Isosteviol Derivative Inhibits Osteoclast Differentiation and Ameliorates Ovariectomy-Induced Osteoporosis.
Huey-En TzengPo-Hao HuangChun-Hao TsaiGregory J TsayYi-Ju LeeTsurng-Juhn HuangTzu-Hung LinYing-Ming ChiuYi-Ying WuPublished in: Scientific reports (2018)
NC-8 (ent-16-oxobeyeran-19-N-methylureido) is an isosteviol-derived analogue with multiple biological effects, including anti-inflammation and anti-bacterial activities and inhibition of HBV viral surface antigen gene expression. In this study, we explored the effects of NC-8 on the formation of osteoclasts from RAW 264.7 cells. We found that NC-8 exerts the novel effect of inhibiting osteoclast-like cell formation. Our experiments showed that RANKL-induced ERK, p38, and JNK phosphorylation were inhibited by NC-8. An ovariectomy-induced osteoporosis animal model was used to examine the protective effects of oral treatment with NC-8. Serum analysis was used to examine markers of osteoblasts, osteoclasts, and renal and hepatic function in rats. Micro CT scanning and histological analysis were used to measure bone loss in ovariectomized rats. Oral administration of NC-8 effectively decreased excess bone resorption and significantly antagonized trabecular bone loss in ovariectomized rats. Serum analysis of C-terminal telopeptide of type-I collagen, an osteoclast marker, also showed that NC-8 administration inhibited excess bone resorption. Furthermore, serum analysis showed that renal and liver function were not affected by these doses of NC-8 during long-term treatment. Our results demonstrate that NC-8 inhibits osteoclast differentiation and effectively ameliorates ovariectomy-induced osteoporosis.
Keyphrases
- bone loss
- high glucose
- gene expression
- bone mineral density
- diabetic rats
- postmenopausal women
- signaling pathway
- drug induced
- induced apoptosis
- computed tomography
- mouse model
- stem cells
- sars cov
- hepatitis b virus
- endothelial cells
- immune response
- magnetic resonance imaging
- cell therapy
- nuclear factor
- pi k akt
- combination therapy
- cell cycle arrest
- endoplasmic reticulum stress
- stress induced
- soft tissue
- pet ct
- tissue engineering