Literature DB >> 16046794

Zebrafish and cardiac toxicology.

Warren Heideman1, Dagmara S Antkiewicz, Sara A Carney, Richard E Peterson.   

Abstract

Model systems are a mainstay in toxicological research. Zebrafish are rapidly becoming an important model organism for studying vertebrate development. The advantages of zebrafish: short reproductive cycle, production of numerous transparent, synchronously developing embryos, low cost, and standardization make zebrafish an attractive model for toxicologists as well. The use of these fish to study heart development has moved forward very rapidly, laying the groundwork for studying the effects of chemicals on cardiac development and function. Here we describe approaches that can be used to study cardiac toxicity in developing zebrafish, focusing on examples where zebrafish embryos have been especially useful in understanding the impact of specific toxicants on heart development and function.

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Year:  2005        PMID: 16046794     DOI: 10.1385/ct:5:2:203

Source DB:  PubMed          Journal:  Cardiovasc Toxicol        ISSN: 1530-7905            Impact factor:   3.231


  15 in total

1.  Sensitivity to dioxin decreases as zebrafish mature.

Authors:  Kevin A Lanham; Richard E Peterson; Warren Heideman
Journal:  Toxicol Sci       Date:  2012-03-08       Impact factor: 4.849

Review 2.  Reproductive and developmental toxicity of dioxin in fish.

Authors:  Tisha C King-Heiden; Vatsal Mehta; Kong M Xiong; Kevin A Lanham; Dagmara S Antkiewicz; Alissa Ganser; Warren Heideman; Richard E Peterson
Journal:  Mol Cell Endocrinol       Date:  2011-09-21       Impact factor: 4.102

3.  Impaired cardiovascular function caused by different stressors elicits a common pathological and transcriptional response in zebrafish embryos.

Authors:  Jing Chen
Journal:  Zebrafish       Date:  2013-07-09       Impact factor: 1.985

4.  Methyl tert butyl ether targets developing vasculature in zebrafish (Danio rerio) embryos.

Authors:  Josephine A Bonventre; Lori A White; Keith R Cooper
Journal:  Aquat Toxicol       Date:  2011-05-13       Impact factor: 4.964

5.  Persistent adverse effects on health and reproduction caused by exposure of zebrafish to 2,3,7,8-tetrachlorodibenzo-p-dioxin during early development and gonad differentiation.

Authors:  Tisha C King Heiden; Jan Spitsbergen; Warren Heideman; Richard E Peterson
Journal:  Toxicol Sci       Date:  2009-03-11       Impact factor: 4.849

6.  Sox9b is required for epicardium formation and plays a role in TCDD-induced heart malformation in zebrafish.

Authors:  Peter Hofsteen; Jessica Plavicki; Shaina D Johnson; Richard E Peterson; Warren Heideman
Journal:  Mol Pharmacol       Date:  2013-06-17       Impact factor: 4.436

7.  Dioxin inhibits zebrafish epicardium and proepicardium development.

Authors:  Jessica Plavicki; Peter Hofsteen; Richard E Peterson; Warren Heideman
Journal:  Toxicol Sci       Date:  2012-11-07       Impact factor: 4.849

8.  Lrrc10 is required for early heart development and function in zebrafish.

Authors:  Ki-Hyun Kim; Dagmara S Antkiewicz; Long Yan; Kevin W Eliceiri; Warren Heideman; Richard E Peterson; Youngsook Lee
Journal:  Dev Biol       Date:  2007-06-13       Impact factor: 3.582

9.  A dominant negative zebrafish Ahr2 partially protects developing zebrafish from dioxin toxicity.

Authors:  Kevin A Lanham; Amy L Prasch; Kasia M Weina; Richard E Peterson; Warren Heideman
Journal:  PLoS One       Date:  2011-12-15       Impact factor: 3.240

10.  Cardiac development in zebrafish and human embryonic stem cells is inhibited by exposure to tobacco cigarettes and e-cigarettes.

Authors:  Nathan J Palpant; Peter Hofsteen; Lil Pabon; Hans Reinecke; Charles E Murry
Journal:  PLoS One       Date:  2015-05-15       Impact factor: 3.240

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