DOI: 10.17151/vetzo.2015.9.2.5
How to Cite
Pinzón-Osorio, C. A. ., Acosta-Galindez, P. ., Cristancho-Mendoza, R. ., Vélez-Jaramillo, C. ., Pinzón-Porras, J. ., Berdugo-Gutiérrez, J. ., Zambrano-Varón, J. ., & Jiménez-Escoba, C. (2015). Use of the vagina as an alternative for bovine embryo production . Revista Veterinaria Y Zootecnia (On Line), 9(2), 54–64. https://doi.org/10.17151/vetzo.2015.9.2.5

Authors

Cesar Augusto Pinzón-Osorio
Universidad Nacional de Colombia
a@a.com
Pablo Acosta-Galindez
Universidad Nacional de Colombia
a@a.com
Richard Cristancho-Mendoza
Universidad Nacional de Colombia
a@a.com
Catalina Vélez-Jaramillo
Universidad Nacional de Colombia
a@a.com
Jorge Pinzón-Porras
Universidad Nacional de Colombia
a@a.com
Jesús Berdugo-Gutiérrez
Universidad Nacional de Colombia
a@a.com
Jorge Zambrano-Varón
Universidad Nacional de Colombia
a@a.com
Claudia Jiménez-Escoba
Universidad Nacional de Colombia
cjimeneze@unal.edu.co

Abstract

In vitro embryo production (IVEP) is an alternative for multiplying genetically superior animals. The high cost for the establishment of laboratories and the low embryo production rates make researchers seek alternatives to simplify and improve the procedure. The Intra Vaginal Embryo Culture is a system using a device (INVO) inserted into the vagina that creates the conditions of temperature and humidity necessary for the development of the embryo. There are no reports of the use of INVO for the in vitro production of bovine embryos. The objective of this study was to evaluate the use of the INVO system for bovine embryo production which evaluated the permanence of the device in the vagina for three (3) days and the production of embryos. In phase one, 14 repetitions were performed in three cows while in phase two 191 presumptive zygotes were cultured. The retention rate of the INVO device in the vagina was 92.9% (13/14). A total of 91.9% (158/172) of the structures placed in culture were recovered. The total cleavage of the INVO group was 47.2% (42/84), and the rate of production of 8 and 16 cell embryos was 9.6% and 4.5%, respectively. The embryos obtained after vaginal culture that were cultured in the laboratory for three additional days produced blastocysts. The results obtained show the feasibility of the INVO system for bovine embryo production, making possible embryo development to stages that can be transferred. The development and cleavage rates are comparable to those obtained under totally in vitro conditions from 8 to 16 cells.

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