ffect of quercetin or butylated hydroxytoluene on cooled or frozen-thawed ram sperm qualit

Author(s)

Ferreira Canuto, Lucas Emanuel ^[1] ; Teixeira Martini Segabinazzi, Lorenzo Garrido ^[1] ; Braga de Araujo, Endrigo Adonis ^[1] ; Merces Chaves Silva, Luis Fernando ^[1] ; de Oliveira, Sidnei Nunes ^[1] ; Dalanezi, Felipe Morales ^[1] ; Dell'Aqua Junior, Jose Antonio ^[1] ; Papa, Frederico Ozanam ^[1] ; Oba, Eunice ^[1]

Affiliation

^[1] Univ Estadual Sao Paulo, UNESP, Sch Vet Med & Anim Sci, Botucatu, SP - Brazil

• Document type: Journal article
• Source: SEMINA-CIENCIAS AGRARIAS; v. 43, n. 2, p. 841-854, MAR-APR 2022.
• Web of Science Citations: 0

Abstract

Cooling and freezing processes cause physical and chemical damage to sperm by cold shock and oxidative stress. This study aimed to evaluate the effect of two antioxidants on sperm parameters of cooled and frozen-thawed ram semen diluted in an egg yolk-based extender. Semen was collected from 30 rams and processed in two consecutive experiments to test the inclusion of different concentrations of quercetin and butylated hydroxytoluene (BHT) in an egg yolk-based semen extender. Dimethyl sulfoxide (DMSO) was added as a solvent to the semen extender in a ratio of 1 mL DMSO for 90 mg of quercetin and 1 mL DMSO for 880 mg of BHT. After collection, semen was diluted at 200 x 106 motile sperm/mL (control) and split into different groups in each experiment. In experiment 1, semen was diluted with the extender containing quercetin (Q5, 5 mu g/mL; Q10, 10 mu g/mL; Q15, 15 mu g/mL) or DMSO alone (DMSO1, 0.055 mu L DMSO per mL; DMSO2, 0.165 mu L DMSO per mL). In experiment 2, semen was diluted with the extender with BHT (BHT1, 0.5 mu g/mL; BHT2, 1 mu g/mL; BHT3, 1.5 mu g/mL) or DMSO alone (DMSO3, 0.375 mu L DMSO per mL; DMSO4, 1.125 mu L DMSO per mL). After dilution, the semen was divided into two aliquots. Treated ram sperm samples were also subjected to different storage methods. The first set of samples was cooled at 5 degrees C for 24 h, whereas the second set of samples was frozen-thawed. Sperm motility parameters and plasma membrane integrity (PMI) were evaluated immediately after dilution (0h) and 24 h after cooling and in the frozen-thawed samples via computer-assisted sperm analysis and epifluorescence microscopy, respectively. The inclusion of quercetin or BHT did not affect sperm motility parameters or PMI of fresh, cooled, or frozen-thawed sperm in this study (P < 0.05). However, further studies are needed to test the effects of these antioxidants on the fertility of cryopreserved ram semen. (AU)

• FAPESP's process: 12/50277-6 - Evaluation of different concentrations of selenium in sheep reproduction
• Grantee: Eunice Oba
• Support Opportunities: Regular Research Grants