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Wiley InterScience

International Journal of Andrology

International Journal of Andrology

Early View (Articles online in advance of print)

Published Online: 16 Nov 2009

Journal compilation © 2010 European Academy of Andrology



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ORIGINAL ARTICLE
Differences in mouse models of diabetes mellitus in studies of male reproduction
J. O'Neill*†, A. Czerwiec*, I. Agbaje*, J. Glenn, A. Stitt, N. McClure* and C. Mallidis*‡
  *Obstetrics and Gynaecology, Queen's University Belfast, Belfast, UK ,   Centre of Vision Sciences, Queen's University Belfast, Belfast, UK , and   Basic Medical Sciences/Anatomy, School of Medicine, Queen's University Belfast, Belfast, UK
Correspondence to Dr Con Mallidis, Centre of Reproductive Medicine and Andrology, University of Munster, Domagkstrasse 11, D-48149 Munster, Germany. E-mail: Con.Mallidis@ukmuenster.de
Copyright Journal compilation © 2009 European Academy of Andrology
KEYWORDS
AGEs • diabetes • DNA • sperm • testis

ABSTRACT

Diabetes Mellitus (DM) has been found to have subtle yet profound effects on the metabolic status of the testis, the expression of numerous spermatogenic genes and is associated with increased numbers of sperm with nuclear DNA damage. The precise mechanism causing these detrimental effects remains unknown. The presence of increased levels of the most prominent member (carboxymethyllysine – CML) of the advanced glycation end product adducts and their receptor (RAGE) in the reproductive tract of DM men has provided a new avenue for research. As there are suspicions that the antibiotic (streptozotocin – STZ) employed to induce DM is also capable of causing oxidative stress and DNA damage, we compared CML and RAGE levels in the reproductive tract and sperm nDNA status of STZ mice with the levels in the Ins2Akita mouse to determine which more closely mimics the situation described in the human diabetic. CML was observed in the testes, epididymes and sperm of all animals. Sperm from DM mice showed particularly strong CML immunolocalization in the acrosomal cap, the equatorial region and whenever present, cytoplasmic droplets. Although increased, the level of CML on the sperm of the STZ and Ins2Akita DM mice did not reach statistical significance. RAGE was present on the developing acrosome and epididymal sperm of all animals and in discrete regions of the epididymes of the DM models. Only the epididymal sperm of the Ins2Akita mice were found to have significantly increased (p < 0.0001) nDNA damage. The Ins2Akita mouse therefore appears to more accurately reflect the conditions found in the human and, as such, is a more representative model for the study of diabetes and glycation's influence on male fertility.


Received 30 June 2009; revised 29 September 2009; accepted 4 October 2009

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1365-2605.2009.01013.x About DOI

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