Skip Navigation


Hum. Reprod. Advance Access originally published online on March 11, 2004
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF ) Freely available
Right arrow All Versions of this Article:
19/4/932    most recent
deh194v1
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (7)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Isachenko, E.
Right arrow Articles by Nawroth, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Isachenko, E.
Right arrow Articles by Nawroth, F.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Reproduction, Vol. 19, No. 4, 932-939, April 2004
© 2004 European Society of Human Reproduction and Embryology

DNA integrity and motility of human spermatozoa after standard slow freezing versus cryoprotectant-free vitrification

E. Isachenko1,5, V. Isachenko2, I.I. Katkov3, G. Rahimi1, T. Schöndorf1, P. Mallmann1, S. Dessole4 and F. Nawroth1

1 Department of Obstetrics and Gynecology, University of Cologne, Kerpener Str. 34, D-50931 Cologne, 2 Department of Gynecological Endocrinology and Reproductive Medicine, University of Bonn, Bonn, Germany, 3 Cancer Center, University of California at San Diego, La Jolla, CA, USA and 4 Department of Obstetrics and Gynecology, University of Sassari, Sassari, Italy

5 To whom correspondence should be addressed. e-mail: jeniaisachenko{at}yahoo.de

BACKGROUND: In contrast to the technique of conventional freezing, the vitrification of spermatozoa requires high cooling rates (720 000°K/min), which could be damaging for spermatozoa. The aim of our study was to compare slowly frozen and vitrified spermatozoa in terms of their post-thaw DNA integrity and motility. METHODS: Semen samples were prepared according to the routine swim-up technique and divided into aliquots for comparison of fresh, conventionally frozen and vitrified spermatozoa from the same ejaculate in the presence or absence of cryoprotectants. Spermatozoa motility and DNA integrity were determined. RESULTS: The motility of spermatozoa conventionally (slowly) frozen with a cryoprotectant was similar to that recorded for spermatozoa vitrified in the absence of cryoprotectant (47 versus 52%). The DNA integrity was unaffected by the cryopreservation method or presence of cryoprotectants. CONCLUSION: The vitrification of human spermatozoa in the absence of conventional cryoprotectants is indeed feasible. The DNA integrity of vitrified sperm is comparable with that shown by standard slow-frozen/thawed spermatozoa, yet the method is quick and simple and does not require special cryobiological equipment.

Key words: comet assay/cryopreservation/human/sperm DNA/vitrification


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
ReproductionHome page
E Isachenko, V Isachenko, J M Weiss, R Kreienberg, I I Katkov, M Schulz, A G-M I Lulat, M J Risopatron, and R Sanchez
Acrosomal status and mitochondrial activity of human spermatozoa vitrified with sucrose
Reproduction, August 1, 2008; 136(2): 167 - 173.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
G.J. Morris
Rapidly cooled human sperm: no evidence of intracellular ice formation
Hum. Reprod., August 1, 2006; 21(8): 2075 - 2083.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.