2,4-Dinitrotoluene (DNT) Perturbs Yolk Absorption, Liver Development and Lipid Metabolism/Oxygen Transport Gene Expression in Zebrafish Embryos and Larvae

被引:8
作者
Xiong, Jianglin [1 ]
Sha, Hang [2 ]
Zhou, Hualin [3 ]
Peng, Lijuan [4 ]
Wu, Lingying [1 ]
Qiu, Yinsheng [1 ]
Wang, Rui [1 ]
Hu, Xianqin [1 ]
机构
[1] Wuhan Polytech Univ, Hubei Key Lab Anim Nutr & Feed Sci, Wuhan 430023, Hubei, Peoples R China
[2] Chinese Acad Fishery Sci, Yangtze River Fisheries Res Inst, Wuhan 430223, Hubei, Peoples R China
[3] Xiangyang Vocat & Tech Coll, Agr Coll, Xiangyang 441050, Peoples R China
[4] Wuhan Polytech Univ, Sch Food Sci & Engn, Wuhan 430023, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
2; 4-dinitrotoluene; zebrafish (Danio rerio); embryos; liver; yolk; MAMMARY EPITHELIAL-CELLS; TRANSCRIPTIONAL ACTIVATION; HYPOXIA; 2,4,6-TRINITROTOLUENE; TOXICITY; EXPOSURE;
D O I
10.3390/ijms20153632
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
2,4-dinitrotoluene (2,4-DNT) is a common environmental pollutant, and was classified as a group 2B human carcinogenic compound by the International Agency for Research on Cancer. This study determined the toxic effects of 2,4-DNT exposure on zebrafish at the embryo-larvae stage, in terms of organ morphogenesis and the expression pattern of selected target genes related to lipid metabolism and oxygen transportation. The results showed that the 120-h post-fertilization LC50 of 2,4-DNT was 9.59 mg/L with a 95% confidence interval of 8.89-10.44 mg/L. The larvae treated with 2,4-DNT showed toxic symptoms including smaller body, less skin pigment production, yolk malabsorption, and disordered liver development. Further studies on the expression of genes related to lipid transport and metabolism, and respiration indicated that they were significantly affected by 2,4-DNT. It is concluded that 2,4-DNT exposure perturbed liver development and yolk absorption in early-life zebrafish, and disturbed the lipid metabolism /oxygen transport gene expression.
引用
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页数:16
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共 39 条
[1]  
[Anonymous], 1996, IARC MON EV CARC RIS
[2]   A CRITICAL-REVIEW OF THE LITERATURE ON NITROBENZENE TOXICITY [J].
BEAUCHAMP, RO ;
IRONS, RD ;
RICKERT, DE ;
COUCH, DB ;
HAMM, TE .
CRC CRITICAL REVIEWS IN TOXICOLOGY, 1982, 11 (01) :33-84
[3]  
Bugel Sean M, 2014, Curr Environ Health Rep, V1, P341
[4]   Analysis of Common and Specific Mechanisms of Liver Function Affected by Nitrotoluene Compounds [J].
Deng, Youping ;
Meyer, Sharon A. ;
Guan, Xin ;
Escalon, Barbara Lynn ;
Ai, Junmei ;
Wilbanks, Mitchell S. ;
Welti, Ruth ;
Garcia-Reyero, Natalia ;
Perkins, Edward J. .
PLOS ONE, 2011, 6 (02)
[5]   Quantification of Lipid Abundance and Evaluation of Lipid Distribution in Caenorhabditis elegans by Nile Red and Oil Red O Staining [J].
Escorcia, Wilber ;
Ruter, Dana L. ;
Nhan, James ;
Curran, Sean P. .
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2018, (133)
[6]  
Ishaque Ali B, 2005, Int J Environ Res Public Health, V2, P304, DOI 10.3390/ijerph2005020015
[7]   Identity and distribution of residues of energetic compounds at army live-fire training ranges [J].
Jenkins, T. F. ;
Hewitt, A. D. ;
Grant, C. L. ;
Thiboutot, S. ;
Ampleman, G. ;
Walsh, M. E. ;
Ranney, T. A. ;
Ramsey, C. A. ;
Palazzo, A. J. ;
Pennington, J. C. .
CHEMOSPHERE, 2006, 63 (08) :1280-1290
[8]   PPAR-γ agonists inhibit production of monocyte inflammatory cytokines [J].
Jiang, CY ;
Ting, AT ;
Seed, B .
NATURE, 1998, 391 (6662) :82-86
[9]   Peroxisome proliferator-activated receptor-γ activation and long-chain fatty acids alter lipogenic gene networks in bovine mammary epithelial cells to various extents [J].
Kadegowda, A. K. G. ;
Bionaz, M. ;
Piperova, L. S. ;
Erdman, R. A. ;
Loor, J. J. .
JOURNAL OF DAIRY SCIENCE, 2009, 92 (09) :4276-4289
[10]   STAGES OF EMBRYONIC-DEVELOPMENT OF THE ZEBRAFISH [J].
KIMMEL, CB ;
BALLARD, WW ;
KIMMEL, SR ;
ULLMANN, B ;
SCHILLING, TF .
DEVELOPMENTAL DYNAMICS, 1995, 203 (03) :253-310