MAPK/ERK通路
高尿酸血症
p38丝裂原活化蛋白激酶
活性氧
氧化应激
医学
药理学
代谢物
化学
尿酸
信号转导
生物化学
作者
Qingqing Han,Nan Chen,Kun Peng,Miaofen Wang,Mo Chen,Nilufar Z. Mamadalieva,Yuhong Zhang,Chao Liu,Qidong Ren
标识
DOI:10.1021/acs.jafc.5c09146
摘要
Hyperuricemia (HUA) is a prevalent metabolic disorder, with limited therapeutic options. This study investigated the effects and mechanisms of urolithin C (UroC), a gut-microbiota-derived bioactive metabolite from ellagitannin-rich foods, in the management of HUA. In HUA mice, UroC significantly reduced serum uric acid (SUA) levels, outperforming its analogs, UroA and UroB. UFLC-MS/MS identified free UroC as the primary active form in vivo. Mechanistically, UroC alleviated HUA by enhancing renal UA excretion, while concurrently ameliorating renal oxidative stress and fibrosis. Moreover, UroC inhibited UA-induced p38/ERK MAPK activation by reducing the level of reactive oxygen species (ROS) production. Rescue experiments further confirmed that UroC improved the expression of renal UA transporters and fibrosis markers via p38/ERK MAPK inhibition. These findings highlight UroC as a promising food-derived candidate for HUA management, promoting renal protection and enhancing UA excretion via the ROS-p38/ERK MAPK axis.
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