Literature DB >> 27232715

Xenobiotics Produce Distinct Metabolomic Responses in Zebrafish Larvae (Danio rerio).

Susie S Y Huang1, Jonathan P Benskin1,2, Bharat Chandramouli1, Heather Butler1, Caren C Helbing3, John R Cosgrove1.   

Abstract

Sensitive and quantitative protocols for characterizing low-dose effects are needed to meet the demands of 21st century chemical hazard assessment. To test the hypothesis that xenobiotic exposure at environmentally relevant concentrations produces specific biochemical fingerprints in organisms, metabolomic perturbations in zebrafish (Danio rerio) embryo/larvae were measured following 24 h exposures to 13 individual chemicals covering a wide range of contaminant classes. Measured metabolites (208 in total) included amino acids, biogenic amines, fatty acids, bile acids, sugars, and lipids. The 96-120 h post-fertilization developmental stage was the most appropriate model for detecting xenobiotic-induced metabolomic perturbations. Metabolomic fingerprints were largely chemical- and dose-specific and were reproducible in multiple exposures over a 16-month period. Furthermore, chemical-specific responses were detected in the presence of an effluent matrix; importantly, in the absence of morphological response. In addition to improving sensitivity for detecting biological responses to low-level xenobiotic exposures, these data can aid the classification of novel contaminants based on the similarity of metabolomic responses to well-characterized "model" compounds. This approach is clearly of use for rapid, sensitive, and specific analyses of chemical effect on organisms, and can supplement existing methods, such as the Zebrafish Embryo Toxicity assay (OECD TG236), with molecular-level information.

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Year:  2016        PMID: 27232715     DOI: 10.1021/acs.est.6b01128

Source DB:  PubMed          Journal:  Environ Sci Technol        ISSN: 0013-936X            Impact factor:   9.028


  6 in total

Review 1.  Advantages of omics technology for evaluating cadmium toxicity in zebrafish.

Authors:  Eun Ki Min; Ahn Na Lee; Ji-Young Lee; Ilseob Shim; Pilje Kim; Tae-Young Kim; Ki-Tae Kim; Sangkyu Lee
Journal:  Toxicol Res       Date:  2021-01-25

2.  Development, characterization and comparisons of targeted and non-targeted metabolomics methods.

Authors:  Anton Ribbenstedt; Haizea Ziarrusta; Jonathan P Benskin
Journal:  PLoS One       Date:  2018-11-15       Impact factor: 3.240

3.  Evaluating Chemicals for Thyroid Disruption: Opportunities and Challenges with in Vitro Testing and Adverse Outcome Pathway Approaches.

Authors:  Pamela D Noyes; Katie Paul Friedman; Patience Browne; Jonathan T Haselman; Mary E Gilbert; Michael W Hornung; Stan Barone; Kevin M Crofton; Susan C Laws; Tammy E Stoker; Steven O Simmons; Joseph E Tietge; Sigmund J Degitz
Journal:  Environ Health Perspect       Date:  2019-09-05       Impact factor: 9.031

4.  Toxicometabolomics and Biotransformation Product Elucidation in Single Zebrafish Embryos Exposed to Carbamazepine from Environmentally-Relevant to Morphologically Altering Doses.

Authors:  Anton Ribbenstedt; Malte Posselt; Jonathan P Benskin
Journal:  Chem Res Toxicol       Date:  2022-02-15       Impact factor: 3.739

5.  Carbon Nanotubes Induce Metabolomic Profile Disturbances in Zebrafish: NMR-Based Metabolomics Platform.

Authors:  Raja Ganesan; Prabhakaran Vasantha-Srinivasan; Deepa Rani Sadhasivam; Raghunandhakumar Subramanian; Selvaraj Vimalraj; Ki Tae Suk
Journal:  Front Mol Biosci       Date:  2021-07-02

6.  Evaluation of Three Prokaryote Primers for Identification of Prokaryote Community Structure and Their Abode Preference in Three Distinct Wetland Ecosystems.

Authors:  Kavita Kumari; Malay Naskar; Md Aftabuddin; Soma Das Sarkar; Bandana Das Ghosh; Uttam Kumar Sarkar; Subir Kumar Nag; Chayna Jana; Basanta Kumar Das
Journal:  Front Microbiol       Date:  2021-07-14       Impact factor: 5.640

  6 in total

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