Is fine morphology of the human sperm nuclei affected by in vitro incubation at 37 degrees C?

Fertil Steril. 2007 Dec;88(6):1589-94. doi: 10.1016/j.fertnstert.2007.01.069. Epub 2007 May 3.

Abstract

Objective: Incubation of ejaculated spermatozoa at 37 degrees C is recommended for IVF-intracytoplasmic sperm injection. Preselection of sperm cells with morphologically normal nuclei before microinjection, adapted in our laboratory, is usually a time-consuming procedure. Therefore, we aimed to verify whether incubation at 37 degrees C could affect the morphologic integrity of sperm nuclei.

Design: Time-kinetics studies testing fine morphology of the sperm nuclei upon prolonged in vitro incubation.

Setting: Male Fertility Laboratory at Bar-Ilan University, Ramat Gan, Israel.

Patient(s): Forty-two males selected at random, who were referred for sperm preselection before ICSI.

Main outcome measure(s): Morphologic integrity of the sperm nuclei, obtained by motile sperm organelle morphology examination.

Result(s): After 2 hours of incubation at 37 degrees C a significant decrease occurred in the morphologic integrity of the sperm nuclei, compared with the initial state (4.7% +/- 2.8% vs. 6.8% +/- 3.5%, t = 3.2, P<or=.01). Correspondingly, a significant increase occurred in the frequency of vacuolated nuclei (80.8% +/- 7.2% vs. 75.0% +/- 7.6%, t = -2.8, P<or=.01). No significant morphologic changes in sperm nuclei were observed upon prolonged incubation at 21 degrees C. After 2 hours of incubation, the incidence of spermatozoa with vacuolated nuclei was significantly higher at 37 degrees C compared with 21 degrees C (56.5% +/- 10.8% vs. 45.5% +/- 10%, t = 6.6, P<or=.01).

Conclusion(s): Prolonged (>or=2 hours) sperm manipulations for assisted reproduction therapy should be performed at 21 degrees C rather than 37 degrees C.

Publication types

  • Comparative Study
  • Evaluation Study

MeSH terms

  • Cell Nucleus / ultrastructure*
  • Cell Shape
  • Humans
  • Incubators / adverse effects
  • Male
  • Specimen Handling / methods*
  • Sperm Motility
  • Spermatozoa / cytology
  • Spermatozoa / ultrastructure*
  • Temperature*
  • Time Factors
  • Vacuoles / ultrastructure