Abstract

Objective To observe the effect of conjugated linoleic acid (c9,t11-CLA and t10,c12-CLA) on the mRNA expression of peroxisome proliferator activated receptorγ2 (PPARγ2),receptor activator of NF-κB ligand ( RANKL),alkaline phosphatase ( ALP),osteoprotegerin ( OPG),receptor activator of NF-κB (RANK) and tartrate-resistant acid phosphatase (TRAP) of bone marrow cells,and study the effect of c9,t11-CLA and t10,c12-CLA on bone metabolism.Methods Bone marrow cells of Wistar rats were cultured in vitro and then the cells were cultured in DMEM with c9,t11-CLA or t10,c12-CLA at different concentrations (the final concentration was 0,12.5,25.0,50.0 μmol/L,respectively) for 24 h.Reverse transcription-polymerase chain reaction (RT-PCR) was performed to detect the mRNA expression of PPARγ2,RANKL,ALP,OPG,RANK and TRAP.Results Semi-quantitative RT-PCR analysis showed that c9,t11-CLA down-regulated the mRNA expression of RANK and TRAP in a dose-dependent manner,and statistically significant difference was found in interclass comparison (P < 0.05,P < 0.01 ),while it had no effect on the mRNA expression of RANKL,ALP,OPG and PPARγ2.The results also showed that t10,c12-CLA up-regulated the mRNA expression of RANKL and OPG in a dose-dependent manner and down-regnlated the mRNA expression of RANK,TRAP and PPARγ2 in a dose-dependent manner,statistically significant difference was found in interclass comparison ( P < 0.05,P < 0.01 ),while it had no effect on the mRNA expression of ALP.Conclusion Our findings suggest that c9,t11-CLA and t10,c12-CLA can suppress the expression of osteoclastogenesis genes and t10,c12-CLA can also promote the expression of osteogenic genes,which suggests a possible benecial effect on bone formation. Key words: Peroxisome proliferator activated receptoryγ; Conjugated linoleic acid; Osteoporosis

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.