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首页> 外文期刊>Current Diabetes Reviews >Relaxin, Insulin and Diabetes: An Intriguing Connection
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Relaxin, Insulin and Diabetes: An Intriguing Connection

机译:松弛素,胰岛素和糖尿病:一个有趣的联系

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Until recently, relaxin and insulin were grouped into the same hormone superfamily because of substantial biochemicalnhomologies. This notion has then changed with the understanding that insulin and relaxin are ligands for differentnreceptors and signal transduction systems, namely, tyrosine kinase and G-protein-coupled receptors respectively. As anmatter of fact, relaxin does not mimic the metabolic effects of insulin. The biological effects of insulin are much morenclearly delineated than those of relaxin, which is traditionally viewed as a reproductive hormone involved in the maternalnadjustments of pregnancy. In the last decade, evidence has been accumulating that relaxin has major effects on the heart,nblood vessels and the extracellular matrix within connective tissues. In particular, pertaining to the relationships betweennrelaxin and diabetes, relaxin was shown to promote arterial and microvascular dilation, thereby increasing organnperfusion, counteract ischemic injury, improve adverse cardiac and vascular remodeling, and promote extracellular matrixnturn-over, thereby exerting anti-fibrotic effects. Thus, relaxin could blunt or delay the vascular and organ complication ofndiabetes. Whether relaxin may also synergize with insulin to optimize blood glucose homeostasis remains an unconfirmednissue. However, there are clues in the literature which, if gathered, speak in favor of this perspective. Moreover,npreliminary data suggest that exogenous relaxin administration may improve insulin sensitivity in diabetic patients.nConsidering that human recombinant relaxin is under study as a novel, promising drug for the treatment of heart failure, anbroader knowledge of the possible beneficial effects of relaxin in diabetes and its complications can be of interest to thenscientific community.
机译:直到最近,由于大量的生化同源性,松弛素和胰岛素被归为同一激素超家族。在认识到胰岛素和松弛素是不同的受体和信号转导系统的配体后,这一观念发生了变化,分别是酪氨酸激酶和G蛋白偶联受体。实际上,松弛素不能模拟胰岛素的代谢作用。胰岛素的生物学作用比松弛素要清楚得多,松弛素在传统上被认为是与孕产妇适应有关的生殖激素。在过去的十年中,越来越多的证据表明,松弛素对结缔组织内的心脏,血管和细胞外基质具有重大影响。特别地,关于神经松弛素和糖尿病之间的关系,松弛素显示出促进动脉和微血管的扩张,从而增加了器官灌注,抵消了缺血性损伤,改善了不良的心脏和血管重塑,并促进了细胞外基质的转变,从而发挥了抗纤维化作用。因此,松弛素可钝化或延迟糖尿病的血管和器官并发症。松弛素是否也可与胰岛素协同以优化血糖稳态仍未得到证实。但是,文献中有一些线索,如果收集起来,就会支持这种观点。此外,初步数据表明,外源性松弛素的给药可能会改善糖尿病患者的胰岛素敏感性。n考虑到人类重组松弛素正在研究作为一种新的,有前途的治疗心力衰竭的药物,对松弛素在糖尿病和糖尿病中可能产生的有益作用的认识更加广泛它的复杂性可能是科学界感兴趣的。

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