Effect of rhodiola extracts on UVA -induced collagen decrement in human fibroblast cell line

碩士 === 嘉南藥理科技大學 === 化妝品科技研究所 === 96 === Ultraviolet irradiation (especially UVA) is thought to main cause to evoke skin photoageing. UVA irradiation can increase amounts of free radicals and make dermal extracellular matrix alteration; hence it may lead to collagen degeneration. Thereby, UVA can acc...

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Main Authors: Jung-Hsiu Liu, 劉容秀
Other Authors: Chia-Chyuan Liu
Format: Others
Language:zh-TW
Published: 2008
Online Access:http://ndltd.ncl.edu.tw/handle/17249963334533721041
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spelling ndltd-TW-096CNUP57930302015-10-13T15:42:16Z http://ndltd.ncl.edu.tw/handle/17249963334533721041 Effect of rhodiola extracts on UVA -induced collagen decrement in human fibroblast cell line 紅景天萃取在人類纖維母細胞中對紫外線A引起膠原蛋白減少之影響 Jung-Hsiu Liu 劉容秀 碩士 嘉南藥理科技大學 化妝品科技研究所 96 Ultraviolet irradiation (especially UVA) is thought to main cause to evoke skin photoageing. UVA irradiation can increase amounts of free radicals and make dermal extracellular matrix alteration; hence it may lead to collagen degeneration. Thereby, UVA can accelerate to display the ageing appearances such as wrinkling and slackening on the skin. The previous studies indicated that the Chinese traditional herbal medicine, rhodiola (Rhodiola rosea L.), had various efficacies on the aspects of anti-hypoxia, anti-fatigue, anti-cancer, anti-bacteria, and anti-irridation. Meanwhile, rhodiola also had great work on anti-oxidation. However, so far, there is less study to investigate the application of rhodiola in the skin field, particularly in evaluation of anti-ageing function. Presently, the purpose of this study is mainly to observe whether the treatment of rhodiola extracts can ameliorate the UVA irradiation-induced collagen decrement, and attempt to find out its probable mechanism. After treatment with or without the rhodiola extracts, expressions of type I procollagen and matrix metalloproteinase (MMP-1, MMP-2, and MMP-9) in human fibroblast cell line (HS68) under UVA irradiation were respectively assessed by using the methods of western blot analysis and gelatin zymography. The studying results find that the UVA irradiation may increase the amounts of free radicals (our previous results). Expressions of type I procollagen are significantly reduced under UVA irradiation with 20 J/cm2, but expressions of MMP-1 are apparently increased. However, those situations of the type I procollagen decrement and the MMP-1 expressions increment can be greatly improved by giving treatment with methanolic rhodiola extracts, but expressions of MMP-2 are uninfluenced (Expressions of MMP-9 are undetectable). Our findings obtain that the rhodiola extracts can ameliorate the UV irradiation- induced collagen decreases via diminishing the MMP-1 expressions, and thereby lead to increase the collagen expressions. Hence, we speculate that rhodiola may have great potential to further develop and apply on skin anti-oxidation and anti-ageing efficacies. Chia-Chyuan Liu Tsai-Hsiu Yang 劉家全 楊彩秀 2008 學位論文 ; thesis 56 zh-TW
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description 碩士 === 嘉南藥理科技大學 === 化妝品科技研究所 === 96 === Ultraviolet irradiation (especially UVA) is thought to main cause to evoke skin photoageing. UVA irradiation can increase amounts of free radicals and make dermal extracellular matrix alteration; hence it may lead to collagen degeneration. Thereby, UVA can accelerate to display the ageing appearances such as wrinkling and slackening on the skin. The previous studies indicated that the Chinese traditional herbal medicine, rhodiola (Rhodiola rosea L.), had various efficacies on the aspects of anti-hypoxia, anti-fatigue, anti-cancer, anti-bacteria, and anti-irridation. Meanwhile, rhodiola also had great work on anti-oxidation. However, so far, there is less study to investigate the application of rhodiola in the skin field, particularly in evaluation of anti-ageing function. Presently, the purpose of this study is mainly to observe whether the treatment of rhodiola extracts can ameliorate the UVA irradiation-induced collagen decrement, and attempt to find out its probable mechanism. After treatment with or without the rhodiola extracts, expressions of type I procollagen and matrix metalloproteinase (MMP-1, MMP-2, and MMP-9) in human fibroblast cell line (HS68) under UVA irradiation were respectively assessed by using the methods of western blot analysis and gelatin zymography. The studying results find that the UVA irradiation may increase the amounts of free radicals (our previous results). Expressions of type I procollagen are significantly reduced under UVA irradiation with 20 J/cm2, but expressions of MMP-1 are apparently increased. However, those situations of the type I procollagen decrement and the MMP-1 expressions increment can be greatly improved by giving treatment with methanolic rhodiola extracts, but expressions of MMP-2 are uninfluenced (Expressions of MMP-9 are undetectable). Our findings obtain that the rhodiola extracts can ameliorate the UV irradiation- induced collagen decreases via diminishing the MMP-1 expressions, and thereby lead to increase the collagen expressions. Hence, we speculate that rhodiola may have great potential to further develop and apply on skin anti-oxidation and anti-ageing efficacies.
author2 Chia-Chyuan Liu
author_facet Chia-Chyuan Liu
Jung-Hsiu Liu
劉容秀
author Jung-Hsiu Liu
劉容秀
spellingShingle Jung-Hsiu Liu
劉容秀
Effect of rhodiola extracts on UVA -induced collagen decrement in human fibroblast cell line
author_sort Jung-Hsiu Liu
title Effect of rhodiola extracts on UVA -induced collagen decrement in human fibroblast cell line
title_short Effect of rhodiola extracts on UVA -induced collagen decrement in human fibroblast cell line
title_full Effect of rhodiola extracts on UVA -induced collagen decrement in human fibroblast cell line
title_fullStr Effect of rhodiola extracts on UVA -induced collagen decrement in human fibroblast cell line
title_full_unstemmed Effect of rhodiola extracts on UVA -induced collagen decrement in human fibroblast cell line
title_sort effect of rhodiola extracts on uva -induced collagen decrement in human fibroblast cell line
publishDate 2008
url http://ndltd.ncl.edu.tw/handle/17249963334533721041
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