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Inhibitory effects of different fractions of Nepeta satureioides on melanin synthesis through reducing oxidative stress
Nepeta satureioides Boiss. has been used in traditional medicine of eastern countries and is famous for its medicinal properties. The aim of this study was to evaluate the effect of methanol (MeOH), n-hexane and dichloromethane (CH(2)Cl(2)) fractions of the extract on melanin synthesis and oxidative...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5385731/ https://www.ncbi.nlm.nih.gov/pubmed/28515769 http://dx.doi.org/10.4103/1735-5362.202455 |
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author | Emami, Seyed Ahmad Yazdian-Robati, Rezvan Sadeghi, Mohammad Baharara, Javad Amini, Elaheh Salek, Farzaneh Tayarani-Najaran, Zahra |
author_facet | Emami, Seyed Ahmad Yazdian-Robati, Rezvan Sadeghi, Mohammad Baharara, Javad Amini, Elaheh Salek, Farzaneh Tayarani-Najaran, Zahra |
author_sort | Emami, Seyed Ahmad |
collection | PubMed |
description | Nepeta satureioides Boiss. has been used in traditional medicine of eastern countries and is famous for its medicinal properties. The aim of this study was to evaluate the effect of methanol (MeOH), n-hexane and dichloromethane (CH(2)Cl(2)) fractions of the extract on melanin synthesis and oxidative stress in B16F10 melanoma cell line. The B16F10 cell line viability after treatment with increasing concentrations of different fractions of the plant (5-60 μg/mL) was measured using MTT assay. The inhibitory effect on synthesis of melanin, mushroom tyrosinase activity, cellular tyrosinase and oxidative stress were determined by the colorimetric and fluorometric methods. The data showed that at concentrations below 60 μg/mL, fractions did not show significant toxicity on melanoma cells. The amount of melanin synthesis by MeOH and CH(2)Cl(2) fractions and mushroom tyrosinase activity by the MeOH fraction declined in B16F10 cells. In addition to the capacity of MeOH, n-hexane and CH(2)Cl(2) fractions in decreasing the amount of reactive oxygen species (ROS) in melanoma cells, all fractions revealed remarkable antioxidant activity. The melanogenesis inhibitory and antioxidant effects of N. satureioides on B16F10 cells may suggest this plant as a new pharmaceutical agent in reducing skin pigment and skin aging in cosmetic industry. |
format | Online Article Text |
id | pubmed-5385731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53857312017-05-17 Inhibitory effects of different fractions of Nepeta satureioides on melanin synthesis through reducing oxidative stress Emami, Seyed Ahmad Yazdian-Robati, Rezvan Sadeghi, Mohammad Baharara, Javad Amini, Elaheh Salek, Farzaneh Tayarani-Najaran, Zahra Res Pharm Sci Original Article Nepeta satureioides Boiss. has been used in traditional medicine of eastern countries and is famous for its medicinal properties. The aim of this study was to evaluate the effect of methanol (MeOH), n-hexane and dichloromethane (CH(2)Cl(2)) fractions of the extract on melanin synthesis and oxidative stress in B16F10 melanoma cell line. The B16F10 cell line viability after treatment with increasing concentrations of different fractions of the plant (5-60 μg/mL) was measured using MTT assay. The inhibitory effect on synthesis of melanin, mushroom tyrosinase activity, cellular tyrosinase and oxidative stress were determined by the colorimetric and fluorometric methods. The data showed that at concentrations below 60 μg/mL, fractions did not show significant toxicity on melanoma cells. The amount of melanin synthesis by MeOH and CH(2)Cl(2) fractions and mushroom tyrosinase activity by the MeOH fraction declined in B16F10 cells. In addition to the capacity of MeOH, n-hexane and CH(2)Cl(2) fractions in decreasing the amount of reactive oxygen species (ROS) in melanoma cells, all fractions revealed remarkable antioxidant activity. The melanogenesis inhibitory and antioxidant effects of N. satureioides on B16F10 cells may suggest this plant as a new pharmaceutical agent in reducing skin pigment and skin aging in cosmetic industry. Medknow Publications & Media Pvt Ltd 2017-04 /pmc/articles/PMC5385731/ /pubmed/28515769 http://dx.doi.org/10.4103/1735-5362.202455 Text en Copyright: © 2017 Research in Pharmaceutical Sciences 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 Emami, Seyed Ahmad Yazdian-Robati, Rezvan Sadeghi, Mohammad Baharara, Javad Amini, Elaheh Salek, Farzaneh Tayarani-Najaran, Zahra Inhibitory effects of different fractions of Nepeta satureioides on melanin synthesis through reducing oxidative stress |
title | Inhibitory effects of different fractions of Nepeta satureioides on melanin synthesis through reducing oxidative stress |
title_full | Inhibitory effects of different fractions of Nepeta satureioides on melanin synthesis through reducing oxidative stress |
title_fullStr | Inhibitory effects of different fractions of Nepeta satureioides on melanin synthesis through reducing oxidative stress |
title_full_unstemmed | Inhibitory effects of different fractions of Nepeta satureioides on melanin synthesis through reducing oxidative stress |
title_short | Inhibitory effects of different fractions of Nepeta satureioides on melanin synthesis through reducing oxidative stress |
title_sort | inhibitory effects of different fractions of nepeta satureioides on melanin synthesis through reducing oxidative stress |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5385731/ https://www.ncbi.nlm.nih.gov/pubmed/28515769 http://dx.doi.org/10.4103/1735-5362.202455 |
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