Heidari Akbar, Hamidi Gholamali, Soleimani Alireza, Aghadavod Esmat, Asemi Zatollah
Research Center for Biochemistry and Nutrition in Metabolic Diseases, Kashan University of Medical Sciences, Kashan, Iran.
Iran J Kidney Dis. 2018 Jan;12(1):14-21.
Data on the effects of coenzyme Q10 (CQ10) on gene expression related to insulin, lipid, and inflammation in patients with diabetic nephropathy (DN) are scarce. This study aimed to determine the effects of CQ10 supplementation on gene expression related to insulin, lipid, and inflammation pathways in patients with DN.
Forty patients with DN, aged 40 to 85 years old, were randomly assigned into 2 groups to receive either 100 mg/d of CQ10 supplements (n = 20) or placebo (n = 20), for 12 weeks. Gene expression related to signaling pathway of insulin, lipid, and inflammation were determined in blood samples using a reverse transcriptase polymerase chain reaction method.
Quantitative results of reverse transcriptase polymerase chain reaction demonstrated that compared with the placebo, CQ10 administration upregulated gene expression of peroxisome proliferator-activated receptor-γ (P = .02) in peripheral blood mononuclear cells of the patients with DN. In addition, compared with the placebo, CQ10 supplementation downregulated gene expression of interleukin-1 (P = .003) and tumor necrosis factor-α (P = .02). No significant effects were observed on gene expression of oxidized low-density lipoprotein, lipoprotein(a), glucose transporter-1, transforming growth factor-β in the CQ10 group.
Overall, CQ10 supplementation for 12 weeks in DN patients significantly improved gene expression of peroxisome proliferator-activated receptor-γ, interleukin-1, and tumor necrosis factor-α.
关于辅酶Q10(CQ10)对糖尿病肾病(DN)患者胰岛素、脂质和炎症相关基因表达影响的数据稀缺。本研究旨在确定补充CQ10对DN患者胰岛素、脂质和炎症信号通路相关基因表达的影响。
40例年龄在40至85岁之间的DN患者被随机分为两组,分别接受100mg/d的CQ10补充剂(n = 20)或安慰剂(n = 20),持续12周。使用逆转录聚合酶链反应方法测定血样中与胰岛素、脂质和炎症信号通路相关的基因表达。
逆转录聚合酶链反应的定量结果表明,与安慰剂相比,CQ10给药上调了DN患者外周血单核细胞中过氧化物酶体增殖物激活受体-γ的基因表达(P = 0.02)。此外,与安慰剂相比,补充CQ10下调了白细胞介素-1(P = 0.003)和肿瘤坏死因子-α(P = 0.02)的基因表达。在CQ10组中,未观察到对氧化型低密度脂蛋白、脂蛋白(a)、葡萄糖转运蛋白-1、转化生长因子-β基因表达的显著影响。
总体而言,DN患者补充CQ10 12周可显著改善过氧化物酶体增殖物激活受体-γ、白细胞介素-1和肿瘤坏死因子-α的基因表达。