계명대학교 의학도서관 Repository

The effects of the melatonin on ultraviolet-B irradiated cultured dermal fibroblasts

Metadata Downloads
Author(s)
Young Wook RyooSeong Il SuhKyo Cheol MunByung Chun KimKyu Suk Lee
Keimyung Author(s)
Suh, Seong IlRyoo, Young WookKim, Byung ChunLee, Kyu SukMun, Kyo Cheol
Department
Dept. of Microbiology (미생물학)
Dept. of Dermatology (피부과학)
Dept. of Biochemistry (생화학)
Journal Title
Journal of Dermatological Science
Issued Date
2001
Volume
27
Issue
3
Keyword
Ultraviolet-BMelatoninFibroblast
Abstract
It has been reported that reactive oxygen species (ROS) and oxygen-derived free radicals are generated by ultraviolet (UV) radiation and various chemicals and their important roles in cellular damage and apoptosis are being increasingly recognized. Melatonin is a hormone with multiple functions in humans, produced by the pineal gland and stimulated by beta-adrenergic receptors. Melatonin has been shown to have photo protection properties, but there has been little progress toward identifying the specific mechanisms of its action. To clarify the role of melatonin as a free radical scavenger, in response to ultraviolet-B (UVB) irradiation, we investigated the effects of UVB and melatonin on cytotoxicity, lipid peroxidation, terminal deoxynucleotidyl transferase-mediated digoxigenin-dUTP nick end-labeling (TUNEL) assay and alteration of cell cycle in cultured skin fibroblast. Cell survival curves after UVB irradiation showed dose dependent decrement pattern by trypan blue exclusion assay. Only 56% of dermal fibroblasts were survived at 140 mJ/cm2 UVB irradiation. The damage was associated with cell membrane lipid peroxidation, as shown by accumulation malondialdehyde (MDA). By pre-cultivation with melatonin (10−9 M), a significant preventive effect was noted on the increase in the absolute number of surviving cells (up to 92.5% of cells were survived) and the levels of MDA were markedly decreased. These finding suggest significant correlation between an increase of lipid peroxide and cell viability. Morphological changes associated with apoptotic cell death were easily distinguished by TUNEL stain. Quantitative analysis of DNA content of skin fibroblasts was evaluated by flow cytometric analysis performed after vital staining with propidium iodide. UVB suppresses the G1 progression induced pre-G1 arrest leading to apoptotic changes of dermal fibroblast and those are blocked by melatonin pre-treatment. The results show the photodynamic effects of UVB that supposes the production of ROS and arrest the cell cycle. Melatonin, which have newly accepted as a potential UV protection properties, is effective membrane peroxidation inhibitor and prevent the pre-G1 arrest when present in relevant concentration during UVB irradiation.
Keimyung Author(s)(Kor)
서성일
류영욱
김병천
이규석
문교철
Publisher
School of Medicine
Citation
Young Wook Ryoo et al. (2001). The effects of the melatonin on ultraviolet-B irradiated cultured dermal fibroblasts. Journal of Dermatological Science, 27(3), 162–169. doi: 10.1016/S0923-1811(01)00133-5
Type
Article
ISSN
0923-1811
Source
http://lps3.linkinghub.elsevier.com.proxy.dsmc.or.kr/retrieve/pii/S0923181101001335
DOI
10.1016/S0923-1811(01)00133-5
URI
https://kumel.medlib.dsmc.or.kr/handle/2015.oak/33774
Appears in Collections:
1. School of Medicine (의과대학) > Dept. of Biochemistry (생화학)
1. School of Medicine (의과대학) > Dept. of Dermatology (피부과학)
1. School of Medicine (의과대학) > Dept. of Microbiology (미생물학)
공개 및 라이선스
  • 공개 구분공개
  • 엠바고Forever
파일 목록

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.