Milton Flora Aparecida, Cvoro Aleksandra, Amato Angelica A, Sieglaff Douglas H, Filgueira Carly S, Arumanayagam Anithachristy Sigamani, de Lima Maria do Carmo Alves, Pitta Ivan Rocha, de Assis Rocha Neves Francisco, Webb Paul
Faculdade de Ciências da Saúde, Laboratório de Farmacologia Molecular, Universidade de Brasília, Brazil; Genomic Medicine, Houston Methodist Research Institute, Houston, TX, USA.
Genomic Medicine, Houston Methodist Research Institute, Houston, TX, USA.
Biochem Biophys Res Commun. 2015 Aug 28;464(3):718-23. doi: 10.1016/j.bbrc.2015.07.011. Epub 2015 Jul 10.
Thiazolidinediones (TZDs) are peroxisome proliferator-activated receptor gamma (PPARγ) agonists that improve insulin resistance but trigger side effects such as weight gain, edema, congestive heart failure and bone loss. GQ-16 is a PPARγ partial agonist that improves glucose tolerance and insulin sensitivity in mouse models of obesity and diabetes without inducing weight gain or edema. It is not clear whether GQ-16 acts as a partial agonist at all PPARγ target genes, or whether it displays gene-selective actions. To determine how GQ-16 influences PPARγ activity on a gene by gene basis, we compared effects of rosiglitazone (Rosi) and GQ-16 in mature 3T3-L1 adipocytes using microarray and qRT-PCR. Rosi changed expression of 1156 genes in 3T3-L1, but GQ-16 only changed 89 genes. GQ-16 generally showed weak effects upon Rosi induced genes, consistent with partial agonist actions, but a subset of modestly Rosi induced and strongly repressed genes displayed disproportionately strong GQ-16 responses. PPARγ partial agonists MLR24 and SR1664 also exhibit disproportionately strong effects on transcriptional repression. We conclude that GQ-16 displays a continuum of weak partial agonist effects but efficiently represses some negatively regulated PPARγ responsive genes. Strong repressive effects could contribute to physiologic actions of GQ-16.
噻唑烷二酮类药物(TZDs)是过氧化物酶体增殖物激活受体γ(PPARγ)激动剂,可改善胰岛素抵抗,但会引发体重增加、水肿、充血性心力衰竭和骨质流失等副作用。GQ-16是一种PPARγ部分激动剂,在肥胖和糖尿病小鼠模型中可改善葡萄糖耐量和胰岛素敏感性,且不会导致体重增加或水肿。目前尚不清楚GQ-16是否在所有PPARγ靶基因上都作为部分激动剂起作用,或者它是否表现出基因选择性作用。为了逐基因确定GQ-16如何影响PPARγ活性,我们使用微阵列和定量逆转录聚合酶链反应(qRT-PCR)比较了罗格列酮(Rosi)和GQ-16在成熟3T3-L1脂肪细胞中的作用。Rosi改变了3T3-L1中1156个基因的表达,但GQ-16仅改变了89个基因。GQ-16对Rosi诱导的基因通常显示出较弱的作用,这与部分激动剂的作用一致,但一小部分Rosi适度诱导和强烈抑制的基因对GQ-16表现出不成比例的强烈反应。PPARγ部分激动剂MLR24和SR1664对转录抑制也表现出不成比例的强烈作用。我们得出结论,GQ-16表现出一系列微弱的部分激动剂作用,但能有效抑制一些负调控的PPARγ反应性基因。强烈的抑制作用可能有助于GQ-16的生理作用。