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In vitro and In vivo Activity of Myrsine africana on Elastase Inhibition and Anti-wrinkle Activity
BACKGROUND: Myrsine africana (MA) is a plant traditionally used in South Africa to treat various diseases. OBJECTIVE: The ethanolic extract of MA, was used for in vitro and in vivo studies to determine its elastase inhibitory activity. MATERIALS AND METHODS: MA and its isolated compound, myrsinoside...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701395/ https://www.ncbi.nlm.nih.gov/pubmed/29200717 http://dx.doi.org/10.4103/pm.pm_145_17 |
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author | Lall, Namrita Kishore, Navneet Fibrich, Bianca Lambrechts, Isa Anina |
author_facet | Lall, Namrita Kishore, Navneet Fibrich, Bianca Lambrechts, Isa Anina |
author_sort | Lall, Namrita |
collection | PubMed |
description | BACKGROUND: Myrsine africana (MA) is a plant traditionally used in South Africa to treat various diseases. OBJECTIVE: The ethanolic extract of MA, was used for in vitro and in vivo studies to determine its elastase inhibitory activity. MATERIALS AND METHODS: MA and its isolated compound, myrsinoside B, were tested in vitro for their elastase inhibitory activity. The MA extract was also evaluated for mutagenicity using two strains of Salmonella typhimurium (TA 98 and TA 100), microbial count, metal analysis, and stability. In vivo studies included irritancy and wrinkle reduction trials using Visioscan and Visioface. RESULTS: The leaf extract showed good elastase inhibition with a 50% inhibitory concentration (IC(50)) of 28.04 μg/ml. Myrsinoside B inhibited the elastase enzyme at an IC(50) of 4.68 ± 0.34 μg/ml. No colony growth observed during mutagenicity studies and it was concluded that MA ethanolic extract is a nonmutagen. MA extract was found to be a nonirritant during the patch test clinical trial. MA was found to contain negligible amounts of microorganisms and heavy metals. Gel cream containing MA crude extract was found to be stable for 2 years when kept at temperatures below 30°C. In clinical trials (in vivo), it was found that the test product containing 5% ethanolic extract of MA was effective in reducing wrinkles after application 2 times a day for 14 days and 28 days compared to the placebo aqueous cream. CONCLUSION: MA is effective in reducing the appearance of wrinkles. SUMMARY: This is a first time report of the elastase inhibitory potential of Myrsine africana and myrsinoside B and the anti-wrinkle potential of Myrsine africana. Myrsine africana ethanolic extract effectively inhibited the elastase enzyme. Myrsine africana was effective in in vivo studies to reduce the appearance of wrinkles after 14 days. [Image: see text] Abbreviations used: 4-NQO: 4-nitroquinoline, D14-BL: Baseline to day fourteen, D28-BL: Baseline to day twenty-eight, CFU: Colony forming units, IC(50): 50% inhibitory concentration, MA: Myrsine africana, MOU: Measurement of uncertainty, NaCl: Sodium chloride, NaH(2) PO(4).H(2)O: Sodium phosphate monobasic monohydrate, SEM: Standard error of the mean, TA 98: Salmonella typhimurium strain 98, TA 100: S. typhimurium strain 100, TLC: Thin layer chromatography, TMA: Total microbial activity, XVB salt: Vogel-Bonner medium E. |
format | Online Article Text |
id | pubmed-5701395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-57013952017-12-01 In vitro and In vivo Activity of Myrsine africana on Elastase Inhibition and Anti-wrinkle Activity Lall, Namrita Kishore, Navneet Fibrich, Bianca Lambrechts, Isa Anina Pharmacogn Mag Original Article BACKGROUND: Myrsine africana (MA) is a plant traditionally used in South Africa to treat various diseases. OBJECTIVE: The ethanolic extract of MA, was used for in vitro and in vivo studies to determine its elastase inhibitory activity. MATERIALS AND METHODS: MA and its isolated compound, myrsinoside B, were tested in vitro for their elastase inhibitory activity. The MA extract was also evaluated for mutagenicity using two strains of Salmonella typhimurium (TA 98 and TA 100), microbial count, metal analysis, and stability. In vivo studies included irritancy and wrinkle reduction trials using Visioscan and Visioface. RESULTS: The leaf extract showed good elastase inhibition with a 50% inhibitory concentration (IC(50)) of 28.04 μg/ml. Myrsinoside B inhibited the elastase enzyme at an IC(50) of 4.68 ± 0.34 μg/ml. No colony growth observed during mutagenicity studies and it was concluded that MA ethanolic extract is a nonmutagen. MA extract was found to be a nonirritant during the patch test clinical trial. MA was found to contain negligible amounts of microorganisms and heavy metals. Gel cream containing MA crude extract was found to be stable for 2 years when kept at temperatures below 30°C. In clinical trials (in vivo), it was found that the test product containing 5% ethanolic extract of MA was effective in reducing wrinkles after application 2 times a day for 14 days and 28 days compared to the placebo aqueous cream. CONCLUSION: MA is effective in reducing the appearance of wrinkles. SUMMARY: This is a first time report of the elastase inhibitory potential of Myrsine africana and myrsinoside B and the anti-wrinkle potential of Myrsine africana. Myrsine africana ethanolic extract effectively inhibited the elastase enzyme. Myrsine africana was effective in in vivo studies to reduce the appearance of wrinkles after 14 days. [Image: see text] Abbreviations used: 4-NQO: 4-nitroquinoline, D14-BL: Baseline to day fourteen, D28-BL: Baseline to day twenty-eight, CFU: Colony forming units, IC(50): 50% inhibitory concentration, MA: Myrsine africana, MOU: Measurement of uncertainty, NaCl: Sodium chloride, NaH(2) PO(4).H(2)O: Sodium phosphate monobasic monohydrate, SEM: Standard error of the mean, TA 98: Salmonella typhimurium strain 98, TA 100: S. typhimurium strain 100, TLC: Thin layer chromatography, TMA: Total microbial activity, XVB salt: Vogel-Bonner medium E. Medknow Publications & Media Pvt Ltd 2017 2017-11-13 /pmc/articles/PMC5701395/ /pubmed/29200717 http://dx.doi.org/10.4103/pm.pm_145_17 Text en Copyright: © 2017 Pharmacognosy Magazine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Lall, Namrita Kishore, Navneet Fibrich, Bianca Lambrechts, Isa Anina In vitro and In vivo Activity of Myrsine africana on Elastase Inhibition and Anti-wrinkle Activity |
title | In vitro and In vivo Activity of Myrsine africana on Elastase Inhibition and Anti-wrinkle Activity |
title_full | In vitro and In vivo Activity of Myrsine africana on Elastase Inhibition and Anti-wrinkle Activity |
title_fullStr | In vitro and In vivo Activity of Myrsine africana on Elastase Inhibition and Anti-wrinkle Activity |
title_full_unstemmed | In vitro and In vivo Activity of Myrsine africana on Elastase Inhibition and Anti-wrinkle Activity |
title_short | In vitro and In vivo Activity of Myrsine africana on Elastase Inhibition and Anti-wrinkle Activity |
title_sort | in vitro and in vivo activity of myrsine africana on elastase inhibition and anti-wrinkle activity |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701395/ https://www.ncbi.nlm.nih.gov/pubmed/29200717 http://dx.doi.org/10.4103/pm.pm_145_17 |
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