Standaert Mary L, Sajan Mini P, Miura Atsushi, Kanoh Yoshinori, Chen Hubert C, Farese Robert V, Farese Robert V
Research Service, James A. Haley Veterans Medical Center and Department of Internal Medicine, University of South Florida College of Medicine, Tampa, Florida 33612, USA.
J Biol Chem. 2004 Jun 11;279(24):24929-34. doi: 10.1074/jbc.M402440200. Epub 2004 Apr 6.
Insulin resistance in type 2 diabetes is characterized by defects in muscle glucose uptake and hepatic overproduction of both glucose and lipids. These hepatic defects are perplexing because insulin normally suppresses glucose production and increases lipid synthesis in the liver. To understand the mechanisms for these seemingly paradoxical defects, we examined the activation of atypical protein kinase C (aPKC) and protein kinase B (PKB), two key signaling factors that operate downstream of phosphatidylinositol 3-kinase and regulate various insulin-sensitive metabolic processes. Livers and muscles of three insulin-resistant rodent models were studied. In livers of type 2 diabetic non-obese Goto-Kakazaki rats and ob/ob-diabetic mice, the activation of PKB was impaired, whereas activation of aPKC was surprisingly maintained. In livers of non-diabetic high fatfed mice, the activation of both aPKC and PKB was maintained. In contrast to the maintenance of aPKC activation in the liver, insulin activation of aPKC was impaired in muscles of Goto-Kakazaki-diabetic rats and ob/ob-diabetic and non-diabetic high fat-fed mice. These findings suggest that, at least in these rodent models, (a) defects in aPKC activation contribute importantly to skeletal muscle insulin resistance observed in both high fat feeding and type 2 diabetes; (b) insulin signaling defects in muscle are not necessarily accompanied by similar defects in liver; (c) defects in hepatic PKB activation occur in association with, and probably contribute importantly to, the development of overt diabetes; and (d) maintenance of hepatic aPKC activation may explain the continued effectiveness of insulin for stimulating certain metabolic actions in the liver.
2型糖尿病中的胰岛素抵抗表现为肌肉葡萄糖摄取缺陷以及肝脏葡萄糖和脂质过度生成。这些肝脏缺陷令人困惑,因为胰岛素通常会抑制肝脏中的葡萄糖生成并增加脂质合成。为了理解这些看似矛盾的缺陷的机制,我们研究了非典型蛋白激酶C(aPKC)和蛋白激酶B(PKB)的激活情况,这两种关键信号因子在磷脂酰肌醇3激酶下游发挥作用,并调节各种胰岛素敏感的代谢过程。我们研究了三种胰岛素抵抗啮齿动物模型的肝脏和肌肉。在2型糖尿病非肥胖的Goto-Kakazaki大鼠和ob/ob糖尿病小鼠的肝脏中,PKB的激活受损,而aPKC的激活却令人惊讶地维持着。在非糖尿病高脂喂养小鼠的肝脏中,aPKC和PKB的激活均得以维持。与肝脏中aPKC激活的维持情况相反,Goto-Kakazaki糖尿病大鼠、ob/ob糖尿病和非糖尿病高脂喂养小鼠的肌肉中,胰岛素对aPKC的激活受损。这些发现表明,至少在这些啮齿动物模型中,(a)aPKC激活缺陷对高脂喂养和2型糖尿病中观察到的骨骼肌胰岛素抵抗起重要作用;(b)肌肉中的胰岛素信号缺陷不一定伴随着肝脏中的类似缺陷;(c)肝脏PKB激活缺陷与显性糖尿病的发生相关,并且可能对其发展起重要作用;(d)肝脏aPKC激活的维持可能解释了胰岛素对刺激肝脏某些代谢作用持续有效的原因。