| Literature DB >> 30342225 |
Manabu Tsukamoto1, Toshiharu Mori2, Ke-Yong Wang3, Yasuaki Okada4, Hokuto Fukuda4, Keisuke Naito5, Yoshiaki Yamanaka4, Ken Sabanai4, Eiichiro Nakamura4, Kazuhiro Yatera5, Akinori Sakai4.
Abstract
Although it is suggested that chronic obstructive pulmonary disease (COPD) and bone are related, almost all of the pathological mechanisms of COPD-related osteoporosis remain unknown. There is a mouse model showing a deterioration of bone quality after cigarette smoke exposure; however, in smoking exposure models, various factors exist that affect bone metabolism, such as smoking and body weight loss (muscle and fat mass loss). We considered it appropriate to use an elastase-induced emphysema model to exclude factors influencing bone metabolism and to investigate the influence of pulmonary emphysema on bone metabolism. The purpose of this study was to establish a COPD/emphysema-related osteoporosis mouse model by using the elastase-induced emphysema model. The lumbar vertebrae and femurs/tibiae exhibited trabecular bone loss and impaired osteogenic activity in 24-week-old male elastase-induced emphysema model mice. In addition, the model mice showed atrophy of type I muscle fibers without atrophy of type II muscle fibers. We believe that the mice described in this experimental protocol will be accepted as a COPD/emphysema-related osteoporosis mouse model and contribute to further investigations.Entities:
Keywords: Bone formation; Chronic obstructive pulmonary disease; Histomorphometry; Muscle wasting; Slow twitch
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Year: 2018 PMID: 30342225 DOI: 10.1016/j.bone.2018.10.017
Source DB: PubMed Journal: Bone ISSN: 1873-2763 Impact factor: 4.398