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Introduction
Docosahexaenoic acid is an Omega-3 fatty acid renowned for its anti-inflammatory and antioxidant effects. A major benefit of docosahexaenoic acid as a nutraceutical or topical agent is its high safety profile, making it suitable for a wide range of applications. DHA can be incorporated into the phospholipid bilayer of cell membranes to support physiological homeostasis, and act as a precursor for various metabolites with anti-inflammatory and anti- oxidative properties. A well-known metabolite type of DHA is the specialised pro-resolving mediator, which works to stop excessive or prolonged immune responses following acute inflammation. DHA supporting the function of our skin as a protective barrier Our skin acts as a protective barrier against damaging agents and factors in the outside world. One of these damaging factors is somewhat paradoxically also something that is essential for our health: sunlight. Even though sunlight is important in supporting our health, the UV radiation in sun rays poses a constant risk factor to the integrity of our skin cells. UV radiation can cause oxidative and inflammatory damage called photoaging (damage sustained through exposure to light) and even skin cancer. It can also break down collagen, a protein critical for the structural integrity of our cells, which causes a loss of skin elasticity that presents itself as wrinkles. Oral supplementation of mice with DHA-rich krill oil has been reported to protect against the UV radiation-induced decrease in skin collagen, together with improvements in levels of wrinkling and skin hydration (J. Kim et al. 2023). Although dietary intake provides the main source of DHA in our body, the anti-oxidative and anti-inflammatory properties of DHA can be realised through topical application as well. This is especially relevant for the skin, both in health and disease. Topical application of DHA may enhance its uptake in the skin compared to dietary intake, which can enhance the anti- oxidative and anti-inflammatory effects. This method of DHA administration has therefore been chosen in many studies by a prominent research group led by Dr. Surh of the Seoul National University. Using animal models replicating human skin, the laboratory of Dr. Surh has proven over the years how topical DHA administration protects against UV-B damage and skin cancer (S. H. Kim et al. 2023; Rahman et al. 2011; Yum et al. 2017). Using a hairless mouse model, this laboratory has proven how the topical administration of a DHA metabolite is able to reduce the levels of markers for oxidative stress following UV-induced skin damage. Moreover, using similar models, the research group showed that topical DHA administration prior to exposure to damaging UV radiation can protect against the activation of inflammatory and oxidative stress mechanisms in the skin (Rahman et al. 2011; Yum et al. 2017). As these treatments aim to prevent skin damage and cancer development following UV damage, ethical constraints do not allow the same study setup being tested in a clinical trial. This is due to the fact that study participant would have to be exposed to potentially cancer- causing levels of UV-radiation. Furthermore, clinical intervention trials are not suitable to investigate general ageing of the skin in humans, as this is a process of accumulating damage and increasing inflammatory reactions over many years. Nevertheless, studies using human skin cells report that DHA resolves inflammatory reactions and improves its barrier function (Jia et al. 2019; Serini et al. 2019). A commonality between general ageing of the skin (for example through UV damage) and skin conditions and is the similarity of inflammatory mechanisms that are at play. Over the years, our skin accumulates damage from constant exposure to harmful agents and radiation from sunlight; this coincides with a general increase in levels of inflammation that occurs with age, referred to as ‘inflammaging’. As with protecting against inflammation due to UV damage, research has put forward the protective role of DHA against skin conditions where inflammation plays a central role. Positive role of DHA in conditions of the skin Many skin conditions are characterized by persistent inflammatory reactions, such as psoriasis, acne, and eczema. The symptoms of these conditions lead to a significant decrease in the quality of life; the altered aesthetics can be a large burden for affected individuals. Perhaps not surprisingly, a deficit in anti-inflammatory Omega-3 acids is associated with certain skin conditions (Guertler, Fiedler, et al. 2024; Kim et al. 2025; Myśliwiec et al. 2017). Research has shown that DHA supplementation has a positive influence on skin health in these conditions, as detailed below. In persons with psoriasis, higher relative levels of