A quinoxaline-based compound ameliorates bone loss in ovariectomized mice. Issue 23 (December 2021)

• Record Type: Journal Article
• Authors: Zhou, Ying; Xue, Xiaoyan; Guo, Yanyan; Liu, Huan; Hou, Zheng; Chen, Zhou; Wang, Ning; Li, Fen; Wang, Yang
• Is Part Of: Experimental biology and medicine. Volume 246:Issue 23(2021)
• Page Start: 2502
• Page End: 2510
• Publication Date: 2021-12
• Subjects: Osteoporosis -- glucagon-like peptide 1 receptor -- small molecule agonist -- 6, 7-dichloro-2-methylsulfonyl-3-Ntert-butylaminoquinoxaline -- bone metabolism; Physiology -- Periodicals; Biology, Experimental -- Periodicals; Medicine, Experimental -- Periodicals; 610.72
• DOI: 10.1177/15353702211032133
• Languages: English
• ISSNs: 1535-3702

Abstract

DMB (6, 7-dichloro-2-methylsulfonyl-3-Ntert-butylaminoquinoxaline) is a quinoxaline-based compound that has been investigated as a glucagon-like peptide-1 receptor (GLP-1R) agonist. To clarify anti-osteoporosis effect of DMB, an osteoporotic mice model was established by ovariectomy (OVX) operation. The OVX mice were given intraperitoneally DMB, exendin-4 (EX-4), or 17β-estradiol (E2 ) for two months. Then bone mass and structure, and bone morphometric parameters were examined by micro-CT. Weight gain and food consumption, bone turnover markers, and biomechanical strength of the femur were tested, and bone histomorphometry was analyzed. The food intake and weight gain was obviously reduced by E2 or EX-4, but not DMB. However, DMB or EX-4 treatment obviously inhibited skeletal deterioration and enhanced bone strength. The improvement involved in the increased osteoblast number and level of bone formation markers, and reduced osteoclasts number and level of bone resorption markers. In addition, DMB was found to stimulate osteoblastogenesis-related marker gene expression. These results demonstrated that DMB ameliorated bone loss mainly via induction of bone formation, which suggests that the small molecule compound might be applied to the management of postmenopausal osteoporosis.