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迷迭香酸可减轻游离脂肪酸诱导的肌细胞和脂肪细胞胰岛素抵抗。

Carnosic Acid Attenuates the Free Fatty Acid-Induced Insulin Resistance in Muscle Cells and Adipocytes.

机构信息

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

Centre for Bone and Muscle Health, Brock University, St. Catharines, ON L2S 3A1, Canada.

出版信息

Cells. 2022 Jan 5;11(1):167. doi: 10.3390/cells11010167.

Abstract

Elevated blood free fatty acids (FFAs), as seen in obesity, impair insulin action leading to insulin resistance and Type 2 diabetes mellitus. Several serine/threonine kinases including JNK, mTOR, and p70 S6K cause serine phosphorylation of the insulin receptor substrate (IRS) and have been implicated in insulin resistance. Activation of AMP-activated protein kinase (AMPK) increases glucose uptake, and in recent years, AMPK has been viewed as an important target to counteract insulin resistance. We reported previously that carnosic acid (CA) found in rosemary extract (RE) and RE increased glucose uptake and activated AMPK in muscle cells. In the present study, we examined the effects of CA on palmitate-induced insulin-resistant L6 myotubes and 3T3L1 adipocytes. Exposure of cells to palmitate reduced the insulin-stimulated glucose uptake, GLUT4 transporter levels on the plasma membrane, and Akt activation. Importantly, CA attenuated the deleterious effect of palmitate and restored the insulin-stimulated glucose uptake, the activation of Akt, and GLUT4 levels. Additionally, CA markedly attenuated the palmitate-induced phosphorylation/activation of JNK, mTOR, and p70S6K and activated AMPK. Our data indicate that CA has the potential to counteract the palmitate-induced muscle and fat cell insulin resistance.

摘要

血液中游离脂肪酸(FFAs)水平升高,如肥胖症患者中所见,会损害胰岛素作用,导致胰岛素抵抗和 2 型糖尿病。几种丝氨酸/苏氨酸激酶,包括 JNK、mTOR 和 p70 S6K,会导致胰岛素受体底物(IRS)的丝氨酸磷酸化,并与胰岛素抵抗有关。AMP 激活蛋白激酶(AMPK)的激活会增加葡萄糖摄取,近年来,AMPK 被视为对抗胰岛素抵抗的重要靶点。我们之前曾报道,迷迭香提取物(RE)中的鼠尾草酸(CA)可增加肌肉细胞中的葡萄糖摄取并激活 AMPK。在本研究中,我们研究了 CA 对棕榈酸诱导的胰岛素抵抗 L6 肌管和 3T3L1 脂肪细胞的影响。细胞暴露于棕榈酸会降低胰岛素刺激的葡萄糖摄取、质膜上的 GLUT4 转运体水平和 Akt 激活。重要的是,CA 可减轻棕榈酸的有害作用,并恢复胰岛素刺激的葡萄糖摄取、Akt 的激活和 GLUT4 水平。此外,CA 还显著减弱了棕榈酸诱导的 JNK、mTOR 和 p70S6K 的磷酸化/激活,并激活了 AMPK。我们的数据表明,CA 有可能对抗棕榈酸诱导的肌肉和脂肪细胞胰岛素抵抗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b39b/8750606/59a4cd8357c6/cells-11-00167-g001a.jpg

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