Figure 3.
Experimental design. (A) Group 1 animals underwent bilateral ovariohysterectomy (OSH). Hemi-ovaries were cryopreserved and stored in liquid nitrogen (− 196 °C) for seven days. (B) Seven days after cryopreservation, hemi-ovaries were thawed and transplanted to Group 2 animals, forming the Cryopreserved transplanted group. Group 2 animals underwent OSH in the same surgical procedure, with the hemi-ovaries immediately transplanted to Group 3 animals, constituting the Fresh transplanted group. Hemi-ovaries from Group 3 animals were obtained by OSH, cryopreserved and thawed after 7 days, but not transplanted (Cryopreserved non-transplanted group). Group 4 animals were euthanized, and the hemi-ovaries obtained immediately evaluated as a fresh tissue (Fresh non-transplanted group). Seven days after hemi-ovary transplantation to Groups 2 and 3, animals were euthanized, and hemi-ovaries retrieved for analysis. Hemi-ovary samples from all groups, were distributed between the analysis, with half of the hemi-ovaries fixed for histological analysis, and the other used to evaluate mitochondrial oxygen consumption. OSH = ovariohysterectomy; OT = ovarian tissue, corresponding to a hemi-ovary. This figure was created by the authors using Biorender (https://biorender.com/).