Carvalheira José B C, Torsoni Márcio A, Ueno Mirian, Amaral Maria E, Araújo Eliana P, Velloso Lício A, Gontijo José A R, Saad Mario J A
Department of Internal Medicine, State University of Campinas (UNICAMP), Campinas SP, Brazil.
Obes Res. 2005 Jan;13(1):48-57. doi: 10.1038/oby.2005.7.
To investigate whether insulin and leptin share common intracellular signal transduction pathways and to determine whether these hormonal signaling systems modulate each other's action in rat hypothalamus.
Male Wistar rats were studied after chronic implantation of an intracerebroventricular catheter into the third ventricle. Immunoprecipitation and immunoblotting were used to examine the activation of insulin and leptin signaling molecules in the rat hypothalamus.
Insulin alone is able to produce molecular activation of insulin receptor substrates (IRSs)/phosphatidylinositol 3-kinase (PI 3-kinase)/Akt and mitogen-activated protein (MAP) kinase signaling pathways in hypothalamus, whereas leptin alone activates MAP kinase and IRSs/PI 3-kinase signaling with no effect on Akt. Combined infusion of leptin and insulin provokes a dual action. There was no quantitative potentialization of any single hormone's action on the elements of the insulin signaling pathway, IRSs/PI 3-kinase/Akt, and MAP kinase. Conversely, leptin plus insulin leads to quantitative potentialization of molecular signaling through the Janus kinase/signal transducer and activator of transcription pathway.
We provide evidence for a convergence of leptin and insulin signaling at the level of IRSs-PI 3-kinase and a divergence at the level of Akt. Moreover, our results indicate a direct and positive cross-talk between insulin and leptin at the level of Janus kinase 2 and signal transducer and activator of transcription 3 tyrosine phosphorylation. This mechanism may serve to potentiate the activity of both insulin and leptin pathways and to increase stimulation in physiological processes such as the control of food intake and body weight, which are under the combined control of insulin and leptin.
研究胰岛素和瘦素是否共享共同的细胞内信号转导途径,并确定这些激素信号系统是否在大鼠下丘脑调节彼此的作用。
雄性Wistar大鼠在将脑室内导管慢性植入第三脑室后进行研究。免疫沉淀和免疫印迹用于检测大鼠下丘脑胰岛素和瘦素信号分子的激活情况。
单独胰岛素能够在下丘脑中产生胰岛素受体底物(IRSs)/磷脂酰肌醇3激酶(PI 3激酶)/Akt和丝裂原活化蛋白(MAP)激酶信号通路的分子激活,而单独瘦素激活MAP激酶和IRSs/PI 3激酶信号通路,对Akt无影响。联合输注瘦素和胰岛素引发双重作用。任何单一激素对胰岛素信号通路元件IRSs/PI 3激酶/Akt和MAP激酶的作用均无定量增强。相反,瘦素加胰岛素导致通过Janus激酶/信号转导和转录激活因子途径的分子信号定量增强。
我们提供了瘦素和胰岛素信号在IRSs-PI 3激酶水平汇聚以及在Akt水平发散的证据。此外,我们的结果表明胰岛素和瘦素在Janus激酶2和信号转导和转录激活因子3酪氨酸磷酸化水平存在直接且正向的相互作用。这种机制可能有助于增强胰岛素和瘦素途径的活性,并增加对诸如食物摄入和体重控制等生理过程的刺激,这些过程受胰岛素和瘦素的联合控制。