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Green tea catechin inhibits the activity and neutrophil release of Matrix Metalloproteinase-9
Green tea (Camellia sinensis; 綠茶 lǜ chá) extracts have been shown to possess anti-oxidant and anti-inflammatory effects in various cell types. Green tea extract (GTX) has been shown to significantly inhibit the activity of collagenase-3 (matrix metalloproteinase-13 (MMP-13)) in vitro. MMPs, such as...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067860/ https://www.ncbi.nlm.nih.gov/pubmed/27774417 http://dx.doi.org/10.1016/j.jtcme.2015.02.002 |
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author | Kim-Park, Wan K. Allam, Eman S. Palasuk, Jadesada Kowolik, Michael Park, Kichuel K. Windsor, L. Jack |
author_facet | Kim-Park, Wan K. Allam, Eman S. Palasuk, Jadesada Kowolik, Michael Park, Kichuel K. Windsor, L. Jack |
author_sort | Kim-Park, Wan K. |
collection | PubMed |
description | Green tea (Camellia sinensis; 綠茶 lǜ chá) extracts have been shown to possess anti-oxidant and anti-inflammatory effects in various cell types. Green tea extract (GTX) has been shown to significantly inhibit the activity of collagenase-3 (matrix metalloproteinase-13 (MMP-13)) in vitro. MMPs, such as MMP-9, are known to be involved in many inflammatory diseases including periodontal disease. GTX and a major catechin, epigallocatechin-gallate (EGCG), were examined for their ability to inhibit purified MMP-9 activity and its release from stimulated neutrophils. Methanol extract of Green tea and commercially purchased EGCG (>95 % purity) were tested in vitro for their ability to inhibit MMP-9 activity and/or its release from neutrophils using a β-casein cleavage assay and gelatin zymography, respectively. Statistical analysis was performed by Student's t-test. GTX and EGCG at 0.1% (w/v) completely inhibited the activity of MMP-9. In addition, GTX and EGCG (0.1 %) significantly inhibited (p < 0.001) the release of MMP-9 from formyl-Met-Leu-Phe (FMLP)-stimulated human neutrophils by 62.01% ± 6.717 and 79.63% ± 1.308, respectively. The inhibitory effects of GTX and EGCG occurred in unstimulated neutrophils (52.42% ± 3.443 and 62.33% ± 5.809, respectively). When the inhibitory effect of EGCG was further characterized, it significantly inhibited the release of MMP-9 from the FMLP-stimulated human neutrophils in a dose-dependent manner. The effects of GTX and EGCG on MMPs could be extrapolated to clinical/in vivo studies for the development of oral care products to prevent or treat chronic inflammatory diseases including periodontal diseases. |
format | Online Article Text |
id | pubmed-5067860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-50678602016-10-21 Green tea catechin inhibits the activity and neutrophil release of Matrix Metalloproteinase-9 Kim-Park, Wan K. Allam, Eman S. Palasuk, Jadesada Kowolik, Michael Park, Kichuel K. Windsor, L. Jack J Tradit Complement Med Article Green tea (Camellia sinensis; 綠茶 lǜ chá) extracts have been shown to possess anti-oxidant and anti-inflammatory effects in various cell types. Green tea extract (GTX) has been shown to significantly inhibit the activity of collagenase-3 (matrix metalloproteinase-13 (MMP-13)) in vitro. MMPs, such as MMP-9, are known to be involved in many inflammatory diseases including periodontal disease. GTX and a major catechin, epigallocatechin-gallate (EGCG), were examined for their ability to inhibit purified MMP-9 activity and its release from stimulated neutrophils. Methanol extract of Green tea and commercially purchased EGCG (>95 % purity) were tested in vitro for their ability to inhibit MMP-9 activity and/or its release from neutrophils using a β-casein cleavage assay and gelatin zymography, respectively. Statistical analysis was performed by Student's t-test. GTX and EGCG at 0.1% (w/v) completely inhibited the activity of MMP-9. In addition, GTX and EGCG (0.1 %) significantly inhibited (p < 0.001) the release of MMP-9 from formyl-Met-Leu-Phe (FMLP)-stimulated human neutrophils by 62.01% ± 6.717 and 79.63% ± 1.308, respectively. The inhibitory effects of GTX and EGCG occurred in unstimulated neutrophils (52.42% ± 3.443 and 62.33% ± 5.809, respectively). When the inhibitory effect of EGCG was further characterized, it significantly inhibited the release of MMP-9 from the FMLP-stimulated human neutrophils in a dose-dependent manner. The effects of GTX and EGCG on MMPs could be extrapolated to clinical/in vivo studies for the development of oral care products to prevent or treat chronic inflammatory diseases including periodontal diseases. Elsevier 2015-04-29 /pmc/articles/PMC5067860/ /pubmed/27774417 http://dx.doi.org/10.1016/j.jtcme.2015.02.002 Text en Copyright © 2016, Center for Food and Biomolecules, National Taiwan University. Production and hosting by Elsevier Taiwan LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Kim-Park, Wan K. Allam, Eman S. Palasuk, Jadesada Kowolik, Michael Park, Kichuel K. Windsor, L. Jack Green tea catechin inhibits the activity and neutrophil release of Matrix Metalloproteinase-9 |
title | Green tea catechin inhibits the activity and neutrophil release of Matrix Metalloproteinase-9 |
title_full | Green tea catechin inhibits the activity and neutrophil release of Matrix Metalloproteinase-9 |
title_fullStr | Green tea catechin inhibits the activity and neutrophil release of Matrix Metalloproteinase-9 |
title_full_unstemmed | Green tea catechin inhibits the activity and neutrophil release of Matrix Metalloproteinase-9 |
title_short | Green tea catechin inhibits the activity and neutrophil release of Matrix Metalloproteinase-9 |
title_sort | green tea catechin inhibits the activity and neutrophil release of matrix metalloproteinase-9 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067860/ https://www.ncbi.nlm.nih.gov/pubmed/27774417 http://dx.doi.org/10.1016/j.jtcme.2015.02.002 |
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