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本文引用的文献

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Estrogen, a female hormone involved in spermatogenesis.雌激素,一种参与精子发生的女性激素。
Adv Med Sci. 2012 Jun 1;57(1):31-6. doi: 10.2478/v10039-012-0005-y.
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Testosterone signaling and the regulation of spermatogenesis.睾酮信号传导与精子发生的调控。
Spermatogenesis. 2011 Apr;1(2):116-120. doi: 10.4161/spmg.1.2.16956.
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Epigenetic alterations in sperm DNA associated with testicular cancer treatment.精子 DNA 中的表观遗传改变与睾丸癌治疗相关。
Toxicol Sci. 2012 Feb;125(2):532-43. doi: 10.1093/toxsci/kfr307. Epub 2011 Nov 10.
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Sperm methylation profiles reveal features of epigenetic inheritance and evolution in primates.精子甲基化谱揭示了灵长类动物中表观遗传遗传和进化的特征。
Cell. 2011 Sep 16;146(6):1029-41. doi: 10.1016/j.cell.2011.08.016.
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Effect of low-dose fenvalerate on semen quality capacitation in adult mice.低剂量氰戊菊酯对成年小鼠精液质量获能的影响。
Chin Med J (Engl). 2011 May;124(10):1529-33.
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Intracellular colocalization of HAP1/STBs with steroid hormone receptors and its enhancement by a proteasome inhibitor.HAP1/STBs 与甾体激素受体的细胞内共定位及其被蛋白酶体抑制剂增强。
Exp Cell Res. 2011 Jul 15;317(12):1689-700. doi: 10.1016/j.yexcr.2011.05.004. Epub 2011 May 14.
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Epigenetics, spermatogenesis and male infertility.表观遗传学、精子发生与男性不育。
Mutat Res. 2011 May-Jun;727(3):62-71. doi: 10.1016/j.mrrev.2011.04.002. Epub 2011 Apr 16.
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Gender-specific impairments on cognitive and behavioral development in mice exposed to fenvalerate during puberty.青春期接触氰戊菊酯会导致雌雄小鼠认知和行为发育出现特定性别缺陷。
Toxicol Lett. 2011 Jun 24;203(3):245-51. doi: 10.1016/j.toxlet.2011.03.024. Epub 2011 Mar 31.
9
Effects of pubertal fenvalerate exposure on testosterone and estradiol synthesis and the expression of androgen and estrogen receptors in the developing brain.青春期氰戊菊酯暴露对睾丸酮和雌二醇合成的影响,以及对发育中大脑雄激素和雌激素受体表达的影响。
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The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders.人类类固醇生成及其疾病的分子生物学、生物化学和生理学。
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父亲接触氰戊菊酯会影响后代的生殖功能。

Paternal fenvalerate exposure influences reproductive functions in the offspring.

机构信息

1Institute of Animal Husbandry & Veterinary Sciences, Shanghai Academy of Agricultural Sciences, Shanghai, China.

出版信息

Reprod Sci. 2013 Nov;20(11):1308-15. doi: 10.1177/1933719113483015. Epub 2013 Apr 2.

DOI:10.1177/1933719113483015
PMID:23548413
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3795420/
Abstract

Fenvalerate (Fen), a synthetic pyrethroid insecticide, has been shown to have adverse effects on male reproductive system. Thus, the aim of the present study was to elucidate whether these adverse effects are passed from exposed male mice to their offspring. Adult male mice received Fen (10 mg/kg) daily for 30 days and mated with untreated females to produce offspring. Fenvalerate significantly changed the methylation status of angiotensin I-converting enzyme (Ace), forkhead box O3 (Foxo3a), huntingtin-associated protein 1 (Hap1), nuclear receptor subfamily 3 (Nr3c2), promyelocytic leukemia (Pml), and Prostaglandin F2 receptor negative regulator (Ptgfrn) genes in paternal mice sperm genomic DNA. Further, Fen significantly increased sperm abnormalities; serum testosterone and estradiol-17ß level in adult male (F0) and their male offspring (F1). Further, paternal Fen treatment significantly increased the length of estrous cycle, serum estradiol-17ß concentration in estrus, and progesterone levels in diestrus in female offspring (F1). These findings suggest that adverse effects of paternal Fen exposure on reproductive functions can be seen not only in treated males (F0) but also in their offsprings.

摘要

氰戊菊酯(Fen)是一种合成拟除虫菊酯杀虫剂,已被证明对雄性生殖系统有不良影响。因此,本研究旨在阐明这些不良影响是否会从暴露的雄性小鼠传递给它们的后代。成年雄性小鼠每天接受 Fen(10mg/kg)处理 30 天,并与未处理的雌性小鼠交配以产生后代。Fen 显著改变了雄性小鼠精子基因组 DNA 中血管紧张素 I 转化酶(Ace)、叉头框 O3(Foxo3a)、亨廷顿相关蛋白 1(Hap1)、核受体亚家族 3(Nr3c2)、早幼粒细胞白血病(Pml)和前列腺素 F2 受体负调节剂(Ptgfrn)基因的甲基化状态。此外,Fen 还显著增加了成年雄性(F0)及其雄性后代(F1)的精子畸形率和血清睾酮和雌二醇-17β水平。此外,父代 Fen 处理还显著增加了雌性后代(F1)的动情周期长度、动情期血清雌二醇-17β浓度和动情后期孕激素水平。这些发现表明,父代 Fen 暴露对生殖功能的不良影响不仅可以在处理过的雄性(F0)中看到,也可以在它们的后代中看到。