Dietary supplementation with sulforaphane ameliorates skin aging through activation of the Keap1-Nrf2 pathway |
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| Institution: | 1. Department of Science and Environment, Roskilde University, Roskilde, Denmark;2. Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal;3. Institute for Interdisciplinary Research, University of Coimbra, Coimbra, Portugal;4. Department of Internal Medicine, Division of Hematology and Oncology Texas Tech University Medical Sciences Center, Lubbock, Texas, USA;5. Department of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, AR, USA;6. Department of Pediatrics, University of Arkansas for Medical Sciences; Arkansas Children''s Research Institute, Little Rock, AR, USA;7. Department of Geriatrics, University of Arkansas for Medical Sciences, Little Rock, AR, USA;1. PhD program in Experimental Biology and Biomedicine, Institute for Interdisciplinary Research, Coimbra, Portugal;2. Centre for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal;3. Institute for Interdisciplinary Research, University of Coimbra, Coimbra, Portugal;4. Arkansas Children''s Research Institute, Little Rock, AR, United States;5. Department of Science and Environment, Roskilde University, Roskilde, Denmark;6. Dept. of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, AR, United States;7. Arkansas Children''s Nutrition Center, Little Rock, AR, United States;8. Dept. of Geriatrics, University of Arkansas for Medical Sciences, Little Rock, AR, United States;9. APDP-Portuguese Diabetes Association, Lisbon, Portugal |
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| Abstract: | Visible impairments in skin appearance, as well as a subtle decline in its functionality at the molecular level, are hallmarks of skin aging. Activation of the nuclear factor (erythroid-derived 2)-like 2 (Nrf2)-pathway, which is important in controlling inflammation and oxidative stress that occur during aging, can be triggered by sulforaphane (SFN), an isothiocyanate found in plants from the Brassicaceae family. This study aimed to assess the effects of SFN intake on age-related skin alterations. Male C57BL6 young (2 months) and old (21 months) mice were treated for 3 months with SFN diet (442.5 mg per kg) or control diet. The antioxidant capacities of the skin were increased in old SFN-treated animals as measured by mRNA levels of Nrf2 (P<.001) and its target genes NQO1 (P<.001) and HO1 (P<.01). Protein expression for Nrf2 was also increased in old SFN fed animals (P<.01), but not the protein expression of NQO1 or HO1. Additionally, ROS and MMP9 protein levels were significantly decreased (P<.05) in old SFN fed animals. Histopathological analysis confirmed that there was no difference in epidermal thickness in old, when compared to young, SFN treated animals, while the dermal layer thickness was lower in old vs. young, treated animals (P<.05). Moreover, collagen deposition was improved with SFN treatment in young (P<.05) and structurally significantly improved in the old mice (P<.001). SFN dietary supplementation therefore ameliorates skin aging through activation of the Nrf2-pathway. |
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