Touba Nadri; saeed zeinoaldini; Armin towhodi; Gholamhossein Riazi; Mahdi zhandi; Mohsen Sharafi
Volume 22, Issue 3 , September 2020, , Pages 471-477
Abstract
This study was designed to add the reduced glutathione to a lecithin nanoparticle-based extender and evaluate the quality of bull sperm after freezing and thawing. In the present study, the effect of four different levels of glutathione (0, 1, 2.5 and 5 mM) in extender-based on lecithin nanoparticles ...
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This study was designed to add the reduced glutathione to a lecithin nanoparticle-based extender and evaluate the quality of bull sperm after freezing and thawing. In the present study, the effect of four different levels of glutathione (0, 1, 2.5 and 5 mM) in extender-based on lecithin nanoparticles was evaluated. The lecithin nanoparticles were prepared and the particle size was reduced by using a sonicator device. During three weeks, 48 ejaculates from six Holstein bulls were collected and frozen. Properties evaluated after freezing and thawing were kinetic parameters (CASA), membrane activity (HOST), membrane integrity (eosin-nigrosine) and morphology (Hancock solution). The results showed that using 2.5 mM glutathione in the extender significantly increased total and progressive motility (63.38±1.5 and 43.1±1.1 respectively, P <0.05). The results of eosin-nigrosine staining and Host test showed that the highest viability and cell membrane functionality were related to 2.5 mM treatment (64.8±1.5 and 58.1±1.1 respectively) (p < 0.05). In general, 2.5 mM glutathione could improve the quality of bull sperm compared with other concentrations after freezing and thawing process. It seems that the 2.5 mM glutathione is optimum concentration for bull extender based on the lecithin nanoparticles.
toktam sadat Vafa; heshmat Sepehri moghadam; Mozhdeh Emadi; Alireza Hasani Bafarani
Volume 21, Issue 4 , January 2020, , Pages 569-577
Abstract
To examine the effect of glycyrrhizic acid on lipid peroxidation and vital parameters of Holstein bull sperm after freeze-thawing process, semen samples were collected from four mature Holstein bulls twice a week using artificial vagina. Ejaculates were pooled in order to eliminate the individual ...
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To examine the effect of glycyrrhizic acid on lipid peroxidation and vital parameters of Holstein bull sperm after freeze-thawing process, semen samples were collected from four mature Holstein bulls twice a week using artificial vagina. Ejaculates were pooled in order to eliminate the individual effects of bull. Semen samples were divided into four equal groups (8 reps) including Zero (control), 20, 30 and 40 mg/ml of glycyrrhizic acid along with diluents based on egg yolk-citrate. Following cooling and equilibration stage, semen samples were stored in nitrogen tank for 30 days. After thawing procedure, level of malondialdehyde in sperm samples were measured by ELISA. Also, membrane integrity, motility and viability of sperm were examined. Statistical analysis was carried out using one-way ANOVA and post-hoc Tukey tests (p<0.05). According to the results, membrane integrity, motility and viability of sperm samples treated with concentration of 20, 30 and 40 mg/ml glycyrrhizic acid dose dependent manner significantly increased and level of malondialdehyde dose dependent manner significantly decreased ccompared to control groups (p<0.05). Therefore, use of glycyrrhizic acid in bull semen diluent can improve sperm vital parameters and decreases lipid peroxidation of sperm after freeze-thawing process.