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邻苯二甲酸二乙酯暴露通过损害脂蛋白功能,与胚胎毒性、脂肪肝变化和低脂血症相关。

Diethyl phthalate exposure is associated with embryonic toxicity, fatty liver changes, and hypolipidemia via impairment of lipoprotein functions.

作者信息

Kim Seong-Min, Yoo Jeong-Ah, Baek Ji-Mi, Cho Kyung-Hyun

机构信息

School of Biotechnology, Yeungnam University, Gyeongsan 712-749, South Korea; Research Institute of Protein Sensor, Yeungnam University, Gyeongsan 712-749, Republic of Korea; BK21Plus Program Serum Biomedical Research and Education Team, Yeungnam University, Gyeongsan 712-749, Republic of Korea.

School of Biotechnology, Yeungnam University, Gyeongsan 712-749, South Korea; Research Institute of Protein Sensor, Yeungnam University, Gyeongsan 712-749, Republic of Korea; BK21Plus Program Serum Biomedical Research and Education Team, Yeungnam University, Gyeongsan 712-749, Republic of Korea.

出版信息

Toxicol In Vitro. 2015 Dec 25;30(1 Pt B):383-93. doi: 10.1016/j.tiv.2015.09.026. Epub 2015 Sep 28.

Abstract

Diethyl phthalates (DEPs) are notorious for their high potential toxicity in endocrinological and reproduction systems in humans and animals. In this study, we investigated the toxic effects of DEP on human lipoproteins, macrophages, and zebrafish embryos. Treatment of human high-density lipoprotein (HDL) with DEP caused oxidation, aggregation, and degradation of lipoproteins. DEP treatment promoted foam cell formation via accelerated phagocytosis of LDL by macrophages as well as exacerbated cellular senescence in human dermal fibroblasts. Injection of DEP (final 5 μM and 10 μM) into zebrafish embryos caused severe embryo death and slower developmental speed. Exposure of zebrafish embryos to water containing DEP (final 11 and 22 ppm) caused early embryonic death along with the increased oxidized products and impairment of skeletal development. Adult zebrafish exposed to water containing DEP (final 11 and 22 ppm) for 4 weeks showed severe loss of body weight under both normal diet (ND) and high cholesterol diet (HCD) conditions. ND and HCD groups showed 59% and 49% reduction of plasma total cholesterol (TC), respectively. Serum levels of hepatic inflammation enzymes along with fatty liver changes were significantly elevated by DEP exposure. In conclusion, DEP showed strong pro-atherogenic and pro-senescence effects via severe lipoprotein modification in human cells. DEP caused impairment of embryonic development and severe loss of body weight, hypolipidemia, and fatty liver changes in zebrafish.

摘要

邻苯二甲酸二乙酯(DEPs)因其对人类和动物内分泌及生殖系统具有高潜在毒性而声名狼藉。在本研究中,我们调查了DEP对人类脂蛋白、巨噬细胞和斑马鱼胚胎的毒性作用。用DEP处理人类高密度脂蛋白(HDL)会导致脂蛋白氧化、聚集和降解。DEP处理通过加速巨噬细胞对低密度脂蛋白(LDL)的吞噬促进泡沫细胞形成,并加剧人类皮肤成纤维细胞的细胞衰老。向斑马鱼胚胎注射DEP(终浓度5 μM和10 μM)会导致严重的胚胎死亡和发育速度减慢。将斑马鱼胚胎暴露于含有DEP的水中(终浓度11 ppm和22 ppm)会导致早期胚胎死亡,同时氧化产物增加和骨骼发育受损。成年斑马鱼在正常饮食(ND)和高胆固醇饮食(HCD)条件下暴露于含有DEP的水中(终浓度11 ppm和22 ppm)4周后,体重均出现严重下降。ND组和HCD组血浆总胆固醇(TC)分别降低了59%和49%。DEP暴露显著提高了肝脏炎症酶的血清水平以及脂肪肝变化。总之,DEP通过对人类细胞脂蛋白的严重修饰表现出强烈的促动脉粥样硬化和促衰老作用。DEP导致斑马鱼胚胎发育受损、体重严重下降、低脂血症和脂肪肝变化。

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