| Literature DB >> 27237975 |
Wei Ming1, Gan Lu2, Sha Xin3, Lu Huanyu4, Jiang Yinghao5, Lei Xiaoying6, Xu Chengming7, Ruan Banjun8, Wang Li9, Lu Zifan10.
Abstract
Therapeutic targeting bone loss has been the focus of the study in osteoporosis. The present study is intended to evaluate whether MOTS-c, a novel mitochondria related 16 aa peptide, can protect mice from ovariectomy-induced osteoporosis. After ovary removal, the mice were injected with MOTS-c at a dose of 5 mg/kg once a day for 12 weeks. Our results showed that MOTS-c treatment significantly alleviated bone loss, as determined by micro-CT examination. Mechanistically, we found that the receptor activator of nuclear factor-κB ligand (RANKL) induced osteoclast differentiation was remarkably inhibited by MOTS-c. Moreover, MOTS-c increased phosphorylated AMPK levels, and compound C, an AMPK inhibitor, could partially abrogate the effects of the MOTS-c on osteoclastogenesis. Thus, our findings provide evidence that MOTS-c may exert as an inhibitor of osteoporosis via AMPK dependent inhibition of osteoclastogenesis.Entities:
Keywords: AMPK; MOTS-c; Osteoblast; Osteoclast; Osteoporosis
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Year: 2016 PMID: 27237975 DOI: 10.1016/j.bbrc.2016.05.135
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575