,有利于有益类群并抑制有害类群。此外,在KRG治疗组中观察到β-连环蛋白/转录因子-4蛋白表达改善,这是与上皮细胞再生相关的关键信号,同时肠壁得到改善。

结论

这些发现表明,KRG通过调节肠道微生物群和创造有利的肠道环境在结肠炎中发挥生物学作用,从而减少再生信号。有必要进一步研究以阐明KRG与肠道微生物群相互作用的细胞和分子机制,并为有效的IBD治疗铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe29/11584195/8240ed51c881/ga1.jpg

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