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Protective effects of different anti-inflammatory drugs on tracheal stenosis following injury and potential mechanisms

Tracheal stenosis following injury cannot be effectively treated. The current study compared the protective effects of different anti-inflammatory drugs on tracheal stenosis and investigated their possible mechanisms. Rabbit tracheal stenosis models following injury were constructed and confirmed us...

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Autores principales: Huang, Zhenjie, Wei, Peng, Gan, Luoman, Li, Wentao, Zeng, Tonghua, Qin, Caicheng, Chen, Zhiyu, Liu, Guangnan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7974317/
https://www.ncbi.nlm.nih.gov/pubmed/34240225
http://dx.doi.org/10.3892/mmr.2021.11953
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author Huang, Zhenjie
Wei, Peng
Gan, Luoman
Li, Wentao
Zeng, Tonghua
Qin, Caicheng
Chen, Zhiyu
Liu, Guangnan
author_facet Huang, Zhenjie
Wei, Peng
Gan, Luoman
Li, Wentao
Zeng, Tonghua
Qin, Caicheng
Chen, Zhiyu
Liu, Guangnan
author_sort Huang, Zhenjie
collection PubMed
description Tracheal stenosis following injury cannot be effectively treated. The current study compared the protective effects of different anti-inflammatory drugs on tracheal stenosis and investigated their possible mechanisms. Rabbit tracheal stenosis models following injury were constructed and confirmed using hematoxylin and eosin (H&E) staining. A total of 30 rabbits were divided into the control (CON), penicillin (PEN), erythromycin (ERY), budesonide (BUD) and PEN + ERY + BUD groups (n=6). Stenotic tracheal tissue, serum and bronchoalveolar lavage fluid (BALF) were collected 10 days after continuous treatment. Pathological changes in the tracheas were observed by H&E staining. Histone deacetylase 2 (HDAC2) expression in tracheal tissues was detected by immunofluorescence. Immunohistochemistry was performed to detect collagen I (Col-I) and collagen III (Col-III) levels in tracheal tissues. Transforming growth factor β1 (TGF-β1), vascular endothelial growth factor (VEGF) and interleukin 8 (IL-8) levels in serum and BALF samples were determined using ELISA kits. Western blotting detected HDAC2, IL-8, TGF-β1 and VEGF levels in tracheal tissues. H&E staining demonstrated that tracheal epithelial hyperplasia and fibroblast proliferation in the ERY and PEN + ERY + BUD groups markedly improved compared with the CON group. Furthermore, in tracheal tissues, HDAC2 expression was significantly increased and IL-8, TGF-β1, VEGF, Col-I and Col-III levels were significantly decreased in the ERY and PEN + ERY + BUD groups compared with the CON group. Additionally, the results for the PEN + ERY + BUD were more significant compared with the ERY group. In serum and BALF samples, IL-8, TGF-β1 and VEGF levels in the ERY and PEN + ERY + BUD groups were significantly lower compared with the CON group, with the results of the PEN + ERY + BUD group being more significant compared with the ERY group. There were no significant differences between the PEN, BUD and CON groups. ERY inhibited tracheal granulation tissue proliferation and improved tracheal stenosis following injury and synergistic effects with PEN and BUD further enhanced these protective effects. The mechanism may involve HDAC2 upregulation and inhibition of local airway and systemic inflammatory responses.
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spelling pubmed-79743172021-03-24 Protective effects of different anti-inflammatory drugs on tracheal stenosis following injury and potential mechanisms Huang, Zhenjie Wei, Peng Gan, Luoman Li, Wentao Zeng, Tonghua Qin, Caicheng Chen, Zhiyu Liu, Guangnan Mol Med Rep Articles Tracheal stenosis following injury cannot be effectively treated. The current study compared the protective effects of different anti-inflammatory drugs on tracheal stenosis and investigated their possible mechanisms. Rabbit tracheal stenosis models following injury were constructed and confirmed using hematoxylin and eosin (H&E) staining. A total of 30 rabbits were divided into the control (CON), penicillin (PEN), erythromycin (ERY), budesonide (BUD) and PEN + ERY + BUD groups (n=6). Stenotic tracheal tissue, serum and bronchoalveolar lavage fluid (BALF) were collected 10 days after continuous treatment. Pathological changes in the tracheas were observed by H&E staining. Histone deacetylase 2 (HDAC2) expression in tracheal tissues was detected by immunofluorescence. Immunohistochemistry was performed to detect collagen I (Col-I) and collagen III (Col-III) levels in tracheal tissues. Transforming growth factor β1 (TGF-β1), vascular endothelial growth factor (VEGF) and interleukin 8 (IL-8) levels in serum and BALF samples were determined using ELISA kits. Western blotting detected HDAC2, IL-8, TGF-β1 and VEGF levels in tracheal tissues. H&E staining demonstrated that tracheal epithelial hyperplasia and fibroblast proliferation in the ERY and PEN + ERY + BUD groups markedly improved compared with the CON group. Furthermore, in tracheal tissues, HDAC2 expression was significantly increased and IL-8, TGF-β1, VEGF, Col-I and Col-III levels were significantly decreased in the ERY and PEN + ERY + BUD groups compared with the CON group. Additionally, the results for the PEN + ERY + BUD were more significant compared with the ERY group. In serum and BALF samples, IL-8, TGF-β1 and VEGF levels in the ERY and PEN + ERY + BUD groups were significantly lower compared with the CON group, with the results of the PEN + ERY + BUD group being more significant compared with the ERY group. There were no significant differences between the PEN, BUD and CON groups. ERY inhibited tracheal granulation tissue proliferation and improved tracheal stenosis following injury and synergistic effects with PEN and BUD further enhanced these protective effects. The mechanism may involve HDAC2 upregulation and inhibition of local airway and systemic inflammatory responses. D.A. Spandidos 2021-05 2021-03-02 /pmc/articles/PMC7974317/ /pubmed/34240225 http://dx.doi.org/10.3892/mmr.2021.11953 Text en Copyright: © Huang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Huang, Zhenjie
Wei, Peng
Gan, Luoman
Li, Wentao
Zeng, Tonghua
Qin, Caicheng
Chen, Zhiyu
Liu, Guangnan
Protective effects of different anti-inflammatory drugs on tracheal stenosis following injury and potential mechanisms
title Protective effects of different anti-inflammatory drugs on tracheal stenosis following injury and potential mechanisms
title_full Protective effects of different anti-inflammatory drugs on tracheal stenosis following injury and potential mechanisms
title_fullStr Protective effects of different anti-inflammatory drugs on tracheal stenosis following injury and potential mechanisms
title_full_unstemmed Protective effects of different anti-inflammatory drugs on tracheal stenosis following injury and potential mechanisms
title_short Protective effects of different anti-inflammatory drugs on tracheal stenosis following injury and potential mechanisms
title_sort protective effects of different anti-inflammatory drugs on tracheal stenosis following injury and potential mechanisms
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7974317/
https://www.ncbi.nlm.nih.gov/pubmed/34240225
http://dx.doi.org/10.3892/mmr.2021.11953
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