Literature DB >> 19919578

Differences in mouse models of diabetes mellitus in studies of male reproduction.

J O'Neill1, A Czerwiec, I Agbaje, J Glenn, A Stitt, N McClure, C Mallidis.   

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 Ins(2Akita) 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 Ins(2Akita) 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 Ins(2Akita) mice were found to have significantly increased (p < 0.0001) nDNA damage. The Ins(2Akita) 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.

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Year:  2009        PMID: 19919578     DOI: 10.1111/j.1365-2605.2009.01013.x

Source DB:  PubMed          Journal:  Int J Androl        ISSN: 0105-6263


  4 in total

1.  Germ cell abnormalities in streptozotocin induced diabetic mice do not correlate with blood glucose level.

Authors:  Rohini Bose; Satish K Adiga; Fiona D'Souza; Sujith R Salian; Shubhashree Uppangala; Guruprasad Kalthur; Navya Jain; Raghu A Radhakrishnan; Nalini Bhat; Hanumantappa Krishnamurthy; Pratap Kumar
Journal:  J Assist Reprod Genet       Date:  2012-10-16       Impact factor: 3.412

2.  Diabetes-induced oxidative DNA damage alters p53-p21CIP1/Waf1 signaling in the rat testis.

Authors:  Narayana Kilarkaje; Maie M Al-Bader
Journal:  Reprod Sci       Date:  2014-05-14       Impact factor: 3.060

3.  Effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice.

Authors:  Esmat Mangoli; Ali Reza Talebi; Morteza Anvari; Majid Pourentezari
Journal:  Iran J Reprod Med       Date:  2013-01

4.  Animal Models of Diabetes-Related Male Hypogonadism.

Authors:  Anastasia Dimakopoulou; Channa N Jayasena; Utsav K Radia; Metab Algefari; Suks Minhas; Nick Oliver; Waljit S Dhillo
Journal:  Front Endocrinol (Lausanne)       Date:  2019-09-18       Impact factor: 5.555

  4 in total

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