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Formation of lamellar body-like structure may be an initiator of didecyldimethylammonium chloride-induced toxic response.
Park, Eun-Jung; Seong, Eunsol; Kang, Min-Sung; Lee, Gwang-Hee; Kim, Dong-Wan; Han, Ji-Seok; Lim, Hyun-Ji; Lee, Seung Hyeun; Han, Hyoung-Yun.
  • Park EJ; East-West Medical Science Research Institute, Kyung Hee University, Seoul 02447, Republic of Korea. Electronic address: pejtoxic@khu.ac.kr.
  • Seong E; East-West Medical Science Research Institute, Kyung Hee University, Seoul 02447, Republic of Korea.
  • Kang MS; In vivo Hazard Evaluation & Research Division, General Toxicology & Research Group, Jeonbuk Branch Institute, Korea Institute of Toxicology, Jeongeup-si, Jeollabuk-do, Republic of Korea.
  • Lee GH; School of Civil, Environmental, Architectural Engineering, Korea University, Seoul 136-713, Republic of Korea.
  • Kim DW; School of Civil, Environmental, Architectural Engineering, Korea University, Seoul 136-713, Republic of Korea.
  • Han JS; Department of Advanced Toxicology Research, Korea Institute of Toxicology, 141 Gajeong-ro, Yuseong-gu, Daejeon, Republic of Korea.
  • Lim HJ; East-West Medical Science Research Institute, Kyung Hee University, Seoul 02447, Republic of Korea.
  • Lee SH; Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, School of Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.
  • Han HY; Department of Predictive Toxicology, Korea Institute of Toxicology, Daejeon 34114, Republic of Korea.
Toxicol Appl Pharmacol ; 404: 115182, 2020 10 01.
Artículo en Inglés | MEDLINE | ID: covidwho-694488
ABSTRACT
Due to the pandemic of coronavirus disease 2019, the use of disinfectants is rapidly increasing worldwide. Didecyldimethylammonium chloride (DDAC) is an EPA-registered disinfectant, it was also a component in humidifier disinfectants that had caused idiopathic pulmonary diseases in Korea. In this study, we identified the possible pulmonary toxic response and mechanism using human bronchial epithelial (BEAS-2B) cells and mice. First, cell viability decreased sharply at a 4 µg/mL of concentration. The volume of intracellular organelles and the ROS level reduced, leading to the formation of apoptotic bodies and an increase of the LDH release. Secretion of pro-inflammatory cytokines (IL-1ß, IL-6, and TNF-α) and matrix metalloproteinase-1 also significantly increased. More importantly, lamellar body-like structures were formed in both the cells and mice exposed to DDAC, and the expression of both the indicator proteins for lamellar body (ABCA3 and Rab11a) and surfactant proteins (A, B, and D) was clearly enhanced. In addition, chronic fibrotic pulmonary lesions were notably observed in mice instilled twice (weekly) with DDAC (500 µg), ultimately resulting in death. Taken together, we suggest that disruption of pulmonary surfactant homeostasis may contribute to DDAC-induced cell death and subsequent pathophysiology and that the formation of lamellar body-like structures may play a role as the trigger. In addition, we propose that the cause of sudden death of mice exposed to DDAC should be clearly elucidated for the safe application of DDAC.
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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Asunto principal: Neumonía Viral / Supervivencia Celular / Infecciones por Coronavirus / Pandemias / Betacoronavirus / Compuestos de Amonio Cuaternario Tipo de estudio: Estudio pronóstico Límite: Animales / Femenino / Humanos / Masculino Idioma: Inglés Revista: Toxicol Appl Pharmacol Año: 2020 Tipo del documento: Artículo

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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Asunto principal: Neumonía Viral / Supervivencia Celular / Infecciones por Coronavirus / Pandemias / Betacoronavirus / Compuestos de Amonio Cuaternario Tipo de estudio: Estudio pronóstico Límite: Animales / Femenino / Humanos / Masculino Idioma: Inglés Revista: Toxicol Appl Pharmacol Año: 2020 Tipo del documento: Artículo