In vitro supplementation of testosterone or prolactin affects spermatozoa freezability in small ruminants
2020
Martínez-Fresneda, Lucía | O'Brien, Emma | López Sebastián, Antonio | Velázquez, Rosario | Toledano-Díaz, A. | Tesfaye, Dawit | Schellander, Karl | García-Vázquez, Francisco Alberto | Santiago-Moreno, Julián | European Commission | Ministerio de Economía, Industria y Competitividad (España) | Martínez-Fresneda, Lucía [0000-0002-0967-8593] | López Sebastián, Antonio [0000-0001-8695-7441] | Velázquez, Rosario [0009-0009-2115-4715] | Toledano-Diaz, A. [0000-0001-8695-7441] | Tesfaye, Dawit [0000-0001-8166-0606] | García-Vázquez, Francisco Alberto [0000-0001-7665-3858] | Santiago Moreno, Julián [0000-0001-5551-8120] | Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72]
9 Pág.
显示更多 [+] 显示较少 [-]In small ruminants, testosterone and prolactin plasma concentrations show circannual fluctuations as an adaptation mechanism to their seasonal breeding behavior. Sperm resistance to the freezing-thawing process shows seasonal fluctuation throughout the year, with lower sperm freezability at the beginning of the breeding season when prolactin and testosterone levels reach their maximum concentration. Nevertheless, whether these hormones directly affect post-thaw sperm quality parameters is still unclear. The objective was to study the effect of testosterone or prolactin added in vitro on sperm freezability in domestic ram (Ovis aries) and buck (Capra hircus). Sperm samples were incubated for 1 h with a range of testosterone (0, 2, 4, or 6 ng/mL; Exp. 1) or prolactin (0, 20, 100, 200, or 400 ng/mL; Exp. 2) concentrations. Samples were cryopreserved by slow freezing in straws at 0 h and after 1 h incubation. Sperm viability, acrosome integrity, motility, and kinetic parameters were assessed at 0 and 1 h in fresh and frozen-thawed samples. Results showed no hormone effect in fresh sperm, whereas these hormones affected post-thaw sperm parameters. In Exp. 1, in vitro incubation with testosterone decreased the post-thaw acrosome integrity of ram sperm (from 68.1 ± 6.3% to 49.6 ± 3.9%; P < 0.05). In Exp. 2, in vitro incubation with prolactin decreased the post-thaw acrosome integrity of ram (from 78.2 ± 3.4% to 66.3 ± 3.5%; P < 0.05) and buck sperm (from 81.7 ± 2.5% to 67.6 ± 3.5%; P < 0.05). Moreover, prolactin increased the post-thaw amplitude of lateral head displacement in ram sperm (from 3.3 ± 0.1 μm to 3.8 ± 0.2 μm; P < 0.05). In conclusion, either testosterone or prolactin added in vitro decreased the post-thaw acrosome integrity of ram and buck sperm. This suggests a destabilization process that could be decreasing sperm freezability when physiological levels of these hormones are high in vivo.
显示更多 [+] 显示较少 [-]This work was supported by European Union Horizon 2020 Marie Sklodowska-Curie Action (REPBIOTECH 675526) and the Spanish “Ministerio de Economía, Industria y Competitividad” (MINECO/AEI/FEDER and EU grants AGL2014-52081-R and AGL2017-85753-R).
显示更多 [+] 显示较少 [-]Peer reviewed
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