O 22. Differential expression of the Wnt/β - catenin pathway in the genital tubercle (GT) of fetal male rat following maternal exposure to di-n-butyl phthalate (DBP)
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O 22. Differential expression of the Wnt/β - catenin pathway in the genital tubercle (GT) of fetal male rat following maternal exposure to di-n-butyl phthalate (DBP)

Li-Feng Zhang1†, Chao Qin1†, Yun-Fei Wei2†, Yong Wang1, Jun-Kai Chang3, Yuan-Yuan Mi1, Long Ma2, Jun-Tao Jiang4, Ning-Han Feng1, Zeng-Jun Wang1, Wei Zhang1

1Department of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China; 2Department of Urology, Jiangsu Province Hospital of TCM, Nanjing, China; 3Department of Urology, Huaihe Hospital of Henan University, Kaifeng, China; 4Department of Urology, Shanghai First People's Hospital affiliated to Shanghai Jiaotong University, Shanghai, PR China; These authors contributed equally to this work


Di-n-butyl phthalate (DBP) is one of the most abundantly produced endocrine disruptors that leaches out from polyvinyl chloride plas-tics and can cause hypospadias in male rats during maternal exposure. The objective of this study was to first explore the roles of Wnt/β-catenin pathway in the fetal rat genital tubercle (GT) following in-utero exposure to DBP. Timedpregnant rats were given DBP by gastric intubation at a dose of 750 mg/kg body weight (bw)/day from gestation day (GD) 14 to (GD) 18 to establish a rat model of hypospadias. On (GD) 19, genital tubercle down-regulation of β-catenin, Phospho- GSK-3β, andup-regulation of GSK-3β (glycogen synthase kinase-3β), NFκB in fetal male rats was observed by western blot analysis. β-catenin was located in the urethral plate epithelium (UPE). Immunochemistry showed that the relative expression of β-catenin decreased in the DBP-trea-ted fetal rat GT compared to the normal control. These findings, for the first time, indicate that DBP may affect the development of GT by down-regulating the Wnt/β-catenin pathway in fetal male rats.

Key words

β-catenin; di-n-butyl phthalate; genital tubercle; hypospadias; male rats

DOI: 10.3978/j.issn.2223-4683.2012.s147

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