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Testicular effect of a mixture of 2-methoxyethanol and 2-ethoxyethanol in rats.
Starek-Swiechowicz, Beata; Szymczak, Wieslaw; Budziszewska, Boguslawa; Starek, Andrzej.
Afiliación
  • Starek-Swiechowicz B; Department of Biochemical Toxicology, Chair of Toxicology, Medical College, Jagiellonian University, Kraków, Poland. Electronic address: beata.starek@gmail.com.
  • Szymczak W; Institute of Psychology, University of Lodz, Lódz, Poland.
  • Budziszewska B; Department of Biochemical Toxicology, Chair of Toxicology, Medical College, Jagiellonian University, Kraków, Poland; Department of Experimental Neuroendocrinology, Institute of Pharmacology, Polish Academy of Sciences, Kraków, Poland.
  • Starek A; Department of Biochemical Toxicology, Chair of Toxicology, Medical College, Jagiellonian University, Kraków, Poland.
Pharmacol Rep ; 67(2): 289-93, 2015 Apr.
Article en En | MEDLINE | ID: mdl-25712652
ABSTRACT

BACKGROUND:

2-Methoxyethanol (ME) and 2-ethoxyethanol (EE) represent a large group of chemicals which are used separately or as mixtures. These compounds exert multidirectional toxic effects. The present studies aimed to demonstrate the effects of ME and EE alone and their mixture on the reproductive organs in the rats.

METHODS:

Male Wistar rats were treated subcutaneously with ME and EE alone (1.25-5.0mM/kg/day) or with their mixture (11) for 4 weeks. After completion of the experiment, the testes, epididymides, and prostate were weighed. In post-mitochondrial supernatant of the testes, the level of total protein, non-protein and protein sulfhydryl groups, malondialdehyde, total antioxidant status, and glutathione peroxidase and glutathione reductase activities were determined.

RESULTS:

Exposure to ME alone resulted in a dose-dependent decrease in the organ weights, the total protein, non-protein and protein sulfhydryl groups. EE alone led to less marked alterations. Co-exposure to ME and EE caused alterations similar as in the rats treated with ME alone.

CONCLUSIONS:

Marked testicular atrophy, decrease in epididymis and prostate weights are predominant effects of the repeated exposure to relatively low doses of ME and EE. A decrease in the total protein level, and protein sulfhydryl groups may be responsible for testicular atrophy. A significant depletion of non-protein sulfhydryl groups and occasionally elevated glutathione peroxidase activity may indicate that ME and EE resulted in disturbances of pro-oxidant/antioxidant balance. The study suggests that testicular toxicity in male rats co-exposed to ME and EE is mainly caused by the former compound.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Atrofia / Testículo / Glicoles de Etileno Límite: Animals Idioma: En Revista: Pharmacol Rep Asunto de la revista: FARMACOLOGIA Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Atrofia / Testículo / Glicoles de Etileno Límite: Animals Idioma: En Revista: Pharmacol Rep Asunto de la revista: FARMACOLOGIA Año: 2015 Tipo del documento: Article