The dietary antioxidant piceatannol inhibits adipogenesis of human adipose mesenchymal stem cells and limits glucose transport and lipogenic activities in adipocytes

Carpéné, C. ; Pejenaute, H. ; Del Moral, R. ; Boulet, N. ; Hijona, E. ; Andrade, F. ; Villanueva-Millán, M.J. ; Aguirre, L. ; Arbones-Mainar, J.M.

Resumen: Phenolic compounds are among the most investigated herbal remedies, as is especially the case for resveratrol. Many reports have shown its anti-aging properties and the ability to reduce obesity and diabetes induced by high-fat diet in mice. However, such beneficial effects hardly translate from animal models to humans. The scientific community has therefore tested whether other plant phenolic compounds may surpass the effects of resveratrol. In this regard, it has been reported that piceatannol reproduces in rodents the anti-obesity actions of its parent polyphenol. However, the capacity of piceatannol to inhibit adipocyte differentiation in humans has not been characterized so far. Here, we investigated whether piceatannol was antiadipogenic and antilipogenic in human preadipocytes. Human mesenchymal stem cells (hMSC), isolated from adipose tissues of lean and obese individuals, were differentiated into mature adipocytes with or without piceatannol, and their functions were explored. Fifty µM of piceatannol deeply limited synthesis/accumulation of lipids in both murine and hMSC-derived adipocytes. Interestingly, this phenomenon occurred irrespective of being added at the earlier or later stages of adipocyte differentiation. Moreover, piceatannol lowered glucose transport into adipocytes and decreased the expression of key elements of the lipogenic pathway (PPAR¿, FAS, and GLUT4). Thus, the confirmation of the antiadipogenic properties of piceatanol in vitro warrants the realization of clinical studies for the application of this compound in the treatment of the metabolic complications associated with obesity.

Idioma: Inglés

DOI: 10.3390/ijms19072081

Año: 2018

Publicado en: International Journal of Molecular Sciences 19, 7 (2018), [14 pp]
ISSN: 1661-6596

Factor impacto JCR: 4.183 (2018)

Categ. JCR: CHEMISTRY, MULTIDISCIPLINARY rank: 45 / 172 = 0.262 (2018) - Q2 - T1
Categ. JCR: BIOCHEMISTRY & MOLECULAR BIOLOGY rank: 77 / 294 = 0.262 (2018) - Q2 - T1

Factor impacto SCIMAGO: 1.312 - Catalysis (Q1) - Computer Science Applications (Q1) - Inorganic Chemistry (Q1) - Spectroscopy (Q1) - Molecular Biology (Q1) - Organic Chemistry (Q1) - Physical and Theoretical Chemistry (Q1) - Medicine (miscellaneous) (Q1)

Financiación: info:eu-repo/grantAgreement/ES/FEDER/Una manera de hacer Europa
Financiación: info:eu-repo/grantAgreement/EUR/INTERREG POCTEFA/Refbio-Pyrenees Biomedical Network
Financiación: info:eu-repo/grantAgreement/ES/ISCIII/FIS/PI17-02268

Tipo y forma: Artículo (Versión definitiva)