Dendrobium nobile Lindl. alkaloids regulate metabolism gene expression in livers of mice

Author:

Xu Yun-Yan1,Xu Ya-Sha1,Wang Yuan1,Wu Qin1,Lu Yuan-Fu1,Liu Jie1ORCID,Shi Jing-Shan1

Affiliation:

1. Key Laboratory of Basic Pharmacology of Ministry of Education and Joint International Research Laboratory of Ethnomedicine of Ministry of Education, Zunyi Medical University, Zunyi, Guizhou, China

Abstract

Abstract Objectives In our previous studies, Dendrobium nobile Lindl. alkaloids (DNLA) has been shown to have glucose-lowering and antihyperlipidaemia effects in diabetic rats, in rats fed with high-fat diets, and in mice challenged with adrenaline. This study aimed to examine the effects of DNLA on the expression of glucose and lipid metabolism genes in livers of mice. Methods Mice were given DNLA at doses of 10–80 mg/kg, po for 8 days, and livers were removed for total RNA and protein isolation to perform real-time RT-PCR and Western blot analysis. Key findings Dendrobium nobile Lindl. alkaloids increased PGC1α at mRNA and protein levels and increased glucose metabolism gene Glut2 and FoxO1 expression. DNLA also increased the expression of fatty acid β-oxidation genes Acox1 and Cpt1a. The lipid synthesis regulator Srebp1 (sterol regulatory element-binding protein-1) was decreased, while the lipolysis gene ATGL was increased. Interestingly, DNLA increased the expression of antioxidant gene metallothionein-1 and NADPH quinone oxidoreductase-1 (Nqo1) in livers of mice. Western blot on selected proteins confirmed these changes including the increased expression of GLUT4 and PPARα. Conclusions DNLA has beneficial effects on liver glucose and lipid metabolism gene expressions, and enhances the Nrf2-antioxidant pathway gene expressions, which could play integrated roles in regulating metabolic disorders.

Funder

Guizhou Education Department

Chinese National Science Foundation

Science and Technology Cooperation Project of Zunyi Science and Technology Bureau

Zunyi Medical University

Science Foundation of Zunyi Medical University

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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