Oral and systemic photoprotection
- 12 January 2014
- journal article
- review article
- Published by Wiley in Photodermatology, Photoimmunology & Photomedicine
- Vol. 30 (2-3) , 102-111
Abstract
Summary: Photoprotection can be provided not only by ultraviolet (UV) blockers but also by oral substances. Epidemiologically identified associations between foods and skin cancer and interventional experiments have discovered mechanisms of UV skin damage. These approaches have identified oral substances that are photoprotective in humans. UV inhibits adenosine triphosphate (ATP) production causing an energy crisis, which prevents optimal skin immunity and DNA repair. Enhancing ATP production with oral nicotinamide protects from UV immunosuppression, enhances DNA repair and reduces skin cancer in humans. Reactive oxygen species also contribute to photodamage. Nontoxic substances consumed in the diet, or available as oral supplements, can protect the skin by multiple potential mechanisms. These substances include polyphenols in fruit, vegetables, wine, tea and caffeine‐containing foods. UV‐induced prostaglandin E2 (PGE2) contributes to photodamage. Nonsteroidal anti‐inflammatory drugs and food substances reduce production of this lipid mediator. Fish oils are photoprotective, at least partially by reducing PGE2. Orally consumed substances, either in the diet or as supplements, can influence cutaneous responses to UV. A current research goal is to develop an oral supplement that could be used in conjunction with other sun protective strategies in order to provide improved protection from sunlight.Keywords
This publication has 78 references indexed in Scilit:
- Molecular mechanisms of garlic‐derived allyl sulfides in the inhibition of skin cancer progressionAnnals of the New York Academy of Sciences, 2012
- Pomegranate Fruit Extract Inhibits UVB‐induced Inflammation and Proliferation by Modulating NF‐κB and MAPK Signaling Pathways in Mouse Skin†Photochemistry and Photobiology, 2011
- Effects of high-fat diets rich in either omega-3 or omega-6 fatty acids on UVB-induced skin carcinogenesis in SKH-1 miceCarcinogenesis, 2011
- Prostaglandin E2–prostoglandin E receptor subtype 4 (EP4) signaling mediates UV irradiation-induced systemic immunosuppressionProceedings of the National Academy of Sciences, 2011
- Chemoprevention of Nonmelanoma Skin Cancer With Celecoxib: A Randomized, Double-Blind, Placebo-Controlled TrialJNCI: Journal of the National Cancer Institute, 2010
- A Randomized, Double-Blind, Placebo-Controlled Phase 3 Skin Cancer Prevention Study of α-Difluoromethylornithine in Subjects with Previous History of Skin CancerCancer Prevention Research, 2010
- Skin photoprotection by natural polyphenols: anti-inflammatory, antioxidant and DNA repair mechanismsArchives of Dermatological Research, 2009
- Inhibition of UVB-Induced Skin Tumor Development by Drinking Green Tea Polyphenols Is Mediated Through DNA Repair and Subsequent Inhibition of InflammationJournal of Investigative Dermatology, 2009
- Multiple Signaling Pathways Are Responsible for Prostaglandin E2–Induced Murine Keratinocyte ProliferationMolecular Cancer Research, 2008
- Polyamines and nonmelanoma skin cancerToxicology and Applied Pharmacology, 2007