Isosteviol Derivative Inhibits Osteoclast Differentiation and Ameliorates Ovariectomy-Induced Osteoporosis

被引:7
作者
Tzeng, Huey-En [1 ,2 ,3 ]
Huang, Po-Hao [4 ,5 ,6 ]
Tsai, Chun-Hao [5 ,7 ]
Tsay, Gregory J. [4 ,5 ,6 ]
Lee, Yi-Ju [8 ]
Huang, Tsurng-Juhn [9 ]
Lin, Tzu-Hung [10 ]
Chiu, Ying-Ming [11 ,12 ]
Wu, Yi-Ying [13 ,14 ,15 ]
机构
[1] Taipei Med Univ, Taipei Canc Ctr, Taipei, Taiwan
[2] Taipei Med Univ, Grad Inst Canc Biol & Drug Discovery, Coll Med Sci & Technol, Taipei, Taiwan
[3] Taipei Med Univ, Dept Internal Med, Div Hematol Oncol, Shuang Ho Hosp, Taipei, Taiwan
[4] China Med Univ Hosp, Sch Med, Dept Internal Med, Taichung, Taiwan
[5] China Med Univ, Taichung, Taiwan
[6] China Med Univ Hosp, Div Rheumatol & Immunol, Dept Internal Med, Taichung, Taiwan
[7] China Med Univ Hosp, Sch Med, Dept Orthoped, Taichung, Taiwan
[8] Chung Shan Med Univ, Inst Biochem Microbiol & Immunol, Taichung, Taiwan
[9] China Med Univ, Dept Biochem, Taichung, Taiwan
[10] Ind Technol Res Inst, Mat & Chem Res Labs, Chutung, Hsinchu County, Taiwan
[11] Changhua Christian Hosp, Div Allergy Immunol & Rheumatol, Changhua, Taiwan
[12] Hungkuang Univ, Coll Med & Nursing, Dept Nursing, Taichung, Taiwan
[13] China Med Univ, Dept Med Lab Sci & Biotechnol, Taichung, Taiwan
[14] China Med Univ, Chinese Med Res Ctr, Taichung, Taiwan
[15] China Med Univ, Res Ctr Chinese Herbal Med, Taichung, Taiwan
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
NF-KAPPA-B; EXPRESSION; TRANSFORMATION; ACTIVATION; MECHANISMS; APOPTOSIS; PRODUCTS; NFATC1; ERK;
D O I
10.1038/s41598-018-29257-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
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页数:12
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