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Association of L-arginine with heparin on the sperm capacitation improves in vitro embryo production in bovine
Aguiar, Gester Breda; Caldas-Bussiere, Maria Clara; Maciel Júnior, Valter Luiz; Carvalho, Carla Sobrinho Paes de; Souza, Cláudio Luiz Melo de.
Afiliação
  • Aguiar, Gester Breda; Universidade Estadual do Norte Fluminense Darcy Ribeiro. Laboratório de Reprodução e Melhoramento Genético Animal. Campos dos Goytacazes. BR
  • Caldas-Bussiere, Maria Clara; Universidade Estadual do Norte Fluminense Darcy Ribeiro. Laboratório de Reprodução e Melhoramento Genético Animal. Campos dos Goytacazes. BR
  • Maciel Júnior, Valter Luiz; Universidade Estadual do Norte Fluminense Darcy Ribeiro. Laboratório de Reprodução e Melhoramento Genético Animal. Campos dos Goytacazes. BR
  • Carvalho, Carla Sobrinho Paes de; Universidade Estadual do Norte Fluminense Darcy Ribeiro. Laboratório de Reprodução e Melhoramento Genético Animal. Campos dos Goytacazes. BR
  • Souza, Cláudio Luiz Melo de; Universidade Estadual do Norte Fluminense Darcy Ribeiro. Laboratório de Engenharia Agrícola. Campos dos Goytacazes. BR
Anim. Reprod. (Online) ; 16(4): 938-944, 2019. graf
Article em En | VETINDEX | ID: biblio-1461481
Biblioteca responsável: BR68.1
Localização: BR68.1
ABSTRACT
We aimed to evaluate the effects of L-arginine (L-arg) in the quality of in vitro heparin-induced capacitation of cryopreserved bovine spermatozoa and its effects on IVP. The experimental groups were Control 0 hour without pre-capacitation, and groups of sperm capacitated for 30 min in the absence of COC with heparin (Control 30 min), with 1 mM L-arg and with 1 mM L-arg + heparin. The capacitation pattern was evaluated by chlortetracycline assay and the integrity of the plasma membrane (PM) and acrosome membrane (AM) by the association of Hoescht 33342 and propidium iodide. Further, we assess the sperm quality by the rate of in vitro blastocysts production. Treatment with 1 mM L-arg + heparin increased the percentage of capacitated sperm when compared to Control 0 hour and the treatment with heparin (61.1 vs. 18.2 and 47.0%, respectively, P0.05). The group capacitated with 1 mM L-arg + heparin for 30 min increased the blastocyst rate compared to Control IVF (53.7 vs. 40.8%, P<0.05). We conclude that the addition of L-arg with heparin increases the number of capacitated spermatozoa in vitro with 30 min of pre-incubation in the absence of COC not altering the integrity of plasma and acrosomal membrane. This treatment in the absence of COC was the most effective method for blastocysts production, and the method of pre-incubation could be used to assess the role of other substances in the sperm capacitation and its effect on IVP.
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