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Journal of Diabetes Research - Volume 2015 2015, Article ID 973287, 12 pages -

Research Article

National Drug Screening Center and Jiangsu Key Laboratory of TCM Evaluation and Translational Research, China Pharmaceutical University, 24 Tongjiaxiang, Nanjing 210009, China

Center for Drug Discovery, State Key Laboratory of Natural Medicines, China Pharmaceutical University, 24 Tongjiaxiang, Nanjing 210009, China

Received 13 August 2014; Revised 13 December 2014; Accepted 15 December 2014

Academic Editor: Giuseppe Paolisso

Copyright © 2015 Xue Wang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Aims and Background. Type 2 diabetes is a chronic disease that cannot be treated adequately using the known monotherapies, especially when the disease progresses to an advanced stage. In this study, we explore the possibility of treating the disease with a novel combination approach of oleanolic acid OA, a glycogen phosphorylase GP inhibitor, and metformin. Methods. Db-db mice were randomly divided into four groups: a db-db control group, db-db mice treated with OA 250 mg-kg, db-db mice treated with metformin 100 mg-kg, and db-db mice treated with a combination of OA and metformin. All mice were treated for four weeks. The effects of the treatments on glucose homeostasis were measured using an OGTT, an assessment of insulin sensitivity and signaling in the liver, and the hepatic glucose production. Results. Combination therapy with OA and metformin significantly reduced the blood glucose and insulin levels and improved the liver pathology compared with that for the monotherapy in the db-db diabetic mouse model. We also found that the combination therapy significantly increased the mRNA expression of glycogen synthesis and decreased the GP, PGC-1α, PEPCK1, and G-6-Pase levels. In addition, the combination therapy with OA and metformin significantly increased the phosphorylation of AKT, PI3K, AMPK, and ACC and decreased the protein expression levels of G-6-Pase, PEPCK1, and TORC compared with those for either monotherapy. The combination therapy also reduced the phosphorylation of mTOR and CREB. Conclusions. Our results suggest that the combination therapy with OA and metformin has synergistic effects on the symptoms of db-db diabetic mice by improving glucose and insulin homeostasis.





Autor: Xue Wang, Yupeng Chen, Daoud Abdelkader, Waseem Hassan, Hongbin Sun, and Jun Liu

Fuente: https://www.hindawi.com/



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