| Literature DB >> 26482405 |
Manel Jallouli1, Ines El Bini Dhouib2, Hanène Dhouib2, Najoua Gharbi2, Saloua El Fazaa2.
Abstract
The aim of the current study was to investigate the ability of dimethoate (DMT) to induce reprotoxicity in male mice. The dose (20 mg/kg/day) was given orally for 30 days. A significant decrease in sperm count, motility and viability and a significant increase of morphologically abnormal spermatozoa percent in DMT treated mice was observed. Testicular Acetylcholinesterase (AChE) and Butyrylcholinesterase (BChE) activities were inhibited. Also, a significant increase in lipid peroxidation level and a significant decrease in the activities of antioxidant enzymes were observed in testis of DMT mice. In addition, gene expression of glutathione peroxidase 4 (GPx4) was quantified in RNA samples extracted from the testis by real-time reverse transcription-polymerase chain reaction (RT-PCR). Compared with control, mRNA expression of GPx4 was slightly decreased after DMT-exposure.Entities:
Keywords: Dimethoate; Mice; Oxidative stress; Reprotoxicity; Testis
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Year: 2015 PMID: 26482405 DOI: 10.1016/j.yrtph.2015.10.010
Source DB: PubMed Journal: Regul Toxicol Pharmacol ISSN: 0273-2300 Impact factor: 3.271