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

• Published in: Foods 2024-09, Vol.13 (18), p.2994
• Main Authors: Zhou, Qiaoyi, Gao, Jinjing, Sun, Xueyan, Du, Junyuan, Wu, Zhiyi, Liang, Dongxia, Ling, Caijin, Fang, Binghu
• Format: Article
• Language: English
• Subjects: Agricultural commodities; Atrophy; Body weight; Cecum; Cyclophosphamide; Enzymes; Feces; Flora; Food composition; Gene sequencing; gut microbiota flora; immune regulation; Immune system; Immunoglobulins; Immunomodulation; Immunoregulation; Immunosuppression; Immunotherapy; Interleukins; Intestinal microflora; Leaves; Metabolic disorders; Metabolites; metabolomic; Metabolomics; Microbiota; Microbiota (Symbiotic organisms); Microorganisms; Natural & organic foods; Negative ions; Nitric oxide; Nitric-oxide synthase; Plasma levels; Polysaccharides; Positive ions; rRNA 16S; Saccharides; Spleen; Tea; tea polysaccharide; Thymus gland; Tryptophan; Tumor necrosis factor; Tumor necrosis factor-TNF
• ISSN: 2304-8158; 2304-8158
• DOI: 10.3390/foods13182994

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.