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Oxidative Stress and Cytotoxic Potential of Anticholinesterase Insecticide, Malathion in Reproductive Toxicology of Male Adolescent Mice After Acute Exposure

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Specialty General Medicine
Date 2014 Nov 28
PMID 25429344
Citations 12
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Abstract

Objectives: The present study was undertaken to determine the effects of acute exposure to malathion on oxidative stress and cytotoxic potential of anticholinesterase insecticide, malathion in reproductive toxicology of adolescent male mice.

Materials And Methods: Thirty two adolescent male mice at pubertal age were treated with 500 mg/kg body weight (BW) of malathion for three days. After exposure, biochemical markers and sperm analysis were evaluated and finally histological modifications of testis and sperm were assessed.

Results: Our data showed that treatment of male mice with malathion (500 mg/kg, BW) could lead to oxidative stress. Induced oxidative stress status can be assessed due to increased malondialdhyde (MDA) content, decreased thiol group content, as well as increased antioxidant enzyme activities. On the other hand, exposure to malathion at the pubertal age led to alteration of semen parameters; sperm production and percentage of motile sperm were decreased in the treated groups compared to the control. Furthermore, exposure of male mice to malathion led to a decrease of testosterone level, inhibition of acetylcholinesterase, and decrease of the reproductive performance of male mice after three days of treatment at the age of puberty.

Conclusion: The importance to carry out in vitro reproductive toxicology assays lies on the need of knowing the alterations these insecticides may cause at cellular level, since they are endocrine disruptors that interfere with reproductive functions.

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References
1.
Rubin C, Esteban E, Kieszak S, Hill Jr R, Dunlop B, Yacovac R . Assessment of human exposure and human health effects after indoor application of methyl parathion in Lorain County, Ohio, 1995-1996. Environ Health Perspect. 2003; 110 Suppl 6:1047-51. PMC: 1241291. DOI: 10.1289/ehp.02110s61047. View

2.
Pope C . Organophosphorus pesticides: do they all have the same mechanism of toxicity?. J Toxicol Environ Health B Crit Rev. 1999; 2(2):161-81. DOI: 10.1080/109374099281205. View

3.
Vega S, Guzman P, Garcia L, Espinosa J, Cortinas de Nava C . Sperm shape abnormality and urine mutagenicity in mice treated with niclosamide. Mutat Res. 1988; 204(2):269-76. DOI: 10.1016/0165-1218(88)90099-7. View

4.
Fortunato J, Feier G, Vitali A, Petronilho F, Dal-Pizzol F, Quevedo J . Malathion-induced oxidative stress in rat brain regions. Neurochem Res. 2006; 31(5):671-8. DOI: 10.1007/s11064-006-9065-3. View

5.
Kakinuma K, Yamaguchi T, Kaneda M, Shimada K, Tomita Y, Chance B . A determination of H2O2 release by the treatment of human blood polymorphonuclear leukocytes with myristate. J Biochem. 1979; 86(1):87-95. View