慢性阻塞性肺病
医学
骨质疏松症
弹性蛋白酶
骨重建
萎缩
内科学
内分泌学
肌肉萎缩
病理
生物
生物化学
酶
作者
Manabu Tsukamoto,Toshiharu Mori,Ke‐Yong Wang,Yasuaki Okada,Hokuto Fukuda,Keisuke Naito,Yoshiaki Yamanaka,Ken Sabanai,Eiichiro Nakamura,Kazuhiro Yatera,Akinori Sakai
出处
期刊:Bone
[Elsevier BV]
日期:2018-10-17
卷期号:120: 114-124
被引量:23
标识
DOI:10.1016/j.bone.2018.10.017
摘要
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.
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