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The effects of BRL-50481 on ovalbumin-induced asthmatic lung inflammation exacerbated by co-exposure to Asian sand dust in the murine model

Asian sand dust (ASD), which mainly originates in China and Mongolia in the spring and blows into Korea, can exacerbate respiratory and immunological diseases. This study aims to observe effects of co-exposure to ASD on ovalbumin (OVA)-induced asthmatic lung inflammation and of treatment with a phos...

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Autores principales: Kim, Hong Jo, Song, Jin Yong, Park, Tae Il, Choi, Won Seok, Kim, Jong Heon, Kwon, Oh Seong, Lee, Ji-Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pharmaceutical Society of Korea 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8726530/
https://www.ncbi.nlm.nih.gov/pubmed/34984603
http://dx.doi.org/10.1007/s12272-021-01367-x
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author Kim, Hong Jo
Song, Jin Yong
Park, Tae Il
Choi, Won Seok
Kim, Jong Heon
Kwon, Oh Seong
Lee, Ji-Yun
author_facet Kim, Hong Jo
Song, Jin Yong
Park, Tae Il
Choi, Won Seok
Kim, Jong Heon
Kwon, Oh Seong
Lee, Ji-Yun
author_sort Kim, Hong Jo
collection PubMed
description Asian sand dust (ASD), which mainly originates in China and Mongolia in the spring and blows into Korea, can exacerbate respiratory and immunological diseases. This study aims to observe effects of co-exposure to ASD on ovalbumin (OVA)-induced asthmatic lung inflammation and of treatment with a phosphodiesterase 7 (PDE7) inhibitor in a mouse model. The challenge with OVA increased airway hyperresponsiveness (AHR) and inflammatory cell infiltration into the lung tissue. Interleukin (IL)-13, tumor necrosis factor-alpha, monocyte-protein-1, mucin, and antigen-specific IgE and IgG1 production increased in mouse serum. The co-exposure of ASD significantly exacerbated these effects in this asthma model. Notably, the administration of a PDE7 inhibitor, BRL-50481 (BRL), significantly reduced AHR, infiltration of inflammatory cells into the lungs, and the levels of type 2 T helper cell-related cytokines, antigen-specific immunoglobulins, and mucin. Thus, the administration of BRL ameliorated OVA-induced allergic asthmatic responses exacerbated by co-exposure to ASD. This study suggests that PDE7 inhibition can be a therapeutic strategy for inflammatory lung diseases and asthma via the regulation of T lymphocytes and reduction of IL-13, and, consequently, mucin production. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12272-021-01367-x.
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spelling pubmed-87265302022-01-05 The effects of BRL-50481 on ovalbumin-induced asthmatic lung inflammation exacerbated by co-exposure to Asian sand dust in the murine model Kim, Hong Jo Song, Jin Yong Park, Tae Il Choi, Won Seok Kim, Jong Heon Kwon, Oh Seong Lee, Ji-Yun Arch Pharm Res Research Article Asian sand dust (ASD), which mainly originates in China and Mongolia in the spring and blows into Korea, can exacerbate respiratory and immunological diseases. This study aims to observe effects of co-exposure to ASD on ovalbumin (OVA)-induced asthmatic lung inflammation and of treatment with a phosphodiesterase 7 (PDE7) inhibitor in a mouse model. The challenge with OVA increased airway hyperresponsiveness (AHR) and inflammatory cell infiltration into the lung tissue. Interleukin (IL)-13, tumor necrosis factor-alpha, monocyte-protein-1, mucin, and antigen-specific IgE and IgG1 production increased in mouse serum. The co-exposure of ASD significantly exacerbated these effects in this asthma model. Notably, the administration of a PDE7 inhibitor, BRL-50481 (BRL), significantly reduced AHR, infiltration of inflammatory cells into the lungs, and the levels of type 2 T helper cell-related cytokines, antigen-specific immunoglobulins, and mucin. Thus, the administration of BRL ameliorated OVA-induced allergic asthmatic responses exacerbated by co-exposure to ASD. This study suggests that PDE7 inhibition can be a therapeutic strategy for inflammatory lung diseases and asthma via the regulation of T lymphocytes and reduction of IL-13, and, consequently, mucin production. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12272-021-01367-x. Pharmaceutical Society of Korea 2022-01-04 2022 /pmc/articles/PMC8726530/ /pubmed/34984603 http://dx.doi.org/10.1007/s12272-021-01367-x Text en © The Pharmaceutical Society of Korea 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Research Article
Kim, Hong Jo
Song, Jin Yong
Park, Tae Il
Choi, Won Seok
Kim, Jong Heon
Kwon, Oh Seong
Lee, Ji-Yun
The effects of BRL-50481 on ovalbumin-induced asthmatic lung inflammation exacerbated by co-exposure to Asian sand dust in the murine model
title The effects of BRL-50481 on ovalbumin-induced asthmatic lung inflammation exacerbated by co-exposure to Asian sand dust in the murine model
title_full The effects of BRL-50481 on ovalbumin-induced asthmatic lung inflammation exacerbated by co-exposure to Asian sand dust in the murine model
title_fullStr The effects of BRL-50481 on ovalbumin-induced asthmatic lung inflammation exacerbated by co-exposure to Asian sand dust in the murine model
title_full_unstemmed The effects of BRL-50481 on ovalbumin-induced asthmatic lung inflammation exacerbated by co-exposure to Asian sand dust in the murine model
title_short The effects of BRL-50481 on ovalbumin-induced asthmatic lung inflammation exacerbated by co-exposure to Asian sand dust in the murine model
title_sort effects of brl-50481 on ovalbumin-induced asthmatic lung inflammation exacerbated by co-exposure to asian sand dust in the murine model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8726530/
https://www.ncbi.nlm.nih.gov/pubmed/34984603
http://dx.doi.org/10.1007/s12272-021-01367-x
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