Abstract: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… Show more
“…Oxidative stress occurs due to excessive increase in reactive oxygen species depending on the deterioration of oxidant–antioxidant balance in the body (Ak & Gulcin, ; Aksu et al, ; Bursal & Gülçin, ; Gulcin, ). Due to oxidative stress, damage occurs in lipids, proteins and DNA, which are the macromolecules that make up the cell; that is why, cell integrity is impaired (Aksu et al, ). In the studies on mice and monkeys, methyl mercury has been reported to reduce sperm count and motility (Mohamed, Burbacher, & Mottet, ; Rao, ).…”
This study investigated the effects of rutin against reproductive damage caused by toxic mercury in male rats. Thirty‐five Sprague Dawley rats were used. Control group was injected with saline for 7 days. The rutin‐100 group received 100 mg/kg/b.w. rutin for 7 days. Mercuric chloride (HgCl2) group received 1.23 mg/kg/b.w. of HgCl2 for 7 days. Mercury chloride + rutin‐50 group received 50 mg/kg/b.w. rutin and HgCl2 1.23 mg/kg/b.w. for 7 days. HgCl2 + rutin‐100 group received 100 mg/kg/b.w. rutin and HgCl2 1.23 mg/kg/b.w. for 7 days. It was detected that HgCl2 treatment increased malondialdehyde (MDA) levels, tumour necrosis factor‐α (TNF‐α) and cyclooxygenase‐2 (COX‐2) expressions, necrosis and degeneration of spermatogonium, dead and abnormal sperm percentages; tubular walls thinning; and decreased antioxidant enzyme activities and sperm motility. It was determined that rutin application reduced testicular damage caused by HgCl2. In conclusion, rutin administration may treat HgCl2 toxicity in testes.
“…Oxidative stress occurs due to excessive increase in reactive oxygen species depending on the deterioration of oxidant–antioxidant balance in the body (Ak & Gulcin, ; Aksu et al, ; Bursal & Gülçin, ; Gulcin, ). Due to oxidative stress, damage occurs in lipids, proteins and DNA, which are the macromolecules that make up the cell; that is why, cell integrity is impaired (Aksu et al, ). In the studies on mice and monkeys, methyl mercury has been reported to reduce sperm count and motility (Mohamed, Burbacher, & Mottet, ; Rao, ).…”
This study investigated the effects of rutin against reproductive damage caused by toxic mercury in male rats. Thirty‐five Sprague Dawley rats were used. Control group was injected with saline for 7 days. The rutin‐100 group received 100 mg/kg/b.w. rutin for 7 days. Mercuric chloride (HgCl2) group received 1.23 mg/kg/b.w. of HgCl2 for 7 days. Mercury chloride + rutin‐50 group received 50 mg/kg/b.w. rutin and HgCl2 1.23 mg/kg/b.w. for 7 days. HgCl2 + rutin‐100 group received 100 mg/kg/b.w. rutin and HgCl2 1.23 mg/kg/b.w. for 7 days. It was detected that HgCl2 treatment increased malondialdehyde (MDA) levels, tumour necrosis factor‐α (TNF‐α) and cyclooxygenase‐2 (COX‐2) expressions, necrosis and degeneration of spermatogonium, dead and abnormal sperm percentages; tubular walls thinning; and decreased antioxidant enzyme activities and sperm motility. It was determined that rutin application reduced testicular damage caused by HgCl2. In conclusion, rutin administration may treat HgCl2 toxicity in testes.
“…A rich composition of polyunsaturated fatty acids in the mammalian sperm cell membrane makes the cell sensitive to free radicals. There are many experimental studies reporting that increased ROS levels decrease sperm motility and quality and increase the rate of sperm death in the semen . Using antioxidant compounds may be a useful and important strategy for preventing male infertility caused by chemotherapy.…”
This study aimed to investigate the effect of curcumin (CUR) on doxorubicin (DOX)‐induced testicular damage in male rats. Thirty‐five adult male Wistar rats were used. Control group was received saline for 7 days. CUR group received CUR for 7 days. DOX group received single dose DOX on the 5th day. DOX+ CUR‐100 group received 100 mg/kg/day CUR for 7 days and DOX injection on the 5th day. DOX + CUR‐200 group received 200 mg/kg/day CUR for 7 days and DOX injection on the 5th day. DOX treatment decreased in sperm motility rate, live sperm percentages, cellular antioxidants, and increased malondialdehyde (MDA) levels, necrosis, degenerations, and slimming in seminiferous tubules, and DNA damages in testes by inducing oxidative stress. CUR treatment mitigated significantly these side effects when compared with DOX group in a dose‐dependent manner. In conclusion, CUR treatment can be used in the mitigation of DOX‐induced testicular toxicity.
“…Many studies have examined the adverse effects of CP on sperm quality and reproductive organ weights (Aksu et al, , ; Saral et al, ). Aksu et al () demonstrated that CP administration resulted in a decrease in total testicular weight, sperm motility and sperm concentration and an increase in abnormal sperm rates as compared to these parameters in a control group.…”
Section: Discussionmentioning
confidence: 99%
“…The average of the values from these observations was used as the final motility score (Aksu et al, ). To determine the percentage of morphological sperm abnormalities, the method of Aksu et al () was used. Briefly, slides were prepared by staining each semen sample with eosin–nigrosin dye.…”
The aim of this study was to investigate the potential beneficial effects of β‐glucan treatment against oxidative, histological and spermatological damage caused by cisplatin on the male reproductive system. Twenty‐eight Sprague Dawley male rats were used in the study. The rats were randomly divided into four equal‐sized groups: a control group, cisplatin group (7 mg/kg in a single‐dose cisplatin administered intraperitoneally), β‐glucan group (β‐glucan given at a dose of 50 mg kg−1 d−1 for 14 day) and a cisplatin plus β‐glucan group (cisplatin and β‐glucan administered together at the same dose). Cisplatin administration induced an increase in the level of thiobarbituric acid‐reactive substances, a lipid peroxidation indicator. It induced a decrease in enzymatic (superoxide dismutase, catalase and glutathione peroxidase) activities and nonenzymatic (reduced glutathione) antioxidant levels. In addition, cisplatin caused both histological and spermatological damage, as shown by a decrease in sperm motility and epididymal sperm concentrations and an increase in abnormal sperm rates. The β‐glucan treatment improved cisplatin‐induced oxidative, histological and spermatological damage. This study revealed that β‐glucan treatment provided prevention against male reproductive system damage caused by cisplatin. These preventative effects were likely due to its antioxidant properties.
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