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全氟辛酸对类固醇激素和生长因子水平的影响介导 C57BL/6 小鼠青春期乳腺发育的刺激作用。

Perfluorooctanoic acid effects on steroid hormone and growth factor levels mediate stimulation of peripubertal mammary gland development in C57BL/6 mice.

机构信息

Department of Physiology, Michigan State University, East Lansing, Michigan 48824, USA.

出版信息

Toxicol Sci. 2010 May;115(1):214-24. doi: 10.1093/toxsci/kfq030. Epub 2010 Jan 29.

Abstract

Perfluorooctanoic acid (PFOA) is a synthetic, widely used perfluorinated carboxylic acid and a persistent environmental pollutant. It is an agonist of peroxisome proliferator-activated receptor alpha (PPARalpha). Studies have shown that PFOA causes hepatocellular hypertrophy, tumorigenesis, and developmental toxicity in rodents, and some of its toxicity depends on the expression of PPARalpha. Our recent study revealed a stimulatory effect of peripubertal PFOA treatment (5 mg/kg) on mammary gland development in C57Bl/6 mice. The present study was designed to examine the underlying mechanism(s). It was found that mammary gland stimulation by PFOA was similarly observed in PPARalpha knockout and wild-type C57Bl/6 mice. The presence of ovaries was required for PFOA treatment (5 mg/kg) to stimulate mammary gland development with significant increases in the levels of enzymes involved in steroid hormone synthesis in both PFOA-treated wild-type and PPARalpha knockout mouse ovaries. PFOA treatment significantly increased serum progesterone (P) levels in ovary-intact mice and also enhanced mouse mammary gland responses to exogenous estradiol (E), P, and E + P. In addition, PFOA treatment resulted in elevated mammary gland levels of epidermal growth factor receptor (EGFR), estrogen receptor alpha, amphiregulin (Areg, a ligand of EGFR), hepatocyte growth factor, cyclin D1, and proliferating cell nuclear antigen (PCNA) in both wild-type and PPARalpha knockout mouse mammary glands. These results indicate that PFOA stimulates mammary gland development in C57Bl/6 mice by promoting steroid hormone production in ovaries and increasing the levels of a number of growth factors in mammary glands, which is independent of the expression of PPARalpha.

摘要

全氟辛酸(PFOA)是一种合成的、广泛使用的全氟羧酸,也是一种持久性的环境污染物。它是过氧化物酶体增殖物激活受体α(PPARα)的激动剂。研究表明,PFOA 可导致啮齿动物的肝细胞肥大、肿瘤形成和发育毒性,其部分毒性依赖于 PPARα 的表达。我们最近的研究揭示了青春期前 PFOA 处理(5mg/kg)对 C57Bl/6 小鼠乳腺发育的刺激作用。本研究旨在探讨其潜在机制。研究发现,PPARα 敲除和野生型 C57Bl/6 小鼠的乳腺均受到 PFOA 的刺激。卵巢的存在是 PFOA 处理(5mg/kg)刺激乳腺发育所必需的,并且在 PFOA 处理的野生型和 PPARα 敲除小鼠的卵巢中,参与类固醇激素合成的酶的水平显著增加。PFOA 处理显著增加了卵巢完整小鼠的血清孕激素(P)水平,也增强了小鼠乳腺对外源性雌二醇(E)、P 和 E+P 的反应。此外,PFOA 处理导致乳腺中表皮生长因子受体(EGFR)、雌激素受体α、双调蛋白(Areg,EGFR 的配体)、肝细胞生长因子、细胞周期蛋白 D1 和增殖细胞核抗原(PCNA)的水平升高在野生型和 PPARα 敲除小鼠的乳腺中。这些结果表明,PFOA 通过促进卵巢中类固醇激素的产生和增加乳腺中多种生长因子的水平来刺激 C57Bl/6 小鼠的乳腺发育,这与 PPARα 的表达无关。

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