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Effects of Several Cosmetic Preservatives on ROS-Dependent Apoptosis of Rat Neural Progenitor Cells
Benzalkonium chloride, diazolidinyl urea, and imidazolidinyl urea are commonly used preservatives in cosmetics. Recent reports suggested that these compounds may have cellular and systemic toxicity in high concentration. In addition, diazolidinyl urea and imidazolidinyl urea are known formaldehyde (...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Applied Pharmacology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254638/ https://www.ncbi.nlm.nih.gov/pubmed/29429147 http://dx.doi.org/10.4062/biomolther.2017.221 |
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author | Ryu, Onjeon Park, Bo Kyung Bang, Minji Cho, Kyu Suk Lee, Sung Hoon Gonzales, Edson Luck T. Yang, Sung Min Kim, Seonmin Eun, Pyeong Hwa Lee, Joo Young Kim, Kyu-Bong Shin, Chan Young Kwon, Kyoung Ja |
author_facet | Ryu, Onjeon Park, Bo Kyung Bang, Minji Cho, Kyu Suk Lee, Sung Hoon Gonzales, Edson Luck T. Yang, Sung Min Kim, Seonmin Eun, Pyeong Hwa Lee, Joo Young Kim, Kyu-Bong Shin, Chan Young Kwon, Kyoung Ja |
author_sort | Ryu, Onjeon |
collection | PubMed |
description | Benzalkonium chloride, diazolidinyl urea, and imidazolidinyl urea are commonly used preservatives in cosmetics. Recent reports suggested that these compounds may have cellular and systemic toxicity in high concentration. In addition, diazolidinyl urea and imidazolidinyl urea are known formaldehyde (FA) releasers, raising concerns for these cosmetic preservatives. In this study, we investigated the effects of benzalkonium chloride, diazolidinyl urea, and imidazolidinyl urea on ROS-dependent apoptosis of rat neural progenitor cells (NPCs) in vitro. Cells were isolated and cultured from embryonic day 14 rat cortices. Cultured cells were treated with 1–1,000 nM benzalkonium chloride, and 1–50 μM diazolidinyl urea or imidazolidinyl urea at various time points to measure the reactive oxygen species (ROS). PI staining, MTT assay, and live-cell imaging were used for cell viability measurements. Western blot was carried out for cleaved caspase-3 and cleaved caspase-8 as apoptotic protein markers. In rat NPCs, ROS production and cleaved caspase-8 expression were increased while the cell viability was decreased in high concentrations of these substances. These results suggest that several cosmetic preservatives at high concentrations can induce neural toxicity in rat brains through ROS induction and apoptosis. |
format | Online Article Text |
id | pubmed-6254638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Korean Society of Applied Pharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-62546382018-11-27 Effects of Several Cosmetic Preservatives on ROS-Dependent Apoptosis of Rat Neural Progenitor Cells Ryu, Onjeon Park, Bo Kyung Bang, Minji Cho, Kyu Suk Lee, Sung Hoon Gonzales, Edson Luck T. Yang, Sung Min Kim, Seonmin Eun, Pyeong Hwa Lee, Joo Young Kim, Kyu-Bong Shin, Chan Young Kwon, Kyoung Ja Biomol Ther (Seoul) Original Article Benzalkonium chloride, diazolidinyl urea, and imidazolidinyl urea are commonly used preservatives in cosmetics. Recent reports suggested that these compounds may have cellular and systemic toxicity in high concentration. In addition, diazolidinyl urea and imidazolidinyl urea are known formaldehyde (FA) releasers, raising concerns for these cosmetic preservatives. In this study, we investigated the effects of benzalkonium chloride, diazolidinyl urea, and imidazolidinyl urea on ROS-dependent apoptosis of rat neural progenitor cells (NPCs) in vitro. Cells were isolated and cultured from embryonic day 14 rat cortices. Cultured cells were treated with 1–1,000 nM benzalkonium chloride, and 1–50 μM diazolidinyl urea or imidazolidinyl urea at various time points to measure the reactive oxygen species (ROS). PI staining, MTT assay, and live-cell imaging were used for cell viability measurements. Western blot was carried out for cleaved caspase-3 and cleaved caspase-8 as apoptotic protein markers. In rat NPCs, ROS production and cleaved caspase-8 expression were increased while the cell viability was decreased in high concentrations of these substances. These results suggest that several cosmetic preservatives at high concentrations can induce neural toxicity in rat brains through ROS induction and apoptosis. The Korean Society of Applied Pharmacology 2018-11 2018-02-12 /pmc/articles/PMC6254638/ /pubmed/29429147 http://dx.doi.org/10.4062/biomolther.2017.221 Text en Copyright ©2018, The Korean Society of Applied Pharmacology http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Ryu, Onjeon Park, Bo Kyung Bang, Minji Cho, Kyu Suk Lee, Sung Hoon Gonzales, Edson Luck T. Yang, Sung Min Kim, Seonmin Eun, Pyeong Hwa Lee, Joo Young Kim, Kyu-Bong Shin, Chan Young Kwon, Kyoung Ja Effects of Several Cosmetic Preservatives on ROS-Dependent Apoptosis of Rat Neural Progenitor Cells |
title | Effects of Several Cosmetic Preservatives on ROS-Dependent Apoptosis of Rat Neural Progenitor Cells |
title_full | Effects of Several Cosmetic Preservatives on ROS-Dependent Apoptosis of Rat Neural Progenitor Cells |
title_fullStr | Effects of Several Cosmetic Preservatives on ROS-Dependent Apoptosis of Rat Neural Progenitor Cells |
title_full_unstemmed | Effects of Several Cosmetic Preservatives on ROS-Dependent Apoptosis of Rat Neural Progenitor Cells |
title_short | Effects of Several Cosmetic Preservatives on ROS-Dependent Apoptosis of Rat Neural Progenitor Cells |
title_sort | effects of several cosmetic preservatives on ros-dependent apoptosis of rat neural progenitor cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254638/ https://www.ncbi.nlm.nih.gov/pubmed/29429147 http://dx.doi.org/10.4062/biomolther.2017.221 |
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