Fujiwara T, Horikoshi H
Pharmacology and Molecular Biol. Res. Labs., Sankyo. Co. Ltd., Tokyo, Japan.
Life Sci. 2000 Oct 6;67(20):2405-16. doi: 10.1016/s0024-3205(00)00829-8.
Troglitazone and structurally related compounds (pioglitazone, rosiglitazone etc.) containing thiazolidinediones (TZD) are a novel class of antidiabetic agents which decrease blood glucose in diabetic animal models and in patients with Non-Insulin-Dependent Diabetes Mellitus (NIDDM) through alleviating insulin resistance. A large body of evidence is now accumulating indicating that insulin resistance and/or resulting hyperinsulinemia underlie the pathogenesis of not only diabetes but also of the clustering syndrome called "syndrome X" or "insulin resistance syndrome" which includes hypertension, dislipidemia and hypercoagulation. Therefore, TZD class of insulin sensitizers seem to have therapeutic potential to improve this clustering syndrome in addition to diabetes. Moreover, it was demonstrated that the TZD class of insulin sensitizers including troglitazone bind and activate the peroxisome proliferator-activated receptor gamma (PPARgamma), a nuclear hormone receptor. Although PPARgamma is predominantly expressed in adipose tissue, one of the target tissues for insulin, it have been subsequently found to be expressed in macrophages, vascular smooth muscle cells (VSMC), endothelial cells and several cancer cell lines. PPARgamma activation by PPARgamma agonists such as TZD class of insulin sensitizers in these cells modulates these cell functions such as the production of inflammatory cytokine by macrophages, proliferation and migration of VSMC, and growth or differentiation in cancer cells. In addition, troglitazone has potent antioxidant effect, and suppresses both L-type and receptor operated Ca2+ channel and protein kinase C. Thus since TZD class of insulin sensitizers has many kind of therapeutic effect in addition to lowering blood glucose, these agents expect to have therapeutic potential beyond diabetes.
曲格列酮以及含有噻唑烷二酮(TZD)的结构相关化合物(吡格列酮、罗格列酮等)是一类新型抗糖尿病药物,它们通过减轻胰岛素抵抗,降低糖尿病动物模型和非胰岛素依赖型糖尿病(NIDDM)患者的血糖。现在大量证据不断积累,表明胰岛素抵抗和/或由此导致的高胰岛素血症不仅是糖尿病发病机制的基础,也是被称为“X综合征”或“胰岛素抵抗综合征”的聚集综合征发病机制的基础,该综合征包括高血压、血脂异常和高凝状态。因此,TZD类胰岛素增敏剂除了对糖尿病有治疗潜力外,似乎对改善这种聚集综合征也有治疗潜力。此外,已证明包括曲格列酮在内的TZD类胰岛素增敏剂能结合并激活过氧化物酶体增殖物激活受体γ(PPARγ),一种核激素受体。尽管PPARγ主要在脂肪组织(胰岛素的靶组织之一)中表达,但随后发现它也在巨噬细胞、血管平滑肌细胞(VSMC)、内皮细胞和几种癌细胞系中表达。在这些细胞中,TZD类胰岛素增敏剂等PPARγ激动剂激活PPARγ可调节这些细胞功能,如巨噬细胞产生炎性细胞因子、VSMC的增殖和迁移以及癌细胞的生长或分化。此外,曲格列酮具有强大的抗氧化作用,并抑制L型和受体操纵的Ca2+通道以及蛋白激酶C。因此,由于TZD类胰岛素增敏剂除了降低血糖外还有多种治疗作用,这些药物有望具有超越糖尿病的治疗潜力。