Targeting PPARβ/δ for the treatment of type 2 diabetes mellitus

被引:36
作者
Salvado, Laia
Serrano-Marco, Lucia
Barroso, Emma
Palomer, Xavier
Vazquez-Carrera, Manuel [1 ,2 ]
机构
[1] Univ Barcelona, Dept Pharmacol & Therapeut Chem, CIBER Diabet & Enfermedades Metab Asociadas CIBER, Inst Salud Carlos III, E-08028 Barcelona, Spain
[2] IBUB, Fac Pharm, E-08028 Barcelona, Spain
关键词
fatty acids; IL-6; NF-kappa B; PPAR beta/delta; STAT-3; PROLIFERATOR-ACTIVATED RECEPTORS; INDUCED INSULIN-RESISTANCE; PROTEIN-KINASE-C; DENSITY-LIPOPROTEIN CHOLESTEROL; TUMOR-NECROSIS-FACTOR; FACTOR-KAPPA-B; PEROXISOME-PROLIFERATOR; FATTY-ACIDS; METABOLIC SYNDROME; ADIPOSE-TISSUE;
D O I
10.1517/14728222.2012.658370
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: The nuclear receptors Peroxisome Proliferator-Activated Receptors (PPAR)alpha and PPAR gamma are therapeutic targets for hypertriglyceridemia and insulin resistance, respectively. Evidence is now emerging that the PPAR beta/delta isotype is a potential pharmacological target for the treatment of insulin resistance and type 2 diabetes mellitus. Areas covered: In this review, the capacity of PPAR beta/delta to prevent the development of insulin resistance and type 2 diabetes mellitus is discussed. Special emphasis is placed on preclinical studies and the molecular mechanisms responsible for its actions in the main cell types involved in these pathologies: adipocytes, beta-cells, skeletal muscle cells and hepatocytes. Expert opinion: While several concerns remain for the development of PPAR beta/delta agonists, these drugs have demonstrated their efficacy in the treatment of insulin resistance and type 2 diabetes mellitus in preclinical studies, as well as in a few short clinical studies in humans. Although this data is promising, additional studies must be performed to confirm the efficacy and safety of these drugs in the treatment of type 2 diabetes mellitus.
引用
收藏
页码:209 / 223
页数:15
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