Bergeron Raynald, Yao Jun, Woods John W, Zycband Emanuel I, Liu Cherrie, Li Zhihua, Adams Alan, Berger Joel P, Zhang Bei B, Moller David E, Doebber Thomas W
Department of Metabolic Disorders, Merck Research Laboratories, Rahway, New Jersey 07065, USA.
Endocrinology. 2006 Sep;147(9):4252-62. doi: 10.1210/en.2005-1535. Epub 2006 May 25.
Peroxisome proliferator-activated receptor (PPAR)-gamma agonists are insulin sensitizers, whereas PPAR alpha agonists are lipid-lowering agents in humans. Chronic treatment with PPAR gamma agonists has been shown to prevent the onset of diabetes in young Zucker diabetic fatty (ZDF) rats; however, the effects of PPAR alpha agonists have not been well characterized in this model. Here we investigated chronic efficacy of PPAR alpha and nonthiazolidinedione (nTZD) PPAR gamma agonists on the onset of diabetes in 6-wk-old male ZDF rats. Whereas treatment with the nTZD PPAR gamma agonist completely prevented development of hyperglycemia, PPAR alpha activation was associated with lowering of food intake and body weight and reductions in fed and fasting hyperglycemia, with prevention of the hyperinsulinemic peak preceding the development of hyperglycemia in ZDF rats. Both compounds improved glucose tolerance during an oral glucose tolerance test with concomitant increases in insulin response. Such improvements of insulin secretion were associated with increased islet to total pancreatic area ratio and pancreatic insulin contents. Hyperinsulinemic-euglycemic clamp studies demonstrated that nTZD PPAR gamma reduced basal endogenous glucose production and increased insulin-stimulated glucose disposal, consistent with an improved insulin action as a cause of the improved glucose homeostasis. In contrast, activation of PPAR alpha did not significantly improve glucose metabolism during the hyperinsulinemic-euglycemic clamp. In conclusion, chronic treatment of ZDF rats with a PPAR gamma agonist completely prevented the onset of diabetes by improving both insulin action and secretion, whereas PPAR alpha agonism was partially effective, primarily by improving the pancreatic islet insulin response. Unlike the PPAR gamma agonist, the PPAR alpha agonist demonstrated efficacy without inducing body weight gain and cardiomegaly. This study suggests a possible role for PPAR alpha agonists in the prevention of type 2 diabetes mellitus.
过氧化物酶体增殖物激活受体(PPAR)-γ激动剂是胰岛素增敏剂,而PPARα激动剂在人类中是降脂药物。已证明用PPARγ激动剂进行慢性治疗可预防年轻的 Zucker 糖尿病肥胖(ZDF)大鼠患糖尿病;然而,PPARα激动剂在该模型中的作用尚未得到充分表征。在此,我们研究了PPARα和非噻唑烷二酮(nTZD)PPARγ激动剂对6周龄雄性ZDF大鼠糖尿病发病的慢性疗效。虽然用nTZD PPARγ激动剂治疗可完全预防高血糖的发展,但PPARα激活与食物摄入量和体重降低以及进食和空腹高血糖的降低有关,并可预防ZDF大鼠高血糖发展之前的高胰岛素血症峰值。两种化合物在口服葡萄糖耐量试验期间均改善了葡萄糖耐量,同时胰岛素反应增加。胰岛素分泌的这种改善与胰岛与胰腺总面积之比以及胰腺胰岛素含量增加有关。高胰岛素-正常血糖钳夹研究表明,nTZD PPARγ降低了基础内源性葡萄糖生成并增加了胰岛素刺激的葡萄糖处置,这与胰岛素作用改善导致葡萄糖稳态改善一致。相比之下,在高胰岛素-正常血糖钳夹期间,PPARα激活并未显著改善葡萄糖代谢。总之,用PPARγ激动剂对ZDF大鼠进行慢性治疗可通过改善胰岛素作用和分泌完全预防糖尿病的发生,而PPARα激动作用部分有效,主要是通过改善胰岛胰岛素反应。与PPARγ激动剂不同,PPARα激动剂在不诱导体重增加和心脏肥大的情况下显示出疗效。这项研究表明PPARα激动剂在预防2型糖尿病中可能发挥作用。