Alternative cryoprotectans suitable for a slow freezing method of epididymal spermatozoa of alpaca (Vicugna pacos)

The objective of this study was to use alternative cryoprotectans suitable for freezing epididymal spermatozoa of alpaca (Vicugna pacos) in a slow freezing method. Epididymides obtained in the slaughterhouse of Huancavelica city were transported at 4 °C in saline solution to the laboratory in Lima,...

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Detalhes bibliográficos
Autores: Canorio Pariona, Nadia, Paredes Arnedo, Fernando, Valdivia Cuya, Martha
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2015
País:Perú
Recursos:Universidad Nacional Mayor de San Marcos
Repositorio:Revistas - Universidad Nacional Mayor de San Marcos
Idioma:español
OAI Identifier:oai:revistasinvestigacion.unmsm.edu.pe:article/11185
Acesso em linha:https://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/11185
Access Level:acceso abierto
Palavra-chave:alpaca
sperm
cryopreservation
dimethylacetamide
dimethylsulfoxide
espermatozoide
criopreservación
dimetilacetamida
dimetilsulfóxido
Descrição
Resumo:The objective of this study was to use alternative cryoprotectans suitable for freezing epididymal spermatozoa of alpaca (Vicugna pacos) in a slow freezing method. Epididymides obtained in the slaughterhouse of Huancavelica city were transported at 4 °C in saline solution to the laboratory in Lima, Peru. The sperm cells were extracted from the epididymis and incubated in HAMF10 medium. The Tes-Tris-Yolk-Citrate medium was used and supplemented with the cryoprotectants dimethyl sulfoxide (Me2SO4) at 0.5, 0.25 and 0.125M concentrations, and dimethylacetamide (DMA) at 0.75, 0.385 and 0.18M concentrations, and compared with a control group cryopreserved with glycerol 0.6M. Motility, viability and integrity of membrane before and after freezing were assessed. The results showed a better viability and membrane integrity post-freezing when using DMA 0.375M (p<0.05). Motility was better with Me2SO4 0.25 and 05M and DMA 0.375 and 0.75M (p<0.05).