Evidence map›Paper›PMID 32763356›Full record

ArticleToxicology and applied pharmacology2020

Formation of lamellar body-like structure may be an initiator of didecyldimethylammonium chloride-induced toxic response.

Eun-Jung Park, Eunsol Seong, Min-Sung Kang, Gwang-Hee Lee, Dong-Wan Kim, Ji-Seok Han, Hyun-Ji Lim, Seung Hyeun Lee, Hyoung-Yun Han

Open access · greenAbstract read
In one paragraph

Article in Toxicology and applied pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 34% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Eun-Jung ParkEast-West Medical Science Research Institute, Kyung Hee University, Seoul 02447, Republic of Korea. Electronic address: pejtoxic@khu.ac.kr.
Eunsol SeongEast-West Medical Science Research Institute, Kyung Hee University, Seoul 02447, Republic of Korea.
Min-Sung KangIn vivo Hazard Evaluation & Research Division, General Toxicology & Research Group, Jeonbuk Branch Institute, Korea Institute of Toxicology, Jeongeup-si, Jeollabuk-do, Republic of Korea.
Gwang-Hee LeeSchool of Civil, Environmental, Architectural Engineering, Korea University, Seoul 136-713, Republic of Korea.
Dong-Wan KimSchool of Civil, Environmental, Architectural Engineering, Korea University, Seoul 136-713, Republic of Korea.
Ji-Seok HanDepartment of Advanced Toxicology Research, Korea Institute of Toxicology, 141 Gajeong-ro, Yuseong-gu, Daejeon, Republic of Korea.
Hyun-Ji LimEast-West Medical Science Research Institute, Kyung Hee University, Seoul 02447, Republic of Korea.
Seung Hyeun LeeDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, School of Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.
Hyoung-Yun HanDepartment of Predictive Toxicology, Korea Institute of Toxicology, Daejeon 34114, Republic of Korea.
Korea Institute of Toxicology · KRKyung Hee University East-West Neo Medical Center · KRKorea University · KRKyung Hee University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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-1β, 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.

Indexed as

AnimalsApoptosisBetacoronavirusCell LineCell SurvivalCoronavirus InfectionsCOVID-19Dose-Response Relationship, DrugFemaleGene Expression RegulationHumansMaleMiceMice, Inbred ICRPandemicsPneumonia, ViraldidecyldimethylammoniumQuaternary Ammonium CompoundsDidecyldimethylammonium chlorideDisinfectantsIdiopathic pulmonary fibrosisLamella bodyMatrix metalloproteinase-1Quaternary ammonium compounds

Identifiers

PMID32763356
PMCPMC7403870
OpenAlexW3047455272

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.