Stingl Harald, Roden Michael
Klinische Abteilung für Endokrinologie und Stoffwechsel, Universitätsklinik für Innere Medizin III, Medizinische Universität Wien, Osterreich.
Wien Klin Wochenschr. 2004 Apr 30;116(7-8):217-29. doi: 10.1007/BF03041051.
Prevention and treatment of type 2 diabetes mellitus (T2DM) and the metabolic syndrome represent a major clinical challenge, because effective strategies such as fat restriction and exercise are difficult to implement into diabetes treatment. Based on the increasing knowledge on the pathogenesis of T2DM, new therapeutic approaches are currently under investigation. Potential targets of new therapeutic approaches include: (i) Inhibition of hepatic glucose production, (ii) stimulation of glucose-dependent insulin secretion, (iii) enhancement of insulin signal transduction, and (iv) reduction of body fat mass. Agonists of glucagon-like-peptide 1 (GLP-1) and antagonists of dipeptidylpeptidase IV, which inactivates GLP-1, stimulate glucose-dependent insulin secretion, improve hyperglycemia and are already tested in clinical trials. In humans, glucagon antagonists and an amylin analogue reduce glucagon-dependent glucose production. The glucose-lowering effect of current modulators of lipid oxidation is not pronounced and their use could be limited by side effects. In addition to clinically approved thiazolidendiones, new agonists of the peroxisome proliferator activator receptor gamma (PPAR gamma) as well as combined PPAR alpha/gamma agonists are developed at present. The direct modulation of insulin signal transduction is still limited to experimental studies.
2型糖尿病(T2DM)和代谢综合征的预防与治疗是一项重大临床挑战,因为诸如限制脂肪摄入和运动等有效策略难以应用于糖尿病治疗。基于对T2DM发病机制的认识不断增加,目前正在研究新的治疗方法。新治疗方法的潜在靶点包括:(i)抑制肝糖生成,(ii)刺激葡萄糖依赖性胰岛素分泌,(iii)增强胰岛素信号转导,以及(iv)减少体脂量。胰高血糖素样肽1(GLP-1)激动剂和使GLP-1失活的二肽基肽酶IV拮抗剂可刺激葡萄糖依赖性胰岛素分泌,改善高血糖,并且已在临床试验中进行测试。在人类中,胰高血糖素拮抗剂和一种胰淀素类似物可减少胰高血糖素依赖性糖生成。目前脂质氧化调节剂的降糖作用并不显著,其使用可能会受到副作用的限制。除了临床批准的噻唑烷二酮类药物外,目前还在研发过氧化物酶体增殖物激活受体γ(PPARγ)新激动剂以及PPARα/γ联合激动剂。胰岛素信号转导的直接调节仍仅限于实验研究。