Oral exposure to tire rubber-derived contaminant 6PPD and 6PPD-quinone induce hepatotoxicity in mice

被引:91
作者
Fang, Liya [1 ]
Fang, Chanlin [1 ]
Di, Shanshan [2 ]
Yu, Yundong [1 ,2 ]
Wang, Caihong [1 ]
Wang, Xinquan [2 ,3 ]
Jin, Yuanxiang [1 ,4 ]
机构
[1] Zhejiang Univ Technol, Coll Biotechnol & Bioengn, Hangzhou 310032, Peoples R China
[2] Zhejiang Acad Agr Sci, Inst Agroprod Safety & Nutr, State Key Lab Managing Biot & Chem Threats Qual &, Key Lab Detect Pesticide Residues & Control Zheji, Hangzhou 310021, Peoples R China
[3] Desheng Middle Rd 298, Hangzhou 310021, Zhejiang, Peoples R China
[4] Chaowang Rd 18, Hangzhou 310014, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
6PPD; 6PPDQ; Male mice; Liver toxicity; Transcriptomic analysis; PPAR-GAMMA; LIVER; METABOLISM; EXPRESSION; TOXICITY; RATS;
D O I
10.1016/j.scitotenv.2023.161836
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
N-(1,3-dimethylbutyl)-N '-phenyl-p-phenylenediamine (6PPD) is a widely used additive for protecting various rubber products, and its product of oxidation N-(1,3-Dimethylbutyl)-N '-phenyl-p-phenylenediamine-quinone (6PPDQ) has attracted extensive attention in aquatic toxicity. However, the toxicity of 6PPD and 6PPDQ in mammals has not been reported yet. In this study, the effects of 6PPD and 6PPDQ on the liver of C57BL/6 mice were assessed by orally administering different doses of 6PPD and 6PPDQ (10, 30, and 100 mg/kg) in mice for 6 weeks. 6PPD and 6PPDQ were found to bioaccumulate in the liver in a dose-dependent manner. Moreover, a high dose of 6PPD and 6PPDQ exposure increased not only the liver weights but also liver triglyceride levels, indicating that 6PPD and 6PPDQ exposure induced hepatotoxicity in mice. Furthermore, transcriptomic analysis revealed that 6PPD and 6PPDQ induced differential expression of genes mainly enriched in glycolipid metabolism, immune-related, and glutathione metabolism pathways. Therefore, 6PPD and 6PPDQ altered hepatic metabolism in mice. Furthermore, 6PPDQ could induce an immune response by upregulating the transcription of immune-related genes and promoting macrophage infiltration in the liver. In conclusion, our study revealed the toxic effects of 6PPD and 6PPDQ exposure on multi-endpoints in the liver of mice and improve our understanding of the health risks of 6PPD and 6PPDQ to mammals. The findings of our study may help formulate better safety regulations for the use and disposal of rubber products.
引用
收藏
页数:11
相关论文
共 35 条
  • [1] Acute cerebrovascular effects in juvenile coho salmon exposed to roadway runoff
    Blair, Stephanie, I
    Barlow, Clyde H.
    McIntyre, Jenifer K.
    [J]. CANADIAN JOURNAL OF FISHERIES AND AQUATIC SCIENCES, 2021, 78 (02) : 103 - 109
  • [2] Predicting Hepatic Clearance of Psychotropic Drugs in Isolated Perfused Fish Livers Using a Combination of Two In Vitro Assays br
    Bourgeois, Zoey M.
    Comfort, Jordan
    Schultz, Matthew
    Challis, Jonathan K.
    Cantin, Jenna
    Ji, Xiaowen
    Giesy, John P.
    Brinkmann, Markus
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2022, 56 (22) : 15839 - 15847
  • [3] On the early reaction stages of ozone with N,N′-substituted p-phenylenediamines (6PPD, 77PD) and N,N′,N"-substituted-1,3,5-triazine "Durazone®" : An electron spin resonance (ESR) and electronic absorption spectroscopy study
    Cataldo, Franco
    Faucette, Brad
    Huang, Semone
    Ebenezer, Warren
    [J]. POLYMER DEGRADATION AND STABILITY, 2015, 111 : 223 - 231
  • [4] TOXICITY OF LEACHATE FROM AUTOMOBILE TIRES TO AQUATIC BIOTA
    DAY, KE
    HOLTZE, KE
    METCALFESMITH, JL
    BISHOP, CT
    DUTKA, BJ
    [J]. CHEMOSPHERE, 1993, 27 (04) : 665 - 675
  • [5] Chiral perspective evaluations: Enantioselective hydrolysis of 6PPD and 6PPD-quinone in water and enantioselective toxicity to Gobiocypris rarus and Oncorhynchus mykiss
    Di, Shanshan
    Liu, Zhenzhen
    Zhao, Huiyu
    Li, Ying
    Qi, Peipei
    Wang, Zhiwei
    Xu, Hao
    Jin, Yuanxiang
    Wang, Xinquan
    [J]. ENVIRONMENT INTERNATIONAL, 2022, 166
  • [6] Obesity and Nonalcoholic Fatty Liver Disease: Biochemical, Metabolic, and Clinical Implications
    Fabbrini, Elisa
    Sullivan, Shelby
    Klein, Samuel
    [J]. HEPATOLOGY, 2010, 51 (02) : 679 - 689
  • [7] The organization, promoter analysis, and expression of the human PPAR gamma gene
    Fajas, L
    Auboeuf, D
    Raspe, E
    Schoonjans, K
    Lefebvre, AM
    Saladin, R
    Najib, J
    Laville, M
    Fruchart, JC
    Deeb, S
    VidalPuig, A
    Flier, J
    Briggs, MR
    Staels, B
    Vidal, H
    Auwerx, J
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (30) : 18779 - 18789
  • [8] Lack of induction of chromosome aberrations and micronuclei by N-(1,3-dimethylbutyl)-N-phenylparaphenylenediamine in mouse bone marrow cells
    George, J
    Kuttan, R
    [J]. MUTATION RESEARCH-GENETIC TOXICOLOGY, 1996, 370 (3-4): : 191 - 194
  • [9] Hartwig A., 2016, N 13 DIMETHYLBUTYL N, P746
  • [10] Concentration and leachability of N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine (6PPD) and its quinone transformation product (6PPD-Q) in road dust collected in Tokyo, Japan
    Hiki, Kyoshiro
    Yamamoto, Hiroshi
    [J]. ENVIRONMENTAL POLLUTION, 2022, 302