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Tetradecyl 2,3-Dihydroxybenzoate Improves the Symptoms of Diabetic Mice by Modulation of Insulin and Adiponectin Signaling Pathways

机译:Tetradecyl 2,3-Dihydroxybenzoate通过调节胰岛素和脂联素信号传导途径改善糖尿病小鼠的症状

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Background: Tetradecyl 2,3-dihydroxybenzoate (ABG-001) derived from Chinese medicine, gentiana regescens Franch is a leading compound with NGF mimic effect, it can induce neurite outgrowth of PC12 cells via the IGF-1/PI3K/ERK signaling pathway. Thus, we inferred that this compound had anti-diabetic effect and used streptozocin (STZ)-induced diabetic mice to indicate it. Methods: ABG-001 was synthesized with 2,3-dihydroxybenzoic acid and tetradecyl alcohol under certain reaction conditions. STZ-induced diabetic mice were used to investigate anti-diabetic effect. Oral glucose tolerance test, insulin tolerance test, RT-PCR, Western blot, ELISA assays and histological section were performed to do the analysis of action mechanism. Results: ABG-001 showed anti-diabetic effect in STZ-induced diabetic mice. In diabetic mice, the anti-diabetic effect of ABG-001 at a dose of 20 mg/kg was equal with metformin at a dose of 140 mg/kg. Moreover, glucose tolerance and insulin sensitivity were significantly improved on diabetic mice. The plasma insulin, adiponectin and leptin were notably increased, whereas glucagon remarkably decreased. The gene expressions of adiponectin and leptin in adipose tissue, glucose transporter 4 and adiponectin receptor 1 in liver and gastrocnemius , ADR2 in hypothalamus and pancreas were obviously increased. Conclusion: ABG-001 exerts antidiabetic effects via modulation of insulin and adiponectin signaling pathways. This new type of molecule could be a promising drug candidate for treatment of diabetes.
机译:背景:中药2,3-二羟基苯甲酸酯(ABG-001)是一种中草药,是一种具有NGF模仿作用的领先化合物,它可以通过IGF-1 / PI3K / ERK信号通路诱导PC12细胞的神经突生长。因此,我们推断该化合物具有抗糖尿病作用,并使用链脲佐菌素(STZ)诱导的糖尿病小鼠进行了指示。方法:在一定反应条件下,由2,3-二羟基苯甲酸和十四烷醇合成ABG-001。使用STZ诱导的糖尿病小鼠研究抗糖尿病作用。进行口服葡萄糖耐量试验,胰岛素耐量试验,RT-PCR,Western blot,ELISA测定和组织学切片分析其作用机理。结果:ABG-001在STZ诱导的糖尿病小鼠中显示出抗糖尿病作用。在糖尿病小鼠中,剂量为20 mg / kg的ABG-001的抗糖尿病作用与剂量为140 mg / kg的二甲双胍相同。此外,糖尿病小鼠的葡萄糖耐量和胰岛素敏感性显着提高。血浆胰岛素,脂联素和瘦素明显增加,而胰高血糖素则明显减少。脂肪组织中脂联素和瘦素的基因表达,肝和腓肠肌中葡萄糖转运蛋白4和脂联素受体1的基因表达,下丘脑和胰腺中的ADR2表达明显增加。结论:ABG-001通过调节胰岛素和脂联素信号通路发挥抗糖尿病作用。这种新型分子可能是治疗糖尿病的有希望的候选药物。

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