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Influence of caffeine and hyaluronic acid on collagen biosynthesis in human skin fibroblasts
AIM: The aim of this study was to evaluate the effect of caffeine on collagen biosynthesis in human skin fibroblasts and the influence of hyaluronic acid (HA) on this process. MATERIALS AND METHODS: Collagen, [(3)H]-thymidine incorporation, and prolidase activity were measured in confluent human ski...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206198/ https://www.ncbi.nlm.nih.gov/pubmed/25342885 http://dx.doi.org/10.2147/DDDT.S69791 |
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author | Donejko, Magdalena Przylipiak, Andrzej Rysiak, Edyta Głuszuk, Katarzyna Surażyński, Arkadiusz |
author_facet | Donejko, Magdalena Przylipiak, Andrzej Rysiak, Edyta Głuszuk, Katarzyna Surażyński, Arkadiusz |
author_sort | Donejko, Magdalena |
collection | PubMed |
description | AIM: The aim of this study was to evaluate the effect of caffeine on collagen biosynthesis in human skin fibroblasts and the influence of hyaluronic acid (HA) on this process. MATERIALS AND METHODS: Collagen, [(3)H]-thymidine incorporation, and prolidase activity were measured in confluent human skin fibroblast cultures that had been treated with 1, 2, and 5 mM caffeine and with caffeine and 500 μg/mL HA. Western immunoblot analysis was performed to evaluate expression of β(1)-integrin receptor, insulin-like growth factor receptor phospho-Akt protein and mitogen-activated protein kinase (phospho-extracellular signal-regulated kinase). RESULTS: Caffeine inhibited collagen biosynthesis in a dose-dependent manner. The mechanism of this process was found at the level of prolidase activity. Caffeine significantly inhibited the enzyme activity. The addition of HA had no effect on collagen biosynthesis or prolidase activity in fibroblasts incubated with caffeine. Caffeine also had an inhibitory effect on DNA biosynthesis. HA, however, did not have any significant effect on this process. The inhibition of the expression of β(1)-integrin and insulin-like growth factor receptor in fibroblasts incubated with the caffeine indicates a possible mechanism of inhibition of collagen biosynthesis. CONCLUSION: Caffeine reduces collagen synthesis in human cultured skin fibroblasts. HA did not have any significant protective effect on this process. This is the first study to our knowledge that reports caffeine-induced inhibition of collagen synthesis in human skin fibroblasts. |
format | Online Article Text |
id | pubmed-4206198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-42061982014-10-23 Influence of caffeine and hyaluronic acid on collagen biosynthesis in human skin fibroblasts Donejko, Magdalena Przylipiak, Andrzej Rysiak, Edyta Głuszuk, Katarzyna Surażyński, Arkadiusz Drug Des Devel Ther Original Research AIM: The aim of this study was to evaluate the effect of caffeine on collagen biosynthesis in human skin fibroblasts and the influence of hyaluronic acid (HA) on this process. MATERIALS AND METHODS: Collagen, [(3)H]-thymidine incorporation, and prolidase activity were measured in confluent human skin fibroblast cultures that had been treated with 1, 2, and 5 mM caffeine and with caffeine and 500 μg/mL HA. Western immunoblot analysis was performed to evaluate expression of β(1)-integrin receptor, insulin-like growth factor receptor phospho-Akt protein and mitogen-activated protein kinase (phospho-extracellular signal-regulated kinase). RESULTS: Caffeine inhibited collagen biosynthesis in a dose-dependent manner. The mechanism of this process was found at the level of prolidase activity. Caffeine significantly inhibited the enzyme activity. The addition of HA had no effect on collagen biosynthesis or prolidase activity in fibroblasts incubated with caffeine. Caffeine also had an inhibitory effect on DNA biosynthesis. HA, however, did not have any significant effect on this process. The inhibition of the expression of β(1)-integrin and insulin-like growth factor receptor in fibroblasts incubated with the caffeine indicates a possible mechanism of inhibition of collagen biosynthesis. CONCLUSION: Caffeine reduces collagen synthesis in human cultured skin fibroblasts. HA did not have any significant protective effect on this process. This is the first study to our knowledge that reports caffeine-induced inhibition of collagen synthesis in human skin fibroblasts. Dove Medical Press 2014-10-15 /pmc/articles/PMC4206198/ /pubmed/25342885 http://dx.doi.org/10.2147/DDDT.S69791 Text en © 2014 Donejko et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Donejko, Magdalena Przylipiak, Andrzej Rysiak, Edyta Głuszuk, Katarzyna Surażyński, Arkadiusz Influence of caffeine and hyaluronic acid on collagen biosynthesis in human skin fibroblasts |
title | Influence of caffeine and hyaluronic acid on collagen biosynthesis in human skin fibroblasts |
title_full | Influence of caffeine and hyaluronic acid on collagen biosynthesis in human skin fibroblasts |
title_fullStr | Influence of caffeine and hyaluronic acid on collagen biosynthesis in human skin fibroblasts |
title_full_unstemmed | Influence of caffeine and hyaluronic acid on collagen biosynthesis in human skin fibroblasts |
title_short | Influence of caffeine and hyaluronic acid on collagen biosynthesis in human skin fibroblasts |
title_sort | influence of caffeine and hyaluronic acid on collagen biosynthesis in human skin fibroblasts |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206198/ https://www.ncbi.nlm.nih.gov/pubmed/25342885 http://dx.doi.org/10.2147/DDDT.S69791 |
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