Literature DB >> 15711031

Adverse effects of environmental toxicants, octylphenol and bisphenol A, on male reproductive functions in pubertal rats.

Chandana B Herath1, Wanzhu Jin, Gen Watanabe, Koji Arai, Akira K Suzuki, Kazuyoshi Taya.   

Abstract

It has been proposed that a global decline in sperm counts, semen quality, and several male reproductive disorders are associated with exposure to environmental chemicals. Thus, the present study examined the effects of two estrogenic chemicals, octylphenol (OP) and bisphenol A (BPA), on epididymal sperm counts and sperm motility, luteinizing hormone (LH)-releasing hormone (LHRH)-stimulated plasma LH and steroid hormones, insulin-like growth factor I (IGF-I), and accessory reproductive organs in pubertal male Wistar rats. Fifty-day-old rats in the OP group (n=11) and BPA group (n=11) received daily sc injections of the respective chemical at a dose of 3 mg/kg bw dissolved in 0.2 mL DMSO. Rats in the control group (DMSO group; n=10) received 0.2 mL DMSO alone. After 2 wk of treatment, a jugular blood sample was taken, and, on the next day, a second blood sample was taken 1 h after an sc injection of LHRH (250 ng). After 5 wk of treatment, rats were deeply anesthetized and heart blood was collected. Epididymal sperm motility and sperm head counts were determined. LHRH increased plasma LH to higher levels in all groups, but the increases were significant (p<0.01) in the BPA and OP groups. However, despite higher LH levels after LHRH injection, the incremental responses of testosterone and pro-gesterone in the OP and BPA groups were small compared to those in the DMSO group, which showed a small LH response. After 5 wk of treatment, plasma testosterone levels were significantly (p<0.01) reduced in the OP and BPA groups and this was accompanied by reduced (p<0.05) epididymal sperm counts. However, the chemical-treated groups had high basal progesterone levels. No significant effects of chemicals on sperm motility parameters were noted. The chemical-induced increases (p<0.05) of the weight of ventral prostate gland were coincided with elevated plasma IGF-I levels in the BPA (p<0.05) and OP (p<0.01) groups. The present results demonstrated that OP and BPA can reduce sperm counts resulting from lowered plasma testosterone in male rats just after puberty. The enlarged ventral prostate gland may possibly be associated with increased plasma IGF-I, raising the possibility of a link between these chemicals and prostate diseases because IGF-I has been implicated in the pathogenesis of human prostate cancers.

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Year:  2004        PMID: 15711031     DOI: 10.1385/ENDO:25:2:163

Source DB:  PubMed          Journal:  Endocrine        ISSN: 1355-008X            Impact factor:   3.633


  54 in total

1.  Prepubertal exposure to compounds that increase prolactin secretion in the male rat: effects on the adult prostate.

Authors:  T E Stoker; C L Robinette; B H Britt; S C Laws; R L Cooper
Journal:  Biol Reprod       Date:  1999-12       Impact factor: 4.285

2.  Differing effects of endocrine-disrupting chemicals on basal and FSH-stimulated progesterone production in rat granulosa-luteal cells.

Authors:  H Nejaty; M Lacey; S A Whitehead
Journal:  Exp Biol Med (Maywood)       Date:  2001-06

3.  Effect of a combined trenbolone acetate and estradiol implant on steady-state IGF-I mRNA concentrations in the liver of wethers and the longissimus muscle of steers.

Authors:  B J Johnson; M E White; M R Hathaway; C J Christians; W R Dayton
Journal:  J Anim Sci       Date:  1998-02       Impact factor: 3.159

4.  Effects of bisphenol A on adult male mouse fertility.

Authors:  Ahmad S Al-Hiyasat; Homa Darmani; Ahmed M Elbetieha
Journal:  Eur J Oral Sci       Date:  2002-04       Impact factor: 2.612

5.  The role of estrogen receptor, androgen receptor and growth factors in diethylstilbestrol-induced programming of prostate differentiation.

Authors:  C Gupta
Journal:  Urol Res       Date:  2000-08

6.  Inhibition of hCG-stimulated steroidogenesis in cultured mouse Leydig tumor cells by bisphenol A and octylphenols.

Authors:  H Nikula; T Talonpoika; M Kaleva; J Toppari
Journal:  Toxicol Appl Pharmacol       Date:  1999-06-15       Impact factor: 4.219

7.  In vivo inhibition of insulin-like growth factor I gene expression by tamoxifen.

Authors:  H T Huynh; E Tetenes; L Wallace; M Pollak
Journal:  Cancer Res       Date:  1993-04-15       Impact factor: 12.701

8.  Androgen regulation of the insulin-like growth factor-I and the estrogen receptor in rat uterus and liver.

Authors:  L Sahlin; G Norstedt; H Eriksson
Journal:  J Steroid Biochem Mol Biol       Date:  1994-10       Impact factor: 4.292

9.  Effects of 31 kDa bovine inhibin on FSH and LH in rat pituitary cells in vitro: antagonism of gonadotrophin-releasing hormone agonists.

