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The Effect of γ-Aminobutyric Acid Intake on UVB- Induced Skin Damage in Hairless Mice
The skin, the largest organ in the body, undergoes age-related changes influenced by both intrinsic and extrinsic factors. The primary external factor is photoaging which causes hyperpigmentation, uneven skin surface, deep wrinkles, and markedly enlarged capillaries. In the human dermis, it decrease...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Applied Pharmacology
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10616514/ https://www.ncbi.nlm.nih.gov/pubmed/37524442 http://dx.doi.org/10.4062/biomolther.2023.085 |
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author | Zhao, Hairu Park, Bomi Kim, Min-Jung Hwang, Seok-Hyun Kim, Tae-Jong Kim, Seung-Un Kwon, Iksun Hwang, Jae Sung |
author_facet | Zhao, Hairu Park, Bomi Kim, Min-Jung Hwang, Seok-Hyun Kim, Tae-Jong Kim, Seung-Un Kwon, Iksun Hwang, Jae Sung |
author_sort | Zhao, Hairu |
collection | PubMed |
description | The skin, the largest organ in the body, undergoes age-related changes influenced by both intrinsic and extrinsic factors. The primary external factor is photoaging which causes hyperpigmentation, uneven skin surface, deep wrinkles, and markedly enlarged capillaries. In the human dermis, it decreases fibroblast function, resulting in a lack of collagen structure and also decreases keratinocyte function, which compromises the strength of the protective barrier. In this study, we found that treatment with γ-aminobutyric acid (GABA) had no toxicity to skin fibroblasts and GABA enhanced their migration ability, which can accelerate skin wound healing. UVB radiation was found to significantly induce the production of matrix metalloproteinase 1 (MMP-1), but treatment with GABA resulted in the inhibition of MMP-1 production. We also investigated the enhancement of filaggrin and aquaporin 3 in keratinocytes after treatment with GABA, showing that GABA can effectively improve skin moisturization. In vivo experiments showed that oral administration of GABA significantly improved skin wrinkles and epidermal thickness. After the intake of GABA, there was a significant decrease observed in the increase of skin thickness measured by calipers and erythema. Additionally, the decrease in skin moisture and elasticity in hairless mice exposed to UVB radiation was also significantly restored. Overall, this study demonstrates the potential of GABA as functional food material for improving skin aging and moisturizing. |
format | Online Article Text |
id | pubmed-10616514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Korean Society of Applied Pharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-106165142023-11-01 The Effect of γ-Aminobutyric Acid Intake on UVB- Induced Skin Damage in Hairless Mice Zhao, Hairu Park, Bomi Kim, Min-Jung Hwang, Seok-Hyun Kim, Tae-Jong Kim, Seung-Un Kwon, Iksun Hwang, Jae Sung Biomol Ther (Seoul) Original Article The skin, the largest organ in the body, undergoes age-related changes influenced by both intrinsic and extrinsic factors. The primary external factor is photoaging which causes hyperpigmentation, uneven skin surface, deep wrinkles, and markedly enlarged capillaries. In the human dermis, it decreases fibroblast function, resulting in a lack of collagen structure and also decreases keratinocyte function, which compromises the strength of the protective barrier. In this study, we found that treatment with γ-aminobutyric acid (GABA) had no toxicity to skin fibroblasts and GABA enhanced their migration ability, which can accelerate skin wound healing. UVB radiation was found to significantly induce the production of matrix metalloproteinase 1 (MMP-1), but treatment with GABA resulted in the inhibition of MMP-1 production. We also investigated the enhancement of filaggrin and aquaporin 3 in keratinocytes after treatment with GABA, showing that GABA can effectively improve skin moisturization. In vivo experiments showed that oral administration of GABA significantly improved skin wrinkles and epidermal thickness. After the intake of GABA, there was a significant decrease observed in the increase of skin thickness measured by calipers and erythema. Additionally, the decrease in skin moisture and elasticity in hairless mice exposed to UVB radiation was also significantly restored. Overall, this study demonstrates the potential of GABA as functional food material for improving skin aging and moisturizing. The Korean Society of Applied Pharmacology 2023-11-01 2023-08-01 /pmc/articles/PMC10616514/ /pubmed/37524442 http://dx.doi.org/10.4062/biomolther.2023.085 Text en Copyright © 2023, The Korean Society of Applied Pharmacology https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Zhao, Hairu Park, Bomi Kim, Min-Jung Hwang, Seok-Hyun Kim, Tae-Jong Kim, Seung-Un Kwon, Iksun Hwang, Jae Sung The Effect of γ-Aminobutyric Acid Intake on UVB- Induced Skin Damage in Hairless Mice |
title | The Effect of γ-Aminobutyric Acid Intake on UVB- Induced Skin Damage in Hairless Mice |
title_full | The Effect of γ-Aminobutyric Acid Intake on UVB- Induced Skin Damage in Hairless Mice |
title_fullStr | The Effect of γ-Aminobutyric Acid Intake on UVB- Induced Skin Damage in Hairless Mice |
title_full_unstemmed | The Effect of γ-Aminobutyric Acid Intake on UVB- Induced Skin Damage in Hairless Mice |
title_short | The Effect of γ-Aminobutyric Acid Intake on UVB- Induced Skin Damage in Hairless Mice |
title_sort | effect of γ-aminobutyric acid intake on uvb- induced skin damage in hairless mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10616514/ https://www.ncbi.nlm.nih.gov/pubmed/37524442 http://dx.doi.org/10.4062/biomolther.2023.085 |
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