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Updated: May 19, 2026

Collection of Human Follicular Fluid, Follicle Somatic Cells, and Immature Oocytes from Individuals Undergoing In Vitro Fertilization
Published on: October 24, 2025
The dynamics of in vitro maturation of germinal vesicle oocytes
Laura Escrich1, Noelia Grau, María José de los Santos
1Instituto Universitario IVI Valencia, Valencia, Spain.
Objective:
To evaluate the dynamics of the nuclear maturation (NM) of in vitro-matured (IVM) oocytes and to determine the most favorable duration of meiosis II (MII) arrest in relation to the normal activation response.
Design:
Experimental.
Setting:
University-affiliated infertility clinic.
Patient(S):
Donated immature germinal vesicle oocytes (GV).
Intervention(S):
The GV underwent spontaneous IVM and the dynamics of NM studied by real-time monitoring. The IVM oocytes were parthenogenetically activated at different MII arrest points and their response assessed.
Main Outcome Measure(S):
Moment of GV breakdown; extrusion of the first polar body; duration of MI and MII arrest; activation rate (AR) and type.
Result(S):
Two GV populations-early (E-IVM, 18.4 ± 2.7 hours) and late (L-IVM, 26.3 ± 3.8 hours) maturing-were defined according to the time required for extrusion of the first polar body. Significantly more E-IVM than L-IVM exhibited a normal activation response (61.3% vs. 34.6%), but AR were similar (average, 88.6%) in both groups. Duration of the GV stage differed between the two groups, but MI arrest (14.0 ± 0.3 hours) was constant. The E-IVM arrested at MII for at least 4.3 hours displayed significantly lower AR and similar normal activation rates (61.3%) to E-IVM arrested for a shorter time (83.9% vs. 100%). The L-IVM displayed a similar AR (80.8%), but lower normal activation rates than E-IVM (34.6%), regardless of when activation took place.
Conclusion(S):
The success of IVM depends on the NM timing rather than on the length of MII arrest.
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