Reproduction   citetrack
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS  

Reproduction (2005) 129 505-514
DOI: 10.1530/rep.1.00531
Copyright © 2005 Society for Reproduction and Fertility
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Banks, S.
Right arrow Articles by Saunders, P. T K
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Banks, S.
Right arrow Articles by Saunders, P. T K

RESEARCH

Impact of a mild scrotal heat stress on DNA integrity in murine spermatozoa

Stephen Banks, Sasha A King, D Stewart Irvine and Philippa T K Saunders

MRC Human Reproductive Sciences Unit, The Chancellor’s Building, 49 Little France Crescent, Edinburgh, EH16 4SB, UK

Correspondence should be addressed to P Saunders, MRC Human Reproductive Sciences Unit, 49 Little France Crescent, Edinburgh EH16 4SB, UK; Email: p.saunders{at}ed.ac.uk

An increase in scrotal temperature can lead to the production of poor quality spermatozoa and infertility. In the present study we have used mice to examine the impact of mild, scrotal heat stress (42 °C for 30 min) on numbers of spermatozoa as well as on the integrity of their DNA. Spermatozoa recovered from the epididymides hours (1 to 24) or days (7 to 32) after treatment were analysed using COMET and sperm chromatin structure (SCSA) assays. The treatment induced a stress response in both the testis and the epididymis that was associated with reduced expression of the cold inducible RNA binding protein (Cirp) and an increase in germ cell apoptosis (Apotag positive cells). Although spermatozoa present in the epididymis at the time of heating contained correctly packaged DNA, its integrity was compromised by heat stress. In addition, although some germ cells, which were present within the testis at the time of heat stress, were removed by apoptosis, many germ cells completed their development and were recovered as motile spermatozoa with damaged DNA. In conclusion, these data demonstrate that scrotal heat stress can compromise the DNA integrity of spermatozoa and this may have clinical implications for patients undergoing IVF and intra-cytoplasmic sperm injection (ICSI).




This article has been cited by other articles:


Home page
ReproductionHome page
C. Paul, A. A Murray, N. Spears, and P. T K Saunders
A single, mild, transient scrotal heat stress causes DNA damage, subfertility and impairs formation of blastocysts in mice
Reproduction, July 1, 2008; 136(1): 73 - 84.
[Abstract] [Full Text] [PDF]


Home page
Hum Reprod UpdateHome page
K. Tremellen
Oxidative stress and male infertility--a clinical perspective
Hum. Reprod. Update, May 1, 2008; 14(3): 243 - 258.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
C. Paul, D. W. Melton, and P. T.K. Saunders
Do heat stress and deficits in DNA repair pathways have a negative impact on male fertility?
Mol. Hum. Reprod., January 1, 2008; 14(1): 1 - 8.
[Abstract] [Full Text] [PDF]


Home page
CMAJHome page
A. Zini and J. Libman
Sperm DNA damage: clinical significance in the era of assisted reproduction.
Can. Med. Assoc. J., August 29, 2006; 175(5): 495 - 500.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS  
Copyright © 2005 by the Society for Reproduction and Fertility.