4.7 Article

Transcriptomic Analysis of Polyhexamethyleneguanidine-Induced Lung Injury in Mice after a Long-Term Recovery

Journal

TOXICS
Volume 9, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/toxics9100253

Keywords

polyhexamethyleneguanidine; persistent inflammation; lung dysfunction; transcriptome

Funding

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education of Korea [2017R1D1A1B04032833, 2021R1F1A1061858]
  2. National Research Foundation of Korea [2021R1F1A1061858, 2017R1D1A1B04032833] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Repeated exposure to PHMG-P led to sustained inflammation and fibrotic changes, resulting in downregulation of muscle and vascular development and lung dysfunction. Importantly, the pathological structural remodeling induced by PHMG-P was not reversed even after long-term recovery.
Polyhexamethyleneguanidine phosphate (PHMG-P) is one of the causative agents of humidifier disinfectant-induced lung injury. Direct exposure of the lungs to PHMG-P causes interstitial pneumonia with fibrosis. Epidemiological studies showed that patients with humidifier disinfectant-associated lung injuries have suffered from restrictive lung function five years after the onset of the lung injuries. We investigated whether lung damage was sustained after repeated exposure to PHMG-P followed by a long-term recovery and evaluated the adverse effects of PHMG-P on mice lungs. Mice were intranasally instilled with 0.3 mg/kg PHMG-P six times at two weeks intervals, followed by a recovery period of 292 days. Histopathological examination of the lungs showed the infiltration of inflammatory cells, the accumulation of extracellular matrix in the lung parenchyma, proteinaceous substances in the alveoli and bronchiolar-alveolar hyperplasia. From RNA-seq, the gene expression levels associated with the inflammatory response, leukocyte chemotaxis and fibrosis were significantly upregulated, whereas genes associated with epithelial/endothelial cells development, angiogenesis and smooth muscle contraction were markedly decreased. These results imply that persistent inflammation and fibrotic changes caused by repeated exposure to PHMG-P led to the downregulation of muscle and vascular development and lung dysfunction. Most importantly, this pathological structural remodeling induced by PHMG-P was not reversed even after long-term recovery.

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