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Upregulation of AP1 by Tertiary Butyl Hydroperoxide Induced Oxidative Stress and Subsequent Effect on Spermatogenesis in Mice Testis - Abstract Show Comments PDF Print E-mail
  
Tuesday, 06 November 2007

Department of Biophysics, Panjab University, Chandigarh, 160014, India

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Oxidative stress is detrimental to sperm function and a significant factor in the etiology of male infertility. Present study evaluates the effect of ter butyl hydroperoxide (TBHP)-induced oxidative stress on the spermatogenic process and cell number in the seminiferous tubules. Intraperitoneal injection of TBHP (84 mumol TBHP/100 g body weight) for 2 weeks to male Balb/c mice resulted in enhanced lipid peroxidation (P < 0.0001) decrease in reduced glutathione (P < 0.0001) and increase in the oxidized glutathione levels (P = 0.007) in the testis. Status of spermatogenesis after the treatment was assessed by the quantitative methods of germ cell evaluation in the seminiferous tubules. A significant decrease in the number of young spermatids (P = 0.0003) and pachytene cells (P = 0.022) was observed. A marked reduction was also seen in the mature spermatid number (P < 0.0001). An increase in testicular mRNA levels of redox-regulated cjun (P = 0.008) and cfos (P = 0.0006) subunits of activator protein 1 (AP1) was observed after TBHP treatment. Evaluation of AP1 regulated antioxidant enzymes in the testis revealed an increase in gamma-glutamyl cysteine synthetase (GCS) mRNA expression (P = 0.001). These results suggest a potential role of AP1 in oxidative stress-mediated meiotic and post meiotic changes in the spermatogenic process and regulation of cell number in male reproductive system.

Written by
Kaur P, Kaur G, Bansal MP.

Reference
Mol Cell Biochem. 2007 Oct 13; [Epub ahead of print]
doi:10.1007/s11010-007-9626-z

PubMed Abstract
PMID:17934699

UroToday.com Male Infertility & Reproduction Section

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