Polysaccharides from Alpinia oxyphylla fruit prevent hyperuricemia by inhibiting uric acid synthesis, modulating intestinal flora and reducing renal inflammation

• Published in: International journal of biological macromolecules Vol. 278; no. Pt 2; p. 134782
• Main Authors: Ren, Fei, Lin, Jinji, Zhu, Mengxu, Ma, Rui, Zhang, Ming, Chen, Weijun, Ma, Guobiao, Chen, Haiming, He, Rongrong, Chen, Wenxue
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.10.2024
• Subjects: Alpinia oxyphylla polysaccharide; Gut flora; Hyperuricemia; Metabolomics; Metabolomics; Hyperuricemia; Alpinia oxyphylla polysaccharide; Gut flora
• ISSN: 0141-8130; 1879-0003; 1879-0003
• DOI: 10.1016/j.ijbiomac.2024.134782

Hyperuricemia (HUA) is one of the most common chronic diseases today, with a prevalence exceeding 14 % in both the United States and China. Current clinical treatments for HUA focus on promoting uric acid (UA) excretion and inhibiting UA production, but often neglect the strain on the liver and kidneys. The fruit of Alpinia oxyphylla (A. oxyphylla) is known to improve renal function, regulate metabolism, and exhibit anti-inflammatory effects; however, its effectiveness and mechanisms in treating HUA are not well understood. In this study, HUA mice induced by potassium oxonate and adenine were treated with A. oxyphylla polysaccharide (AFP) for 21 days. The levels associated with HUA were quantified using assay kits to evaluate the impact of AFP on HUA. Serum metabolomics and 16S rRNA sequencing were used to investigate the mechanisms by which AFP ameliorates HUA. The results showed that AFP treatment reduced abnormal biochemical levels, including UA, blood urea nitrogen, and creatinine, in HUA mice. AFP inhibited UA synthesis by regulating pyrimidine metabolism and the metabolism of alanine, aspartate and glutamate, reduced kidney inflammation, and promoted UA excretion by regulating intestinal flora. Thus, AFP appears to be an effective agent for alleviating HUA symptoms. •AFP has an ameliorating effect on HUA.•AFP reduced UA, BUN, Cre and XOD levels in HUA mice.•AFP inhibited UA synthesis by regulating multiple metabolic pathways.•AFP alleviated renal inflammation by regulating the abundance of intestinal flora.