4.7 Article

Ferulic acid in Lolium multiflorum inhibits adipogenesis in 3T3-L1 cells and reduced high-fat-diet-induced obesity in Swiss albino mice via regulating p38MAPK and p44/42 signal pathways

Journal

JOURNAL OF FUNCTIONAL FOODS
Volume 37, Issue -, Pages 293-302

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jff.2017.08.002

Keywords

3T3-L1 cells; Swiss albino mice; Ferulic acid; High fat diet; PPAR-gamma 2; AMPK-alpha; p38MAPK; p44/42 (Erk 1/2)

Funding

  1. Cooperative Research Program for Agriculture Science & Technology Development Project entitled Technical development to increase utilization of Italian ryegrass in livestock - Rural Development Administration, Republic of Korea [PJ010903022016]
  2. National Institute of Animal Science - Rural Development Administration, Republic of Korea
  3. Rural Development Administration (RDA), Republic of Korea [PJ010903022016] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Ferulic acid (FA), a ubiquitous natural phenolic component found in many plants and fruits, has a wide range of biomedical applications. However, action mechanism of FA involved in lipid accumulation remains unclear. In this study, lipid accumulation and changes in expression levels of genes and proteins associated with adipocyte differentiation were investigated. Oil red O staining and glycerol accumulation assay revealed that FA decreased lipid accumulation in cells. FA downregulated expression levels of C/EBP-beta, C/EBP-alpha, PPAR-gamma, and SREBP-1, but upregulated expression levels of p38MAPK, p44/42 (Erk 1/2), and AMPK-alpha phosphorylation in 3T3 -L1 cells. FA effects on high fat diet -induced (HFD) obese mice were also investigated. FA lowered HFD-induced body weight gain of obese mice without affecting regular food intake. FA reduced serum levels of total cholesterol and triglycerides in HFD obese mice. Similar to results of in vitro study, FA inhibited adipogenesis and lipid accumulation via downregulating PPAR-gamma while upregulating p38MAPK, p44/42 (Erk 1/2), and AMPK-ct phosphorylation in Swiss albino mice. (C) 2017 Elsevier Ltd. All rights reserved.

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