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Steroidogenic impairment due to reduced ovarian transcription of cytochrome P450 side-chain-cleavage (P450scc) and steroidogenic acute regulatory protein (StAR) during experimental nephrotic syndrome

机译:实验性肾病综合征期间由于细胞色素P450侧链切割(P450scc)和类固醇生成的急性调节蛋白(StAR)的卵巢转录减少而导致类固醇生成障碍

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The nephrotic syndrome is a renal disease characterized by proteinuria, hypoproteinemia, edema and hyperlipidemia. It has been reported that female nephrotic rats are characterized by loss of the oestrus cycle, follicle atresia, low gonadotropin and steroid concentrations; particularly, undetectable estradiol levels. Therefore, to determine the mechanisms involved in the ovarian steroidogenesis impairment, in this present study we evaluated the ovarian expression of the essential steroidogenesis components: cytochrome P450 side cholesterol chain cleavage enzyme (P450scc) and steroidogenic acute regulatory protein (StAR). The experiments were conducted in the rat experimental model of nephrosis induced by puromycin aminonucleoside (PAN) and in control groups. The evaluation of the expression of P450scc and StAR mRNA were performed during the acute phase of nephrosis as well as after the exogenous administration of I or 4 doses of human chorionic gonadotrophin (hCG), or a daily dose of FSH or FSH+hCG for 10 days. In addition, serum hormone concentrations, intra-ovarian steroid content, and the reproductive capacity were determined. The results revealed a decreased expression of mRNA of P450scc enzyme and StAR during nephrosis, and eventhough they increased after gonadotropins treatment, they did not conduce to a normal cycling rat period or fertility recovery. This study demonstrates that the mechanism by which ovarian steroid biosynthesis is altered during acute nephrosis involves damage at the P450scc and StAR mRNA synthesis and processing. (c) 2006 Elsevier Inc. All rights reserved.
机译:肾病综合征是一种以蛋白尿,低蛋白血症,水肿和高脂血症为特征的肾脏疾病。据报道,雌性肾病大鼠的特征是发情周期丧失,卵泡闭锁,促性腺激素和类固醇浓度低。特别是无法检测到的雌二醇水平。因此,为了确定参与卵巢类固醇生成障碍的机制,在本研究中,我们评估了必需类固醇生成成分的卵巢表达:细胞色素P450侧胆固醇链裂解酶(P450scc)和类固醇生成急性调节蛋白(StAR)。实验在嘌呤霉素氨基核苷(PAN)诱导的大鼠肾病实验模型中和对照组中进行。对P450scc和StAR mRNA表达的评估在肾病急性期以及外用I或4剂人绒毛膜促性腺激素(hCG)或每日剂量FSH或FSH + hCG 10次后进行天。此外,还测定了血清激素浓度,卵巢内类固醇含量和生殖能力。结果表明,肾病期间P450scc酶和StAR的mRNA表达降低,尽管在促性腺激素治疗后它们增加,但并不能帮助大鼠正常骑车或恢复生育能力。这项研究表明,急性肾病期间卵巢类固醇生物合成发生改变的机制涉及P450scc和StAR mRNA合成和加工的破坏。 (c)2006 Elsevier Inc.保留所有权利。

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