Effect of quinestrol on body weight, vital organs, biochemicals and genotoxicity in adult male lesser bandicoot rat, Bandicota bengalensis.
Autor: | Sidhu A; Department of Zoology, Punjab Agricultural University, Ludhiana 141004, India., Singla N; Department of Zoology, Punjab Agricultural University, Ludhiana 141004, India. Electronic address: neenasingla@pau.edu., Lonare M; Department of Veterinary Pharmacology & Toxicology, Guru Angad Dev Veterinary and Animal Sciences University, Ludhiana 141004, India., Mahal AK; Department of Mathematics, Statistics & Physics, Punjab Agricultural University, Ludhiana 141004, India. |
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Jazyk: | angličtina |
Zdroj: | Pesticide biochemistry and physiology [Pestic Biochem Physiol] 2020 May; Vol. 165, pp. 104544. Date of Electronic Publication: 2020 Feb 19. |
DOI: | 10.1016/j.pestbp.2020.02.010 |
Abstrakt: | The present study was aimed to evaluate the toxic effects of quinestrol (a synthetic estradiol) in male lesser bandicoot rat, Bandicota bengalensis. Effect was studied on body weight, weight of vital organs, changes in level of biochemical parameters and genotoxicity. Feeding of bait containing 0.01% quinestrol in bi-choice and 0.02 and 0.03% quinestrol in no-choice for a period of 10 days resulted in total ingestion of 19.50, 67.60 and 243.30 mg/kg bwt, respectively of the active ingredient. Autopsy of rats after 15 and 30 days of treatment withdrawal revealed no significant effect on body weight and weights of vital organs of rats. A significant decrease in the testicular levels of 17-beta hydroxysteroid dehydrogenase and increase in total soluble proteins was observed in rats treated with 0.02 and 0.03% quinestrol. The plasma levels of lipid peroxidation in the form of malondialdehyde concentration and lactate dehydrogenase increased significantly whereas the level of testosterone decreased significantly in treated rats. The plasma levels of acid and alkaline phosphatases, superoxide dismutase and total proteins differed non-significantly among rats of treated and untreated groups. The effect was found reversed partially in rats autopsied after 60 days of treatment withdrawal. No micronuclei in bone marrow cells, no aberrations in chromosomes and no DNA damage in blood cells during comet assay indicated no genotoxic effect of quinestrol on B. bengalensis at the test doses administered. The results thus revealed that quinestrol causes reversible toxic effects in the form of oxidative stress, increased lytic enzyme activity and decreased steroidogenesis which may further lead to testicular damage thereby inhibiting reproductive function. Also more effect was shown at higher doses ingested in no-choice test as compared to low doses ingested in bi-choice tests. (Copyright © 2020 Elsevier Inc. All rights reserved.) |
Databáze: | MEDLINE |
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