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本文引用的文献

1
Neuroestradiol in the hypothalamus contributes to the regulation of gonadotropin releasing hormone release.下丘脑神经雌二醇有助于调节促性腺激素释放激素的释放。
J Neurosci. 2013 Dec 4;33(49):19051-9. doi: 10.1523/JNEUROSCI.3878-13.2013.
2
Sex steroid regulation of kisspeptin circuits.性甾体激素对 kisspeptin 回路的调节。
Adv Exp Med Biol. 2013;784:275-95. doi: 10.1007/978-1-4614-6199-9_13.
3
Bisphenol A exposure during adulthood causes augmentation of follicular atresia and luteal regression by decreasing 17β-estradiol synthesis via downregulation of aromatase in rat ovary.成年期双酚 A 暴露通过下调卵巢芳香化酶减少 17β-雌二醇合成,导致卵泡闭锁和黄体退化增加。
Environ Health Perspect. 2013 Jun;121(6):663-9. doi: 10.1289/ehp.1205823. Epub 2013 Mar 19.
4
Ovarian regulation of kisspeptin neurones in the arcuate nucleus of the rhesus monkey (macaca mulatta).卵巢调节恒河猴弓状核中的 kisspeptin 神经元。
J Neuroendocrinol. 2013 May;25(5):488-96. doi: 10.1111/jne.12025.
5
Tonic control of kisspeptin release in prepubertal monkeys: implications to the mechanism of puberty onset.青春期前猕猴的促性腺激素释放激素对 kisspeptin 释放的调控:对青春期启动机制的启示。
Endocrinology. 2012 Jul;153(7):3331-6. doi: 10.1210/en.2012-1221. Epub 2012 May 14.
6
Developmental increase in kisspeptin-54 release in vivo is independent of the pubertal increase in estradiol in female rhesus monkeys (Macaca mulatta).体内 kisspeptin-54 释放的发育性增加与雌性恒河猴(Macaca mulatta)青春期雌激素增加无关。
Endocrinology. 2012 Apr;153(4):1887-97. doi: 10.1210/en.2011-1701. Epub 2012 Feb 7.
7
Developmental changes in GnRH release in response to kisspeptin agonist and antagonist in female rhesus monkeys (Macaca mulatta): implication for the mechanism of puberty.促性腺激素释放激素释放在雌性恒河猴(Macaca mulatta)对 kisspeptin 激动剂和拮抗剂反应中的发育变化:对青春期机制的影响。
Endocrinology. 2012 Feb;153(2):825-36. doi: 10.1210/en.2011-1565. Epub 2011 Dec 13.
8
Probable gamma-aminobutyric acid involvement in bisphenol A effect at the hypothalamic level in adult male rats.可能的γ-氨基丁酸参与成年雄性大鼠下丘脑水平双酚 A 的作用。
J Physiol Biochem. 2011 Dec;67(4):559-67. doi: 10.1007/s13105-011-0102-6. Epub 2011 Jun 9.
9
Bisphenol A disrupts steroidogenesis in human H295R cells.双酚 A 会破坏人 H295R 细胞中的类固醇生成。
Toxicol Sci. 2011 Jun;121(2):320-7. doi: 10.1093/toxsci/kfr061. Epub 2011 Apr 6.
10
Evidence to suggest glutamic acid involvement in Bisphenol A effect at the hypothalamic level in prepubertal male rats.有证据表明谷氨酸参与双酚A对青春期前雄性大鼠下丘脑水平的影响。
Neuro Endocrinol Lett. 2010;31(4):512-6.

双酚A暴露对雌性恒河猴下丘脑促性腺激素释放激素和吻素释放的急性影响

Acute Influences of Bisphenol A Exposure on Hypothalamic Release of Gonadotropin-Releasing Hormone and Kisspeptin in Female Rhesus Monkeys.

作者信息

Kurian Joseph R, Keen Kim L, Kenealy Brian P, Garcia James P, Hedman Curtis J, Terasawa Ei

机构信息

Wisconsin National Primate Research Center (J.R.K., K.L.K., B.P.K., J.P.G., E.T.), and Department of Pediatrics (E.T.), University of Wisconsin-Madison, Madison, Wisconsin 53715; Wisconsin State Laboratory of Hygeine (C.J.H.), Madison, Wisconsin 53718; and Southern Illinois University School of Medicine (J.R.K.), Springfield, Illinois 62794.

出版信息

Endocrinology. 2015 Jul;156(7):2563-70. doi: 10.1210/en.2014-1634. Epub 2015 Apr 8.

DOI:10.1210/en.2014-1634
PMID:25853665
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4475715/
Abstract

Bisphenol A (BPA) is an industrial compound with pervasive distribution in the environments of industrialized countries. The U.S. Centers for Disease Control recently found that greater than 90% of Americans carry detectable levels of BPA, raising concern over the direct influences of this compound on human physiology. Epidemiologic evidence links elevated BPA serum concentrations to human reproductive dysfunction, although controlled studies on the acute effect of BPA exposure on reproductive function are limited, particularly in primates. We evaluated the effect of direct BPA exposure on female primate hypothalamic peptide release. Specifically, using a microdialysis method, we examined the effects of BPA (0.1, 1, and 10nM) directly infused to the stalk-median eminence on the release of GnRH and kisspeptin (KP) in mid to late pubertal ovarian intact female rhesus monkeys. We found that the highest level of BPA exposure (10nM) suppressed both GnRH and KP release, whereas BPA at lower concentrations (0.1 and 1nM) had no apparent effects. In addition, we measured BPA in plasma and hypothalamic dialysates after an iv bolus injection of BPA (100 μg/kg). We found a relatively stable distribution of BPA between the blood and brain (plasma:brain ≅ 5:1) persists across a wide range of blood BPA concentrations (1-620 ng/mL). Findings of this study suggest that persistent, high-level exposures to BPA could impair female reproductive function by directly influencing hypothalamic neuroendocrine function.

摘要

双酚A(BPA)是一种工业化合物,在工业化国家的环境中广泛分布。美国疾病控制中心最近发现,超过90%的美国人携带可检测水平的双酚A,这引发了人们对该化合物对人体生理直接影响的担忧。流行病学证据将双酚A血清浓度升高与人类生殖功能障碍联系起来,尽管关于双酚A暴露对生殖功能急性影响的对照研究有限,尤其是在灵长类动物中。我们评估了双酚A直接暴露对雌性灵长类动物下丘脑肽释放的影响。具体而言,我们采用微透析方法,研究了直接向青春期中期至晚期卵巢完整的雌性恒河猴的视交叉上核注入双酚A(0.1、1和10nM)对促性腺激素释放激素(GnRH)和亲吻素(KP)释放的影响。我们发现,最高水平的双酚A暴露(10nM)抑制了GnRH和KP的释放,而较低浓度(0.1和1nM)的双酚A没有明显影响。此外,我们在静脉推注双酚A(100μg/kg)后测量了血浆和下丘脑透析液中的双酚A。我们发现,在广泛的血液双酚A浓度范围(1 - 620ng/mL)内,血液和大脑之间双酚A的分布相对稳定(血浆:大脑≈5:1)。本研究结果表明,持续、高水平暴露于双酚A可能通过直接影响下丘脑神经内分泌功能损害雌性生殖功能。