Affiliations 

  • 1 School of Biosciences, Faculty of Health and Medical Sciences Taylor's University Lakeside Campus, No 1 Jalan Taylor's, 47500, Subang Jaya, Malaysia
  • 2 School of Chemistry and Forensic Science, Ingram Building, University of Kent, Canterbury, Kent, CT2 7NH, United Kingdom
  • 3 School of Medicine, Faculty of Health and Medical Sciences Taylor's University Lakeside Campus, No 1 Jalan Taylor's, 47500, Subang Jaya, Malaysia
  • 4 School of Chemistry and Forensic Science, Ingram Building, University of Kent, Canterbury, Kent, CT2 7NH, United Kingdom. Electronic address: C.J.Serpell@kent.ac.uk
  • 5 School of Biosciences, Stacey Building, University of Kent, Canterbury, Kent, CT2 7NJ, United Kingdom
  • 6 School of Pharmacy, Faculty of Health and Medical Sciences Taylor's University Lakeside Campus, No 1 Jalan Taylor's, 47500, Subang Jaya, Malaysia
  • 7 Department of Paraclinical Sciences, Faculty of Medicine and Health Sciences, Universiti Malaysia Sarawak (UNIMAS), 94300, Kota Samarahan, Sarawak, Malaysia
  • 8 School of Medicine, Faculty of Health and Medical Sciences Taylor's University Lakeside Campus, No 1 Jalan Taylor's, 47500, Subang Jaya, Malaysia. Electronic address: EngHwa.Wong@taylors.edu.my
Eur J Pharmacol, 2023 Jan 05;938:175445.
PMID: 36473593 DOI: 10.1016/j.ejphar.2022.175445

Abstract

In this study, the anti-obesity effects of 5,7,3',4',5-pentamethoxyflavone (PMF) and 6,2',4'-trimethoxyflavone (TMF) were evaluated through two distinct mechanisms of action: inhibition of crude porcine pancreatic lipase (PL), and inhibition of adipogenesis in 3T3-L1 pre-adipocytes. Both flavones show dose dependent, competitive inhibition of PL activity. Molecular docking studies revealed binding of the flavones to the active site of PL. In 3T3-L1 adipocytes, both flavones reduced the accumulation of lipids and triglycerides. PMF and TMF also lowered the expression of adipogenic and lipogenic genes. They both reduced the expression of peroxisome proliferator-activated receptor-gamma (PPAR-γ), CCAAT/enhancer-binding protein α and β (C/EBP α and β), sterol regulatory element-binding protein 1 (SREBF 1), fatty acid synthase (FASN), adipocyte binding protein 2 (aP2), and leptin gene. In addition, these flavones enhanced adiponectin mRNA expression, increased lipolysis and enhanced the expression of lipolytic genes: adipose triglycerides lipase (ATGL), hormone sensitive lipase (HSL) and monoglycerides lipase (MAGL) in mature 3T3-L1 adipocytes. Overall, PMF was seen to be a more potent inhibitor of both PL activity and adipogenesis versus TMF. These results suggest that PMF and TMF possess anti-obesity activities and can be further evaluated for their anti-obesity effects.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.