Authors:  P G Farnworth; D M Robertson; D M de Kretser; H G Burger
Journal:  J Endocrinol       Date:  1988-11       Impact factor: 4.286

10.  Relative binding affinity-serum modified access (RBA-SMA) assay predicts the relative in vivo bioactivity of the xenoestrogens bisphenol A and octylphenol.

Authors:  S C Nagel; F S vom Saal; K A Thayer; M G Dhar; M Boechler; W V Welshons
Journal:  Environ Health Perspect       Date:  1997-01       Impact factor: 9.031

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  20 in total

1.  Disrupting actions of bisphenol A and malachite green on growth hormone receptor gene expression and signal transduction in seabream.

Authors:  Baowei Jiao; Christopher H K Cheng
Journal:  Fish Physiol Biochem       Date:  2008-05-28       Impact factor: 2.794

2.  Proceedings of the Summit on Environmental Challenges to Reproductive Health and Fertility: executive summary.

Authors:  Tracey J Woodruff; Alison Carlson; Jackie M Schwartz; Linda C Giudice
Journal:  Fertil Steril       Date:  2008-02       Impact factor: 7.329

3.  Estrogenic environmental contaminants alter the mRNA abundance profiles of genes involved in gonadal differentiation of the American bullfrog.

Authors:  Stephanie E Wolff; Nik Veldhoen; Caren C Helbing; Claire A Ramirez; Janae M Malpas; Catherine R Propper
Journal:  Sci Total Environ       Date:  2015-04-06       Impact factor: 7.963

4.  BPA Directly Decreases GnRH Neuronal Activity via Noncanonical Pathway.

Authors:  Ulrike Klenke; Stephanie Constantin; Susan Wray
Journal:  Endocrinology       Date:  2016-03-02       Impact factor: 4.736

5.  Bisphenol A and Human Reproductive Health.

Authors:  David E Cantonwine; Russ Hauser; John D Meeker
Journal:  Expert Rev Obstet Gynecol       Date:  2013-07-01

6.  Are environmental levels of bisphenol a associated with reproductive function in fertile men?

Authors:  Jaime Mendiola; Niels Jørgensen; Anna-Maria Andersson; Antonia M Calafat; Xiaoyun Ye; J Bruce Redmon; Erma Z Drobnis; Christina Wang; Amy Sparks; Sally W Thurston; Fan Liu; Shanna H Swan
Journal:  Environ Health Perspect       Date:  2010-05-21       Impact factor: 9.031

7.  Higher urinary bisphenol A concentration is associated with unexplained recurrent miscarriage risk: evidence from a case-control study in eastern China.

Authors:  Yueping Shen; Yanmin Zheng; Jingting Jiang; Yinmei Liu; Xiaoming Luo; Zongji Shen; Xin Chen; Yan Wang; Yiheng Dai; Jing Zhao; Hong Liang; Aimin Chen; Wei Yuan
Journal:  PLoS One       Date:  2015-05-26       Impact factor: 3.240

8.  Exposure to bisphenol A disrupts meiotic progression during spermatogenesis in adult rats through estrogen-like activity.

Authors:  C Liu; W Duan; R Li; S Xu; L Zhang; C Chen; M He; Y Lu; H Wu; H Pi; X Luo; Y Zhang; M Zhong; Z Yu; Z Zhou
Journal:  Cell Death Dis       Date:  2013-06-20       Impact factor: 8.469

9.  Exposure to Bisphenol A prenatally or in adulthood promotes T(H)2 cytokine production associated with reduction of CD4CD25 regulatory T cells.

Authors:  Huimin Yan; Masaya Takamoto; Kazuo Sugane
Journal:  Environ Health Perspect       Date:  2008-04       Impact factor: 9.031

10.  Histopathology and Histomorphometric Investigation of Bisphenol A and Nonylphenol on the Male Rat Reproductive System.

Authors:  Sohrab Kazemi; Farideh Feizi; Fahimaeh Aghapour; Gholam Ali Joorsaraee; Ali Akbar Moghadamnia
Journal:  N Am J Med Sci       Date:  2016-05
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