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Photoprotective Effects of Two New Morin-Schiff Base Derivatives on UVB-Irradiated HaCaT Cells.
García-Gil, Sara; Rodríguez-Luna, Azahara; Ávila-Román, Javier; Rodríguez-García, Gabriela; Del Río, Rosa E; Motilva, Virginia; Gómez-Hurtado, Mario A; Talero, Elena.
Afiliação
  • García-Gil S; Department of Pharmacology, Faculty of Pharmacy, Universidad de Sevilla, 41012 Seville, Spain.
  • Rodríguez-Luna A; Department of Pharmacology, Faculty of Pharmacy, Universidad de Sevilla, 41012 Seville, Spain.
  • Ávila-Román J; Faculty of Health Sciences, Universidad Loyola Andalucía, 41704 Seville, Spain.
  • Rodríguez-García G; Department of Pharmacology, Faculty of Pharmacy, Universidad de Sevilla, 41012 Seville, Spain.
  • Del Río RE; Instituto de Investigaciones Químico Biológicas, Universidad Michoacana de San Nicolás de Hidalgo, Ciudad Universitaria, Morelia 58030, Michoacán, Mexico.
  • Motilva V; Instituto de Investigaciones Químico Biológicas, Universidad Michoacana de San Nicolás de Hidalgo, Ciudad Universitaria, Morelia 58030, Michoacán, Mexico.
  • Gómez-Hurtado MA; Department of Pharmacology, Faculty of Pharmacy, Universidad de Sevilla, 41012 Seville, Spain.
  • Talero E; Instituto de Investigaciones Químico Biológicas, Universidad Michoacana de San Nicolás de Hidalgo, Ciudad Universitaria, Morelia 58030, Michoacán, Mexico.
Antioxidants (Basel) ; 13(1)2024 Jan 22.
Article em En | MEDLINE | ID: mdl-38275659
ABSTRACT
Ultraviolet (UV) radiation harms the skin, causing oxidative damage, inflammation, and disruption of the skin's barrier function. There is considerable interest in identifying new natural ingredients with antioxidant and anti-inflammatory properties to serve as adjuvants in sunscreens. The flavonoid morin (1) can undergo structural modifications to enhance its biological properties. The aim of this study was to synthesize two new morin-Schiff base derivatives, morin oxime (2) and morin semicarbazone (3), comparing their photoprotective effects with that of the parent compound on UVB-exposed HaCaT keratinocytes. The chemical structure of the novel compounds was revealed based on spectroscopic data analysis. Our findings demonstrated that derivatives 2 and 3 enhanced the light absorption capability in the UV-visible (vis) range compared to 1. Tested compounds exhibited a higher scavenger capacity than Trolox. Moreover, pre-treatment with all compounds protected HaCaT cells from UVB-induced cell death. Compound 3 demonstrated the strongest antioxidant effect, reducing reactive oxygen species (ROS) generation and, subsequently, malondialdehyde (MDA) levels. Additionally, compounds 2 and 3 exhibited greater anti-inflammatory effects than compound 1, significantly reducing interleukin (IL)-6 production levels at all tested concentrations. These findings have demonstrated, for the first time, a promising photoprotective activity of two new Schiff base derivatives and suggest their use as natural sunscreen ingredients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2024 Tipo de documento: Article