Open AccessCurcumin regulates EZH2/Wnt/β‐Catenin pathway in the mandible and femur of ovariectomized osteoporosis rats
Author(s) -
Jiang Qi,
Lei YongHua,
Krishnadath Dewi Chrystal,
Zhu BingYu,
Zhou XiongWen
Publication year - 2021
Publication title -
the kaohsiung journal of medical sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.439
H-Index - 36
eISSN - 2410-8650
pISSN - 1607-551X
DOI - 10.1002/kjm2.12346
Subject(s) - ovariectomized rat , femur , medicine , mandible (arthropod mouthpart) , bone resorption , osteoporosis , curcumin , wnt signaling pathway , runx2 , endocrinology , osteoblast , surgery , biology , microbiology and biotechnology , pharmacology , in vitro , estrogen , signal transduction , biochemistry , botany , genus
Osteoporosis (OP) behaves in different manners in different parts of the skeleton. This study aims to investigate the effects of curcumin on bone mass of the mandibular and femur from ovariectomized OP rats and to validate whether enhancer of zeste homolog 2 (EZH2)/Wnt/β‐Catenin pathway is involved in this process. Curcumin was administered intragastrically into ovariectomized rats for 12 weeks. The bone parameters and the morphology of the trabecular bone of the left mandible and left femur were assessed by micro‐computed tomography assay. Morphological changes of the left mandible and left femur were evaluated by hematoxylin and eosin staining. The mRNA levels of EZH2, β‐Catenin, and Runx2 in the right mandible and right femur were examined by quantitative real‐time polymerase chain reaction. Immunohistochemistry was performed to assess EZH2 expression. Both the mandible and femur exhibited OP‐like changes in ovariectomized rats, while the mandible bone resorption was less than the femur bone resorption. Curcumin intragastric administration improved bone microstructure and promoted bone formation in the mandible and femur. Curcumin inhibited EZH2 mRNA level and induced that of β‐Catenin and Runx2 in the mandible and femur. Collectively, curcumin exerts protective effects against OP, possibly by regulating the EZH2/Wnt/β‐Catenin pathway.