首页> 外文期刊>Obesity research >Differential regulation of adiponectin receptor gene expression by adiponectin and leptin in myotubes derived from obese and diabetic individuals.
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Differential regulation of adiponectin receptor gene expression by adiponectin and leptin in myotubes derived from obese and diabetic individuals.

机译:脂联素和瘦素在来自肥胖和糖尿病个体的肌管中对脂联素受体基因表达的差异调节。

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OBJECTIVE: This study aimed to investigate the regulation of adiponectin receptors 1 (AdipoR1) and 2 (AdipoR2) gene expression in primary skeletal muscle myotubes, derived from human donors, after exposure to globular adiponectin (gAd) and leptin. RESEARCH METHODS AND PROCEDURES: Four distinct primary cell culture groups were established [Lean, Obese, Diabetic, Weight Loss (Wt Loss); n = 7 in each] from rectus abdominus muscle biopsies obtained from surgical patients. Differentiated myotube cultures were exposed to gAd (0.1 microg/mL) or leptin (2.5 microg/mL) for 6 hours. AdipoR1 and AdipoR2 gene expression was measured by real-time polymerase chain reaction analysis. RESULTS: AdipoR1 mRNA expression in skeletal muscle myotubes derived from Lean subjects (p < 0.05) was stimulated 1.8-fold and 2.5-fold with gAd and leptin, respectively. No increase in AdipoR1 gene expression was measured in myotubes derived from Obese, Diabetic, or Wt Loss subjects. AdipoR2 mRNA expression was unaltered after gAd and leptin exposure in all myotube groups. DISCUSSION: Adiponectin and leptin are rapid and potent stimulators of AdipoR1 in myotubes derived from lean healthy individuals. This effect was abolished in myotubes derived from obese, obese diabetic subjects, and obese-prone individuals who had lost significant weight after bariatric surgery. The incapacity of skeletal muscle of obese and diabetic individuals to respond to exogenous adiponectin and leptin may be further suppressed as a result of impaired regulation of the AdipoR1 gene.
机译:目的:本研究旨在探讨人源性供体骨骼肌肌管中脂联素受体1(AdipoR1)和脂联素2(AdipoR2)基因在暴露于球形脂联素(gAd)和瘦素后的表达调控。研究方法和程序:建立了四个不同的原代细胞培养组[瘦,肥胖,糖尿病,体重减轻(体重减轻);从手术患者获得的腹直肌活检中每人[n = 7]。将分化的肌管培养物暴露于gAd(0.1 microg / mL)或瘦素(2.5 microg / mL)中6小时。通过实时聚合酶链反应分析测量AdipoR1和AdipoR2基因表达。结果:分别用gAd和leptin刺激瘦患者骨骼肌肌管中AdipoR1 mRNA表达(p <0.05),分别为1.8倍和2.5倍。在肥胖,糖尿病或Wt丢失受试者的肌管中未检测到AdipoR1基因表达的增加。在所有肌管组中,暴露于gAd和瘦素后,AdipoR2 mRNA表达未改变。讨论:脂联素和瘦素是来自瘦弱健康个体的肌管中的AdipoR1的快速有效刺激剂。在肥胖患者,肥胖糖尿病患者以及肥胖患者在减肥手术后体重显着减轻的肌管中,这种作用已被消除。肥胖和糖尿病个体的骨骼肌对外源脂联素和瘦素无反应的能力可能会由于AdipoR1基因调控受损而进一步得到抑制。

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