Increase in the expression of inducible nitric oxide synthase on exposure to bisphenol A: A possible cause for decline in steroidogenesis in male mice

被引:39
作者
Chouhan, Shikha [1 ]
Yadav, Satyndra Kumar [1 ]
Prakash, Jay [1 ]
Westfall, Susan [1 ]
Ghosh, Amrita [2 ]
Agarwal, Neeraj Kumar [3 ]
Singh, Surya Pratap [1 ]
机构
[1] Banaras Hindu Univ, Fac Sci, Dept Biochem, Varanasi 221005, Uttar Pradesh, India
[2] Banaras Hindu Univ, Inst Med Sci, Dept Pathol, Varanasi 221005, Uttar Pradesh, India
[3] Banaras Hindu Univ, Inst Med Sci, Dept Endocrinol & Metab, Varanasi 221005, Uttar Pradesh, India
关键词
Bisphenol A; iNOS; StAR; Oxidative stress; Sperm count; Serum testosterone; ENDOCRINE-DISRUPTING CHEMICALS; LUTEINIZING-HORMONE SECRETION; SEMINIFEROUS EPITHELIUM; REPRODUCTIVE TOXICITY; OXIDATIVE STRESS; EPIDIDYMAL SPERM; STAR PROTEIN; ESTROGEN; ADULT; TESTIS;
D O I
10.1016/j.etap.2014.09.014
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Bisphenol A (BPA) is a well-known plasticizer and xenoestrogen that is responsible for many acquired reproductive difficulties, especially in men. Despite the prevalence of BPA in society, the mechanism behind reproductive deficits remains elusive. The present study investigates the mode of BPA's action by evaluating its effect on the expression of inducible nitric oxide synthase (iNOS) and steriodogenic acute regulatoxyprotein (StAR) in male mice testis. Swiss albino mice were treated with a range BPA concentrations of 0.5, 50 and 100 mu g/kg body weight/day intraperitoneally for 60 days. Several markers of oxidative stress and male fertility were investigated. Nitrite levels, malondialdehyde levels and testicular injury scores were elevated whereas the sperm count, serum testosterone levels and catalase activity were reduced in the BPA groups. Mechanistically, an increase in iNOS expression was observed in the testis whereas the expression of the StAR was down regulated in the BPA treated mouse. These results suggest that BPA induces oxidative stress by altering the expression of iNOS, which consequently leads to the down regulation of StAR expression in the testis of male mouse. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:405 / 416
页数:12
相关论文
共 56 条
[1]   Effects of nitric oxide-related agents on opioid regulation of rat testicular steroidogenesis [J].
Adams, ML ;
Meyer, ER ;
Cicero, TJ .
BIOLOGY OF REPRODUCTION, 1996, 54 (05) :1128-1134
[2]   Inhibition of testicular steroidogenesis by the xenoestrogen bisphenol a is associated with reduced pituitary luteinizing hormone secretion and decreased steroidogenic enzyme gene expression in rat Leydig cells [J].
Akingbemi, BT ;
Sottas, CM ;
Koulova, AI ;
Klinefelter, GR ;
Hardy, MP .
ENDOCRINOLOGY, 2004, 145 (02) :592-603
[3]   Effects of bisphenol A on adult male mouse fertility [J].
Al-Hiyasat, AS ;
Darmani, H ;
Elbetieha, AM .
EUROPEAN JOURNAL OF ORAL SCIENCES, 2002, 110 (02) :163-167
[4]  
[Anonymous], 2001, NAT TOX PROGR REP EN
[5]   Permanent effects of neonatal estrogen exposure in rats on reproductive hormone levels, sertoli cell number, and the efficiency of spermatogenesis in adulthood [J].
Atanassova, N ;
McKinnell, C ;
Walker, M ;
Turner, KJ ;
Fisher, JS ;
Morley, M ;
Millar, MR ;
Groome, NP ;
Sharpe, RM .
ENDOCRINOLOGY, 1999, 140 (11) :5364-5373
[6]   Alteration in expression of estrogen receptor isoforms alpha and beta, and aromatase in the testis and its relation with changes in nitric oxide during aging in mice [J].
Banerjee, Arnab ;
Anjum, Shabana ;
Verma, Rachna ;
Krishna, Amitabh .
STEROIDS, 2012, 77 (06) :609-620
[7]  
Basar M.M., 2006, MEDIAT INFLAMM, V27458, P1
[8]  
BROTONS JA, 1995, ENVIRON HEALTH PERSP, V103, P608, DOI 10.2307/3432439
[9]   Induction of oxidative stress by bisphenol A in the epididymal sperm of rats [J].
Chitra, KC ;
Latchoumycandane, C ;
Mathur, PP .
TOXICOLOGY, 2003, 185 (1-2) :119-127
[10]  
Chouhan S., 2013, J SCI RES, V57, P77