Biao Zhou, Muying Ge, Kai Wang, Peiyao Chen, Jin He, Haiting Wu, Wanyu Yang, Hongru Zhou
{"title":"c6f120灭火剂中反式全氟(4-甲基-2-戊烯)副产物的暴露风险:毒理学机制和影响。","authors":"Biao Zhou, Muying Ge, Kai Wang, Peiyao Chen, Jin He, Haiting Wu, Wanyu Yang, Hongru Zhou","doi":"10.1002/jat.4868","DOIUrl":null,"url":null,"abstract":"<p><p>C<sub>6</sub>F<sub>12</sub>O fire agent is widely used in various fire extinguishing scenarios due to its excellent properties. The most abundant byproduct in C<sub>6</sub>F<sub>12</sub>O fire extinguishing agent is perfluoro (4-methyl-2-pentene) (C<sub>6</sub>F<sub>12</sub>). Currently, there is a lack of reports on the toxic mechanisms of trans-C<sub>6</sub>F<sub>12</sub>. This study investigated the acute oral toxicity of trans-C<sub>6</sub>F<sub>12</sub> in rats, the damage mechanisms to major organs, and evaluated the inflammatory status of various organs. The experimental design comprised four treatment groups: a control group, a low-dose group (250 mg/kg), a medium-dose group (500 mg/kg), and a high-dose group (750 mg/kg), encompassing the range from sublethal to lethal concentrations. The median lethal dose (LD50) for trans-C<sub>6</sub>F<sub>12</sub> revealed its mild acute toxicity, with male rats exhibiting significantly higher sensitivity. Clinical observations showed that trans-C<sub>6</sub>F<sub>12</sub> oral exposure caused symptoms such as lethargy and reduced appetite. Pathological analysis revealed that trans-C<sub>6</sub>F<sub>12</sub> primarily caused significant damage to the respiratory and urinary systems, particularly in lung and kidney tissues. Additionally, moderate damage was observed in the liver, heart, and spleen, whereas only mild pathological changes were detected in the classical hippocampus, and no effects were observed in ocular tissues. Further analysis of the inflammatory cytokine IL-1β levels showed that lung and kidney tissues were more sensitive to the toxicity of trans-C<sub>6</sub>F<sub>12</sub>, exhibiting significant inflammatory responses. In contrast, the inflammatory responses in other organs were relatively weak. This study revealed the toxicity of trans-C<sub>6</sub>F<sub>12</sub> and its toxicological mechanisms, providing important references for the safe use of C<sub>6</sub>F<sub>12</sub>O fire extinguishing agent.</p>","PeriodicalId":15242,"journal":{"name":"Journal of Applied Toxicology","volume":" ","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Exposure Risks of Trans-Perfluoro (4-Methyl-2-Pentene) Byproduct in C<sub>6</sub>F<sub>12</sub>O Fire Suppressants: Toxicological Mechanisms and Implications.\",\"authors\":\"Biao Zhou, Muying Ge, Kai Wang, Peiyao Chen, Jin He, Haiting Wu, Wanyu Yang, Hongru Zhou\",\"doi\":\"10.1002/jat.4868\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>C<sub>6</sub>F<sub>12</sub>O fire agent is widely used in various fire extinguishing scenarios due to its excellent properties. The most abundant byproduct in C<sub>6</sub>F<sub>12</sub>O fire extinguishing agent is perfluoro (4-methyl-2-pentene) (C<sub>6</sub>F<sub>12</sub>). Currently, there is a lack of reports on the toxic mechanisms of trans-C<sub>6</sub>F<sub>12</sub>. This study investigated the acute oral toxicity of trans-C<sub>6</sub>F<sub>12</sub> in rats, the damage mechanisms to major organs, and evaluated the inflammatory status of various organs. The experimental design comprised four treatment groups: a control group, a low-dose group (250 mg/kg), a medium-dose group (500 mg/kg), and a high-dose group (750 mg/kg), encompassing the range from sublethal to lethal concentrations. The median lethal dose (LD50) for trans-C<sub>6</sub>F<sub>12</sub> revealed its mild acute toxicity, with male rats exhibiting significantly higher sensitivity. Clinical observations showed that trans-C<sub>6</sub>F<sub>12</sub> oral exposure caused symptoms such as lethargy and reduced appetite. Pathological analysis revealed that trans-C<sub>6</sub>F<sub>12</sub> primarily caused significant damage to the respiratory and urinary systems, particularly in lung and kidney tissues. Additionally, moderate damage was observed in the liver, heart, and spleen, whereas only mild pathological changes were detected in the classical hippocampus, and no effects were observed in ocular tissues. Further analysis of the inflammatory cytokine IL-1β levels showed that lung and kidney tissues were more sensitive to the toxicity of trans-C<sub>6</sub>F<sub>12</sub>, exhibiting significant inflammatory responses. In contrast, the inflammatory responses in other organs were relatively weak. This study revealed the toxicity of trans-C<sub>6</sub>F<sub>12</sub> and its toxicological mechanisms, providing important references for the safe use of C<sub>6</sub>F<sub>12</sub>O fire extinguishing agent.</p>\",\"PeriodicalId\":15242,\"journal\":{\"name\":\"Journal of Applied Toxicology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-07-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Applied Toxicology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1002/jat.4868\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"TOXICOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Applied Toxicology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/jat.4868","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"TOXICOLOGY","Score":null,"Total":0}
Exposure Risks of Trans-Perfluoro (4-Methyl-2-Pentene) Byproduct in C6F12O Fire Suppressants: Toxicological Mechanisms and Implications.
C6F12O fire agent is widely used in various fire extinguishing scenarios due to its excellent properties. The most abundant byproduct in C6F12O fire extinguishing agent is perfluoro (4-methyl-2-pentene) (C6F12). Currently, there is a lack of reports on the toxic mechanisms of trans-C6F12. This study investigated the acute oral toxicity of trans-C6F12 in rats, the damage mechanisms to major organs, and evaluated the inflammatory status of various organs. The experimental design comprised four treatment groups: a control group, a low-dose group (250 mg/kg), a medium-dose group (500 mg/kg), and a high-dose group (750 mg/kg), encompassing the range from sublethal to lethal concentrations. The median lethal dose (LD50) for trans-C6F12 revealed its mild acute toxicity, with male rats exhibiting significantly higher sensitivity. Clinical observations showed that trans-C6F12 oral exposure caused symptoms such as lethargy and reduced appetite. Pathological analysis revealed that trans-C6F12 primarily caused significant damage to the respiratory and urinary systems, particularly in lung and kidney tissues. Additionally, moderate damage was observed in the liver, heart, and spleen, whereas only mild pathological changes were detected in the classical hippocampus, and no effects were observed in ocular tissues. Further analysis of the inflammatory cytokine IL-1β levels showed that lung and kidney tissues were more sensitive to the toxicity of trans-C6F12, exhibiting significant inflammatory responses. In contrast, the inflammatory responses in other organs were relatively weak. This study revealed the toxicity of trans-C6F12 and its toxicological mechanisms, providing important references for the safe use of C6F12O fire extinguishing agent.
期刊介绍:
Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.