Bioassay-guided isolation of active anti-adipogenic compound from royal jelly and the study of possible mechanisms.
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ABSTRACT: BACKGROUND:Royal jelly (RJ) has been used traditionally for dietary, cosmetic and health purposes for a long time in different parts of the world. Scientific studies have also shown its numerous health-promoting properties including hypoglycemic and anti-hypercholesterolemic action. In this study, we investigated the anti-adipogenic activity of RJ in 3?T3-L1 cells and isolated the major responsible root component for the activity. METHODS:An active anti-adipogenic compound was isolated through bioassay-guided isolation process by successive treatment of RJ and its active fractions on 3?T3-L1 cell line. (E)-10-Hydroxy-2-decenoic Acid (10-HDA) was identified using NMR spectroscopy and ultra-performance liquid chromatography (UPLC). As 10-HDA showed significant anti-adipogenic activity with Oil Red O staining and TG content assay on 3?T3-L1 adipocytes, further study was carried out in molecular level for the expression of adipogenic transcription factors such as PPAR?, FABP4, C/EBP?, SREBP-1c, and Leptin. The effect of 10-HDA on preliminary molecules such as pAkt, pERK, C/EBP?, and pCREB were studied in the early stage of adipogenesis. The effect of 10-HDA on reactive oxygen species (ROS) production in fully differentiating adipocytes was measured by nitro blue tetrazolium (NBT) assay. RESULT:Results showed that triacylglycerol accumulation and ROS production was markedly suppressed by 10-HDA. Preliminary molecules such as pAkt, pERK, pCERB, and C/EBP? were found to be down-regulated by 10-HDA, which led to down-regulation of key adipogenic transcription factors such as PPAR?, FABP4, CEBP?, SREBP-1c, and Leptin on 3?T3-L1 adipocytes. CONCLUSION:Our results suggest that anti-adipogenesis of 10-HDA on 3?T3-L1 adipocyte takes place via two mechanisms: inhibition of cAMP/PKA pathway and inhibition of p-Akt and MAPK dependent insulin signaling pathway. So it is considered that 10-HDA, a major component of RJ, can be a potential therapeutic medicine for obesity.
SUBMITTER: Pandeya PR
PROVIDER: S-EPMC6352437 | biostudies-other | 2019 Jan
REPOSITORIES: biostudies-other
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