INVESTIGADORES
LOMBARDO Daniel Marcelo
congresos y reuniones científicas
Título:
RECOVERY CAPACITY ASSESSMENT IN VITRIFIED EMBRYOS OF SUPEROVULATED CF-1 MICE
Autor/es:
TELLO, MF.; LORENZO, MS.; MARURI, A.; CRUZANS, PR.; GULÍN, E.; LOMBARDO, DM.
Lugar:
Varadero
Reunión:
Congreso; Animal Models and Preclinical Research 2019 (ANIMOD); 2019
Institución organizadora:
Centro de Ingeniería Genética y Biotecnología de la Habana, la Sociedad Cubana de Farmacología y el Centro Nacional de Producción de Animales de Laboratorio (CENPALAB)
Resumen:
The vitrification of embryos is a useful tool for assisted reproductive techniques. It is an ultra-rapid cooling technique using a minimum volume with highly concentration of cryoprotectants avoiding ice crystals formation. The aim of this study was to obtain a high number of embryos using a superovulation (SOV)protocol and to evaluate its morphology and recovery capacity after vitrification.The embryos were retrieved from 6 to 8-week-old SOV CF-1 females (n=3).They were injected with 7.5 IU eCG and 7.5 IU of hCG (48 h later); immediately they were single mated overnight with 9-week-old CF1 males. The following morning the presence of a vaginal plug was checked. A total of 116 embryos (blastocyst=58; cleavage=58) were retrieved by uterine flushing. A group of blastocysts (n=37) were exposed to an equilibration solution (5 min), then tovitrification solution (1 min) and finally placed on a vitrification device with a minimum volume and plunged into liquid nitrogen. For warming, they wereplaced into a prewarmed solution at 37ºC (3 min) then diluted and kept in awashing solution. For recovery, they were incubated in 50-μL drops of anenriched blastocyst medium for 10 h. The morphology, re-expansion, andhatching were evaluated using a stereomicroscope, the number of cells withHoechst 33342 (n=21) and in average a 2,7% of blastomeres presented DNAfragmented ? TUNEL assay (n=15). The treated embryos presented a normalmorphology, mitotic figures, cells number and apoptosis rates according to theirdevelopment stage. Embryos obtained with this SOV protocol maintain theircapacity to re-expand and hatching after vitrification protocol.