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Dried Yeast Extracts Curtails Pulmonary Oxidative Stress, Inflammation and Tissue Destruction in a Model of Experimental Emphysema

Pulmonary emphysema is characterized by a loss of alveolar integrity due to prolonged cigarette smoking and inhaled irritants. Dried yeast extracts (YE) are employed as food additives, savory flavorings, or creation of umami taste sensations. Despite being rich in nutrition, their application as nut...

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Autores principales: Kim, Yun-Ho, Kang, Min-Kyung, Lee, Eun-Jung, Kim, Dong Yeon, Oh, Hyeongjoo, Kim, Soo-Il, Oh, Su Yeon, Kim, Kyung-Hee, Park, Sang-Jae, Choi, Yean-Jung, Kang, Young-Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769699/
https://www.ncbi.nlm.nih.gov/pubmed/31480536
http://dx.doi.org/10.3390/antiox8090349
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author Kim, Yun-Ho
Kang, Min-Kyung
Lee, Eun-Jung
Kim, Dong Yeon
Oh, Hyeongjoo
Kim, Soo-Il
Oh, Su Yeon
Kim, Kyung-Hee
Park, Sang-Jae
Choi, Yean-Jung
Kang, Young-Hee
author_facet Kim, Yun-Ho
Kang, Min-Kyung
Lee, Eun-Jung
Kim, Dong Yeon
Oh, Hyeongjoo
Kim, Soo-Il
Oh, Su Yeon
Kim, Kyung-Hee
Park, Sang-Jae
Choi, Yean-Jung
Kang, Young-Hee
author_sort Kim, Yun-Ho
collection PubMed
description Pulmonary emphysema is characterized by a loss of alveolar integrity due to prolonged cigarette smoking and inhaled irritants. Dried yeast extracts (YE) are employed as food additives, savory flavorings, or creation of umami taste sensations. Despite being rich in nutrition, their application as nutraceuticals and functional foods is not investigated much and little is known about the inhibition of pulmonary emphysema. This study examined whether YE ameliorated pulmonary emphysema in mice is evoked by cigarette smoke (CS) and ovalbumin (OVA). Mice were orally administrated with 25–100 mg/kg YE for 8 weeks. Alveolar epithelial A549 cells exposed to lipopolysaccharide or CS extracts (CSE) were supplemented with 10–100 µg/mL YE. Oral YE administration reduced bronchoalveolar lavage fluid leukocytosis in CS-/OVA-exposed mice. YE reduced induction of inflammatory mediators and MMP-12, and diminished reactive oxygen species production and emphysematous alterations in CS-challenged airways. The YE treatment blunted bax/bcl-2 ratio and activation of p53 and caspases in CS-exposed lungs. Apoptotic death was dampened in CSE-loaded YE-supplemented A549 cells. YE curtailed tissue levels of MMP-12 in inflammatory OVA-exposed lungs. YE abrogated the secretion of TNF-α and MCP-1 through blocking NF-κB signaling in endotoxin-loaded A549 cells. Thus, the antioxidant YE may therapeutically ameliorate oxidative stress and inflammatory tissue destruction in emphysematous diseases.
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spelling pubmed-67696992019-10-30 Dried Yeast Extracts Curtails Pulmonary Oxidative Stress, Inflammation and Tissue Destruction in a Model of Experimental Emphysema Kim, Yun-Ho Kang, Min-Kyung Lee, Eun-Jung Kim, Dong Yeon Oh, Hyeongjoo Kim, Soo-Il Oh, Su Yeon Kim, Kyung-Hee Park, Sang-Jae Choi, Yean-Jung Kang, Young-Hee Antioxidants (Basel) Article Pulmonary emphysema is characterized by a loss of alveolar integrity due to prolonged cigarette smoking and inhaled irritants. Dried yeast extracts (YE) are employed as food additives, savory flavorings, or creation of umami taste sensations. Despite being rich in nutrition, their application as nutraceuticals and functional foods is not investigated much and little is known about the inhibition of pulmonary emphysema. This study examined whether YE ameliorated pulmonary emphysema in mice is evoked by cigarette smoke (CS) and ovalbumin (OVA). Mice were orally administrated with 25–100 mg/kg YE for 8 weeks. Alveolar epithelial A549 cells exposed to lipopolysaccharide or CS extracts (CSE) were supplemented with 10–100 µg/mL YE. Oral YE administration reduced bronchoalveolar lavage fluid leukocytosis in CS-/OVA-exposed mice. YE reduced induction of inflammatory mediators and MMP-12, and diminished reactive oxygen species production and emphysematous alterations in CS-challenged airways. The YE treatment blunted bax/bcl-2 ratio and activation of p53 and caspases in CS-exposed lungs. Apoptotic death was dampened in CSE-loaded YE-supplemented A549 cells. YE curtailed tissue levels of MMP-12 in inflammatory OVA-exposed lungs. YE abrogated the secretion of TNF-α and MCP-1 through blocking NF-κB signaling in endotoxin-loaded A549 cells. Thus, the antioxidant YE may therapeutically ameliorate oxidative stress and inflammatory tissue destruction in emphysematous diseases. MDPI 2019-09-01 /pmc/articles/PMC6769699/ /pubmed/31480536 http://dx.doi.org/10.3390/antiox8090349 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Yun-Ho
Kang, Min-Kyung
Lee, Eun-Jung
Kim, Dong Yeon
Oh, Hyeongjoo
Kim, Soo-Il
Oh, Su Yeon
Kim, Kyung-Hee
Park, Sang-Jae
Choi, Yean-Jung
Kang, Young-Hee
Dried Yeast Extracts Curtails Pulmonary Oxidative Stress, Inflammation and Tissue Destruction in a Model of Experimental Emphysema
title Dried Yeast Extracts Curtails Pulmonary Oxidative Stress, Inflammation and Tissue Destruction in a Model of Experimental Emphysema
title_full Dried Yeast Extracts Curtails Pulmonary Oxidative Stress, Inflammation and Tissue Destruction in a Model of Experimental Emphysema
title_fullStr Dried Yeast Extracts Curtails Pulmonary Oxidative Stress, Inflammation and Tissue Destruction in a Model of Experimental Emphysema
title_full_unstemmed Dried Yeast Extracts Curtails Pulmonary Oxidative Stress, Inflammation and Tissue Destruction in a Model of Experimental Emphysema
title_short Dried Yeast Extracts Curtails Pulmonary Oxidative Stress, Inflammation and Tissue Destruction in a Model of Experimental Emphysema
title_sort dried yeast extracts curtails pulmonary oxidative stress, inflammation and tissue destruction in a model of experimental emphysema
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769699/
https://www.ncbi.nlm.nih.gov/pubmed/31480536
http://dx.doi.org/10.3390/antiox8090349
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