| Literature DB >> 29305866 |
Wenjuan Zhang1, Jingjin Xu1, Juhui Qiu2, Cencan Xing3, Xiumin Li1, Bo Leng1, Yi Su1, Jinmei Lin1, Jiaofen Lin1, Xuqiao Mei4, Yiqun Huang4, Yutian Pan5, Yu Xue6.
Abstract
Osteoporosis is a global public health concern and, it can result from numerous pathogenic mechanisms, many of which are closely related with age, nutritional disorders, endocrine imbalance, or adverse drug side effects presented by glucocorticoids, heparin, and anti-epileptics. Given its wide range etiologies, it is crucial to establish an animal model of osteoporosis for use in screening potential drugs quickly and effectively. Previous research has reported that an accumulation of elevated iron in the body is an independent risk factor for osteoporosis. As such, we sought to use both zebrafish larvae and adults to model an osteoporosis phenotype using high iron stress (FAC, ferric ammonium citrate). Skeletal staining results suggested that iron-overload caused a significant decrease in bone calcification as well as severe developmental cartilage defects. In addition, osteoblast and cartilage-specific mRNA expression levels were downregulated after exposure to a high-iron environment. Most importantly, we demonstrated in both larval and adult fish that high iron-induced osteogenic defects were significantly rescued using alendronate (AL), a drug known to be effective against to human osteoporosis. Even more, the repair effect of AL was achieved by facilitating osteoblast differentiation and targeting Bmp signaling. Taken together, our findings propose an rapid and effective osteoporosis model, which could be used widely for future osteoporosis drug screening.Entities:
Keywords: Bone calcification; Cartilage development; High iron; Osteoporosis; Zebrafish
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Year: 2018 PMID: 29305866 DOI: 10.1016/j.bbrc.2017.12.172
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575