Literature DB >> 17604895

Toxic effects of di(2-ethylhexyl)phthalate on mortality, growth, reproduction and stress-related gene expression in the soil nematode Caenorhabditis elegans.

Ji-Yeon Roh1, In-Ho Jung1, Jai-Young Lee1, Jinhee Choi2.   

Abstract

In this study, di(2-ethylhexyl)phthalate (DEHP) toxicities to Caenorhabditis elegans were investigated using multiple toxic endpoints, such as mortality, growth, reproduction and stress-related gene expression, focusing on the identification of chemical-induced gene expression as a sensitive biomarker for DEHP monitoring. The possible use of C. elegans as a sentinel organism in the monitoring of soil ecosystem health was also tested by conducting the experiment on the exposure of nematode to field soil. Twenty-four-hour median lethal concentration (LC50) data suggest that DEHP has a relatively high potential of acute toxicity to C. elegans. Decreases in body length and egg number per worm observed after 24h of DEHP exposure may induce long-term alteration in the growth and reproduction of the nematode population. Based on the result from the C. elegans genome array and indicated in the literatures, stress proteins, metallothionein, vitellogenin, xenobiotic metabolism enzymes, apoptosis-related proteins, and antioxidant enzyme genes were selected as stress-related genes and their expression in C. elegans by DEHP exposure was analyzed semi-quantitatively. Expression of heat shock protein (hsp)-16.1 and hsp-16.2 genes was decreased by DEHP exposure. Expression of cytochrome P450 (cyp) 35a2 and glutathione-S-transferease (gst)-4, phase I and phase II of xenobiotic metabolism enzymes, was increased by DEHP exposure in a concentration-dependent manner. An increase in stress-related gene expressions occurred concomitantly with the deterioration on the physiological level, which suggests an increase in expression of those genes may not be considered as a homeostatic response but as a toxicity that might have physiological consequences. The experiment with the soil from the landfill site suggests that the potential of the C. elegans biomarker identified in laboratory conditions should be calibrated and validated for its use in situ.

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Year:  2007        PMID: 17604895     DOI: 10.1016/j.tox.2007.05.008

Source DB:  PubMed          Journal:  Toxicology        ISSN: 0300-483X            Impact factor:   4.221


  22 in total

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2.  Hormetic effect of methylmercury on Caenorhabditis elegans.

Authors:  Kirsten J Helmcke; Michael Aschner
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Authors:  L Queirós; J L Pereira; F J M Gonçalves; M Pacheco; M Aschner; P Pereira
Journal:  Crit Rev Toxicol       Date:  2019-07-03       Impact factor: 5.635

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Authors:  Suresh Swain; Jodie F Wren; Stephen R Stürzenbaum; Peter Kille; A John Morgan; Tjalling Jager; Martijs J Jonker; Peter K Hankard; Claus Svendsen; Jenifer Owen; B Ann Hedley; Mark Blaxter; David J Spurgeon
Journal:  BMC Syst Biol       Date:  2010-03-23

5.  Characterization of the effects of methylmercury on Caenorhabditis elegans.

Authors:  Kirsten J Helmcke; Tore Syversen; David M Miller; Michael Aschner
Journal:  Toxicol Appl Pharmacol       Date:  2009-03-31       Impact factor: 4.219

6.  Neurotoxicological evaluation of microcystin-LR exposure at environmental relevant concentrations on nematode Caenorhabditis elegans.

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7.  Two organobromines trigger lifespan, growth, reproductive and transcriptional changes in Caenorhabditis elegans.

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Review 8.  A systematic review on the adverse health effects of di-2-ethylhexyl phthalate.

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9.  Caenorhabditis Elegans Mutants Predict Regulation of Fatty Acids and Endocannabinoids by the CYP-35A Gene Family.

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Journal:  Front Pharmacol       Date:  2011-03-18       Impact factor: 5.810

10.  Gene expression modifications by temperature-toxicants interactions in Caenorhabditis elegans.

Authors:  Ana Viñuela; L Basten Snoek; Joost A G Riksen; Jan E Kammenga
Journal:  PLoS One       Date:  2011-09-09       Impact factor: 3.240

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