DHA are associated with a lower psoriasis severity score (Myśliwiec et al. 2017). Furthermore, supplementation of human skin cells with DHA can cause a reduction in the abnormal proliferation of these cells that causes psoriasis (Morin et al. 2021). In persons with acne, dietary supplementation with DHA has been shown to reduce the number of inflammatory and non-inflammatory lesions (Guertler, Neu, et al. 2024; Jung et al. 2014). Another prevalent condition of the skin wherein DHA can play a positive role is atopic dermatitis, commonly referred to as eczema. In this skin condition, oral supplementation with DHA improves dermatological scores of eczema severity in people with this condition (Koch et al. 2008). Taken together, scientific studies such as those mentioned above show us how DHA can counter inflammation and oxidative damage in the skin, both of which play a central role in skin conditions and general ageing of the skin. References Guertler, Anne, Tobias Fiedler, Diana Lill, Anne-Charlotte Kuna, Arina Volsky, Jens Wallmichrath, Till Kämmerer, Lars E. French, and Markus Reinholz. 2024. ‘Deficit of Omega-3 Fatty Acids in Acne Patients—A Cross-Sectional Pilot Study in a German Cohort’. Life 14(4):519. doi:10.3390/life14040519. Guertler, Anne, Katharina Neu, Diana Lill, Benjamin Clanner-Engelshofen, Lars E. French, and Markus Reinholz. 2024. ‘Exploring the Potential of Omega-3 Fatty Acids in Acne Patients: A Prospective Intervention Study’. Journal of Cosmetic Dermatology. doi:10.1111/jocd.16434. Jia, Tinghan, Wu Qiao, Qifeng Yao, Wenhui Wu, and Ken Kaku. 2019. ‘Treatment with Docosahexaenoic Acid Improves Epidermal Keratinocyte Differentiation and Ameliorates Inflammation in Human Keratinocytes and Reconstructed Human Epidermis Models’. Molecules 24(17):3156. doi:10.3390/molecules24173156. Jung, Jae Yoon, Hyuck Hoon Kwon, Jong Soo Hong, Ji Young Yoon, Mi Sun Park, Mi Young Jang, and Dae Hun Suh. 2014. ‘Effect of Dietary Supplementation with Omega-3 Fatty Acid and Gamma-Linolenic Acid on Acne Vulgaris: A Randomised, Double-Blind, Controlled Trial’. Acta Dermato-Venereologica 94(5):521–25. doi:10.2340/00015555-1802. Kim, Bo Ri, Gahyun Kim, Seon-Pil Jin, Chong Won Choi, Jinho Kim, and Hyunsun Park. 2025. ‘The Causal Association between Polyunsaturated Fatty Acids and Acne: A Two-Sample Mendelian Randomization Study’. British Journal of Dermatology ljaf052. doi:10.1093/bjd/ljaf052. Kim, Jongkyu, Namju Lee, Yoon-Seok Chun, Sang-Hoon Lee, and Sae-Kwang Ku. 2023. ‘Krill Oil’s Protective Benefits against Ultraviolet B-Induced Skin Photoaging in Hairless Mice and In Vitro Experiments’. Marine Drugs 21(9):479. doi:10.3390/md21090479. Kim, Seong Hoon, So Eui Lee, Su-Jung Kim, Xizhu Fang, Jihyeon Hur, Erdi Sozen, Nesrin Kartal Özer, Kwang Pyo Kim, and Young-Joon Surh. 2023. ‘Protective Effects of an Electrophilic Metabolite of Docosahexaenoic Acid on UVB-Induced Oxidative Cell Death, Dermatitis, and Carcinogenesis’. Redox Biology 62:102666. doi:10.1016/j.redox.2023.102666. Koch, C., S. Dölle, M. Metzger, C. Rasche, H. Jungclas, R. Rühl, H. Renz, and M. Worm. 2008. ‘Docosahexaenoic Acid (DHA) Supplementation in Atopic Eczema: A Randomized, Double blind,‐ Controlled Trial’. British Journal of Dermatology 158(4):786–92. doi:10.1111/j.1365-2133.2007.08430.x. Morin, Sophie, Mélissa Simard, Nicolas Flamand, and Roxane Pouliot. 2021. ‘Biological Action of Docosahexaenoic Acid in a 3D Tissue-Engineered Psoriatic Skin Model: Focus on the PPAR Signaling Pathway’. Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids 1866(12):159032. doi:10.1016/j.bbalip.2021.159032. Myśliwiec, Hanna, Anna Baran, Ewa Harasim-Symbor, Piotr Myśliwiec, Anna Justyna Milewska, Adrian Chabowski, and Iwona Flisiak. 2017. ‘Serum Fatty Acid Profile in Psoriasis and Its Comorbidity’. Archives of Dermatological Research 309(5):371–80. doi:10.1007/s00403-017-1748-x. Rahman, Md. Mostafizur, Joydeb Kumar Kundu, Jun-Wan Shin, Hye-Kyung Na, and Young-Joon Surh. 2011. ‘Docosahexaenoic Acid Inhibits UVB-Induced Activation of NF-κB and Expression of COX-2 and NOX-4 in HR-1 Hairless Mouse Skin by Blocking MSK1 Signaling’. PLoS ONE 6(11):e28065. doi:10.1371/journal.pone.0028065. Serini, Simona, Roberta Cassano, Enrica Facchinetti, Gaia Amendola, Sonia Trombino, and Gabriella Calviello. 2019. ‘Anti-Irritant and Anti-Inflammatory Effects of DHA Encapsulated in Resveratrol-Based Solid Lipid Nanoparticles in Human Keratinocytes’. Nutrients 11(6):1400. doi:10.3390/nu11061400. Yum, Hye-Won, Jin Park, Hyun-Jung Park, Jun Wan Shin, Yong-Yeon Cho, Su-Jung Kim, Jing X. Kang, and Young-Joon Surh. 2017. ‘Endogenous ω-3 Fatty Acid Production by Fat-1 Transgene and Topically Applied Docosahexaenoic Acid Protect against UVB-Induced Mouse Skin Carcinogenesis’. Scientific Reports 7(1):11658. doi:10.1038/s41598-017-11443-2. |
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