Author/Authors :
Nasiri، Nahid نويسنده Department of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran , , VosoughTaqi Dizaj، Ahmad نويسنده Department of Reproductive Imaging, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran , , Eftekhari-Yazdi، Poopak نويسنده Baghaban Eslaminejad, M.R. , Akhond، Mohammad Reza نويسنده Department of Statistics, Mathematical Science and Computer Faculty, Shahid Chamran University, Ahvaz, Iran ,
Abstract :
Background: There is a lack of studies regarding the effects of ultrasound (US) and replication
of its exposure on pre-implantation events in mammals. Thus, this study assesses the reproductive
performance of mouse oocytes that have been obtained from ovaries irradiated with US waves
versus non-irradiated ovaries. Also comparision of their parthenogenesis, ovulation, fertilization,
and pre-implantation development rates.
Materials and Methods: In this experimental study, we divided extracted ovaries into three
experimental groups that received the same dosage, but different replicates of radiation for each
group. Results were compared with the control and sham groups. Continuous wave (CW) US,
at a spatial average intensity of 355 mW/cm2 and a frequency of 3.28 MHz, was administered
for 5 minutes to the ovaries at an interval between pregnant mare serum gonadotropin (PMSG)
and human chorionic gonadotropin (hCG) injections. Statistical analysis was performed using the
ANOVA test and the level of significance was determined to be 0.05.
Results: Data collection was based on microscopic visualization. According to the obtained results,
metaphase II (MII) oocyte numbers and the percentage of blastocysts significantly reduced in the USexposed
groups versus the unexposed groups. Fertilization rate was comparable between groups while
parthenogenesis was significantly higher in the US-exposed groups compared to the unexposed groups.
Conclusion: Structural damage to cells, intracellular organelles and proteins, as well as changes
in signaling pathways induced by US may be reasons for some of the observed adverse effects in
groups that have received more US exposure.