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Biology of Reproduction 63, 341-346 (2000)
© 2000 Society for the Study of Reproduction, Inc.


Regular article

Sonication Per Se Is Not as Deleterious to Sperm Chromosomes as Previously Inferred1

Hiroyuki Tatenoa,b, Yasuyuki Kimuraa,c, and Ryuzo Yanagimachi2,,a

a Department of Anatomy and Reproductive Biology, University of Hawaii School of Medicine, Honolulu, Hawaii 96822 b Department of Biological Sciences, Asahikawa Medical College, Asahikawa 078-8510, Japan c Department of Obstetrics and Gynecology, Fukushima Medical College, Fukushima 960-1295, Japan

ABSTRACT

Although sonication is a simple way to immobilize ("kill") spermatozoa prior to injection into oocytes, this has been thought to be destructive to sperm chromosomes. Mouse and human spermatozoa were immobilized by sonication and kept in various media for up to 2 h, then their nuclei were individually injected into mouse oocytes for the analysis of chromosomes at the first cleavage metaphase. In both the mouse and human, incidence of structural chromosome aberrations was much higher in the spermatozoa sonicated and stored in Biggers-Whitten-Whittingham medium for 2 h at 37.5°C than in those stored for 5 min in the same medium. We concluded, therefore, that it is not sonication per se but a prolonged exposure of sperm nuclei to extracellular milieu that is detrimental to sperm chromosomes. The incidence of structural chromosome aberrations of mouse and human spermatozoa was significantly reduced when the spermatozoa were sonicated and stored in K+-rich nucleus isolation medium containing EDTA. This suggests that sperm chromosome degradation following sperm immobilization by sonication is partly due to detrimental effects of a Na+-rich medium and of DNase on sperm chromatin. Ideally, it should be possible to prepare artificial media that maintain the integrity of sperm chromosomes for many hours after immobilization.

FOOTNOTES

First decision: 2 February 2000.

1 This study was supported by grants (HD-34362 and HD-38205 to R.Y.) from the National Institutes of Health, the Victoria S. and Bradley L. Geist Foundation, and The Kosasa Family Foundation. H.T. was a research fellow of the Ministry of Education, Science, Sports and Culture of Japan.

2 Correspondence: Ryuzo Yanagimachi, Department of Anatomy and Reproductive Biology, University of Hawaii School of Medicine, 1951 East-West Road, Honolulu, HI 96822. FAX: 808 956 5474; yana{at}hawaii.edu




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