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Antidiabetic Effects of Bisamide Derivative of Dicarboxylic Acid in Metabolic Disorders

机译:二羧酸双酰胺衍生物在代谢紊乱中的抗糖尿病作用

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摘要

In clinical practice, the metabolic syndrome can lead to multiple complications, including diabetes. It remains unclear which component of the metabolic syndrome (obesity, inflammation, hyperglycemia, or insulin resistance) has the strongest inhibitory effect on stem cells involved in beta cell regeneration. This makes it challenging to develop effective treatment options for complications such as diabetes. In our study, experiments were performed on male C57BL/6 mice where metabolic disorders have been introduced experimentally by a combination of streptozotocin-treatment and a high-fat diet. We evaluated the biological effects of Bisamide Derivative of Dicarboxylic Acid (BDDA) and its impact on pancreatic stem cells in vivo. To assess the impact of BDDA, we applied a combination of histological and biochemical methods along with a cytometric analysis of stem cell and progenitor cell markers. We show that in mice with metabolic disorders, BDDA has a positive effect on lipid and glucose metabolism. The pancreatic restoration was associated with a decrease of the inhibitory effects of inflammation and obesity factors on pancreatic stem cells. Our data shows that BDDA increases the number of pancreatic stem cells. Thus, BDDA could be used as a new compound for treating complication of the metabolic syndrome such as diabetes.
机译:在临床实践中,代谢综合征可导致多种并发症,包括糖尿病。尚不清楚代谢综合征的哪些成分(肥胖,炎症,高血糖或胰岛素抵抗)对参与β细胞再生的干细胞具有最强的抑制作用。这使得开发针对诸如糖尿病的并发症的有效治疗选择具有挑战性。在我们的研究中,对雄性C57BL / 6小鼠进行了实验,通过链脲佐菌素治疗和高脂饮食相结合,实验性引入了代谢性疾病。我们评估了双酰胺双羧酸衍生物(BDDA)的生物学效应及其对体内胰腺干细胞的影响。为了评估BDDA的影响,我们结合了组织学和生化方法以及干细胞和祖细胞标记的细胞计数分析。我们表明,在患有代谢异常的小鼠中,BDDA对脂质和葡萄糖代谢具有积极作用。胰腺修复与炎症和肥胖因子对胰腺干细胞抑制作用的降低有关。我们的数据表明BDDA可增加胰腺干细胞的数量。因此,BDDA可以用作治疗诸如糖尿病的代谢综合征的并发症的新化合物。

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