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熟地黄多糖通过调节微生物群增强小鼠肠道免疫力。

Rehmannia glutinosa polysaccharides enhance intestinal immunity of mice through regulating the microbiota.

作者信息

Yu Lin, Lin Fangzhu, Yu Yaming, Deng Xiangwen, Shi Xiaofeng, Lu Xuanqi, Lu Yu, Wang Deyun

机构信息

Institute of Traditional Chinese Veterinary Medicine, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China.

Institute of Traditional Chinese Veterinary Medicine, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China; Institute of Veterinary Immunology & Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China.

出版信息

Int J Biol Macromol. 2024 Dec;283(Pt 3):137878. doi: 10.1016/j.ijbiomac.2024.137878. Epub 2024 Nov 19.

DOI:10.1016/j.ijbiomac.2024.137878
PMID:39571844
Abstract

The Rehmannia glutinosa polysaccharides (RGP) have various benefits such as enhancing immune cell activity, decreasing oxidative stress and delaying or inhibiting tumor occurrence. Although much research has been directed at understanding the role of RGP, its influence on gut immunity is largely understudied. Here, we aimed to dissect the immune-regulating effects of RGP in the mice intestines. In vivo experiments involving the oral administration of RGP to mice at dosages of 100, 200, and 400 mg/kg over seven consecutive days revealed that RGP therapy significantly increased the percentages of CD3 T lymphocytes and CD19 B lymphocytes in intestines and improved the integrity of the mucosal barrier. Moreover, RGP modified the gut microbiota composition by enhancing the abundance of beneficial bacteria like Lactobacillus and Akkermansia. Fecal microbiota transplantation (FMT) experiments further revealed that RGP modulated the host's intestinal immunological function by altering the gut microbiota composition. These findings indicate that RGP may control the immunological function of the intestines.

摘要

地黄多糖(RGP)具有多种益处,如增强免疫细胞活性、降低氧化应激以及延缓或抑制肿瘤发生。尽管已有许多研究致力于了解RGP的作用,但其对肠道免疫的影响在很大程度上仍未得到充分研究。在此,我们旨在剖析RGP在小鼠肠道中的免疫调节作用。连续七天以100、200和400mg/kg的剂量给小鼠口服RGP的体内实验表明,RGP治疗显著提高了肠道中CD3 T淋巴细胞和CD19 B淋巴细胞的百分比,并改善了黏膜屏障的完整性。此外,RGP通过增加有益细菌如乳酸杆菌和阿克曼氏菌的丰度来改变肠道微生物群组成。粪便微生物群移植(FMT)实验进一步表明,RGP通过改变肠道微生物群组成来调节宿主的肠道免疫功能。这些发现表明,RGP可能控制肠道的免疫功能。

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