Yaspelkis Ben B, Kvasha Ilya A, Figueroa Tania Y
Exercise Biochemistry Laboratory, Department of Kinesiology, California State University Northridge, Northridge, 18111 Nordhoff St., Northridge, CA 91330-8287 USA.
Am J Physiol Regul Integr Comp Physiol. 2009 Jun;296(6):R1709-15. doi: 10.1152/ajpregu.00117.2009. Epub 2009 Apr 22.
Suppressor of cytokine signaling (SOCS) proteins and/or activation of the proinflammatory pathway have been postulated as possible mechanisms that may contribute to skeletal muscle insulin resistance. Thus, the aims of the present investigation were to determine in high-fat-fed skeletal muscle: 1) whether SOCS-3 protein concentration is increased, 2) whether coimmunoprecipitation of SOCS-3 with the insulin receptor-beta subunit and/or IRS-1 is increased, and 3) whether select components of the proinflammatory pathway are altered. Thirty-two male Sprague-Dawley rats were assigned to either control (CON, n = 16) or high-fat-fed (HF, n = 16) dietary groups for 12 wk and then subjected to hind limb perfusions in the presence (n = 8/group) or absence (n = 8/group) of insulin. Insulin-stimulated skeletal muscle 3-MG transport rates and PI-3 kinase activity were greater (P < 0.05) in CON. IRS-1 tyrosine phosphorylation was decreased (P < 0.05), and IRS-1 serine 307 phosphorylation was increased (P < 0.05) in HF. Insulin receptor-beta (IR-beta) subunit coimmunoprecipitation with IRS-1 was reduced in HF. SOCS-3 protein concentration and SOCS-3 coimmunoprecipitation with both the IR-beta subunit and IRS-1 was increased (P < 0.05) in HF. IKKalpha/beta serine phosphorylation was increased (P < 0.05), IkappaBalpha protein concentration was decreased (P < 0.05) and IkappaBalpha serine phosphorylation was increased (P < 0.05) in HF. Increased colocalization of SOCS-3 with both the IR-beta subunit and IRS-1 may provide steric hindrance that prevents IRS-1 from interacting with IR-beta, while increased IKKbeta serine phosphorylation may contribute to increasing IRS-1 serine phosphorylation, both of which independently can have deleterious effects on insulin-stimulated PI-3 kinase activation in high-fat-fed rodent skeletal muscle.
细胞因子信号转导抑制蛋白(SOCS)和/或促炎途径的激活被认为是可能导致骨骼肌胰岛素抵抗的机制。因此,本研究的目的是确定高脂喂养的骨骼肌中:1)SOCS-3蛋白浓度是否升高;2)SOCS-3与胰岛素受体β亚基和/或IRS-1的共免疫沉淀是否增加;3)促炎途径的某些成分是否改变。32只雄性Sprague-Dawley大鼠被分为对照组(CON,n = 16)或高脂喂养组(HF,n = 16),喂养12周,然后在有胰岛素(每组n = 8)或无胰岛素(每组n = 8)的情况下进行后肢灌注。胰岛素刺激的骨骼肌3-MG转运速率和PI-3激酶活性在CON组中更高(P < 0.05)。HF组中IRS-1酪氨酸磷酸化降低(P < 0.05),IRS-1丝氨酸307磷酸化增加(P < 0.05)。HF组中胰岛素受体β(IR-β)亚基与IRS-1的共免疫沉淀减少。HF组中SOCS-3蛋白浓度以及SOCS-3与IR-β亚基和IRS-1的共免疫沉淀均增加(P < 0.05)。HF组中IKKα/β丝氨酸磷酸化增加(P < 0.05),IκBα蛋白浓度降低(P < 0.05),IκBα丝氨酸磷酸化增加(P < 0.05)。SOCS-3与IR-β亚基和IRS-1的共定位增加可能会提供空间位阻,阻止IRS-1与IR-β相互作用,而IKKβ丝氨酸磷酸化增加可能有助于增加IRS-1丝氨酸磷酸化,这两者均可独立地对高脂喂养啮齿动物骨骼肌中胰岛素刺激的PI-3激酶激活产生有害影响。