Kefir inhibits 3T3-L1 adipocyte differentiation through down-regulation of adipogenic transcription factor expression

BACKGROUND: Kefir, a traditional fermented milk composed of microbial symbionts, is reported to have various health benefits such as anti‐tumour, anti‐inflammatory, anti‐neoplastic and pro‐digestive effects. In this study, to elucidate the effects of kefir on adipocyte differentiation and lipid accu...

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Veröffentlicht in:Journal of the science of food and agriculture 2013-02, Vol.93 (3), p.485-490
Hauptverfasser: Ho, Jin-Nyoung, Choi, Jae-Woo, Lim, Won-Chul, Kim, Mi-Kyoung, Lee, In-Young, Cho, Hong-Yon
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Sprache:eng
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Zusammenfassung:BACKGROUND: Kefir, a traditional fermented milk composed of microbial symbionts, is reported to have various health benefits such as anti‐tumour, anti‐inflammatory, anti‐neoplastic and pro‐digestive effects. In this study, to elucidate the effects of kefir on adipocyte differentiation and lipid accumulation, three fractions were prepared from kefir culture broth. The inhibitory effects of kefir liquid culture broth fraction (Fr‐1), soluble fraction (Fr‐2) and insoluble fraction (Fr‐3), prepared by sonication of kefir solid culture broth, on adipocyte differentiation in 3T3‐L1 preadipocytes were examined. RESULTS: Fr‐3 (0.1 mg mL−1) significantly decreased lipid accumulation and glycerol‐3‐phosphate dehydrogenase (GPDH) activity by 60 and 68% respectively without affecting cell viability. In addition, Fr‐3 treatment down‐regulated the mRNA expression of adipogenic transcription factors including C/EBPα (32%), PPARγ (46%) and SREBP‐1c (34%) during adipocyte differentiation compared with untreated control cells. The mRNA expression of adipocyte‐specific genes (aP2, FAS and ACC) was also clearly decreased. CONCLUSION: The results suggest that the insoluble fraction of kefir (Fr‐3) mediates anti‐adipogenic effects through the inhibition of adipocyte differentiation, partly via suppression of the C/EBPα‐, SREBP‐1c‐ and PPARγ‐dependent pathways. © 2012 Society of Chemical Industry
ISSN:0022-5142
1097-0010
DOI:10.1002/jsfa.5792