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Bitter melon extracts suppressed differentiation and triglyceride content of 3T3‐L1 adipocytes
Author(s) -
Tam Ka Shing,
Wu Jiajun,
Tse Iris,
Tam Tsun Ming,
Wang Ming Fu,
Li Edmund Tsze Shing
Publication year - 2008
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.22.1_supplement.889.11
Subject(s) - chemistry , triglyceride , ethanol , momordica , endocrinology , acetyl coa carboxylase , 3t3 l1 , fatty acid synthase , medicine , downregulation and upregulation , carnitine , ingredient , pyruvate carboxylase , adipocyte , fatty acid , biochemistry , adipose tissue , food science , enzyme , biology , cholesterol , gene , traditional medicine
Bitter melon (BM; Momordica charantia ) supplementation slows weight gain and tissue fat accumulation in fat diet‐induced obese rat. Liver and muscle carnitine palmitoyl transferase‐I expression was enhanced in BM rats, suggesting increased lipid oxidation. This study was designed to determine if extracts from BM juice can suppress triglyceride (TG) content in the 3T3‐L1 cell line. 3T3‐L1 pre‐adipocytes were induced to differentiate in the presence or absence of an ethanol‐water extract of BM juice. The latter was obtained by stepwise gradient elution of an organic extract of BM juice. Two fractions (eluted by 10% & 30% ethanol respectively and then freeze‐dried; F2 at 350μg/mL & F3 at 50μg/mL) were found to reduce TG content on day 10 ( p <0.01, F3) & day 12 ( p< 0.01, both); and GPDH activity on day 10 & 12 ( p< 0.01, both) of a 12‐day study. Two‐way ANOVA indicated reduced mRNA expression of fatty acid synthase ( p< 0.001), acetyl CoA carboxylase 1 ( p< 0.01) and Glut‐4 ( p <0.01) in BM‐treated adipocytes. With F3, these effects primarily occurred between days 8–10. Downregulation of PPARγ ( p <0.001) and SREBP‐1c ( p <0.001) mRNA expression was observed in F3‐treated cells on day 12. The data suggest that bioactive ingredient(s) in BM may suppress TG synthesis in 3T3‐L1 cells through suppressing the expression of certain lipogenic genes and transcription factors. (Supported by the Faculty Development Fund, HKU)