From the Diabetes Research Program, Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, New York University School of Medicine, NY.
Arterioscler Thromb Vasc Biol. 2019 Jul;39(7):e166-e174. doi: 10.1161/ATVBAHA.119.312005. Epub 2019 Jun 26.
Obesity and diabetes remain leading causes of reduced health span and life span throughout the world. Hence, it is not surprising that these areas are at the center of highly active areas of research. The identification of novel mechanisms underlying these metabolic disorders sets the stage for uncovering new potential therapeutic strategies. In this issue of Highlights in Arteriosclerosis, Thrombosis and Vascular Biology, we review recently published papers in the journal that add to our understanding of causes and consequences of obesity and diabetes and how these disorders impact metabolic function. Collectively, these studies in cultured cells to in vivo animal models to human subjects add to the growing body of evidence that both cell-intrinsic and cell-cell communication mechanisms collaborate in metabolic disorders to cause obesity, insulin resistance and diabetes and its complications.
肥胖和糖尿病仍然是全世界导致健康寿命和预期寿命缩短的主要原因。因此,这些领域成为高度活跃的研究领域的中心也就不足为奇了。这些代谢紊乱的新机制的确定为揭示新的潜在治疗策略奠定了基础。在本期《动脉硬化、血栓形成和血管生物学亮点》中,我们综述了该杂志最近发表的论文,这些论文增加了我们对肥胖和糖尿病的原因和后果的理解,以及这些疾病如何影响代谢功能。总的来说,这些从培养细胞到体内动物模型再到人类受试者的研究增加了越来越多的证据,即细胞内在和细胞间通讯机制在代谢紊乱中协同作用,导致肥胖、胰岛素抵抗和糖尿病及其并发症。