Many A, Hubel C A, Roberts J M
Magee Womens Research Institute, Pittsburgh, PA 15213, USA.
Am J Obstet Gynecol. 1996 Jan;174(1 Pt 1):288-91. doi: 10.1016/s0002-9378(96)70410-6.
Hyperuricemia is associated with the severity of preeclampsia and with fetal outcome. Traditionally the high uric acid concentration in preeclampsia has been attributed soley to renal dysfunction. Preeclampsia is also characterized by increased free radical formation and elevated oxidative stress. Xanthine dehydrogenase/oxidase produces uric acid. Xanthine dehydrogenase/oxidase is present as two isoforms in vivo. Uric acid production is coupled with formation of reactive oxygen species when the enzyme is in the oxidase form. Several factors can increase the holoenzyme activity and the conversion of xanthine dehydrogenase/oxidase to its oxidase form. These factors include hypoxia-reperfusion, cytokines, and increased substrate availability (xanthine and hypoxanthine). Preeclampsia is characterized by hyperuricemia and signs of increased formation of reactive oxygen species and decreased levels of antioxidants. Preeclampsia is also characterized by shallow implantation, producing a relatively hypoxic maternal-fetal interface, and increased turnover of trophoblast tissue, which can result in higher xanthine and hypoxanthine concentrations and higher levels of circulating cytokines. These mechanisms can lead to increased production of uric acid and free radicals and contribute to the hyperuricemia and increased oxidative stress present in preeclampsia.
高尿酸血症与子痫前期的严重程度及胎儿结局相关。传统上,子痫前期中高尿酸浓度一直仅归因于肾功能不全。子痫前期的特征还包括自由基生成增加和氧化应激升高。黄嘌呤脱氢酶/氧化酶可产生尿酸。黄嘌呤脱氢酶/氧化酶在体内以两种同工型存在。当该酶处于氧化酶形式时,尿酸生成与活性氧的形成相关联。几种因素可增加全酶活性以及黄嘌呤脱氢酶/氧化酶向其氧化酶形式的转化。这些因素包括缺氧再灌注、细胞因子以及底物可用性增加(黄嘌呤和次黄嘌呤)。子痫前期的特征是高尿酸血症、活性氧生成增加的迹象以及抗氧化剂水平降低。子痫前期还具有着床浅的特点,导致母胎界面相对缺氧,滋养层组织更新增加,这可导致黄嘌呤和次黄嘌呤浓度升高以及循环细胞因子水平升高。这些机制可导致尿酸和自由基生成增加,并促使子痫前期出现高尿酸血症和氧化应激增加。