安普克
葡萄糖摄取
3T3-L1
胰岛素受体
内科学
IRS1
胰岛素受体底物
胰岛素
内分泌学
化学
蛋白激酶B
胰岛素抵抗
磷酸化
AMP活化蛋白激酶
脂肪组织
蛋白激酶A
脂肪细胞
生物化学
药理学
葡萄糖转运蛋白
生物
医学
作者
Kang-Lin Zhu,Cuihua Jiang,Yushan Tian,Na Xiao,Zhenghong Wu,Y L,Lin Zhang,Shengzuo Fang,Xiao-Ying SHANG,Kun Liu,J Zhang,Bochao Liu,Zhiqi Yin
出处
期刊:Phytomedicine
[Elsevier]
日期:2015-06-20
卷期号:22 (9): 837-846
被引量:54
标识
DOI:10.1016/j.phymed.2015.05.058
摘要
Abstract Purpose The current study investigated the efficacy of Cyclocarya paliurus chloroform extract (CPEC) and its two specific triterpenoids (cyclocaric acid B and cyclocarioside H) on the regulation of glucose disposal and the underlying mechanisms in 3T3-L1 adipocytes. Methods Mice and adipocytes were stimulated by macrophages-derived conditioned medium (Mac-CM) to induce insulin resistance. CPEC was evaluated in mice for its ability by oral glucose tolerance test (OGTT) and insulin tolerance test (ITT). To investigate the hypoglycemic mechanisms of CPEC and its two triterpenoids, glucose uptake, AMP-activated protein kinase (AMPK) activation, inhibitor of NF-κB kinase β (IKKβ) phosphorylation and insulin signaling transduction were detected in 3T3-L1 adipocytes using 2-NBDG uptake assay and Western blot analysis. Results Mac-CM, an inflammatory stimulus which induced the glucose and insulin intolerance, increased phosphorylation of IKKβ, reduced glucose uptake and impaired insulin sensitivity. CPEC and two triterpenoids improved glucose consumption and increased AMPK phosphorylation under basal and inflammatory conditions. Moreover, CPEC and its two triterpenoids not only enhanced glucose uptake in an insulin-independent manner, but also restored insulin-mediated protein kinase B (Akt) phosphorylation by reducing the activation of IKKβ and regulating insulin receptor substrate-1 (IRS-1) serine/tyrosine phosphorylation. These beneficial effects were attenuated by AMPK inhibitor compound C, implying that the effects may be associated with AMPK activation. Conclusions CPEC and its two triterpenoids promoted glucose uptake in the absence of insulin, as well as ameliorated IRS-1/PI3K/Akt pathway by inhibiting inflammation. These effects were related to the regulation of AMPK activity.
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