Effects and mechanisms of Polygonati Rhizoma polysaccharide on potassium oxonate and hypoxanthine-induced hyperuricemia in mice

被引:5
作者
Zhang, Nanxin [1 ]
Zhang, Bichen [1 ]
Chen, Xiangjun [1 ]
Zhang, Yingqiong [1 ]
Wang, Yue [1 ]
Lu, Shuanghui [1 ]
Zhang, Hengbin [1 ]
Chen, Yujia [1 ]
Jiang, Huidi [1 ,2 ]
Zhou, Hui [1 ,2 ]
机构
[1] Zhejiang Univ, Inst Drug Metab & Pharmaceut Anal, Coll Pharmaceut Sci, Zhejiang Prov Key Lab Anticanc Drug Res, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Univ, Jinhua Inst, Jinhua, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Polysaccharide; Polygonati Rhizoma; Polygonatum sibiricum; Hyperuricemia; Nephroprotective; Mitochondrial damage; CHRONIC KIDNEY-DISEASE; URIC-ACID;
D O I
10.1016/j.ijbiomac.2024.135550
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hyperuricemia, a prevalent metabolic disturbance intricately linked to gout and chronic kidney disease (CKD), may be relieved by traditional Chinese medicine Polygonati Rhizoma. It is derived from the rhizomes of Polygonatum sibiricum, Polygonatum kingianum, and Polygonatum cyrtonema, which are rich in polysaccharides and are effective hyperuricemia alleviators. This study investigated the potential of Polygonatum sibiricum polysaccharide (PSP) in managing hyperuricemia. PSP (125, 250, and 500 mg/kg, i.g.) or allopurinol was administered to hyperuricemia mice treated with potassium oxonate and hypoxanthine for two weeks. PSP effectively decreased serum uric acid levels by inhibiting xanthine oxidase and adenosine deaminase activity and expression in the liver and modulating uric acid-related transporters (URAT1, OAT1, and OAT3) in the kidney. PSP lowered serum creatinine and blood urea nitrogen levels, alleviating hyperuricemia-induced renal tubular epithelialmesenchymal fibrosis. In vitro, PSP promoted mitochondrial biogenesis via the PGC-1 alpha/NRF1/TFAM pathway, suppressed reactive oxygen species production, and prevented cytochrome C and dynamin-related protein 1 dysregulation in HK-2 cells. Furthermore, PSPA (Mw 4.0 kDa) and PSPB (Mw 112.2 kDa) isolated from PSP exhibit different uric acid-lowering mechanisms. In conclusion, our findings highlight the therapeutic potential of PSP and its nephroprotective effects in hyperuricemia, thereby supporting its development as a therapeutic agent for hyperuricemia.
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页数:13
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