Study on developmental abnormalities in hypospadiac male rats induced by maternal exposure to di-n-butyl phthalate (DBP) |
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Authors: | Jiang JunTao Ma Long Yuan Lin Wang XinRu Zhang Wei |
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Affiliation: | Department of Urology, Shanghai First People's Hospital, Shanghai Jiaotong University, 85 Wujin road, Shanghai 200080, Shanghai, PR China. |
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Abstract: | The objective of this study was to establish a hypospadiac rat model by maternal exposure to di-n-butyl phthalate (DBP) and to evaluate the developmental abnormalities of hypospadiac male rats. Timed-pregnant rats were given DBP by gastric intubation at doses of 0, 250, 500, 750 or 1000 mg/kg body weight (bw)/day from gestation day (GD) 14 to 18 to establish a hypospadiac rat model. The hypospadias was observed in the 500 and 750 mg/kg bw/day groups, the incidence of which was 6.8 and 41.3%, respectively. Transverse serial histological analysis of genitalia of hypospadiac male rats confirmed the malformation. With exposed dose increasing, the serum testosterone (T) levels of male rats inversely decreased, and in the same dosage group the serum T levels of hypospadiac rats were significantly lower than the levels of nonhypospadiac counterparts. The other reproductive lesions such as cryptorchidism and decreased ratio of anogenital distance/body weight (AGD/bw) were also observed. Autopsy analysis revealed the development of reproductive organs (prostate, testes, epididymis, pituitary gland) and nonreproductive organs (adrenal gland, liver, kidney, heart, spleen) of hypospadiac rats and nonhypospadiac counterparts. The results indicated that the reproductive system and developmental condition of hypospadiac male offspring were damaged severely by DBP. |
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Keywords: | DBP, di-n-butyl phthalate bw, body weight GD, gestation day T, testosterone AGD/bw, anogenital distance/body weight EEDs, environmental endocrine disruptors PND, postnatal day S.D., standard deviation ANOVA, analysis of variance χ2, chi-square TDS, testicular dysgenesis syndrome GT, genital tubercle DHT, dihydrotestosterone 3β-HSD, 3β-hydroxysteroid dehydrogenase P450scc, P450 side-chain cleavage enzyme 17β-HSD, 17β-hydroxysteroid dehydrogenase SRB1, scavebger receptor class B-1 StAR, steroidogenic acute regulatory protein |
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