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Carvacrol and PPARγ agonist, pioglitazone, affects inhaled paraquat-induced lung injury in rats

Exposed rats to normal saline and paraquat (PQ) aerosol as control and PQ group, rats exposed to PQ and treated with 20 and 80 mg/kg/day carvacrol, 5 and 10 mg/kg/day pioglitazone, low dose of pioglitazone + carvacrol and 0.03 mg/kg/day dexamethasone (Dexa) for 16 days after the end of PQ exposure w...

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Autores principales: Amin, Fatemeh, Memarzia, Arghavan, Rad, Hamideh Kazemi, Kazerani, Hamid Reza, Boskabady, Mohammad Hossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047048/
https://www.ncbi.nlm.nih.gov/pubmed/33854134
http://dx.doi.org/10.1038/s41598-021-87546-8
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author Amin, Fatemeh
Memarzia, Arghavan
Rad, Hamideh Kazemi
Kazerani, Hamid Reza
Boskabady, Mohammad Hossein
author_facet Amin, Fatemeh
Memarzia, Arghavan
Rad, Hamideh Kazemi
Kazerani, Hamid Reza
Boskabady, Mohammad Hossein
author_sort Amin, Fatemeh
collection PubMed
description Exposed rats to normal saline and paraquat (PQ) aerosol as control and PQ group, rats exposed to PQ and treated with 20 and 80 mg/kg/day carvacrol, 5 and 10 mg/kg/day pioglitazone, low dose of pioglitazone + carvacrol and 0.03 mg/kg/day dexamethasone (Dexa) for 16 days after the end of PQ exposure were studied (n = 6 in each group). Lung pathological changes, tracheal responsiveness to methacholine and ovalbumin (OVA) as well as transforming growth factor beta (TGF-β) and interleukin (IL)-6 level in the lung tissue homogenize as well as TGF-β, IL-6, oxidant and antioxidant levels oxidant and antioxidants were increased in PQ group (p < 0.01 to p < 0.001). Lung pathological changes, tracheal responsiveness to methacholine and OVA as well as TGF-β, IL-6 oxidant and antioxidant levels were improved in all treated groups except lung pathological changes in treated group with low dose of pioglitazone (p < 0.05 to p < 0.001). The effects of low dose of pioglitazone and carvacrol alone were significantly lower than in the combination group of low dose of pioglitazone + carvacrol (p < 0.05 to p < 0.001). Carvacrol treatment improved inhaled PQ-induced lug injury similar to the effects of dexamethasone. The synergic effect of carvacrol and pioglitazone suggests PPAR-γ receptor mediated effects of carvacrol on inhaled PQ-induced lung injury.
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spelling pubmed-80470482021-04-15 Carvacrol and PPARγ agonist, pioglitazone, affects inhaled paraquat-induced lung injury in rats Amin, Fatemeh Memarzia, Arghavan Rad, Hamideh Kazemi Kazerani, Hamid Reza Boskabady, Mohammad Hossein Sci Rep Article Exposed rats to normal saline and paraquat (PQ) aerosol as control and PQ group, rats exposed to PQ and treated with 20 and 80 mg/kg/day carvacrol, 5 and 10 mg/kg/day pioglitazone, low dose of pioglitazone + carvacrol and 0.03 mg/kg/day dexamethasone (Dexa) for 16 days after the end of PQ exposure were studied (n = 6 in each group). Lung pathological changes, tracheal responsiveness to methacholine and ovalbumin (OVA) as well as transforming growth factor beta (TGF-β) and interleukin (IL)-6 level in the lung tissue homogenize as well as TGF-β, IL-6, oxidant and antioxidant levels oxidant and antioxidants were increased in PQ group (p < 0.01 to p < 0.001). Lung pathological changes, tracheal responsiveness to methacholine and OVA as well as TGF-β, IL-6 oxidant and antioxidant levels were improved in all treated groups except lung pathological changes in treated group with low dose of pioglitazone (p < 0.05 to p < 0.001). The effects of low dose of pioglitazone and carvacrol alone were significantly lower than in the combination group of low dose of pioglitazone + carvacrol (p < 0.05 to p < 0.001). Carvacrol treatment improved inhaled PQ-induced lug injury similar to the effects of dexamethasone. The synergic effect of carvacrol and pioglitazone suggests PPAR-γ receptor mediated effects of carvacrol on inhaled PQ-induced lung injury. Nature Publishing Group UK 2021-04-14 /pmc/articles/PMC8047048/ /pubmed/33854134 http://dx.doi.org/10.1038/s41598-021-87546-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Amin, Fatemeh
Memarzia, Arghavan
Rad, Hamideh Kazemi
Kazerani, Hamid Reza
Boskabady, Mohammad Hossein
Carvacrol and PPARγ agonist, pioglitazone, affects inhaled paraquat-induced lung injury in rats
title Carvacrol and PPARγ agonist, pioglitazone, affects inhaled paraquat-induced lung injury in rats
title_full Carvacrol and PPARγ agonist, pioglitazone, affects inhaled paraquat-induced lung injury in rats
title_fullStr Carvacrol and PPARγ agonist, pioglitazone, affects inhaled paraquat-induced lung injury in rats
title_full_unstemmed Carvacrol and PPARγ agonist, pioglitazone, affects inhaled paraquat-induced lung injury in rats
title_short Carvacrol and PPARγ agonist, pioglitazone, affects inhaled paraquat-induced lung injury in rats
title_sort carvacrol and pparγ agonist, pioglitazone, affects inhaled paraquat-induced lung injury in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047048/
https://www.ncbi.nlm.nih.gov/pubmed/33854134
http://dx.doi.org/10.1038/s41598-021-87546-8
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