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Ameliorative Effect of Carvacrol on Cisplatin‐Induced Reproductive Damage in Male Rats
Author(s) -
Aksu Emrah Hicazi,
Kandemir Fatih Mehmet,
Altun Serdar,
Küçükler Sefa,
Çomaklı Selim,
Ömür Ali Doğan
Publication year - 2016
Publication title -
journal of biochemical and molecular toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.526
H-Index - 58
eISSN - 1099-0461
pISSN - 1095-6670
DOI - 10.1002/jbt.21816
Subject(s) - sperm , carvacrol , saline , oxidative stress , reproductive toxicity , toxicity , cisplatin , antioxidant , intraperitoneal injection , reproductive system , sperm motility , motility , andrology , biology , pharmacology , medicine , chemistry , essential oil , chemotherapy , botany , biochemistry , genetics
Cisplatin (CP) treatment causes the damage in male reproductive system. Carvacrol (CARV) is an antioxidant that is naturally found in some plants. We aimed to investigate the effect of CARV on CP‐induced reproductive toxicity in male rats. Eighteen adult male Sprague–Dawley rats were used. The control group ( n = 6) was treated orally with physiological saline (PS) daily for 14 days and a single intraperitoneal (IP) PS injection on day 10. The CP group ( n = 6) was administered with daily oral PS for 14 days and a single IP injection of 10 mg/kg CP on day 10. The CARV + CP group ( n = 6) was treated with daily 75 mg/kg oral CARV for 14 days and a single IP injection of 10 mg/kg CP on day 10. CP treatment caused the damage on some spermatological parameters (motility, live sperm rate, and abnormal sperm rate), increased the oxidative stress, and induced testicular degeneration and apoptosis. However, CARV treatment mitigates CP‐induced reproductive toxicity.