Roe A L, Howard G, Blouin R A
Graduate Center for Toxicology, University of Kentucky, Lexington 40536-0082, USA.
Life Sci. 1998;63(15):1339-46. doi: 10.1016/s0024-3205(98)00397-x.
There is evidence to suggest that obese populations have an increased susceptibility to various pathologic disorders. Both AP-1 and STAT nuclear binding proteins have been suggested to play a role in certain obesity-related diseases. The objective of our studies reported herein was to compare constitutive binding activity of nuclear proteins (AP-1, GR, and STAT), that may be relevant to obesity-related diseases in the obese (fa/fa) Zucker rat to lean (Fa/?) littermates. AP-1, GR, and STAT liver nuclear protein binding activity was analyzed using the electrophoretic mobility shift assay (EMSA). EMSA analysis of liver nuclear protein from obese and lean Zucker rats revealed high constitutive AP-1 binding activity in the obese animals. AP-1 binding activity in the obese rats was not further elevated by treatment with phenobarbital, a known inducer of AP-1 binding activity. No differences were observed in GR binding to a consensus GRE between obese and lean animals; however, STAT binding activity to a consensus GAS element was lower in liver tissue from obese Zucker rats. Our findings presented herein suggest that the fa/fa Zucker rat may be a suitable obese rodent model for studying the roles AP-1 and STAT may play in the pathologies of these diseases.
有证据表明肥胖人群对各种病理疾病的易感性增加。AP-1和STAT核结合蛋白均被认为在某些与肥胖相关的疾病中起作用。本文报道的我们研究的目的是比较肥胖(fa/fa) Zucker大鼠与瘦(Fa/?)同窝仔鼠中可能与肥胖相关疾病有关的核蛋白(AP-1、GR和STAT)的组成型结合活性。使用电泳迁移率变动分析(EMSA)分析AP-1、GR和STAT肝核蛋白结合活性。对肥胖和瘦Zucker大鼠肝核蛋白的EMSA分析显示肥胖动物中存在高组成型AP-1结合活性。已知AP-1结合活性诱导剂苯巴比妥处理并未进一步提高肥胖大鼠中的AP-1结合活性。在肥胖和瘦动物之间未观察到GR与共有GRE结合的差异;然而,肥胖Zucker大鼠肝组织中STAT与共有GAS元件的结合活性较低。本文提出的我们的研究结果表明,fa/fa Zucker大鼠可能是研究AP-1和STAT在这些疾病病理中可能发挥的作用的合适肥胖啮齿动物模型。