A freezing and thawing method of hamster oocytes designed for both the penetration test and chromosome assay of human spermatozoa.

Abstract:

:Superovulated hamster oocytes were cryopreserved and thawed according to our carefully designed procedures. More than 90% (92 +/- 4%) of oocytes survived freezing and thawing. They were proven to be well conserved, showing excellent performance comparable to freshly ovulated oocytes in the human sperm penetration test (proportion of penetrated ova: 94.7% vs. 93.6%) and human sperm chromosome analysis (proportion of metaphasic ova: 81.8% vs. 83.6%). There was no statistically significant difference in the incidences of sperm chromosome aberrations between assays using fresh and frozen-thawed oocytes. In addition, there was no statistically significant increase of aberrations in female pronuclear (hamster) chromosomes. This freezing-thawing method was found to be reliable, yielding viable hamster oocytes of high quality.

journal_name

Mol Reprod Dev

authors

Tateno H,Kamiguchi Y,Mikamo K

doi

10.1002/mrd.1080330213

keywords:

subject

Has Abstract

pub_date

1992-10-01 00:00:00

pages

202-9

issue

2

eissn

1040-452X

issn

1098-2795

journal_volume

33

pub_type

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