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    Rights statement: This is the author’s version of a work that was accepted for publication in Reproductive Toxicology. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Reproductive Toxicology, 62 2016 DOI: 10.1016/j.reprotox.2016.04.016

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Effects of 4-Nonylphenol on spermatogenesis and induction of testicular apoptosis through oxidative stress-related pathways

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Effects of 4-Nonylphenol on spermatogenesis and induction of testicular apoptosis through oxidative stress-related pathways. / Duan, Peng; Hu, Chunhui; Butler, Holly et al.
In: Reproductive Toxicology, Vol. 62, 01.07.2016, p. 27-38.

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Duan P, Hu C, Butler H, Chen W, Huang W, Tang S et al. Effects of 4-Nonylphenol on spermatogenesis and induction of testicular apoptosis through oxidative stress-related pathways. Reproductive Toxicology. 2016 Jul 1;62:27-38. Epub 2016 Apr 22. doi: 10.1016/j.reprotox.2016.04.016

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@article{0899e59d3f1c4529afcdfaf3a741acc6,
title = "Effects of 4-Nonylphenol on spermatogenesis and induction of testicular apoptosis through oxidative stress-related pathways",
abstract = "This study tested the hypothesis that prepubertal exposure to 4-Nonylphenol (NP) affects reproductive function in male rats. Twenty-four rats at five-weeks-old were randomly divided into four groups and treated with NP at varying concentrations (0, 5, 20, and 60 mg/kg/2d) for thirty days by intra-peritoneal injection. 60 mg/kg NP induced spermatogenic degeneration and pronounced deficits in epididymal sperm count, motility and function, whereas potentially stimulatory effects were observed at 5 NP mg/kg. Moreover, 60 mg/kg NP resulted in a significant reduction in fructose, FSH and LH; induced apoptosis related to oxidative stress; inhibited mRNA and protein levels of Bcl-2 and PCNA; as well as the additional up-regulation of p53, Bax, Apaf-1, cytochrome c, cleaved-caspase-3, Fas and FasL expression. Our data suggest potentially hormetic effects of NP on spermatogenic function. High-dose NP impairs testicular development and function by reducing cell proliferation and inducing apoptosis involving oxidative stress-related p53-Bcl-2/Bax and −Fas/FasL pathways.",
keywords = "4-Nonylphenol, Hormetic effect, Reproductive toxicity, Oxidative stress, Apoptosis, Intrinsic and extrinsic apoptotic pathways, Rats",
author = "Peng Duan and Chunhui Hu and Holly Butler and Wei Chen and Wenting Huang and Sha Tang and Wei Zhou and Meng Yuan and Yuqin Shi and Martin, {Francis Luke} and Kedi Yang",
note = "This is the author{\textquoteright}s version of a work that was accepted for publication in Reproductive Toxicology. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Reproductive Toxicology, 62 2016 DOI: 10.1016/j.reprotox.2016.04.016",
year = "2016",
month = jul,
day = "1",
doi = "10.1016/j.reprotox.2016.04.016",
language = "English",
volume = "62",
pages = "27--38",
journal = "Reproductive Toxicology",
issn = "0890-6238",
publisher = "Elsevier Inc.",

}

RIS

TY - JOUR

T1 - Effects of 4-Nonylphenol on spermatogenesis and induction of testicular apoptosis through oxidative stress-related pathways

AU - Duan, Peng

AU - Hu, Chunhui

AU - Butler, Holly

AU - Chen, Wei

AU - Huang, Wenting

AU - Tang, Sha

AU - Zhou, Wei

AU - Yuan, Meng

AU - Shi, Yuqin

AU - Martin, Francis Luke

AU - Yang, Kedi

N1 - This is the author’s version of a work that was accepted for publication in Reproductive Toxicology. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Reproductive Toxicology, 62 2016 DOI: 10.1016/j.reprotox.2016.04.016

PY - 2016/7/1

Y1 - 2016/7/1

N2 - This study tested the hypothesis that prepubertal exposure to 4-Nonylphenol (NP) affects reproductive function in male rats. Twenty-four rats at five-weeks-old were randomly divided into four groups and treated with NP at varying concentrations (0, 5, 20, and 60 mg/kg/2d) for thirty days by intra-peritoneal injection. 60 mg/kg NP induced spermatogenic degeneration and pronounced deficits in epididymal sperm count, motility and function, whereas potentially stimulatory effects were observed at 5 NP mg/kg. Moreover, 60 mg/kg NP resulted in a significant reduction in fructose, FSH and LH; induced apoptosis related to oxidative stress; inhibited mRNA and protein levels of Bcl-2 and PCNA; as well as the additional up-regulation of p53, Bax, Apaf-1, cytochrome c, cleaved-caspase-3, Fas and FasL expression. Our data suggest potentially hormetic effects of NP on spermatogenic function. High-dose NP impairs testicular development and function by reducing cell proliferation and inducing apoptosis involving oxidative stress-related p53-Bcl-2/Bax and −Fas/FasL pathways.

AB - This study tested the hypothesis that prepubertal exposure to 4-Nonylphenol (NP) affects reproductive function in male rats. Twenty-four rats at five-weeks-old were randomly divided into four groups and treated with NP at varying concentrations (0, 5, 20, and 60 mg/kg/2d) for thirty days by intra-peritoneal injection. 60 mg/kg NP induced spermatogenic degeneration and pronounced deficits in epididymal sperm count, motility and function, whereas potentially stimulatory effects were observed at 5 NP mg/kg. Moreover, 60 mg/kg NP resulted in a significant reduction in fructose, FSH and LH; induced apoptosis related to oxidative stress; inhibited mRNA and protein levels of Bcl-2 and PCNA; as well as the additional up-regulation of p53, Bax, Apaf-1, cytochrome c, cleaved-caspase-3, Fas and FasL expression. Our data suggest potentially hormetic effects of NP on spermatogenic function. High-dose NP impairs testicular development and function by reducing cell proliferation and inducing apoptosis involving oxidative stress-related p53-Bcl-2/Bax and −Fas/FasL pathways.

KW - 4-Nonylphenol

KW - Hormetic effect

KW - Reproductive toxicity

KW - Oxidative stress

KW - Apoptosis

KW - Intrinsic and extrinsic apoptotic pathways

KW - Rats

U2 - 10.1016/j.reprotox.2016.04.016

DO - 10.1016/j.reprotox.2016.04.016

M3 - Journal article

VL - 62

SP - 27

EP - 38

JO - Reproductive Toxicology

JF - Reproductive Toxicology

SN - 0890-6238

ER -