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基于肠道菌群和代谢组学研究茶叶多糖对环磷酰胺诱导免疫抑制小鼠的免疫调节机制

Immunomodulatory Mechanisms of Tea Leaf Polysaccharide in Mice with Cyclophosphamide-Induced Immunosuppression Based on Gut Flora and Metabolomics.

作者信息

Zhou Qiaoyi, Gao Jinjing, Sun Xueyan, Du Junyuan, Wu Zhiyi, Liang Dongxia, Ling Caijin, Fang Binghu

机构信息

Guangdong Provincial Key Laboratory of Tea Plant Resources Innovation and Utilization, Tea Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, China.

National Reference Laboratory of Veterinary Drug Residues, College of Veterinary Medicine, South China Agricultural University, Guangzhou 510640, China.

出版信息

Foods. 2024 Sep 21;13(18):2994. doi: 10.3390/foods13182994.

DOI:10.3390/foods13182994
PMID:39335922
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11431025/
Abstract

Tea polysaccharides (TPSs) are receiving increasing attention because of their diverse pharmacological and biological activities. Here, we explored the immunoregulatory mechanisms of TPSs from fresh tea leaves in a mouse model of cyclophosphamide (CTX)-induced immunosuppression in terms of gut microbiota and metabolites. We observed that TPSs significantly increased the body weight and alleviated CTX-induced thymus atrophy in the immunosuppressed mice; they also increased the plasma levels of immunoglobulins A and M, interleukin (IL) 1β, IL-6, inducible nitric oxide synthase, and tumor necrosis factor α. Furthermore, we conducted 16S rDNA sequencing of cecal contents, resulting in the acquisition of 5008 high-quality bacterial 16S rDNA gene reads from the sequencing of mouse fecal samples. By analyzing the data, we found that TPSs regulated the gut microbiota structure and diversity and alleviated the CTX-induced dysregulation of gut microbiota. The colonic contents of mice were subjected to analysis using the UPLC-Q-TOF/MS/MS technique for the purpose of untargeted metabolomics. In the course of our metabolite identification analysis, we identified a total of 2685 metabolites in positive ion mode and 1655 metabolites in negative ion mode. The analysis of these metabolites indicated that TPSs improved CTX-induced metabolic disorders by regulating the levels of metabolites related to tryptophan, arginine, and proline metabolism. In conclusion, TPSs can alleviate CTX-induced immunosuppression by regulating the structural composition of gut microbiota, indicating the applicability of TPSs as novel innate immune modulators in health foods or medicines.

摘要

茶多糖(TPSs)因其多样的药理和生物学活性而受到越来越多的关注。在此,我们从小鼠肠道微生物群和代谢产物的角度,探讨了新鲜茶叶中TPSs在环磷酰胺(CTX)诱导的免疫抑制小鼠模型中的免疫调节机制。我们观察到,TPSs显著增加了免疫抑制小鼠的体重,并减轻了CTX诱导的胸腺萎缩;它们还提高了免疫球蛋白A和M、白细胞介素(IL)-1β、IL-6、诱导型一氧化氮合酶和肿瘤坏死因子α的血浆水平。此外,我们对盲肠内容物进行了16S rDNA测序,从小鼠粪便样本测序中获得了5008条高质量细菌16S rDNA基因读数。通过分析数据,我们发现TPSs调节了肠道微生物群的结构和多样性,并减轻了CTX诱导的肠道微生物群失调。为了进行非靶向代谢组学分析,我们使用超高效液相色谱-四极杆飞行时间串联质谱(UPLC-Q-TOF/MS/MS)技术对小鼠结肠内容物进行了分析。在代谢物鉴定分析过程中,我们在正离子模式下共鉴定出2685种代谢物,在负离子模式下鉴定出1655种代谢物。对这些代谢物的分析表明,TPSs通过调节与色氨酸、精氨酸和脯氨酸代谢相关的代谢物水平,改善了CTX诱导的代谢紊乱。总之,TPSs可以通过调节肠道微生物群的结构组成来减轻CTX诱导的免疫抑制,这表明TPSs作为新型天然免疫调节剂在保健食品或药品中的适用性。

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