Rebholz Sandra L, Jones Thomas, Herrick Robert L, Xie Changchun, Calafat Antonia M, Pinney Susan M, Woollett Laura A
Department of Pathology and Laboratory Medicine, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA.
Department of Environmental Health, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA.
Toxicol Rep. 2016;3:46-54. doi: 10.1016/j.toxrep.2015.11.004.
Perfluorooctanoic acid (PFOA) is a man-made surfactant with a number of industrial applications. It has a long half-life environmentally and biologically. Past studies suggest a direct relationship between plasma cholesterol and PFOA serum concentrations in humans and an inverse one in rodents fed standard rodent chow, making it difficult to examine mechanisms responsible for the potential PFOA-induced hypercholesterolemia and altered sterol metabolism. To examine dietary modification of PFOA-induced effects, C57BL/6 and BALB/c mice were fed PFOA in a fat- and cholesterol-containing diet. When fed these high fat diets, PFOA ingestion resulted in marked hypercholesterolemia in male and female C57BL/6 mice and less robust hypercholesterolemia in male BALB/c mice. The PFOA-induced hypercholesterolemia appeared to be the result of increased liver masses and altered expression of genes associated with hepatic sterol output, specifically bile acid production. mRNA levels of genes associated with sterol input were reduced only in C57BL/6 females, the mice with the greatest increase in plasma cholesterol levels. Strain-specific PFOA-induced changes in cholesterol concentrations in mammary tissues and ovaries paralleled changes in plasma cholesterol levels. mRNA levels of sterol-related genes were reduced in ovaries of C57BL/6 but not in BALB/c mice and not in mammary tissues. Our data suggest that PFOA ingestion leads to hypercholesterolemia in mice fed fat and cholesterol and effects are dependent upon the genetic background and gender of the mice with C57BL/6 female mice being most responsive to PFOA.
全氟辛酸(PFOA)是一种具有多种工业用途的人造表面活性剂。它在环境和生物体内具有较长的半衰期。过去的研究表明,人体血浆胆固醇与PFOA血清浓度之间存在直接关系,而在喂食标准啮齿动物饲料的啮齿动物中则呈反比关系,这使得难以研究导致潜在的PFOA诱导的高胆固醇血症和固醇代谢改变的机制。为了研究饮食对PFOA诱导效应的影响,给C57BL/6和BALB/c小鼠喂食含脂肪和胆固醇的饮食中的PFOA。当喂食这些高脂肪饮食时,摄入PFOA会导致雄性和雌性C57BL/6小鼠出现明显的高胆固醇血症,而雄性BALB/c小鼠的高胆固醇血症则较弱。PFOA诱导的高胆固醇血症似乎是肝脏质量增加和与肝脏固醇输出相关基因表达改变的结果,特别是胆汁酸的产生。仅在血浆胆固醇水平升高最大的C57BL/6雌性小鼠中,与固醇输入相关基因的mRNA水平降低。PFOA诱导的乳腺组织和卵巢中胆固醇浓度的品系特异性变化与血浆胆固醇水平的变化平行。C57BL/6小鼠卵巢中固醇相关基因的mRNA水平降低,而BALB/c小鼠和乳腺组织中则未降低。我们的数据表明,摄入PFOA会导致喂食脂肪和胆固醇的小鼠出现高胆固醇血症,其影响取决于小鼠的遗传背景和性别,其中C57BL/6雌性小鼠对PFOA最为敏感。