Suppr超能文献

杂合子脂蛋白脂肪酶缺乏对小鼠饮食诱导动脉粥样硬化的影响。

Effects of heterozygous lipoprotein lipase deficiency on diet-induced atherosclerosis in mice.

作者信息

Semenkovich C F, Coleman T, Daugherty A

机构信息

Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

J Lipid Res. 1998 Jun;39(6):1141-51.

PMID:9643345
Abstract

Heterozygous lipoprotein lipase deficiency (LPL+/-) is common and has been implicated in premature atherosclerosis in epidemiologic studies. However, in vitro data suggest that LPL deficiency in the vascular wall may be antiatherogenic. To address the role of LPL in atherosclerosis, LPL+/- mice in the C57BL/6J background were fed an atherogenic diet for 8 months. LPL+/- mice were more dyslipidemic than +/+ animals due to increased concentrations of non-HDL lipoproteins. There was no difference in aortic origin atherosclerosis between LPL+/- (n=56) and +/+ (n=55) mice. LPL+/- mice in the low density lipoprotein receptor knockout (LDLR-/-) background were fed the same atherogenic diet for 3 months. LPL+/-LDLR-/- mice were more dyslipidemic than LPL+/+LDLR-/- animals. There was no difference in atherosclerosis assayed for the entire aorta and no difference in aortic sterol content between LPL+/-LDLR-/- (n=28) and LPL+/+LDLR-/- (n=15) mice. LPL protein was detected in murine lesions in a consistent layered pattern. More luminal, lipid-laden macrophages generally did not stain for LPL, but deeper, lipid-poor macrophages as well as necrotic core regions contained immunoreactive LPL. LPL protein was more abundant in lesions from LPL+/+ LDLR-/- than LPL+/-LDLR-/- mice. After eating an atherogenic diet, LPL+/- as compared to LPL+/+ mice have more dyslipidemia, but no more atherosclerosis, and less LPL protein in atherosclerotic lesions. These data suggest that lipoprotein lipase deficiency in the vascular wall could prevent the retention of atherogenic lipoproteins.

摘要

杂合子脂蛋白脂肪酶缺乏症(LPL+/-)很常见,并且在流行病学研究中与早发性动脉粥样硬化有关。然而,体外数据表明血管壁中的LPL缺乏可能具有抗动脉粥样硬化作用。为了探讨LPL在动脉粥样硬化中的作用,给C57BL/6J背景的LPL+/-小鼠喂食致动脉粥样硬化饮食8个月。由于非高密度脂蛋白浓度升高,LPL+/-小鼠比+/+动物的血脂异常更严重。LPL+/-(n=56)和+/+(n=55)小鼠之间的主动脉起源动脉粥样硬化没有差异。给低密度脂蛋白受体敲除(LDLR-/-)背景的LPL+/-小鼠喂食相同的致动脉粥样硬化饮食3个月。LPL+/-LDLR-/-小鼠比LPL+/+LDLR-/-动物的血脂异常更严重。在整个主动脉中检测到的动脉粥样硬化没有差异,LPL+/-LDLR-/-(n=28)和LPL+/+LDLR-/-(n=15)小鼠之间的主动脉固醇含量也没有差异。在小鼠病变中检测到LPL蛋白呈一致的分层模式。更多位于管腔、富含脂质的巨噬细胞通常不表达LPL,但更深层、脂质较少的巨噬细胞以及坏死核心区域含有免疫反应性LPL。LPL蛋白在LPL+/+LDLR-/-小鼠的病变中比LPL+/-LDLR-/-小鼠中更丰富。与LPL+/+小鼠相比,喂食致动脉粥样硬化饮食后,LPL+/-小鼠有更严重的血脂异常,但动脉粥样硬化程度并没有更严重,并且动脉粥样硬化病变中的LPL蛋白更少。这些数据表明血管壁中的脂蛋白脂肪酶缺乏可能会阻止致动脉粥样硬化脂蛋白的滞留。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验