4.7 Article

Anti-adipogenic activity of maackiain and ononin is mediated via inhibition of PPAR? in human adipocytes

Journal

BIOMEDICINE & PHARMACOTHERAPY
Volume 149, Issue -, Pages -

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2022.112908

Keywords

Obesity; Adipogenesis; PPAR gamma; Ononis spinosa L; Ononin; Maackiain

Funding

  1. European Union [739582, 664620]
  2. European Regional Development Fund through the Science and Education for Smart Growth Operational Programme [BG05M2OP001-1.003-001C01]

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This study investigated the anti-adipogenic capacity of Ononis spinosa L. root and its secondary metabolites in human adipocytes. The results showed that the root, ononin, and maackiain all reduced lipid accumulation during adipocyte differentiation. They also affected the expression of proteins involved in adipogenic regulation. Although the root did not inhibit adipogenic differentiation, it could be used as a source of natural leads with anti-adipogenic potential. The multi-directional mechanism of action of maackiain needs further validation in in vivo obesity models.
Obesity is a global health burden for which we do not yet have effective treatments for prevention or therapy. Plants are an invaluable source of bioactive leads possessing anti-adipogenic potential. Ethnopharmacological use of Ononis spinosa L. roots (OSR) for treatment of obesity and metabolic disorders requires a scientific rationale. The current study examined the anti-adipogenic capacity of OSR and its secondary metabolites ononin (ONON) and maackiain (MACK) in human adipocytes as an in vitro model of obesity. Both ONON and MACK diminished lipid accumulation during adipocyte differentiation. Molecular docking analysis exposed the po-tential interactions between MACK or ONON and target regulatory adipogenic proteins. Furthermore, results from an RT-qPCR analysis disclosed significant upregulation of AMPK by MACK and ONON treatment. In addition, ONON increased SIRT1, PI3K and ACC mRNA expression, while MACK notably downregulated CEBPA, AKT, SREBP1, ACC and ADIPOQ. The protein level of PI3K, C/EBP alpha, PPAR gamma and adiponectin was reduced upon MACK treatment in a concentration-dependent manner. Similarly, ONON suppressed PI3K, PPAR gamma and adipo-nectin protein abundance. Finally, our study provides evidence that ONON exerts anti-adipogenic effect by upregulation of SIRT1 and inhibition of PI3K, PPAR gamma and adiponectin, while MACK induced strong inhibitory effect on adipogenesis via hampering PI3K, PPAR gamma/C/EBP alpha signaling and anti-lipogenic effect through down-regulation of SREBP1 and ACC. Even though OSR does not hamper adipogenic differentiation, it could be exploited as a source of natural leads with anti-adipogenic potential. The multidirectional mechanism of action of MACK warrant further validation in the context of in vivo obesity models.

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