4.7 Article

Antioxidants enhance the recovery of three cycles of bleomycin, etoposide, and cisplatin-induced testicular dysfunction, pituitary-testicular axis, and fertility in rats

Journal

FERTILITY AND STERILITY
Volume 100, Issue 4, Pages 1151-+

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.fertnstert.2013.06.019

Keywords

Anticancer drugs; male infertility; sex hormones; pituitary-testicular axis

Funding

  1. Kuwait University [MA02/08, GM01/01]

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Objective: To investigate the effects of an antioxidant cocktail (AC) on bleomycin, etoposide, and cisplatin (BEP)-induced testicular dysfunction. Design: In vivo study. Setting: Research laboratory. Animal(s): Adult male and female Sprague-Dawley rats. Intervention(s): The rats were treated with three cycles of 21 days each of therapeutically relevant dose levels of BEP (0.75, 7.5, and 1.5 mg/ kg) with or without the AC (a mixture of a-tocopherol, L-ascorbic acid, Zn, and Se). Main Outcome Measure(s): Sperm parameters, fertility, serum hormone levels (ELISA), testicular histopathology, and expression of proliferating cell nuclear antigen (PCNA), and transferrin (Western blotting and immunohistochemistry) were evaluated at the end of treatment and a 63-day recovery period. Result(s): At the end of treatment, the AC improved BEP-induced decrease in sperm motility and increase in abnormality but had no effect on reduced sperm count, fertility, and tubular atrophy, although it up-regulated germ cell proliferation. The AC normalized reduced inhibin B levels, but had no effect on decreased transferrin and testosterone and elevated LH levels. At the end of the recovery period, the AC enhanced the expression of PCNA and transferrin, repopulation of germ cells, LH-testosterone axis, and fertility, but had no effect on reduced FSH and elevated inhibin B levels. Conclusion(s): The antioxidants protect and then enhance the recovery of testicular and reproductive endocrine functions when administered concomitantly with BEP therapy. The AC may be beneficial to regain testicular functions after chemotherapy. (Fertil Steril (R) 2013;100: 1151-9. (C) 2013 by American Society for Reproductive Medicine.)

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