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Altered estrogen receptor expression in skeletal muscle and adipose tissue of female rats fed a high-fat diet

机译:高脂饮食雌性大鼠骨骼肌和脂肪组织中雌激素受体表达的改变

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摘要

Estrogen receptors (ERs) are expressed in adipose tissue and skeletal muscle, with potential implications for glucose metabolism and insulin signaling. Previous studies examining the role of ERs in glucose metabolism have primarily used knockout mouse models of ERα and ERβ, and it is unknown whether ER expression is altered in response to an obesity-inducing high-fat diet (HFD). The purpose of the current study was to determine whether modulation of glucose metabolism in response to a HFD in intact and ovariectomized (OVX) female rats is associated with alterations in ER expression. Our results demonstrate that a 6-wk HFD (60% calories from fat) in female rats induces whole body glucose intolerance with tissue-specific effects isolated to the adipose tissue, and no observed differences in insulin-stimulated glucose uptake, GLUT4, or ERα protein expression levels in skeletal muscle. In chow-fed rats, OVX resulted in decreased ERα with a trend toward decreased GLUT4 expression in adipose tissue. Sham-treated and OVX rats fed a HFD demonstrated a decrease in ERα and GLUT4 in adipose tissue. The HFD also increased activation of stress kinases (c-jun NH2-terminal kinase and inhibitor of κB kinase β) in the sham-treated rats and decreased expression of the protective heat shock protein 72 (HSP72) in both sham-treated and OVX rats. Our findings suggest that decreased glucose metabolism and increased inflammation in adipose tissue with a HFD in female rats could stem from a significant decrease in ERα expression.
机译:雌激素受体(ERs)在脂肪组织和骨骼肌中表达,对葡萄糖代谢和胰岛素信号传导具有潜在的影响。先前研究ERs在葡萄糖代谢中的作用的研究主要使用ERα和ERβ的基因敲除小鼠模型,尚不清楚ER表达是否会因肥胖诱导的高脂饮食(HFD)而改变。本研究的目的是确定完整和去卵巢(OVX)雌性大鼠中响应HFD的葡萄糖代谢调节是否与ER表达改变有关。我们的研究结果表明,雌性大鼠六周高脂饮食(脂肪中60%的卡路里)可诱导全身葡萄糖耐受不良,且对脂肪组织具有组织特异性作用,在胰岛素刺激的葡萄糖摄取,GLUT4或ERα中未观察到差异骨骼肌中蛋白质的表达水平。在用食物喂养的大鼠中,OVX导致ERα降低,并有降低脂肪组织中GLUT4表达的趋势。接受HFD的深水处理和OVX大鼠表现出脂肪组织中ERα和GLUT4的减少。 HFD还增加了假治疗大鼠的应激激酶(c-jun NH2末端激酶和κB激酶β抑制剂)的活化,并降低了假治疗和OVX大鼠中保护性热休克蛋白72(HSP72)的表达。 。我们的研究结果表明,雌性大鼠,HFD降低了葡萄糖代谢,并增加了脂肪组织中的炎症,这可能是由于ERα表达的显着降低所致。

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