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迷迭香提取物通过激活AMPK增加骨骼肌对葡萄糖的摄取。

Increased skeletal muscle glucose uptake by rosemary extract through AMPK activation.

作者信息

Naimi Madina, Tsakiridis Theodoros, Stamatatos Theocharis C, Alexandropoulos Dimitris I, Tsiani Evangelia

机构信息

Department of Health Sciences, Brock University, St. Catharines, ON L2S 3A1, Canada.

出版信息

Appl Physiol Nutr Metab. 2015 Apr;40(4):407-13. doi: 10.1139/apnm-2014-0430. Epub 2014 Dec 22.

Abstract

Stimulation of the energy sensor AMP-activated kinase (AMPK) has been viewed as a targeted approach to increase glucose uptake by skeletal muscle and control blood glucose homeostasis. Rosemary extract (RE) has been reported to activate AMPK in hepatocytes and reduce blood glucose levels in vivo but its effects on skeletal muscle are not known. In the present study, we examined the effects of RE and the mechanism of regulation of glucose uptake in muscle cells. RE stimulated glucose uptake in L6 myotubes in a dose- and time-dependent manner. Maximum stimulation was seen with 5 μg/mL of RE for 4 h (184% ± 5.07% of control, p < 0.001), a response comparable to maximum insulin (207% ± 5.26%, p < 0.001) and metformin (216% ± 8.77%, p < 0.001) stimulation. RE did not affect insulin receptor substrate 1 and Akt phosphorylation but significantly increased AMPK and acetyl-CoA carboxylase phosphorylation. Furthermore, the RE-stimulated glucose uptake was significantly reduced by the AMPK inhibitor compound C, but remained unchanged by the PI3K inhibitor, wortmannin. RE did not affect GLUT4 or GLUT1 glucose transporter translocation in contrast with a significant translocation of both transporters seen with insulin or metformin treatment. Our study is the first to show a direct effect of RE on muscle cell glucose uptake by a mechanism that involves AMPK activation.

摘要

能量传感器AMP激活的蛋白激酶(AMPK)的激活已被视为一种增加骨骼肌葡萄糖摄取和控制血糖稳态的靶向方法。迷迭香提取物(RE)已被报道可在体内激活肝细胞中的AMPK并降低血糖水平,但其对骨骼肌的影响尚不清楚。在本研究中,我们研究了RE对肌肉细胞葡萄糖摄取的影响及其调节机制。RE以剂量和时间依赖性方式刺激L6肌管中的葡萄糖摄取。在5μg/mL的RE处理4小时时观察到最大刺激(为对照的184%±5.07%,p<0.001),该反应与最大胰岛素刺激(207%±5.26%,p<0.001)和二甲双胍刺激(216%±8.77%,p<0.001)相当。RE不影响胰岛素受体底物1和Akt的磷酸化,但显著增加AMPK和乙酰辅酶A羧化酶的磷酸化。此外,AMPK抑制剂化合物C可显著降低RE刺激的葡萄糖摄取,但PI3K抑制剂渥曼青霉素对其无影响。与胰岛素或二甲双胍处理后观察到的两种转运体的显著转位相反,RE不影响GLUT4或GLUT1葡萄糖转运体的转位。我们的研究首次表明RE通过涉及AMPK激活的机制对肌肉细胞葡萄糖摄取有直接影响。

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