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1.
Clinical and Experimental Reproductive Medicine ; : 27-33, 2021.
Article in English | WPRIM | ID: wpr-874425

ABSTRACT

Objective@#The chief outcome of testicular torsion in clinical and experimental contexts is testicular ischemia. Curcumin, a compound with anti-inflammatory and antioxidant properties, has fascinated researchers and clinicians for its promise in the treatment of fertility diseases. @*Methods@#Thirty-five fully grown male mice were randomly classified into five groups: control, sham, testicular torsion, treatment group 1 (testicular torsion+short-term curcumin), and treatment group 2 (testicular torsion+long-term curcumin). Thirty-five days later, spermatozoa from the right cauda epididymis were analyzed with regard to count and motility. Toluidine blue (TB), aniline blue (AB), and chromomycin A3 (CMA3) staining assays were used to evaluate the sperm chromatin integrity. In addition, the terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick-end labeling (TUNEL) test was used to assess apoptosis.Result: Treatment group 1 exhibited a remarkably elevated sperm count compared to the testicular torsion group. Additionally, notably lower sperm motility was found in the testicular torsion group compared to the control, treatment 1, and treatment 2 groups. Staining (CMA3, AB, and TB) and the TUNEL test indicated significantly greater testicular torsion in the torsion group compared to the control group (p<0.05). The data also revealed notably lower results of all sperm chromatin assays and lower apoptosis in both treatment groups relative to the testicular torsion group (p<0.05). Significantly elevated (p<0.05) AB and TB results were noted in treatment group 1 compared to treatment group 2. @*Conclusion@#Curcumin can compensate for the harmful effects of testicular ischemia and improve sperm chromatin quality in mice.

2.
IJRM-International Journal of Reproductive Biomedicine. 2018; 16 (6): 365-372
in English, Persian | IMEMR | ID: emr-199225

ABSTRACT

Background: Prescribing antidepressant drugs is becoming common. These drugs are known to affect sexual functions


Objective: The study is aimed to assess the effects of amitriptyline and venlafaxine on sperm parameters and evaluate Malondialdehyde [MDA] and 1, 1-Diphenyl-2- picryl-hydrazyl values in BALB/ mice spermatozoa


Materials and Methods: Forty adult male BALB/c mice were separated into five groups. Group I [control] received distilled water; group II amitriptyline [4 mg/kg]; group III amitriptyline [4 mg/kg] +vitamin C [10 mg/kg]; group IV venlafaxine [2 mg/kg]; and group V received vitamin C [10 mg/kg] + venlafaxine [2 mg/kg]. All drugs were administered by oral gavage for 35 days. After excision of caudal epididymis, it was located in 1 mL Ham's F10 medium at 37 degree C for 15 min and then analysis of sperm parameters was performed. To examine lipid peroxidation and total antioxidant capacity, the MDA and 1, 1-Diphenyl-2-picryl-hydrazyl were measured, respectively


Results: The mean sperm parameters in the group treated with amitriptyline were significantly lower than in the other groups. MDA tests showed a significant difference between amitriptyline and control groups [p=0.007]


Conclusion: The results of this study showed that amitriptyline consumption can weaken sperm parameters, which can be attributed to the increased production of ROS and toxicity resulting from amitriptyline consumption. Moreover, venlafaxine improved sperm parameters in mice and the lipid peroxidation in this group did not change compared to the control group

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