RESUMEN
We recently showed that prenatal exposure to diesel exhaust (DE) disrupts spermatogenesis in mouse offspring. This study was undertaken to determine whether filtered DE in which 99.97% of diesel exhaust particles >0.3 microm in diameter were removed affects spermatogenesis in growing mice. After prenatal exposure to filtered DE for 2-16 days postcoitum, we examined daily sperm production (DSP), testicular histology, serum testosterone levels and mRNA expression of hormone synthesis process-related factors. In the filtered DE exposed group, DSP was markedly reduced at 12 weeks compared with the control group; clean air exposed group. Histological examination showed multinucleated giant cells and partial vacuolation in the seminiferous tubules of the exposed group. Testosterone was elevated significantly at 5 weeks. Moreover, luteinizing hormone receptor mRNA at 5 and 12 weeks, 17alpha-hydroxylase/C17-20-lyase and 17beta-hydroxysteroid dehydrogenase mRNAs at 12 weeks were significantly elevated. These results suggest that filtered DE retains its toxic effects on the male reproductive system following prenatal exposure.
Asunto(s)
Efectos Tardíos de la Exposición Prenatal , Espermatogénesis/efectos de los fármacos , Testículo/efectos de los fármacos , Emisiones de Vehículos/toxicidad , 17-Hidroxiesteroide Deshidrogenasas/efectos de los fármacos , 17-Hidroxiesteroide Deshidrogenasas/metabolismo , Animales , Femenino , Regulación de la Expresión Génica/efectos de los fármacos , Células Gigantes/efectos de los fármacos , Células Gigantes/metabolismo , Masculino , Ratones , Ratones Endogámicos ICR , Tamaño de la Partícula , Embarazo , ARN Mensajero/efectos de los fármacos , ARN Mensajero/metabolismo , Receptores de HL/efectos de los fármacos , Receptores de HL/metabolismo , Túbulos Seminíferos/efectos de los fármacos , Recuento de Espermatozoides , Esteroide 17-alfa-Hidroxilasa/efectos de los fármacos , Esteroide 17-alfa-Hidroxilasa/metabolismo , Testículo/metabolismo , Testosterona/sangre , Factores de Tiempo , Vacuolas/efectos de los fármacos , Vacuolas/metabolismoRESUMEN
The effect of prenatal exposure to diesel exhaust (DE) was investigated. Twenty pregnant ICR mice were exposed to DE at the particle concentration of 1.0 mg/m3, from d 2 until d 16 postcoitum. Male offspring were kept alive until 12 wk of age, and then male reproductive organ weight, daily sperm production (DSP), serum testosterone level, and mRNA expression of sex steroid hormone synthesis process-related factors were measured. Serum testosterone levels of the exposed group were reduced significantly at 3 wk, whereas they were elevated significantly at 12 wk. DSP was also markedly reduced at 5 and 12 wk. Histological examination showed multinucleated giant cells in the seminiferous tubules of the exposed group as well as partial vacuolation of the seminiferous tubules. Follicle-stimulating hormone receptor (FSHR) mRNA expression and steroidogenesis acute regulatory (StAR) protein were significantly increased at 5 wk and 12 wk, respectively. This study suggests that prenatal exposure to DE has detrimental effects on mouse spermatogenesis in offspring.
Asunto(s)
Feto/efectos de los fármacos , Efectos Tardíos de la Exposición Prenatal , Espermatogénesis/efectos de los fármacos , Emisiones de Vehículos/toxicidad , Animales , Peso Corporal/efectos de los fármacos , Femenino , Masculino , Ratones , Ratones Endogámicos ICR , Tamaño de los Órganos/efectos de los fármacos , Fosfoproteínas/genética , Embarazo , ARN Mensajero/análisis , Testículo/efectos de los fármacos , Testículo/patología , Testosterona/sangreRESUMEN
The effects of in utero exposure to diesel exhaust (DE) on the male mouse reproductive system were examined. Pregnant ICR mice inhaled DE at soot concentrations of 0.3, 1.0, or 3.0 mg DEP/m3 or clean air as the control, for 2-16 days postcoitum. On postnatal day (PND) 28, the weights of the testes and accessory glands and testosterone concentration in serum were significantly higher in the DE-exposed male pups. Testosterone concentration correlated significantly (P<0.01) with the expression levels of steroidogenic enzyme mRNAs, weights of the testes and male reproductive accessory glands, and daily sperm production. These findings indicate that very early stage mouse embryo exposure to DE leads to endocrine disruption after birth and acceleration of male puberty.