Pulmonary Toxicity of Polystyrene, Polypropylene, and Polyvinyl Chloride Microplastics in Mice

Globally, plastics are used in various products. Concerns regarding the human body’s exposure to plastics and environmental pollution have increased with increased plastic use. Microplastics can be detected in the atmosphere, leading to potential human health risks through inhalation; however, the t...

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Main Authors: Isaac Kwabena Danso, Jong-Hwan Woo, Kyuhong Lee
Format: Article
Language:English
Published: MDPI AG 2022-11-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/27/22/7926
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author Isaac Kwabena Danso
Jong-Hwan Woo
Kyuhong Lee
author_facet Isaac Kwabena Danso
Jong-Hwan Woo
Kyuhong Lee
author_sort Isaac Kwabena Danso
collection DOAJ
description Globally, plastics are used in various products. Concerns regarding the human body’s exposure to plastics and environmental pollution have increased with increased plastic use. Microplastics can be detected in the atmosphere, leading to potential human health risks through inhalation; however, the toxic effects of microplastic inhalation are poorly understood. In this study, we examined the pulmonary toxicity of polystyrene (PS), polypropylene (PP), and polyvinyl chloride (PVC) in C57BL/6, BALB/c, and ICR mice strains. Mice were intratracheally instilled with 5 mg/kg of PS, PP, or PVC daily for two weeks. PS stimulation increased inflammatory cells in the bronchoalveolar lavage fluid (BALF) of C57BL/6 and ICR mice. Histopathological analysis of PS-instilled C57BL/6 and PP-instilled ICR mice showed inflammatory cell infiltration. PS increased the NLR family pyrin domain containing 3 (NLRP3) inflammasome components in the lung tissue of C57BL/6 and ICR mice, while PS-instilled BALB/c mice remained unchanged. PS stimulation increased inflammatory cytokines, including IL-1β and IL-6, in BALF of C57BL/6 mice. PP-instilled ICR mice showed increased NLRP3, ASC, and Caspase-1 in the lung tissue compared to the control groups and increased IL-1β levels in BALF. These results could provide baseline data for understanding the pulmonary toxicity of microplastic inhalation.
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spelling doaj.art-1d08a297223d4255afcbc9636edfb89f2023-11-24T09:23:35ZengMDPI AGMolecules1420-30492022-11-012722792610.3390/molecules27227926Pulmonary Toxicity of Polystyrene, Polypropylene, and Polyvinyl Chloride Microplastics in MiceIsaac Kwabena Danso0Jong-Hwan Woo1Kyuhong Lee2Inhalation Toxicology Center for Airborne Risk Factor, Korea Institute of Toxicology, 30 Baekhak 1-gil, Jeongeup 56212, Jeollabuk-do, Republic of KoreaInhalation Toxicology Center for Airborne Risk Factor, Korea Institute of Toxicology, 30 Baekhak 1-gil, Jeongeup 56212, Jeollabuk-do, Republic of KoreaInhalation Toxicology Center for Airborne Risk Factor, Korea Institute of Toxicology, 30 Baekhak 1-gil, Jeongeup 56212, Jeollabuk-do, Republic of KoreaGlobally, plastics are used in various products. Concerns regarding the human body’s exposure to plastics and environmental pollution have increased with increased plastic use. Microplastics can be detected in the atmosphere, leading to potential human health risks through inhalation; however, the toxic effects of microplastic inhalation are poorly understood. In this study, we examined the pulmonary toxicity of polystyrene (PS), polypropylene (PP), and polyvinyl chloride (PVC) in C57BL/6, BALB/c, and ICR mice strains. Mice were intratracheally instilled with 5 mg/kg of PS, PP, or PVC daily for two weeks. PS stimulation increased inflammatory cells in the bronchoalveolar lavage fluid (BALF) of C57BL/6 and ICR mice. Histopathological analysis of PS-instilled C57BL/6 and PP-instilled ICR mice showed inflammatory cell infiltration. PS increased the NLR family pyrin domain containing 3 (NLRP3) inflammasome components in the lung tissue of C57BL/6 and ICR mice, while PS-instilled BALB/c mice remained unchanged. PS stimulation increased inflammatory cytokines, including IL-1β and IL-6, in BALF of C57BL/6 mice. PP-instilled ICR mice showed increased NLRP3, ASC, and Caspase-1 in the lung tissue compared to the control groups and increased IL-1β levels in BALF. These results could provide baseline data for understanding the pulmonary toxicity of microplastic inhalation.https://www.mdpi.com/1420-3049/27/22/7926polystyrenepolypropylenepolyvinyl chlorideC57BL/6 miceBALB/c miceICR mice
spellingShingle Isaac Kwabena Danso
Jong-Hwan Woo
Kyuhong Lee
Pulmonary Toxicity of Polystyrene, Polypropylene, and Polyvinyl Chloride Microplastics in Mice
Molecules
polystyrene
polypropylene
polyvinyl chloride
C57BL/6 mice
BALB/c mice
ICR mice
title Pulmonary Toxicity of Polystyrene, Polypropylene, and Polyvinyl Chloride Microplastics in Mice
title_full Pulmonary Toxicity of Polystyrene, Polypropylene, and Polyvinyl Chloride Microplastics in Mice
title_fullStr Pulmonary Toxicity of Polystyrene, Polypropylene, and Polyvinyl Chloride Microplastics in Mice
title_full_unstemmed Pulmonary Toxicity of Polystyrene, Polypropylene, and Polyvinyl Chloride Microplastics in Mice
title_short Pulmonary Toxicity of Polystyrene, Polypropylene, and Polyvinyl Chloride Microplastics in Mice
title_sort pulmonary toxicity of polystyrene polypropylene and polyvinyl chloride microplastics in mice
topic polystyrene
polypropylene
polyvinyl chloride
C57BL/6 mice
BALB/c mice
ICR mice
url https://www.mdpi.com/1420-3049/27/22/7926
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AT jonghwanwoo pulmonarytoxicityofpolystyrenepolypropyleneandpolyvinylchloridemicroplasticsinmice
AT kyuhonglee pulmonarytoxicityofpolystyrenepolypropyleneandpolyvinylchloridemicroplasticsinmice