Hediger Matthias A, Johnson Richard J, Miyazaki Hiroki, Endou Hitoshi
Membrane Biology Program and Renal Division, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Physiology (Bethesda). 2005 Apr;20:125-33. doi: 10.1152/physiol.00039.2004.
Humans excrete uric acid as the final breakdown product of unwanted purine nucleotides. Urate scavenges potential harmful radicals in our body. However, in conjunction with genetic or environmental (especially dietary) factors, urate may cause gout, nephrolitiasis, hypertension, and vascular disease. Blood levels of urate are maintained by the balance between generation and excretion. Excretion requires specialized transporters located in renal proximal tubule cells, intestinal epithelial cells, and vascular smooth muscle cells. The recently identified human urate transporters URAT1, MRP4, OAT1, and OAT3 are thought to play central roles in homeostasis and may prove interesting targets for future drug development.
人类将尿酸作为不需要的嘌呤核苷酸的最终分解产物排出体外。尿酸盐清除我们体内潜在的有害自由基。然而,与遗传或环境(尤其是饮食)因素一起,尿酸盐可能会导致痛风、肾结石、高血压和血管疾病。尿酸盐的血液水平通过生成和排泄之间的平衡来维持。排泄需要位于肾近端小管细胞、肠上皮细胞和血管平滑肌细胞中的特殊转运蛋白。最近发现的人类尿酸转运蛋白URAT1、MRP4、OAT1和OAT3被认为在体内平衡中起核心作用,并且可能成为未来药物开发的有趣靶点。