Zanquetta Melissa Moreira, Nascimento Monalisa Edi Cabral, Mori Rosana Cristina Tieko, D'Agord Schaan Beatriz, Young Martin E, Machado Ubiratan Fabres
Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, SP 05508-900, Brazil.
Metabolism. 2006 Nov;55(11):1538-45. doi: 10.1016/j.metabol.2006.06.026.
Through in vitro studies, several factors have been reported as modulators of GLUT4 gene expression. However, the role(s) of each potential GLUT4 modulator is not completely understood in the in vivo setting. The present study has investigated the hypothesis that beta-adrenergic stimulation participates in modulation of GLUT4 expression during fasting and refeeding. As such, GLUT4 messenger RNA (mRNA) and protein were investigated in insulin-sensitive tissues during a 48-hour fast. In addition, the effects of 8-hour refeeding on GLUT4 mRNA in the gastrocnemius muscle and interscapular brown adipose tissue (BAT) were investigated. Whether beta-adrenoceptor blockade by propranolol (20 mg/kg) treatment influenced the responsiveness to fasting/refeeding was also investigated. The results show that fasting repressed GLUT4 gene and protein expression in BAT, white adipose tissue, and soleus muscle, but had no effect on the gastrocnemius muscle. Refeeding induced a rapid overexpression of GLUT4 mRNA in both gastrocnemius (approximately 25%, P < .05) and BAT (approximately 200%, P < .001). Propranolol treatment induced an increase (approximately 60%, P < .05) in GLUT4 mRNA at the end of the fasting period. In contrast, propranolol treatment attenuated GLUT4 mRNA induction after refeeding; the latter may be due to attenuation of postprandial insulin levels. These results suggest that sympathetic activity is important for the repression of GLUT4 gene expression during fasting. In contrast, sympathetic control of the GLUT4 gene seems to be overbalanced by metabolic/hormonal modulators during refeeding stage. Taken together, the results suggest that feeding behavior influences GLUT4 gene expression pattern through changes in sympathetic activity, especially during long-term starvation periods.
通过体外研究,已有多种因素被报道为GLUT4基因表达的调节因子。然而,在体内环境中,每种潜在的GLUT4调节因子的作用尚未完全明确。本研究探讨了β-肾上腺素能刺激参与禁食和再喂养期间GLUT4表达调节的假说。因此,在48小时禁食期间,对胰岛素敏感组织中的GLUT4信使核糖核酸(mRNA)和蛋白质进行了研究。此外,还研究了8小时再喂养对腓肠肌和肩胛间棕色脂肪组织(BAT)中GLUT4 mRNA的影响。同时也研究了普萘洛尔(20 mg/kg)治疗引起的β-肾上腺素能受体阻断是否会影响对禁食/再喂养的反应性。结果显示,禁食抑制了BAT、白色脂肪组织和比目鱼肌中GLUT4基因和蛋白质的表达,但对腓肠肌没有影响。再喂养诱导腓肠肌(约25%,P < 0.05)和BAT(约200%,P < 0.001)中GLUT4 mRNA迅速过度表达。普萘洛尔治疗在禁食期结束时诱导GLUT4 mRNA增加(约60%,P < 0.05)。相反,普萘洛尔治疗减弱了再喂养后GLUT4 mRNA的诱导;后者可能是由于餐后胰岛素水平的降低。这些结果表明,交感神经活动对禁食期间GLUT4基因表达的抑制很重要。相比之下,在再喂养阶段,GLUT4基因的交感神经控制似乎被代谢/激素调节因子过度平衡。综上所述,结果表明进食行为通过交感神经活动的变化影响GLUT4基因表达模式,尤其是在长期饥饿期间。