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通过定量类固醇特征评估先兆子痫中的细胞色素 P450 介导的代谢改变。

Cytochrome P450-mediated metabolic alterations in preeclampsia evaluated by quantitative steroid signatures.

机构信息

Future Convergence Research Division, Korea Institute of Science and Technology, Seoul 136-791, Republic of Korea; Department of Chemistry, Yonsei University, Seoul 120-749, Republic of Korea.

出版信息

J Steroid Biochem Mol Biol. 2014 Jan;139:182-91. doi: 10.1016/j.jsbmb.2013.02.014. Epub 2013 Mar 6.

Abstract

Although preeclampsia has been suggested potential risk factors including placental and systemic inflammation, oxidative stress, and abnormal steroid metabolism during pregnancy, the pathogenesis of preeclampsia has not fully been elucidated, particularly in steroid metabolism. The association between various cytochrome P450 (CYP)-mediated steroid metabolic markers and preeclampsia risk was therefore investigated. The serum levels of 54 CYP-mediated regioselective hydroxysteroids and their substrates were quantitatively evaluated from both pregnant women with preeclampsia (n=30; age, 30.8±4.5 years) and normotensive controls (n=30; age, 31.0±3.5 years), who were similar with respect to maternal age, gestational age, and body mass index. The levels of 6ß-, 7a-, and 11ß-hydroxymetabolites of androgens and corticoids were significantly increased in women with preeclampsia. In addition, the levels of oxysterols, including 7a-, 7ß-, 4ß-, 20a-, 24S-, and 27-hydroxycholesterol, were markedly higher, while the levels of 16a-OH-DHEA, 16a-OH-androstenedione, and cholesterol were significantly decreased in patients. The 6ß-hydroxylation of androgens and corticoids by CYP3A4 (P<0.01), the activation of 20,22-desmolase (a cholesterol side-chain cleavage enzyme) by CYP11A1 (P<0.00001), and the multi-hydroxylation of cholesterol at C-4ß, C-7a, C-7ß, C-24S, C-27, and C-20a (P<0.0001) by catalytic or enzymatic reaction (e.g. CYP3A4, CYP7A1, CYP27A1, and CYP46A1) were differed between preeclamptic women and control subjects. In particular, an increased oxysterols (induction>2.0-fold) were positively correlated with the conditions of preeclampsia. Our metabolic profiling suggests the CYP-mediated alterations in steroid metabolism and hydroxylation in pregnancy-induced hypertension. These multiple markers could serve as background information for improved clinical diagnosis and management during pregnancy. This article is part of a Special Issue entitled "Pregnancy and Steroids".

摘要

虽然子痫前期已被提出有多种潜在的危险因素,包括胎盘和全身炎症、氧化应激和怀孕期间类固醇代谢异常,但子痫前期的发病机制尚未完全阐明,特别是在类固醇代谢方面。因此,研究了各种细胞色素 P450(CYP)介导的类固醇代谢标志物与子痫前期风险之间的关系。从患有子痫前期的孕妇(n=30;年龄 30.8±4.5 岁)和正常血压对照组(n=30;年龄 31.0±3.5 岁)中定量评估了 54 种 CYP 介导的区域选择性羟甾类及其底物的血清水平,两组在母亲年龄、妊娠周数和体重指数方面相似。与对照组相比,患有子痫前期的妇女的雄激素和皮质类固醇的 6β-、7α-和 11β-羟代谢物水平显著升高。此外,氧化固醇(包括 7α-、7β-、4β-、20a-、24S-和 27-羟胆固醇)的水平明显升高,而患者的 16α-OH-DHEA、16α-OH-雄烯二酮和胆固醇水平显著降低。CYP3A4 介导的雄激素和皮质类固醇的 6β-羟化(P<0.01)、CYP11A1 介导的 20,22-脱羟酶(胆固醇侧链裂解酶)的激活(P<0.00001)以及胆固醇的 C-4β、C-7α、C-7β、C-24S、C-27 和 C-20a(P<0.0001)的多羟基化通过催化或酶促反应(例如 CYP3A4、CYP7A1、CYP27A1 和 CYP46A1)在子痫前期妇女和对照组之间存在差异。特别是,氧化固醇的增加(诱导>2.0 倍)与子痫前期的状况呈正相关。我们的代谢分析表明,CYP 介导的类固醇代谢和羟化在妊娠高血压中发生改变。这些多标记物可以作为改善怀孕期间临床诊断和管理的背景信息。本文是题为“妊娠和类固醇”的特刊的一部分。

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