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在人类胰岛素抵抗的细胞模型中,性激素结合球蛋白(SHBG)表达与PI3K/AKT信号通路活性相关。

SHBG expression is correlated with PI3K/AKT pathway activity in a cellular model of human insulin resistance.

作者信息

Feng Chong, Jin Zhen, Chi Xinshu, Zhang Bao, Wang Xiaoyan, Sun Lei, Fan Jiehui, Sun Qian, Zhang Xuan

机构信息

a Department of Obstetrics and Gynecology , Shengjing Hospital Affiliated to China Medical University , Shenyang , China.

出版信息

Gynecol Endocrinol. 2018 Jul;34(7):567-573. doi: 10.1080/09513590.2017.1411474. Epub 2018 Jan 3.

Abstract

Decreased sex hormone-binding globulin (SHBG) expression is an independent risk factor for gestational diabetes mellitus(GDM).However, the mechanisms that link low SHBG expression and insulin resistance in GDM is unclear. In this study, we investigated the placenta SHBG in the PI3K/AKT pathway to reveal the mechanism that links decreased SHBG to insulin resistance. A insulin resistance cells model was established by the method of insulin stimulation. Two groups were set up, HTR8/Svneo cells and insulin-resistance cells of HTR8/SVneo. The expression of SHBG and PI3K/AKT associated factors were detected using real-time PCR and western blotting and their correlations were analyzed. The results showed that SHBG protein and mRNA levels in insulin resistance cells were both significantly lower. Along with decreased SHBG expression, the mRNA and protein levels of IRS-1, IRS-2, PI3Kp85α and GLUT-3, GLUT-4 decreased significantly. However, the expression of GLUT-1 increased significantly. Pearson correlation analysis showed that SHBG mRNA expression was positively correlated with IRS-1, IRS-2 and PI3Kp85α mRNA levels. According to the results, low SHBG expression not only participates in the development of local insulin resistance, but may also play an important role in PI3K/AKT pathway-mediated systemic insulin resistance and gestational diabetes.

摘要

性激素结合球蛋白(SHBG)表达降低是妊娠期糖尿病(GDM)的一个独立危险因素。然而,GDM中低SHBG表达与胰岛素抵抗之间的联系机制尚不清楚。在本研究中,我们研究了胎盘SHBG在PI3K/AKT通路中的作用,以揭示SHBG降低与胰岛素抵抗之间的联系机制。通过胰岛素刺激法建立胰岛素抵抗细胞模型。设置两组,HTR8/Svneo细胞和HTR8/SVneo胰岛素抵抗细胞。采用实时PCR和western blotting检测SHBG及PI3K/AKT相关因子的表达,并分析其相关性。结果显示,胰岛素抵抗细胞中SHBG蛋白和mRNA水平均显著降低。随着SHBG表达降低,IRS-1、IRS-2、PI3Kp85α以及GLUT-3、GLUT-4的mRNA和蛋白水平显著降低。然而,GLUT-1的表达显著增加。Pearson相关性分析显示,SHBG mRNA表达与IRS-1、IRS-2和PI3Kp85α mRNA水平呈正相关。根据结果,低SHBG表达不仅参与局部胰岛素抵抗的发生发展,还可能在PI3K/AKT通路介导的全身胰岛素抵抗和妊娠期糖尿病中起重要作用。

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