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Potential anti-skin aging effect of (-)-catechin isolated from the root bark of ulmus davidiana var. Japonica in tumor necrosis factor-α-stimulated normal human dermal fibroblasts
- Lee, S.;
- Yu, J.S.;
- Phung, H.M.;
- Lee, J.G.;
- Kim, K.H.;
- ... Kang, K.S.
WEB OF SCIENCE
41SCOPUS
44초록
Reactive oxygen species (ROS) are generated during skin aging, including intrinsic (chronologic aging) and extrinsic aging (photoaging). Therefore, antioxidants that inhibit ROS generation can delay skin aging. In this study, we evaluated the potential anti-skin aging effect of (-)-phenolic compounds isolated from the root bark of Ulmus davidiana var. japonica. We preferentially investigated the possible preventive effects of isolates against the degradation of skin extracellular matrix. Among the isolates, (-)-catechin suppressed the activity of collagenase MMP-1, and reversed the degradation of collagen induced by tumor necrosis factor-α (TNF-α) in normal human dermal fibroblast. This action mechanism of (-)-catechin was validated by the suppression of tumor necrosis factor-α-induced accumulation of ROS and activation of mitogen-activated protein kinases, protein kinase B (Akt), and cyclooxygenase-2 (COX-2). The proinflammatory cytokines upregulate inflammatory reactions, and ultimately promote aging-related reactions. In this milieu, we demonstrated that (-)-catechin decreased the expression and secretion of proinflammatory cytokines, including interleukin (IL)-1β and IL-6. In conclusion, (-)-catechin is a candidate to ameliorate both intrinsic and extrinsic skin aging. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
키워드
- 제목
- Potential anti-skin aging effect of (-)-catechin isolated from the root bark of ulmus davidiana var. Japonica in tumor necrosis factor-α-stimulated normal human dermal fibroblasts
- 저자
- Lee, S.; Yu, J.S.; Phung, H.M.; Lee, J.G.; Kim, K.H.; Kang, K.S.
- 발행일
- 2020-10
- 유형
- Article
- 저널명
- Antioxidants
- 권
- 9
- 호
- 10
- 페이지
- 1 ~ 13
- 언어
- ENG
- 출판사
- MDPI AG
- 발행국가
- 스위스
- 분량
- 13 페이지
- ISSN
- P 2076-3921