低尿酸血症
高尿酸血症
有机阴离子转运蛋白1
尿酸
痛风
尿酸
丙磺舒
内科学
内分泌学
苯溴马隆
肾脏疾病
医学
重吸收
肾
化学
运输机
生物化学
基因
作者
Atsushi Enomoto,Thosimitsu Niwa,Yoshikatsu Kanai,Hitoshi Endou
出处
期刊:PubMed
日期:2003-09-01
卷期号:51 (9): 892-7
被引量:4
摘要
Urate, a purine metabolite, is a cause of gout(hyperuricemia), which is an independent risk factor for cardiovascular disease. Urate is a scavenger of reactive oxygen radicals that are involved in numerous diseases. Because humans have a renal urate reabsorption system and have lost hepatic uricase by mutational silencing in evolution, urate is present in human blood at high levels. We identified the long-hypothesized urate transporter in the human kidney (URAT1, encoded by SLC22A12), a urate anion exchanger regulating blood urate levels and targeted it with uricosuric and antiuricosuric agents. Moreover, we demonstrated that patients with renal hypouricemia have mutational defects in SLC22A12.
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