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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Pharmaceutical Society of Korea
2022
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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. |
format | Online Article Text |
id | pubmed-8726530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Pharmaceutical Society of Korea |
record_format | MEDLINE/PubMed |
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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