Maiese Kenneth, Morhan Simona Daniela, Chong Zhao Zhong
Department of Neurology, 8C-1 UHC, Wayne State University School of Medicine, 4201 St. Antoine, Detroit, MI 48201, USA.
Curr Neurovasc Res. 2007 Feb;4(1):63-71. doi: 10.2174/156720207779940653.
Diabetes mellitus (DM) affects approximately 170 million individuals worldwide and is expected to alter the lives of at least 366 million individuals within a future span of 25 years. Of even greater concern is the premise that these projections are underestimated since they assume obesity levels will remain constant. Type 1 insulin-dependent DM accounts for only 5-10 percent of all diabetics but represents a highly significant health concern, since this disorder begins early in life and leads to long-term complications. In contrast, Type 2 DM is recognized as the etiology of over 80 percent of all diabetics and is dramatically increasing in incidence as a result of changes in human behavior and increased body mass index. Yet, the pathological consequences of these disorders that involve the both the neuronal and vascular systems are intimately linked through the pathways that mediate oxidative stress. Here we highlight some of the relevant oxidative pathways that determine insulin resistance through reactive oxygen species, mitochondrial dysfunction, uncoupling proteins, and endoplasmic reticulum stress. These pathways are ultimately linked to protein kinase B (Akt) and the insulin signaling pathways that determine the initial onset of glucose intolerance and the subsequent course to apoptotic cell injury. Through the elucidation of these targets, improvement in current strategies as well as the development of future clinical applications can move forward for both the prevention and treatment of Type 1 and Type 2 DM.
糖尿病(DM)在全球约影响1.7亿人,预计在未来25年内将改变至少3.66亿人的生活。更令人担忧的是,这些预测可能被低估了,因为它们假设肥胖水平将保持不变。1型胰岛素依赖型糖尿病仅占所有糖尿病患者的5%-10%,但却是一个高度重要的健康问题,因为这种疾病在生命早期就开始,并会导致长期并发症。相比之下,2型糖尿病被认为是超过80%的糖尿病患者的病因,并且由于人类行为的改变和体重指数的增加,其发病率正在急剧上升。然而,这些涉及神经和血管系统的疾病的病理后果,通过介导氧化应激的途径紧密相连。在这里,我们重点介绍一些相关的氧化途径,这些途径通过活性氧、线粒体功能障碍、解偶联蛋白和内质网应激来决定胰岛素抵抗。这些途径最终与蛋白激酶B(Akt)和胰岛素信号通路相关联,后者决定了葡萄糖不耐受的初始发作以及随后细胞凋亡损伤的进程。通过阐明这些靶点,可以推动当前策略的改进以及未来临床应用的发展,以预防和治疗1型和2型糖尿病。