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1
Arsenic, organic foods, and brown rice syrup.砷、有机食品和糙米糖浆。
Environ Health Perspect. 2012 May;120(5):623-6. doi: 10.1289/ehp.1104619. Epub 2012 Feb 16.
2
Rice consumption contributes to arsenic exposure in US women.食用大米会导致美国女性砷暴露。
Proc Natl Acad Sci U S A. 2011 Dec 20;108(51):20656-60. doi: 10.1073/pnas.1109127108. Epub 2011 Dec 5.
3
Rural children's exposure to well water contaminants: implications in light of the American Academy of Pediatrics' recent policy statement.农村儿童接触井水污染物:鉴于美国儿科学会最近的政策声明所带来的影响。
J Am Acad Nurse Pract. 2011 May;23(5):258-65. doi: 10.1111/j.1745-7599.2011.00609.x. Epub 2011 Apr 19.
4
Cancer excess after arsenic exposure from contaminated milk powder.砷污染奶粉暴露后的癌症高发。
Environ Health Prev Med. 2011 May;16(3):164-70. doi: 10.1007/s12199-010-0182-x. Epub 2010 Sep 29.
5
SEM X-ray microanalysis of nanoparticles present in tissue or cultured cell thin sections.组织或培养细胞薄片中存在的纳米颗粒的扫描电子显微镜X射线微分析。
Methods Mol Biol. 2011;697:93-9. doi: 10.1007/978-1-60327-198-1_9.
6
Elevated circulating IGF-I promotes mammary gland development and proliferation.升高的循环 IGF-I 促进乳腺发育和增殖。
Endocrinology. 2010 Dec;151(12):5751-61. doi: 10.1210/en.2010-0792. Epub 2010 Oct 6.
7
Pathological, immunological and biochemical markers of subchronic arsenic toxicity in rats.大鼠亚慢性砷中毒的病理学、免疫学和生物化学标志物。
Environ Toxicol. 2012 Mar;27(4):244-54. doi: 10.1002/tox.20635. Epub 2010 Aug 19.
8
Chronic exposure to low levels of inorganic arsenic causes alterations in locomotor activity and in the expression of dopaminergic and antioxidant systems in the albino rat.长期接触低水平无机砷会导致白化大鼠运动活动和多巴胺能及抗氧化系统表达的改变。
Neurotoxicol Teratol. 2010 Nov-Dec;32(6):640-7. doi: 10.1016/j.ntt.2010.07.005. Epub 2010 Aug 10.
9
Arsenic alters monocyte superoxide anion and nitric oxide production in environmentally exposed children.砷会改变环境暴露儿童单核细胞超氧阴离子和一氧化氮的产生。
Toxicol Appl Pharmacol. 2010 Jun 1;245(2):244-51. doi: 10.1016/j.taap.2010.03.006. Epub 2010 Mar 11.
10
The role of liver-derived insulin-like growth factor-I.肝脏源性胰岛素样生长因子-I的作用。
Endocr Rev. 2009 Aug;30(5):494-535. doi: 10.1210/er.2009-0010. Epub 2009 Jul 9.

青春期前接触三价砷会抑制循环胰岛素样生长因子-1(IGF-1),从而延迟雌性大鼠的性成熟。

Prepubertal exposure to arsenic(III) suppresses circulating insulin-like growth factor-1 (IGF-1) delaying sexual maturation in female rats.

作者信息

Reilly Michael P, Saca James C, Hamilton Alina, Solano Rene F, Rivera Jesse R, Whitehouse-Innis Wendy, Parsons Jason G, Dearth Robert K

机构信息

Department of Biology, The University of Texas-Pan American, 1021 West University Drive, Edinburg, TX 78539, USA.

Edinburg Regional Academic Health Center (E-RAHC), University of Texas Health Science Center San Antonio Medical Research Division, 1214 West Schunior Street, Edinburg, TX 78541, USA.

出版信息

Reprod Toxicol. 2014 Apr;44:41-9. doi: 10.1016/j.reprotox.2013.09.005. Epub 2013 Sep 30.

DOI:10.1016/j.reprotox.2013.09.005
PMID:24090629
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3969868/
Abstract

Arsenic (As) is a prevalent environmental toxin readily accessible for human consumption and has been identified as an endocrine disruptor. However, it is not known what impact As has on female sexual maturation. Therefore, in the present study, we investigated the effects of prepubertal exposure on mammary gland development and pubertal onset in female rats. Results showed that prepubertal exposure to 10 mg/kg of arsenite (As(III)) delayed vaginal opening (VO) and prepubertal mammary gland maturation. We determined that As accumulates in the liver, disrupts hepatocyte function and suppresses serum levels of the puberty related hormone insulin-like growth factor 1 (IGF-1) in prepubertal animals. Overall, this is the first study to show that prepubertal exposure to As(III) acts peripherally to suppress circulating levels of IGF-1 resulting in delayed sexual maturation. Furthermore, this study identifies a critical window of increased susceptibility to As(III) that may have a lasting impact on female reproductive function.

摘要

砷(As)是一种普遍存在的环境毒素,很容易被人类摄入,并且已被确定为一种内分泌干扰物。然而,目前尚不清楚砷对女性性成熟有何影响。因此,在本研究中,我们调查了青春期前暴露对雌性大鼠乳腺发育和青春期开始的影响。结果表明,青春期前暴露于10 mg/kg的亚砷酸盐(As(III))会延迟阴道开口(VO)和青春期前乳腺成熟。我们确定砷在肝脏中积累,破坏肝细胞功能,并抑制青春期前动物血清中与青春期相关的激素胰岛素样生长因子1(IGF-1)的水平。总体而言,这是第一项表明青春期前暴露于As(III)会在周围发挥作用,抑制IGF-1的循环水平,从而导致性成熟延迟的研究。此外,本研究确定了对As(III)易感性增加的关键窗口期,这可能会对女性生殖功能产生持久影响。