カドミウム依存の肺胞上皮細胞傷害に対するメタロチオネイン誘導剤の保護効果

Exposure to cadmium has been reported to cause respiratory disease in humans by inducing oxidative stress-dependent cellular injury. Metallothioneins are intracellular, cysteine-rich, metal-binding proteins that have a detoxifying action on heavy metals such as cadmium in various organs. In addition...

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Published in日本薬理学会年会要旨集 p. 3-P-310
Main Authors 下田, 実可子, 田中, 健一郎, 木村, 和真, 中野, 由加里, 川原, 正博, 杉崎, 俊文
Format Journal Article
LanguageJapanese
Published 公益社団法人 日本薬理学会 2020
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ISSN2435-4953
DOI10.1254/jpssuppl.93.0_3-P-310

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Summary:Exposure to cadmium has been reported to cause respiratory disease in humans by inducing oxidative stress-dependent cellular injury. Metallothioneins are intracellular, cysteine-rich, metal-binding proteins that have a detoxifying action on heavy metals such as cadmium in various organs. In addition, expression of metallothioneins is induced by metals with low biological toxicity, such as zinc. Therefore, in this study we examined whether polaprezinc, a chelate compound consisting of carnosine and zinc, can suppress cadmium-induced lung epithelial cell death. We found that cell viability and cytotoxicity were decreased and increased, respectively by cadmium treatment; however, polaprezinc significantly reversed these changes. Moreover, cadmium-dependent endoplasmic reticulum stress responses were suppressed by polaprezinc treatment. Cadmium induced the production of reactive oxygen species (ROS) in A549 cells in a dose-dependent manner and polaprezinc significantly suppressed this cadmium-induced ROS production. Finally, we found that polaprezinc dose-dependently induced metallothioneins using real-time RT-PCR, ELISA, and western blotting analyses. These results indicate that polaprezinc can suppress cadmium-induced lung epithelial cell death and oxidative stress by inducing metallothioneins. We therefore suggest that polaprezinc may have therapeutic effects against respiratory diseases, such as chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis.
Bibliography:93_3-P-310
ISSN:2435-4953
DOI:10.1254/jpssuppl.93.0_3-P-310