PPARγ inhibits osteogenesis via the down-regulation of the expression of COX-2 and iNOS in rats
- 作者：Tzu-Hung Lin ; Rong-Sen Yang ; Chih-Hsin Tang ; Chih-Peng Lin ; Wen-Mei Fu
- 关键词：PPARγ ; Osteoblast maturation ; COX-2 ; Osteocalcin ; iNOS
- 刊名：Bone
- 出版年：2007
- 期刊代码：39_87563282
- 类别：med
- 出版时间：October 2007
- 卷：41
- 期：4
- 页码：562-574
- 文件大小：1712 K
摘要
Peroxisome proliferator-activated receptor gamma (PPARγ), a ligand-activated transcription factor, is considered as an anti-osteoblastic factor associated with adiposity and the elderly osteoporosis due to a defect in osteoblastogenesis. We have found that oral administration of PPARγ activator rosiglitazone decreased tibia BMD and serum ALP but left serum calcium and osteoclast marker C-terminal telopeptide unaffected. In addition, we examined the inhibitory mechanisms of PPARγ on the bone formation by using PPARγ activators ciglitazone and 15-deoxy-Δ12,14-prostaglandin-J2 (15d-PGJ2). Our data indicated that PPARγ ligands decreased both mineralized bone nodules and alkaline phosphatase (ALP) activities in cultured primary osteoblasts. Reverse transcription polymerase chain reaction (RT-PCR) showed that the expression of bone morphogenetic protein-2 (BMP-2) and osteocalcin (OCN) was inhibited by ciglitizone and 15d-PGJ2. Furthermore, PPARγ ligands inhibited NF-κB associated downstream COX-2 and iNOS osteogenic signaling. The ultrasound (US)-induced elevation of COX-2 and iNOS expression and nitric oxide (NO) production were attenuated in the presence of PPARγ ligands. Furthermore, local administration of PPARγ ligands into the metaphysis of rat tibia decreased the bone volume in secondary spongiosa. These results suggest that the activation of PPARγ inhibits osteoblastic differentiation and the expression of several anabolic mediators involved in bone formation. These data may reflect osteoporosis and less bone formation in the aging people and patients treated with thiazolidinediones.