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Evaluation of toxic potential of captan: Induction of hsp70 and tissue damage in transgenic drosophila melanogaster (hsp70-lacZ) Bg9

✍ Scribed by Aamir Nazir; Indranil Mukhopadhyay; D. K. Saxena; M. Saeed Siddiqui; D. Kar Chowdhuri


Book ID
102303696
Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
191 KB
Volume
17
Category
Article
ISSN
1095-6670

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✦ Synopsis


Abstract

The study investigated the working hypothesis that a widely used fungicide captan exerts toxic effects on nontarget organisms. Transgenic Drosophila melanogaster (hsp70‐lacZ) was used as a model by assaying stress gene expression as an endpoint for cytotoxicity and also to evaluate whether stress gene expression is sufficient enough to protect and to prevent tissue damage against toxic insult of the chemical. The study was further extended to understand the effect of the pesticide on development, life cycle, and reproduction of the organism and finally to evaluate a concentration of the chemical to be nontoxic to the organism. The study showed that (i) captan causes cytotoxicity at and above 0.015 ppm; (ii) at 0.0015 ppm captan, absence of hsp70 expression in the exposed organism was evaluated as the concentration referred to as no observed adverse effect level (NOAEL) for Drosophila; (iii) emergence pattern of flies was affected only at the highest concentration of captan by 4 days, while hatching and survivorship were unaffected even at this concentration; (iv) reproductive performance was significantly affected only at 125.0 and 1250.0 ppm captan, while in the lower dietary concentrations no such deleterious effects were observed; (v) at 1250.0 ppm, hsp70 failed to protect the cells from toxicant assault after 48 h exposure, thus leading to tissue damage as revealed by Trypan Blue staining. The present study shows the cytotoxic potential of captan and further reveals the application of stress genes in determining NOAEL and its expression as bioindicator of exposure to environmental contaminants. Β© 2003 Wiley Periodicals, Inc. J Biochem Mol Toxicol 17:98–107, 2003; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/jbt.10066


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