Publication | Open Access
Retinoic acid inhibits inducible nitric oxide synthase expression in 3T3-L1 adipocytes
13
Citations
30
References
2002
Year
3T3-l1 AdipocytesSynthase ExpressionLipid PeroxidationImmunologyMetabolic RemodelingInsulin SignalingOxidative StressTnf-induced Inos InductionInflammationMetabolic SyndromeAll-trans-retinoic AcidMetabolic SignalingAtherosclerosisCell SignalingHealth SciencesBiochemistryChronic InflammationPharmacologyCell BiologyAnti-inflammatoryTnf-induced Lpl SuppressionPhysiologyMetabolic RegulationMetabolismMedicineNitrosative StressLipid Synthesis
The present study was undertaken to explore whether retinoids, which are known to have immunomodulatory actions, could attenuate tumor necrosis factor-alpha (TNF)-stimulated inducible nitric oxide synthase (iNOS) expression in 3T3-L1 adipocytes. Adipocytes incubated with TNF induced dose- and time-dependent accumulation of nitrite in the culture medium through the iNOS induction as confirmed by Western blotting. Treatment of cells with TNF in the presence of all-trans-retinoic acid (RA) significantly decreased their ability to produce nitrite and iNOS induction. Both 13-cis- and all- trans-RA-induced suppression was dose-dependent, and all-trans-RA was somewhat potent than 13-cis-RA. The inhibitory effect of RA on TNF-induced iNOS induction was reversible, completely recovered after 2 days, and was exerted through the inhibition of NF-kappaB activation. TNF also suppressed the lipoprotein lipase (LPL) activity of 3T3-L1 adipocytes. RA could not reverse the TNF- induced LPL suppression at RA levels causing near complete inhibition of the TNF-induced NO production. These results indicate that RAs attenuate iNOS expression reversibly in TNF-stimulated 3T3-L1 adipocytes, and that the TNF-induced LPL suppression is not the result of NO overproduction.
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