Abstract
Objective
The aim of this study was to evaluate the folliculogenesis progression in mice ovaries after vitrification/devitrification followed by ectopic autotransplantation.
Methods
Female Balbc mice (60days, n=12), were anesthetized and bilaterally ovariectomized. One ovary was kept in buffer (PBS) during the procedure (control group – fresh). The other ovary was placed in PBS and then vitrified/devitrified using the IngáMed® kits, following the manufacturer’s instructions. Both ovaries were subcutaneously transplanted and after 21 days some animals (n=6) received 5UI of eCG (equine chorionic gonadotropin, Novormon 5000®) and, after 48h, 5UI of hCG (human chorionic gonadotropin, Vetecor®), analogous to FSH and LH respectively; other animals received PBS (n=6; control). Three days later, the hosts were euthanized and grafts were recovered, processed to histology (HE) and qualitatively analyzed.
Results
Primordial, primary, multilaminar and antral follicles were observed in fresh ovaries, with or without hormonal stimulation. In vitrified/devitrified tissues without stimulation, folliculogenesis were observed up to the multilaminar stage and in those with exogenous stimulation, a higher follicular density was observed, with follicles in preovulatory stage. Atretic follicles also were observed in all groups.
Conclusions
Folliculogenesis progression was observed in fresh and vitrified tissues; however, hormonal superstimulation using exogenous gonadotropins brought better results. This study showed, for the first time in the literature, the feasibility of the ovarian tissue vitrification technique, without morpho- functional damages. So, this technique could be used for fertility preservation and should be more investigated.