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In vitro and in vivo assessment of the genotoxic effects of ceric ammonium nitrate and 1,3-propane sultone.
Kim, Ji-Young; Lee, A-Ram; Choi, Young Jae; Back, Sen-Min; Kim, Ok-Hee; Moon, Kyoung-Sik; Kim, Sang Kyum.
Afiliación
  • Kim JY; Department of Toxicological Evaluation and Research, Korea Institute of Toxicology, Daejeon 34114, Republic of Korea; College of Pharmacy, Chungnam National University, Daejeon 34134, Republic of Korea.
  • Lee AR; Department of Toxicological Evaluation and Research, Korea Institute of Toxicology, Daejeon 34114, Republic of Korea.
  • Choi YJ; College of Pharmacy, Chungnam National University, Daejeon 34134, Republic of Korea.
  • Back SM; Department of Toxicological Evaluation and Research, Korea Institute of Toxicology, Daejeon 34114, Republic of Korea.
  • Kim OH; Department of Toxicological Evaluation and Research, Korea Institute of Toxicology, Daejeon 34114, Republic of Korea.
  • Moon KS; Department of Toxicological Evaluation and Research, Korea Institute of Toxicology, Daejeon 34114, Republic of Korea.
  • Kim SK; College of Pharmacy, Chungnam National University, Daejeon 34134, Republic of Korea. Electronic address: sangkim@cnu.ac.kr.
Toxicol Lett ; 332: 202-212, 2020 Oct 10.
Article en En | MEDLINE | ID: mdl-32659469
A variety of methods have been developed for accurate and systematic evaluation of chemical genotoxicity. Ceric ammonium nitrate (CAN) and 1,3-propane sultone (1,3-PS) have been extensively applied in industrial fields. Although 1,3-PS, but not CAN, has been reported as a potent carcinogen, systematic assessment of the genotoxic properties of these chemicals has not been conducted. The purpose of this study was to establish a decision tree for evaluating genotoxicity based on the good laboratory practices (GLP) system using 1,3-PS and CAN as test chemicals. In vitro studies were performed including the bacterial reverse mutation assay, chromosomal aberration assay, and micronucleus assay. We conducted in vivo studies using a combined micronucleus and alkaline comet (MN-CMT) assay and the Pig-a gene mutation assay, which is a promising method for detecting gene mutations in vivo. CAN showed negative responses in all in vitro genotoxicity assays and the in vivo combined MN-CMT assay. Meanwhile, 1,3-PS had positive results in all in vitro and in vivo genotoxicity assays. In this study, we confirmed the genotoxicity of 1,3-PS and CAN using both in vitro and in vivo assays. We propose a decision tree for evaluating chemical-induced genotoxicity.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tiofenos / Árboles de Decisión / Cerio / Mutágenos Límite: Animals / Female / Humans / Male Idioma: En Revista: Toxicol Lett Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tiofenos / Árboles de Decisión / Cerio / Mutágenos Límite: Animals / Female / Humans / Male Idioma: En Revista: Toxicol Lett Año: 2020 Tipo del documento: Article
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