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Exposure to cigarette smoke exacerbates polyhexamethylene guanidine-induced lung fibrosis in mice.
Shin, Young-Jun; Kim, Sung-Hwan; Park, Chul Min; Kim, Hyeon-Young; Kim, In-Hyeon; Yang, Mi-Jin; Lee, Kyuhong; Kim, Min-Seok.
Afiliación
  • Shin YJ; Inhalation Toxicity Research Group, Korea Institute of Toxicology, Korea.
  • Kim SH; Inhalation Toxicology Center for Airborne Risk Factors, Korea Institute of Toxicology, Korea.
  • Park CM; Inhalation Toxicity Research Group, Korea Institute of Toxicology, Korea.
  • Kim HY; Inhalation Toxicology Center for Airborne Risk Factors, Korea Institute of Toxicology, Korea.
  • Kim IH; Inhalation Toxicology Center for Airborne Risk Factors, Korea Institute of Toxicology, Korea.
  • Yang MJ; Pathology Research Group, Korea Institute of Toxicology, Korea.
  • Lee K; Inhalation Toxicology Center for Airborne Risk Factors, Korea Institute of Toxicology, Korea.
  • Kim MS; Department of Human and Environmental Toxicology, University of Science & Technology, Korea.
J Toxicol Sci ; 46(10): 487-497, 2021.
Article en En | MEDLINE | ID: mdl-34602533
Cigarette smoke (CS) is the leading cause of chronic pulmonary diseases, including lung cancer, chronic obstructive pulmonary disease, and pulmonary fibrosis. In this study, we aimed to investigate the effects of repeated CS exposure on polyhexamethylene guanidine (PHMG)-induced pulmonary fibrosis in mice. A single intratracheal instillation of 0.6 mg/kg PHMG enhanced the immune response of mice by increasing the number of total and specific inflammatory cell types in the bronchoalveolar lavage fluid. It induced histopathological changes such as granulomatous inflammation/fibrosis and macrophage infiltration in the lungs. These responses were upregulated upon exposure to a combination of PHMG and CS. In contrast, a 4-hr/day exposure to 300 mg/m3 CS alone for 2 weeks by nose-only inhalation resulted in minimal inflammation in the mouse lung. Furthermore, PHMG administration increased the expression of fibrogenic mediators, especially in the pulmonary tissues of the PHMG + CS group compared with that in the PHMG alone group. However, there was no upregulation in the expression of inflammatory cytokines following exposure to a combination of PHMG and CS. Our results demonstrate that repeated exposure to CS may promote the development of PHMG-induced pulmonary fibrosis.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fibrosis Pulmonar Límite: Animals Idioma: En Revista: J Toxicol Sci Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fibrosis Pulmonar Límite: Animals Idioma: En Revista: J Toxicol Sci Año: 2021 Tipo del documento: Article