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Tracing of zinc and iron in experimentally induced varicocele: correlation with oxidative, nitrosative and carbonyl stress
Author(s) -
Gholirad S.,
Razi M.,
Hassani Bafrani H.
Publication year - 2017
Publication title -
andrologia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.633
H-Index - 59
eISSN - 1439-0272
pISSN - 0303-4569
DOI - 10.1111/and.12687
Subject(s) - oxidative stress , malondialdehyde , varicocele , sperm , lipid peroxidation , dna fragmentation , chemistry , andrology , dna damage , toxicity , nitric oxide , sperm motility , zinc , epididymis , medicine , endocrinology , biochemistry , biology , dna , infertility , pregnancy , apoptosis , organic chemistry , programmed cell death , genetics
Summary This study was designed to evaluate how varicocele ( VCL ) can time dependently induce zinc (Zn) and iron (Fe) toxicity in testicular tissue and to analyse the relation between heavy metals toxicity and lipid peroxidation, sperm DNA damage, nitrosative and carbonyl stresses. Twenty‐four mature male Wistar rats were divided into control‐sham and test groups, which were then submitted to experimentally induced VCL . Non‐ VCL ‐induced rats were considered as control‐sham. The test groups were subdivided into three groups based on the sample collecting date (2, 6 and 8 months after VCL induction). Zn and Fe distribution in testicles, DNA ladder for sperm DNA fragmentation, testicular total antioxidant capacity ( TAC ), malondialdehyde ( MDA ), nitrite oxide ( NO ) and carbonyl groups ( CG ) were analysed. A significant ( p < .05) enhancement in the percentage of tubules with negative tubular repopulation, differentiation and spermiogenesis indices was revealed. The VCL increased Zn and Fe distribution in testicles. The VCL , time dependently, reduced sperm count, motility and enhanced sperm DNA damage ( p < .05). The VCL downregulated the testicular TAC and enhanced the MDA , NO and CG contents. Our data showed that the VCL results in intensive Fe and Zn toxicities. Produced Zn‐ and Fe‐mediated‐oxidative stress increases sperm DNA damage associated with NO and CG ‐induced stresses.