首页> 外文期刊>Molecular and Cellular Endocrinology >Treatment with a constitutive androstane receptor ligand ameliorates the signs of preeclampsia in high-fat diet-induced obese pregnant mice
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Treatment with a constitutive androstane receptor ligand ameliorates the signs of preeclampsia in high-fat diet-induced obese pregnant mice

机译:用组成型雄烷受体配体治疗可改善高脂饮食诱导的肥胖妊娠小鼠先兆子痫的症状

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摘要

Constitutive androstane receptor (CAR) has been reported to decrease insulin resistance, while obesity and insulin resistance may also be involved in the pathogenesis of preeclampsia. We examined whether a CAR ligand, 1,4-bis(2-(3,5-dichloropyridyloxy)) benzene (TCPOBOP), can ameliorate the signs of preeclampsia in high-fat diet (HFD)-induced obese pregnant mice to examine a possibility of CAR as a therapeutic target. We employed six groups including non-pregnant, HFD-fed or control diet-fed pregnant mice with or without TCPOBOP treatment (n=6). In HFD pregnant mice, insulin resistance increased with increasing expression of gluconeogenic and lipogenic genes and abnormal adipocytokine levels. TCPOBOP treatment, which was once-weekly intraperitoneal injections (0.5. mg/kg) and started at day 0.5 of pregnancy, improved glucose tolerance with significant changes of gluconeogenic, lipogenic and adipocytokine genes. HFD pregnant mice had hypertension and proteinuria, while TCPOBOP treatment ameliorated these signs. Our data suggested CAR might be a potential therapeutic target for obese preeclampsia patients with insulin resistance.
机译:据报道,组成型雄甾烷受体(CAR)可降低胰岛素抵抗,而肥胖和胰岛素抵抗也可能与先兆子痫的发病机理有关。我们检查了CAR配体1,4-双(2-(3,5-二氯吡啶氧基))苯(TCPOBOP)是否可以减轻高脂饮食(HFD)诱导的肥胖妊娠小鼠的先兆子痫症状,以检查CAR作为治疗靶标的可能性。我们采用六组,包括未妊娠,HFD喂养或对照饮食喂养的妊娠小鼠,接受或不接受TCPOBOP治疗(n = 6)。在HFD妊娠小鼠中,胰岛素抵抗随着糖原异生和脂肪原基因的表达增加以及异常的脂肪细胞因子水平而增加。 TCPOBOP治疗是每周一次腹膜内注射(0.5。mg / kg),从妊娠的第0.5天开始,可改善糖耐量,并显着改变糖原异生性,脂肪生成和脂肪细胞因子基因。 HFD妊娠小鼠患有高血压和蛋白尿,而TCPOBOP治疗则改善了这些症状。我们的数据表明CAR可能是肥胖的先兆子痫患者胰岛素抵抗的潜在治疗靶点。

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