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Background & objectives: exposure to lead has a wide range side effects on fertility. Vitamin D is one of the most important vitamins required for the body. This study was conducted to determine the effect of vitamin D on spermatogenesis in male rats treated with lead nitrate.
Methods: In this experimental study, 25 adult male Wistar rats (250-300 gr) were randomly divided into 5 groups (n=5). Control group without any treatment, the group receiving lead by gavage and experimental groups receiving lead plus vitamin D at doses of 25, 50 and 75 mg/kg body weight by gavage  for 28 days. At the end of the study, after anesthetizing the rats, blood samples were collected directly from heart and serum levels of testosterone hormone, Follicle-stimulating Hormone (FSH) andLuteinizing Hormone (LH) were measured. Histological studies were performed to count the spermatocyte and examine the diameter of the seminal tube. Data were analyzed by SPSS software using one-way ANOVA, at significance level of p>0.05.
Results: Compared to the control group,  the mean serum testosterone level in the lead group significantly decreased (p<0.001) and the mean LH and FSH serum levels significantly increased (p<0.001) . Also, spermatocytes and seminiferous tubule diameter significantly decreased (p<0.001). Vitamin D consumption reduced the effects of lead intake, and  this effectiveness was completely dose-dependent.
Conclusion: Our data showed that vitamin D has a significant effect on serum testosterone levels and gonadotropins.

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Background & objectives: The present study investigated the effects of royal jelly on lead acetate induced toxicity on sperm parameters, reproductive hormone assay, and bak gene expression in NMRI male mice.
Methods: In this study, fifty four male mice were randomly divided into nine groups: control group (without royal jelly) (n=6); sham group(10 ml normal saline) (n=6); lead group (1000 ppm, oral) (n=6); Group 4: royal jelly (100 mg/kg/day, oral) (n=6); Group 5: royal jelly (250 mg/kg/day, oral)(n=6); Group 6: royal jelly (500 mg/kg/day, oral)(n=6); Group 7: royal jelly (100 mg/kg/day, oral) + 1000 ppm lead (n=6); Group 8: royal jelly (250 mg/kg/day, oral) + 1000 ppm lead (n=6) and Group 9: royal jelly (500 mg/kg/day, oral) + 1000 ppm lead (n=6). On day 35, blood samples were collected from anaesthetized mice by cardiac puncture to assess reproductive hormones and the testes were harvested for determination of sperm parameters and expression bak gene. Sperm parameters including motility, viability, DNA damage, morphology and total antioxidant capacity (TAC) levels were determined.
Results: The results showed that administration of royal jelly significantly enhanced sperm parameters and all reproductive hormone levels compared to control mice, (p<0.05). Also, treatment with lead acetate caused a significant reduction in levels of all reproductive hormones and a significant diminution in sperm motility, morphology, viability; with an increase in percentage of dead spermatocytes (p<0.05). The co-administration of the 250 and 500 mg/kg/day royal jelly with lead acetate could ameliorate the deleterious effects of lead acetate resulting in a significant increase in sperm parameters and all reproductive hormones and increase the total antioxidant capacity (TAC) levels (p<0.05). Also, the expression of bak gene in all treated (sham, royal jelly groups) and control groups was significantly lower than the lead acetate group (p<0.05).
Conclusion: In conclusion, our findings suggest that the royal jelly has a beneficial effect on male reproductive parameters following lead acetate induced toxicity in mice.