Abstract

To investigate the effect of chronic moderate exercise on male reproductive tract of Wistar rats submitted to a single dose of cyclophosphamide (CP). Animals were submitted to swimming exercise during 21 days or maintained at sedentary state. Trained (TCP) and sedentary (SCP) groups received a single dose of CP (200 mg kg -1 , i.p.). Trained (TCo) and sedentary (SCo) control animals received sterile PBS. Animals were killed after one week and testis, epidydimis and seminal vesicle contend were weighted. Testis were embebbed in parafim and stained with hemotaxilin and eosin. Fifty seminiferous tubules of each animal were analyzed by Johnsen score. Mean Sertoli cells counts per tubule and Leydig cells counts per area were evaluated. CP treatment impairs body weight gain in trained and sedentary animals. Liver and seminal vesicle contend were reduced only in SCo group. SCP animals presented decreased Johnsen scores, indicating a slight toxicity over germinative cells, whereas trained (TCo and TCP) animals presented increased Johnsen scores. Training increased Sertoli cell counts and prevented their loss in TCP group. Leydig cells counts were increased in trained animals, but decreased in CP treated ones (TCP). We conclude that exercise have some protective effect on male reproductive tract submitted to a single dose of CP.

Highlights

  • Cyclophosphamide (CP) is an alkylating agent widely used as an anticancer drug as well as an immunosupressive drug

  • The animals were divided into four groups (n = 6): sedentary control (SCo), sedentary treated with CF (SCP), trained control (TCo) and trained and treated with CF (TCP) groups

  • TCo and tratados com CP (TCP) groups were submitted to training protocol, during 21 days, while SCo and SCP animals were not submitted to training

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Summary

Introduction

Cyclophosphamide (CP) is an alkylating agent widely used as an anticancer drug as well as an immunosupressive drug. CP toxic effects on testis were mainly attributed to oxidative stress on seminiferous tubules and Sertoli cells, impairing spermatogenis and androgenesis, and inducing germinal cells apoptosis (ILBEY et al, 2009; MOTAWI et al, 2010; REZVANFAR et al, 2008; TURK et al, 2010). It was observed decreased testis, seminal vesicles and epididymal weights, damage and decreased number of spermatogonial cells in the seminiferous tubules, low levels of plasma testosterone and infertility (ELANGOVAN et al, 2006; REZVANFAR et al, 2008). A single dose of CP (200 mg kg-1) can induce atrophy and degeneration of germinative epithelium, haemorrhage and edema replacing Leydig cells (MOTAWI et al, 2010)

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