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Topical anti-inflammatory activity of Polygonum cuspidatum extract in the TPA model of mouse ear inflammation
BACKGROUND: This study tested the ability of a characterized extract of Polygonum cuspidatum (PCE) to inhibit mouse ear inflammation in response to topical application of 12-O-tetradecanoylphorbol-13-acetate (TPA). METHODS: A 50% (wt:vol) ethanolic solution of commercial 200:1 PCE was applied to bot...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267461/ https://www.ncbi.nlm.nih.gov/pubmed/18261214 http://dx.doi.org/10.1186/1476-9255-5-1 |
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author | Bralley, Eve E Greenspan, Phillip Hargrove, James L Wicker, Louise Hartle, Diane K |
author_facet | Bralley, Eve E Greenspan, Phillip Hargrove, James L Wicker, Louise Hartle, Diane K |
author_sort | Bralley, Eve E |
collection | PubMed |
description | BACKGROUND: This study tested the ability of a characterized extract of Polygonum cuspidatum (PCE) to inhibit mouse ear inflammation in response to topical application of 12-O-tetradecanoylphorbol-13-acetate (TPA). METHODS: A 50% (wt:vol) ethanolic solution of commercial 200:1 PCE was applied to both ears of female Swiss mice (n = 8) at 0.075, 0.15, 0.3, 1.25 and 2.5 mg/ear 30 min after TPA administration (2 μg/ear). For comparison, 3 other groups were treated with TPA and either 1) the vehicle (50% ethanol) alone, 2) indomethacin (0.5 mg/ear), or 3) trans-resveratrol (0.62 mg/ear). Ear thickness was measured before TPA and at 4 and 24 h post-TPA administration to assess ear edema. Ear punch biopsies were collected at 24 h and weighed as a second index of edema. Myeloperoxidase activity was measured in each ear punch biopsy to assess neutrophil infiltration. RESULTS: PCE treatment at all doses significantly reduced ear edema compared to the TPA control. The PCE response was dose-dependent and 2.5 mg PCE significantly inhibited all markers of inflammation to a greater extent than indomethacin (0.5 mg). MPO activity was inhibited at PCE doses ≥ 1.25 mg/ear. Trans-resveratrol inhibited inflammation at comparable doses. CONCLUSION: PCE inhibits development of edema and neutrophil infiltration in the TPA-treated mouse ear model of topical inflammation. |
format | Text |
id | pubmed-2267461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22674612008-03-14 Topical anti-inflammatory activity of Polygonum cuspidatum extract in the TPA model of mouse ear inflammation Bralley, Eve E Greenspan, Phillip Hargrove, James L Wicker, Louise Hartle, Diane K J Inflamm (Lond) Research BACKGROUND: This study tested the ability of a characterized extract of Polygonum cuspidatum (PCE) to inhibit mouse ear inflammation in response to topical application of 12-O-tetradecanoylphorbol-13-acetate (TPA). METHODS: A 50% (wt:vol) ethanolic solution of commercial 200:1 PCE was applied to both ears of female Swiss mice (n = 8) at 0.075, 0.15, 0.3, 1.25 and 2.5 mg/ear 30 min after TPA administration (2 μg/ear). For comparison, 3 other groups were treated with TPA and either 1) the vehicle (50% ethanol) alone, 2) indomethacin (0.5 mg/ear), or 3) trans-resveratrol (0.62 mg/ear). Ear thickness was measured before TPA and at 4 and 24 h post-TPA administration to assess ear edema. Ear punch biopsies were collected at 24 h and weighed as a second index of edema. Myeloperoxidase activity was measured in each ear punch biopsy to assess neutrophil infiltration. RESULTS: PCE treatment at all doses significantly reduced ear edema compared to the TPA control. The PCE response was dose-dependent and 2.5 mg PCE significantly inhibited all markers of inflammation to a greater extent than indomethacin (0.5 mg). MPO activity was inhibited at PCE doses ≥ 1.25 mg/ear. Trans-resveratrol inhibited inflammation at comparable doses. CONCLUSION: PCE inhibits development of edema and neutrophil infiltration in the TPA-treated mouse ear model of topical inflammation. BioMed Central 2008-02-08 /pmc/articles/PMC2267461/ /pubmed/18261214 http://dx.doi.org/10.1186/1476-9255-5-1 Text en Copyright © 2008 Bralley et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Bralley, Eve E Greenspan, Phillip Hargrove, James L Wicker, Louise Hartle, Diane K Topical anti-inflammatory activity of Polygonum cuspidatum extract in the TPA model of mouse ear inflammation |
title | Topical anti-inflammatory activity of Polygonum cuspidatum extract in the TPA model of mouse ear inflammation |
title_full | Topical anti-inflammatory activity of Polygonum cuspidatum extract in the TPA model of mouse ear inflammation |
title_fullStr | Topical anti-inflammatory activity of Polygonum cuspidatum extract in the TPA model of mouse ear inflammation |
title_full_unstemmed | Topical anti-inflammatory activity of Polygonum cuspidatum extract in the TPA model of mouse ear inflammation |
title_short | Topical anti-inflammatory activity of Polygonum cuspidatum extract in the TPA model of mouse ear inflammation |
title_sort | topical anti-inflammatory activity of polygonum cuspidatum extract in the tpa model of mouse ear inflammation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267461/ https://www.ncbi.nlm.nih.gov/pubmed/18261214 http://dx.doi.org/10.1186/1476-9255-5-1 |
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