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全氟辛烷磺酸诱导雄性 Sprague Dawley 大鼠肝脂肪变性,膳食胆碱补充不能使其减轻。

Perfluorooctane Sulfonate-Induced Hepatic Steatosis in Male Sprague Dawley Rats Is Not Attenuated by Dietary Choline Supplementation.

机构信息

Medical Department, 3M Company, St. Paul, Minnesota 55144.

Charles River Laboratories, Durham, North Carolina 27703.

出版信息

Toxicol Sci. 2017 Dec 1;160(2):284-298. doi: 10.1093/toxsci/kfx185.

Abstract

Perfluorooctane sulfonate (PFOS) is an environmentally persistent chemical. Dietary 100 ppm PFOS fed to male mice and rats for 4 weeks caused hepatic steatosis through an unknown mechanism. Choline deficient diets can cause hepatic steatosis. A hepatic choline:PFOS ion complex was hypothesized to cause this effect in mice. This study tested whether dietary choline supplementation attenuates PFOS-induced hepatic steatosis in rats. Sprague Dawley rats (12/sex/group) were fed control, choline supplemented (CS), 100 ppm PFOS, or 100 ppm PFOS + CS diets for 3 weeks. Male rats fed both PFOS-containing diets had decreased serum cholesterol and triglycerides (TGs) on days 9, 16, and/or 23 and increased hepatic free fatty acids and TG (ie, steatosis). Female rats fed both PFOS diets had decreased serum cholesterol on days 9 and 16 and decreased hepatic free fatty acid and TG at termination (ie, no steatosis). Liver PFOS concentrations were similar for both sexes. Liver choline concentrations were increased in male rats fed PFOS (±CS), but the increase was lower in the PFOS + CS group. Female liver choline concentrations were not altered by any diet. These findings demonstrate a clear sex-related difference in PFOS-induced hepatic steatosis in the rat. Additional evaluated mechanisms (ie, nuclear receptor activation, mRNA upregulation, and choline kinase activity inhibition) did not appear to be involved in the hepatic steatosis. Dietary PFOS (100 ppm) induced hepatic steatosis in male, but not female, rats that was not attenuated by choline supplementation. The mechanism of lipid accumulation and the sex-related differences warrant further investigation.

摘要

全氟辛烷磺酸 (PFOS) 是一种环境持久性化学物质。雄性小鼠和大鼠连续 4 周喂食含 100ppm PFOS 的饮食会导致肝脂肪变性,但具体机制尚不清楚。胆碱缺乏饮食可导致肝脂肪变性。研究人员假设,肝内胆碱与 PFOS 的离子复合物是导致这种现象的原因。本研究旨在测试饮食中添加胆碱是否能减轻 PFOS 诱导的大鼠肝脂肪变性。将 Sprague Dawley 大鼠(每组 12 只,雌雄各半)分别喂食对照饮食、添加胆碱(CS)饮食、含 100ppm PFOS 的饮食和含 100ppm PFOS 加 CS 的饮食,持续 3 周。喂食含 PFOS 饮食的雄性大鼠在第 9、16 和/或 23 天血清胆固醇和甘油三酯(TG)降低,肝脏游离脂肪酸和 TG 增加(即出现脂肪变性)。喂食两种 PFOS 饮食的雌性大鼠在第 9 和 16 天血清胆固醇降低,在实验结束时肝脏游离脂肪酸和 TG 降低(即没有脂肪变性)。雌雄大鼠的肝脏 PFOS 浓度相似。雄性大鼠喂食 PFOS(±CS)时肝脏胆碱浓度增加,但 PFOS+CS 组的增加幅度较低。雌性大鼠的肝脏胆碱浓度不受任何饮食影响。这些发现表明,PFOS 诱导的大鼠肝脂肪变性存在明显的性别差异。此外,评估的其他机制(核受体激活、mRNA 上调和胆碱激酶活性抑制)似乎与肝脂肪变性无关。饮食中添加 PFOS(100ppm)可诱导雄性大鼠出现肝脂肪变性,但雌性大鼠未出现,且添加胆碱不能减轻这种现象。脂类堆积的机制和性别差异值得进一步研究。

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