Ginsenoside Rc, an active component of Panax ginseng, stimulates glucose uptake in C2C12 myotubes through an AMPK-dependent mechanism
- PMID: 19961916
- DOI: 10.1016/j.jep.2009.11.022
Ginsenoside Rc, an active component of Panax ginseng, stimulates glucose uptake in C2C12 myotubes through an AMPK-dependent mechanism
Abstract
Ethnopharmacological relevance: Panax ginseng and its major component, ginsenosides, are widely used for the prevention of various disorders in oriental medicine.
Aim of the study: To evaluate the effect of ginsenoside Rc (Rc), one of the active constituents in Panax ginseng, on glucose uptake in C2C12 myotubes.
Results: Treatment of the C2C12 myotubes with Rc significantly increased glucose uptake. To determine the mechanism of Rc-induced glucose uptake, either insulin-dependent signaling or insulin-independent signaling pathway activities were measured using western blot analysis. We showed that Rc significantly activated an insulin-independent AMPK signaling pathway. However, Rc had no effect on the components of the insulin-dependent signaling pathway, such as receptor substrates (IRS)-1 and protein kinase B or Akt (PKB/Akt). Moreover, we found that treatment with an AMPK inhibitor abolished both glucose uptake and p38 MAPK phosphorylation. This result implies that AMPK activity is critical for the Rc-induced glucose uptake and that AMPK is situated upstream of p38 MAPK. In addition, we also showed that the activation of AMPK and p38 induced by ginsenoside Rc is mediated by reactive oxygen species (ROS) production, suggesting that upstream regulators of AMPK- and p38 MAPK-mediated glucose uptake.
Conclusion: Ginsenoside Rc significantly enhances glucose uptake by inducing ROS generation, which leads to AMPK and p38 MAPK activation. Consequently, ginsenoside Rc can be used as a potent natural anti-diabetic agent.
Copyright 2009 Elsevier Ireland Ltd. All rights reserved.
Similar articles
-
Curcumin stimulates glucose uptake through AMPK-p38 MAPK pathways in L6 myotube cells.J Cell Physiol. 2010 Jun;223(3):771-8. doi: 10.1002/jcp.22093. J Cell Physiol. 2010. PMID: 20205235
-
Ketone bodies alter dinitrophenol-induced glucose uptake through AMPK inhibition and oxidative stress generation in adult cardiomyocytes.Am J Physiol Endocrinol Metab. 2007 May;292(5):E1325-32. doi: 10.1152/ajpendo.00186.2006. Epub 2007 Jan 16. Am J Physiol Endocrinol Metab. 2007. PMID: 17227964
-
Clozapine activates AMP-activated protein kinase (AMPK) in C2C12 myotube cells and stimulates glucose uptake.Life Sci. 2010 Jul 3;87(1-2):42-8. doi: 10.1016/j.lfs.2010.05.017. Epub 2010 May 31. Life Sci. 2010. PMID: 20515698
-
Production of ginseng saponins: elicitation strategy and signal transductions.Appl Microbiol Biotechnol. 2015 Sep;99(17):6987-96. doi: 10.1007/s00253-015-6806-8. Epub 2015 Jul 21. Appl Microbiol Biotechnol. 2015. PMID: 26194557 Review.
-
The promising therapeutic potentials of ginsenosides mediated through p38 MAPK signaling inhibition.Heliyon. 2021 Nov 12;7(11):e08354. doi: 10.1016/j.heliyon.2021.e08354. eCollection 2021 Nov. Heliyon. 2021. PMID: 34825082 Free PMC article. Review.
Cited by
-
Ginseng and obesity.J Ginseng Res. 2018 Jan;42(1):1-8. doi: 10.1016/j.jgr.2016.12.005. Epub 2017 Jan 10. J Ginseng Res. 2018. PMID: 29348715 Free PMC article. Review.
-
The role of triterpenes in the management of diabetes mellitus and its complications.Phytochem Rev. 2015;14(4):675-690. doi: 10.1007/s11101-014-9369-x. Epub 2014 Jun 24. Phytochem Rev. 2015. PMID: 26213526 Free PMC article. Review.
-
Herb-Drug Interaction of Red Ginseng Extract and Ginsenoside Rc with Valsartan in Rats.Molecules. 2020 Jan 31;25(3):622. doi: 10.3390/molecules25030622. Molecules. 2020. PMID: 32023909 Free PMC article.
-
Ginsenosides: the need to move forward from bench to clinical trials.J Ginseng Res. 2019 Jul;43(3):361-367. doi: 10.1016/j.jgr.2018.09.001. Epub 2018 Sep 7. J Ginseng Res. 2019. PMID: 31308807 Free PMC article. Review.
-
Ginsenoside Rc Promotes Bone Formation in Ovariectomy-Induced Osteoporosis In Vivo and Osteogenic Differentiation In Vitro.Int J Mol Sci. 2022 May 31;23(11):6187. doi: 10.3390/ijms23116187. Int J Mol Sci. 2022. PMID: 35682866 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous