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Updated: Jul 17, 2026

Vitrification of In Vitro Matured Oocytes Collected from Adult and Prepubertal Ovaries in Sheep
Published on: July 10, 2021
Cryopreservation of ovine primordial follicles using dimethyl sulfoxide
Christiani Andrade Amorim1, Ana Paula Ribeiro Rodrigues, Davide Rondina
1Laboratorio Renzo Giuliani, Dipartimento di Scienze Zootecniche, University of Florence, Florence, Italy. amorimc-kleinj@yahoo.com
Objective:
To verify the viability of isolated primordial follicles after exposure to different concentrations of dimethyl sulfoxide (DMSO) and after cryopreservation.
Design:
Randomized control trial.
Setting:
Laboratorio Renzo Giuliani, University of Florence, Italy.
Animal(S):
Thirty- to 40-day-old lambs.
Main Outcome Measure(S):
Isolated primordial follicles were stained with trypan blue to evaluate the effect of different DMSO concentrations before and after the cryopreservation. Histological structure and follicular mortality were evaluated.
Result(S):
After the isolation procedure (control), a mean (+/-SE) of 800 +/- 203.86 live primordial follicles/mL were obtained. The number of live follicles in the toxicity test using the DMSO at 0, 0.5, 1.0, 1.5, 2.0, and 2.5 M was 782 +/- 193.96, 754 +/- 172.03, 778 +/- 191.58, 736 +/- 191.92, 476 +/- 122.9, and 316 +/- 83.52, respectively. The number of live follicles at 2.5 M was lower than that in the control procedure. After cryopreservation, the numbers decreased to 0 +/- 0, 232 +/- 44.20, 636 +/- 161.82, 628 +/- 181.28, 208 +/- 11.57, and 184 +/- 47.07, respectively at 0, 0.5, 1.0, 1.5, 2.0, and 2.5 M. The number of live follicles at 0, 0.5, 2.0, and 2.5 M were lower than that in the control procedure.
Conclusion(S):
After cryopreservation, only DMSO concentrations of 1.0 and 1.5 M showed a number of live follicles similar to that of the control procedure.
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