“Perfluorooctane sulfonate (PFOS) is widely used in indust


“Perfluorooctane sulfonate (PFOS) is widely used in industry; it is nonbiodegradable and persistent in the human body and in the environment. Although reports have indicated that young people might have higher PFOS levels in serum or blood than do older people, its adverse effects on neonatal testicular cells had not been investigated previously. PCB 153 is one of the most prevalent polychlorinated CA3 chemical structure biphenyl (PCB) congeners in biological tissues, but the direct adverse effect of

PCB 153 on neonatal testis remains unclear. In this study, we exposed a neonatal Sertoli cell/gonocyte coculture system to PFOS and PCB 153 individually at concentrations of 0, 1, 10, 50, and 100 M for 24 h. Exposure to either compound reduced the cell viability and induced the production of reactive oxygen species (ROS) buy S3I-201 in dose-dependent manners, with PCB 153 having a greater effect than PFOS. Whereas PCB 153 induced apoptosis significantly from 10 M, PFOS induced no obvious change. Morphologically, both PCB 153 and PFOS induced changes in the vimentin and actin filaments

in the Sertoli cells, as investigated using confocal argon ion laser scanning microscopy; here, PFOS exhibited a more dramatic effect than did PCB 153. Furthermore, doses of 50 M for PFOS and 10 M for PCB 153 were the key concentrations that produced significant differences between the control and exposure groups. We suggest that both PCB 153 and PFOS directly affect neonatal gonocyte and Sertoli cells; the production of ROS and the change in the cytoskeleton in Sertoli cells might be causes. (c) 2011

Wiley Periodicals, Inc. Environ Toxicol, 2013.”
“Objective. To identify risk factors for hernia repair following open retropubic, pure laparoscopic and robot-assisted laparoscopic radical prostatectomy. Material and methods. The medical records of 632 patients who had undergone radical prostatectomy (open retropubic n == 430, pure laparoscopic n == 49, and robot-assisted laparoscopic n == 202) were reviewed retrospectively. Patients with postprostatectomy inguinal hernia were defined as those who had undergone subsequent hernia repair. The mean period of follow-up was 19.5 months (median 19, range 1 to 42). Results. Hernia repairs were performed in 27 of the 632 patients find more (4.3%). The site of the repair was right in 15 patients (55.6%), left in 9 patients (33.3%), and bilateral in 3 patients (11.1%). The timing of the hernia repair ranged from 4 to 35 months (mean 13.1) following radical prostatectomy. No difference in hernia-repair-free rates was observed between the extraperitoneal open and transperitoneal pure or robot-assisted laparoscopic radical prostatectomy procedures (p == 0.225, log-rank test). The log-rank test revealed that the nerve sparing procedure (p == 0.019) and the absence of diabetes (p == 0.017) were significant risk factors for postprostatectomy hernia repair.

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