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Codium fragile reduces adipose tissue expansion and fatty liver incidence by downregulating adipo‐ and lipogenesis.

Authors :
Seo, Hyo‐Deok
Lee, Eunyoung
Ahn, Jiyun
Hahm, Jeong‐Hoon
Ha, Tae‐Youl
Lee, Dae‐Hee
Jung, Chang Hwa
Source :
Journal of Food Biochemistry. Dec2022, Vol. 46 Issue 12, p1-9. 9p.
Publication Year :
2022

Abstract

Codium fragile (C. fragile) is a marine alga with high functional food potential. Recent studies have proven C. fragile extract (CFE) effective against obesity. However, the exact underlying mechanism of CFE's anti‐obesity effects remains unclear. Herein, CFE was orally administered to male C57BL/6 mice for 7 weeks, along with a high‐fat diet. CFE (100 mg/kg) effectively induced weight loss, lowered serum cholesterol levels, and suppressed adipocyte differentiation in white adipose tissue (WAT). Furthermore, CFE effectively reduced hepatic total triglyceride, cholesterol, and lipid levels, while significantly improving liver size and color. mRNA expression analysis in WAT and liver tissue revealed that CFE significantly suppressed the expression of PPARγ and aP‐2 in adipocyte differentiation, and SREBP‐1c and FAS in de novo lipogenesis, suggesting that CFE's anti‐obesity effect is exerted by gene inhibition. Practical applications: Research on marine plants with anti‐obesity effects has been increasing recently. This study demonstrated that C. fragile extract (CFE) is effective in reducing body weight and suppressing adipocyte differentiation, along with the improvement of fatty liver in mice fed with a high‐fat diet (HFD). The anti‐obesity effect of CFE was exhibited by the down‐regulation of adipogenesis and lipogenesis, respectively. Based on these results, C. fragile could be useful, not only to effectively combat obesity but also in improving obesity‐induced liver dysfunction. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01458884
Volume :
46
Issue :
12
Database :
Academic Search Index
Journal :
Journal of Food Biochemistry
Publication Type :
Academic Journal
Accession number :
161006630
Full Text :
https://doi.org/10.1111/jfbc.14395