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Siegesbeckiae Herba Extract and Chlorogenic Acid Ameliorate the Death of HaCaT Keratinocytes Exposed to Airborne Particulate Matter by Mitigating Oxidative Stress

Airborne particulate matter with a size of 10 μm or less (PM(10)) can cause oxidative damages and inflammatory reactions in the skin. This study was conducted to discover natural products that are potentially useful in protecting the skin from PM(10). Among the hot water extracts of a total of 23 me...

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Autores principales: Ha, Jae Won, Boo, Yong Chool
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8615115/
https://www.ncbi.nlm.nih.gov/pubmed/34829633
http://dx.doi.org/10.3390/antiox10111762
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author Ha, Jae Won
Boo, Yong Chool
author_facet Ha, Jae Won
Boo, Yong Chool
author_sort Ha, Jae Won
collection PubMed
description Airborne particulate matter with a size of 10 μm or less (PM(10)) can cause oxidative damages and inflammatory reactions in the skin. This study was conducted to discover natural products that are potentially useful in protecting the skin from PM(10). Among the hot water extracts of a total of 23 medicinal plants, Siegesbeckiae Herba extract (SHE), which showed the strongest protective effect against PM(10) cytotoxicity, was selected, and its mechanism of action and active constituents were explored. SHE ameliorated PM(10)-induced cell death, lactate dehydrogenase (LDH) release, lipid peroxidation, and reactive oxygen species (ROS) production in HaCaT cells. SHE decreased the expression of KEAP1, a negative regulator of NRF2, and increased the expression of NRF2 target genes, such as HMOX1 and NQO1. SHE selectively induced the enzymes involved in the synthesis of GSH (GCL-c and GCL-m), the regeneration of GSH (GSR and G6PDH), and GSH conjugation of xenobiotics (GSTκ1), rather than the enzymes that directly scavenge ROS (SOD1, CAT, and GPX1). SHE increased the cellular content of GSH and mitigated the oxidation of GSH to GSSG caused by PM(10) exposure. Of the solvent fractions of SHE, the n-butyl alcohol (BA) fraction ameliorated cell death in both the absence and presence of PM(10). The BA fraction contained a high amount of chlorogenic acid. Chlorogenic acid reduced PM(10)-induced cell death, LDH release, and ROS production. This study suggests that SHE protects cells from PM(10) toxicity by increasing the cellular antioxidant capacity and that chlorogenic acid may be an active phytochemical of SHE.
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spelling pubmed-86151152021-11-26 Siegesbeckiae Herba Extract and Chlorogenic Acid Ameliorate the Death of HaCaT Keratinocytes Exposed to Airborne Particulate Matter by Mitigating Oxidative Stress Ha, Jae Won Boo, Yong Chool Antioxidants (Basel) Article Airborne particulate matter with a size of 10 μm or less (PM(10)) can cause oxidative damages and inflammatory reactions in the skin. This study was conducted to discover natural products that are potentially useful in protecting the skin from PM(10). Among the hot water extracts of a total of 23 medicinal plants, Siegesbeckiae Herba extract (SHE), which showed the strongest protective effect against PM(10) cytotoxicity, was selected, and its mechanism of action and active constituents were explored. SHE ameliorated PM(10)-induced cell death, lactate dehydrogenase (LDH) release, lipid peroxidation, and reactive oxygen species (ROS) production in HaCaT cells. SHE decreased the expression of KEAP1, a negative regulator of NRF2, and increased the expression of NRF2 target genes, such as HMOX1 and NQO1. SHE selectively induced the enzymes involved in the synthesis of GSH (GCL-c and GCL-m), the regeneration of GSH (GSR and G6PDH), and GSH conjugation of xenobiotics (GSTκ1), rather than the enzymes that directly scavenge ROS (SOD1, CAT, and GPX1). SHE increased the cellular content of GSH and mitigated the oxidation of GSH to GSSG caused by PM(10) exposure. Of the solvent fractions of SHE, the n-butyl alcohol (BA) fraction ameliorated cell death in both the absence and presence of PM(10). The BA fraction contained a high amount of chlorogenic acid. Chlorogenic acid reduced PM(10)-induced cell death, LDH release, and ROS production. This study suggests that SHE protects cells from PM(10) toxicity by increasing the cellular antioxidant capacity and that chlorogenic acid may be an active phytochemical of SHE. MDPI 2021-11-04 /pmc/articles/PMC8615115/ /pubmed/34829633 http://dx.doi.org/10.3390/antiox10111762 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ha, Jae Won
Boo, Yong Chool
Siegesbeckiae Herba Extract and Chlorogenic Acid Ameliorate the Death of HaCaT Keratinocytes Exposed to Airborne Particulate Matter by Mitigating Oxidative Stress
title Siegesbeckiae Herba Extract and Chlorogenic Acid Ameliorate the Death of HaCaT Keratinocytes Exposed to Airborne Particulate Matter by Mitigating Oxidative Stress
title_full Siegesbeckiae Herba Extract and Chlorogenic Acid Ameliorate the Death of HaCaT Keratinocytes Exposed to Airborne Particulate Matter by Mitigating Oxidative Stress
title_fullStr Siegesbeckiae Herba Extract and Chlorogenic Acid Ameliorate the Death of HaCaT Keratinocytes Exposed to Airborne Particulate Matter by Mitigating Oxidative Stress
title_full_unstemmed Siegesbeckiae Herba Extract and Chlorogenic Acid Ameliorate the Death of HaCaT Keratinocytes Exposed to Airborne Particulate Matter by Mitigating Oxidative Stress
title_short Siegesbeckiae Herba Extract and Chlorogenic Acid Ameliorate the Death of HaCaT Keratinocytes Exposed to Airborne Particulate Matter by Mitigating Oxidative Stress
title_sort siegesbeckiae herba extract and chlorogenic acid ameliorate the death of hacat keratinocytes exposed to airborne particulate matter by mitigating oxidative stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8615115/
https://www.ncbi.nlm.nih.gov/pubmed/34829633
http://dx.doi.org/10.3390/antiox10111762
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