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Trigonelline attenuates the adipocyte differentiation and lipid accumulation in 3T3-L1 cells

  • Soundharrajan Ilavenil
  • , Mariadhas Valan Arasu
  • , Jeong Chae Lee
  • , Da Hye Kim
  • , Sang Gun Roh
  • , Hyung Su Park
  • , Gi Jun Choi
  • , Vijayakumar Mayakrishnan
  • , Ki Choon Choi*
  • *Corresponding author for this work
  • United States Food and Drug Administration
  • Shimane University
  • Tottori University
  • Tohoku University
  • University of Malaya

Research output: Contribution to journalJournal articlepeer-review

Abstract

Trigonelline is a natural alkaloid mainly found in Trigonella Foenum Graecum (fenugreek) Fabaceae and other edible plants with a variety of medicinal applications. Therefore, we investigated the molecular mechanism of trigonelline (TG) on the inhibition of adipocyte differentiation and lipid accumulation in 3T3-L1 cells. Trigonelline suppressed lipid droplet accumulation in a concentration (75 and 100 μM) dependent manner. Treatment of adipocyte with of TG down regulates the peroxisome proliferator-activated receptor (PPARγ) and CCAAT element binding protein (C/EBP-α) mRNA expression, which leads to further down regulation of other gene such as adiponectin, adipogenin, leptin, resistin and adipocyte fatty acid binding protein (aP2) as compared with respective control cells on 5th and 10th day of differentiation. Further, addition of triognelline along with troglitazone to the adipocyte attenuated the troglitazone effects on PPARγ mediated differentiation and lipid accumulation in 3T3-L1 cells. Trigonelline might compete against troglitazone for its binding to the PPARγ. In addition, adipocyte treated with trigonelline and isoproterenol separately. Isoproterenol, a lipolytic agent which inhibits the fatty acid synthase and GLUT-4 transporter expression via cAMP mediated pathway, we found that similar magnitude response of fatty acid synthase and GLUT-4 transporter expression in trigonelline treated adipocyte. These results suggest that the trigonelline inhibits the adipogenesis by its influences on the expression PPARγ, which leads to subsequent down regulation of PPAR-γ mediated pathway during adipogenesis. Our findings provide key approach to the mechanism underlying the anti-adipogenic activity of trigonelline.

Original languageEnglish
Pages (from-to)758-765
Number of pages8
JournalPhytomedicine
Volume21
Issue number5
DOIs
StatePublished - 2014.04.15

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Adipogenesis
  • cAMP
  • Isoproterenol
  • PPARγ
  • Trigonelline
  • Troglitazone

Quacquarelli Symonds(QS) Subject Topics

  • Medicine
  • Pharmacy & Pharmacology

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