Cannabidiol and Cannabigerol Modify the Composition and Physicochemical Properties of Keratinocyte Membranes Exposed to UVA

The action of UVA radiation (both that derived from solar radiation and that used in the treatment of skin diseases) modifies the function and composition of keratinocyte membranes. Therefore, this study aimed to assess the effects of phytocannabinoids (CBD and CBG), used singly and in combination,...

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Main Authors: Adam Wroński, Izabela Dobrzyńska, Szymon Sękowski, Wojciech Łuczaj, Ewa Olchowik-Grabarek, Elżbieta Skrzydlewska
Format: Article
Language:English
Published: MDPI AG 2023-08-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/24/15/12424
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author Adam Wroński
Izabela Dobrzyńska
Szymon Sękowski
Wojciech Łuczaj
Ewa Olchowik-Grabarek
Elżbieta Skrzydlewska
author_facet Adam Wroński
Izabela Dobrzyńska
Szymon Sękowski
Wojciech Łuczaj
Ewa Olchowik-Grabarek
Elżbieta Skrzydlewska
author_sort Adam Wroński
collection DOAJ
description The action of UVA radiation (both that derived from solar radiation and that used in the treatment of skin diseases) modifies the function and composition of keratinocyte membranes. Therefore, this study aimed to assess the effects of phytocannabinoids (CBD and CBG), used singly and in combination, on the contents of phospholipids, ceramides, lipid rafts and sialic acid in keratinocyte membranes exposed to UVA radiation, together with their structure and functionality. The phytocannabinoids, especially in combination (CBD+CBG), partially prevented increased levels of phosphatidylinositols and sialic acid from occurring and sphingomyelinase activity after the UVA exposure of keratinocytes. This was accompanied by a reduction in the formation of lipid rafts and malondialdehyde, which correlated with the parameters responsible for the integrity and functionality of the keratinocyte membrane (membrane fluidity and permeability and the activity of transmembrane transporters), compared to UVA-irradiated cells. This suggests that the simultaneous use of two phytocannabinoids may have a protective effect on healthy cells, without significantly reducing the therapeutic effect of UV radiation used to treat skin diseases such as psoriasis.
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spelling doaj.art-6a2edf3aa83a4ce8a14baaed75ce77262023-11-18T23:04:52ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672023-08-0124151242410.3390/ijms241512424Cannabidiol and Cannabigerol Modify the Composition and Physicochemical Properties of Keratinocyte Membranes Exposed to UVAAdam Wroński0Izabela Dobrzyńska1Szymon Sękowski2Wojciech Łuczaj3Ewa Olchowik-Grabarek4Elżbieta Skrzydlewska5Dermatological Specialized Center “DERMAL” NZOZ in Białystok, Nowy Swiat 17/5, 15-453 Białystok, PolandLaboratory of Bioanalysis, Faculty of Chemistry, University in Białystok, Ciołkowskiego 1K, 15-245 Białystok, PolandLaboratory of Molecular Biophysics, Department of Microbiology and Biotechnology, Faculty of Biology, University in Białystok, Ciołkowskiego 1J, 15-245 Białystok, PolandDepartment of Analytical Chemistry, Medical University of Białystok, Mickiewicza 2D, 15-222 Białystok, PolandLaboratory of Molecular Biophysics, Department of Microbiology and Biotechnology, Faculty of Biology, University in Białystok, Ciołkowskiego 1J, 15-245 Białystok, PolandDepartment of Analytical Chemistry, Medical University of Białystok, Mickiewicza 2D, 15-222 Białystok, PolandThe action of UVA radiation (both that derived from solar radiation and that used in the treatment of skin diseases) modifies the function and composition of keratinocyte membranes. Therefore, this study aimed to assess the effects of phytocannabinoids (CBD and CBG), used singly and in combination, on the contents of phospholipids, ceramides, lipid rafts and sialic acid in keratinocyte membranes exposed to UVA radiation, together with their structure and functionality. The phytocannabinoids, especially in combination (CBD+CBG), partially prevented increased levels of phosphatidylinositols and sialic acid from occurring and sphingomyelinase activity after the UVA exposure of keratinocytes. This was accompanied by a reduction in the formation of lipid rafts and malondialdehyde, which correlated with the parameters responsible for the integrity and functionality of the keratinocyte membrane (membrane fluidity and permeability and the activity of transmembrane transporters), compared to UVA-irradiated cells. This suggests that the simultaneous use of two phytocannabinoids may have a protective effect on healthy cells, without significantly reducing the therapeutic effect of UV radiation used to treat skin diseases such as psoriasis.https://www.mdpi.com/1422-0067/24/15/12424phospholipidsceramideslipid raftsmembrane fluiditymembrane electrical chargetransmembrane transporters
spellingShingle Adam Wroński
Izabela Dobrzyńska
Szymon Sękowski
Wojciech Łuczaj
Ewa Olchowik-Grabarek
Elżbieta Skrzydlewska
Cannabidiol and Cannabigerol Modify the Composition and Physicochemical Properties of Keratinocyte Membranes Exposed to UVA
International Journal of Molecular Sciences
phospholipids
ceramides
lipid rafts
membrane fluidity
membrane electrical charge
transmembrane transporters
title Cannabidiol and Cannabigerol Modify the Composition and Physicochemical Properties of Keratinocyte Membranes Exposed to UVA
title_full Cannabidiol and Cannabigerol Modify the Composition and Physicochemical Properties of Keratinocyte Membranes Exposed to UVA
title_fullStr Cannabidiol and Cannabigerol Modify the Composition and Physicochemical Properties of Keratinocyte Membranes Exposed to UVA
title_full_unstemmed Cannabidiol and Cannabigerol Modify the Composition and Physicochemical Properties of Keratinocyte Membranes Exposed to UVA
title_short Cannabidiol and Cannabigerol Modify the Composition and Physicochemical Properties of Keratinocyte Membranes Exposed to UVA
title_sort cannabidiol and cannabigerol modify the composition and physicochemical properties of keratinocyte membranes exposed to uva
topic phospholipids
ceramides
lipid rafts
membrane fluidity
membrane electrical charge
transmembrane transporters
url https://www.mdpi.com/1422-0067/24/15/12424
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