4.6 Article

Mangostanin, a Xanthone Derived from Garcinia mangostana Fruit, Exerts Protective and Reparative Effects on Oxidative Damage in Human Keratinocytes

期刊

PHARMACEUTICALS
卷 15, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/ph15010084

关键词

mangostanin; Garcinia mangostana; oxidative stress; apoptosis; cosmeceuticals

资金

  1. Associazione Italiana Ricerca sul Cancro (AIRC) [IG 13312, IG 18999]
  2. AIRC [17216]
  3. Regione Campania POR Campania FESR 2014-2020 Combattere la resistenza tumorale: piattaforma integrata multidisciplinare per un approccio tecnologico innovativo alle oncoterapie-Campania Oncoterapie [B61G18000470007]
  4. Fondazione Cariplo TRIDEO 2015 [17216]

向作者/读者索取更多资源

The fruit of Garcinia mangostana, known as mangosteen, has antioxidant, anti-inflammatory, immunomodulatory, and anticancer activities. This study demonstrates that the polyphenols called xanthones in mangosteen can protect the skin from oxidative damage and prevent skin aging. Mangostanin, one of the xanthone derivatives, reduces the generation of reactive oxygen species, preventing cell damage and apoptosis activation. This research highlights the potential of mangostanin for development in the nutraceutical and cosmeceutical fields.
The fruit of Garcinia mangostana (mangosteen) is known in ancient traditional Asian medicine for its antioxidant, anti-inflammatory, immunomodulatory and anticancer activities. These effects are mainly due to the action of polyphenols known as xanthones, which are contained in the pericarp of the fruit. In recent years, there has been a growing interest from pharmaceutical companies in formulating new topicals based on mangosteen full extracts to prevent skin aging. However, the molecules responsible for these effects and the mechanisms involved have not been investigated so far. Here, the arils and shells of Garcinia mangostana were extracted with chloroform and methanol, and the extracts were further purified to yield 12 xanthone derivatives. Their effects were evaluated using in vitro cultures of human epidermal keratinocytes. After confirming the absence of cytotoxicity, we evaluated the antioxidant potential of these compounds, identifying mangostanin as capable of both protecting and restoring oxidative damage induced by H2O2. We showed how mangostanin, by reducing the generation of intracellular reactive oxygen species (ROS), prevents the activation of AKT (protein kinase B), ERK (extracellular signal-regulated kinase), p53, and other cellular pathways underlying cell damage and apoptosis activation. In conclusion, our study is the first to demonstrate that mangostanin is effective in protecting the skin from the action of free radicals, thus preventing skin aging, confirming a potential toward its development in the nutraceutical and cosmeceutical fields.

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