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Biochem Biophys Res Commun ; 508(1): 97-101, 2019 01 01.
Article in English | MEDLINE | ID: mdl-30471854

ABSTRACT

Nobiletin has protective effects on cardiovascular diseases, but the mechanism is not clear. In this study, we examined whether nobiletin affects the expression of miR-590/LPL and its relative effects on lipid accumulation and pro-inflammatory cytokine secretion in human THP-1 macrophages. RT-qPCR analysis showed that nobiletin increased the expression of miR-590. Western blot analysis showed that nobiletin-suppressed LPL expression was enhanced by miR-590 mimic and abrogated by miR-590 inhibitor. Oil Red O staining and high-performance liquid chromatography assays showed that nobiletin attenuated lipid accumulation in macrophages. Treatment with nobiletin and miR-590 mimic decreased cellular lipid accumulation, whereas treatment with miR-590 inhibitor increased cellular lipid accumulation. ELISA illustrated that nobiletin alleviated pro-inflammatory cytokine secretion in macrophages as measured by, which was reduced by miR-590 mimic and increased by miR-590 inhibitor. In conclusion, nobiletin may alleviate lipid accumulation and secretion of pro-inflammatory cytokines by enhancing the inhibitory effect of miR-590 on LPL expression, suggesting a promising strategy for potential drug development for atherosclerosis.


Subject(s)
Flavones/pharmacology , Lipid Metabolism/drug effects , Lipoprotein Lipase/metabolism , MicroRNAs/genetics , MicroRNAs/metabolism , Atherosclerosis/drug therapy , Atherosclerosis/genetics , Atherosclerosis/metabolism , Cardiotonic Agents/pharmacology , Cytokines/metabolism , Down-Regulation/drug effects , Drug Development , Humans , Inflammation Mediators/metabolism , Lipoprotein Lipase/antagonists & inhibitors , Macrophages/drug effects , Macrophages/metabolism , THP-1 Cells , Up-Regulation/drug effects
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