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首页> 外文期刊>Cardiovascular Diabetology >Antidiabetic treatment restores adiponectin serum levels and APPL1 expression, but does not improve adiponectin-induced vasodilation and endothelial dysfunction in Zucker diabetic fatty rats
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Antidiabetic treatment restores adiponectin serum levels and APPL1 expression, but does not improve adiponectin-induced vasodilation and endothelial dysfunction in Zucker diabetic fatty rats

机译:抗糖尿病治疗可恢复脂联素的血清水平和APPL1表达,但不能改善脂联素诱导的Zucker糖尿病脂肪大鼠的血管舒张和内皮功能障碍

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Background Adiponectin is able to induce NO-dependent vasodilation in Zucker lean (ZL) rats, but this effect is clearly alleviated in their diabetic littermates, the Zucker diabetic fatty (ZDF) rats. ZDF rats also exhibit hypoadiponectinemia and a suppressed expression of APPL1, an adaptor protein of the adiponectin receptors, in mesenteric resistance arteries. Whether an antidiabetic treatment can restore the vasodilatory effect of adiponectin and improve endothelial function in diabetes mellitus type 2 is not known. Methods During our animal experiment from week 11 to 22 in each case seven ZDF rats received an antidiabetic treatment with either insulin (ZDF+I) or metformin (ZDF+M). Six normoglycemic ZL and six untreated ZDF rats served as controls. Blood glucose was measured at least weekly and serum adiponectin levels were quantified via ELISA in week 11 and 22. The direct vasodilatory response of their isolated mesenteric resistance arteries to adiponectin as well as the endothelium-dependent and -independent function was evaluated in a small vessel myograph. Additionally, the expression of different components of the adiponectin signaling pathway in the resistance arteries was quantified by real-time RT-PCR. Results In ZDF rats a sufficient blood glucose control could only be reached by treatment with insulin, but both treatments restored the serum levels of adiponectin and the expression of APPL1 in small resistance arteries. Nevertheless, both therapies were not able to improve the vasodilatory response to adiponectin as well as endothelial function in ZDF rats. Concurrently, a downregulation of the adiponectin receptors 1 and 2 as well as endothelial NO-synthase expression was detected in insulin-treated ZDF rats. Metformin-treated ZDF rats showed a reduced expression of adiponectin receptor 2. Conclusions An antidiabetic treatment with either insulin or metformin in ZDF rats inhibits the development of hypoadiponectinemia and downregulation of APPL1 in mesenteric resistance arteries, but is not able to improve adiponectin induced vasodilation and endothelial dysfunction. This is possibly due to alterations in the expression of adiponectin receptors and eNOS.
机译:背景脂联素能够在Zucker lean(ZL)大鼠中诱导NO依赖性血管舒张,但在其糖尿病同窝人Zucker糖尿病性脂肪(ZDF)大鼠中,这种作用明显减轻。 ZDF大鼠在肠系膜阻力动脉中还表现出低脂联素血症和APPL1(脂联素受体的衔接蛋白)表达受到抑制。在2型糖尿病患者中,抗糖尿病药物能否恢复脂联素的血管舒张作用并改善其内皮功能尚不清楚。方法在我们的动物实验从第11周到第22周,每种情况下有7只ZDF大鼠接受了胰岛素(ZDF + I)或二甲双胍(ZDF + M)的抗糖尿病治疗。六只血糖正常的ZL和六只未经治疗的ZDF大鼠作为对照。至少每周测量一次血糖,并在第11和22周通过ELISA对血清脂联素水平进行定量。在一个小血管中评估其分离的肠系膜抗性动脉对脂联素的直接血管舒张反应以及内皮依赖性和非依赖性功能myograph。另外,通过实时RT-PCR定量了脂联素信号传导途径的不同成分在阻力动脉中的表达。结果在ZDF大鼠中,只有通过胰岛素治疗才能达到足够的血糖控制,但是这两种治疗均能恢复小抵抗性动脉的血清脂联素水平和APPL1的表达。然而,这两种疗法均不能改善ZDF大鼠对脂联素的血管舒张反应以及内皮功能。同时,在用胰岛素治疗的ZDF大鼠中检测到脂联素受体1和2的下调以及内皮一氧化氮合酶的表达。用二甲双胍治疗的ZDF大鼠显示脂联素受体2的表达降低。结论在ZDF大鼠中用胰岛素或二甲双胍对糖尿病进行抗糖尿病治疗可抑制肠系膜阻力动脉的低脂联素血症的发生和APPL1的下调,但不能改善脂联素诱导的血管舒张和内皮功能障碍。这可能是由于脂联素受体和eNOS表达的改变。

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