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首页> 外文期刊>Bioscience, Biotechnology, and Biochemistry >Enteric lactoferrin attenuates the development of high-fat and high-cholesterol diet-induced hypercholesterolemia and atherosclerosis in Microminipigs
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Enteric lactoferrin attenuates the development of high-fat and high-cholesterol diet-induced hypercholesterolemia and atherosclerosis in Microminipigs

机译:肠乳铁蛋白衰减了高脂肪和高胆固醇饮食诱导的高胆固醇血症和动脉粥样硬化的发展

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摘要

Previously, we found that enteric lactoferrin (eLF) could reduce the visceral fat accumulation known to associate strongly with metabolic syndrome symptoms and consequently with an increased risk of atherosclerosis. In this study, the atherosclerosis-preventive potential of LF was assessed in a high-fat and high-cholesterol diet (HFCD)-induced hypercholesterolemia and atherosclerosis model using Microminipig. Eight-week orally administered eLF remarkably reduced the HFCD-induced serum total and low-density lipoprotein cholesterol levels but not high-density lipoprotein cholesterol levels. A histological analysis of 15 arteries revealed that eLF systemically inhibited the development of atherosclerotic lesions. Pathway analysis using identified genes that characterized eLF administration in liver revealed significant changes in the steroid biosynthesis pathway (ssc00100) and all affected genes in this pathway were upregulated, suggesting that cholesterol synthesis inhibited by HFCD was recovered by eLF. In summary, eLF could potentially prevent the hypercholesterolemia and atherosclerosis through protecting homeostasis from HFCD-induced dysfunction of cholesterol metabolism.
机译:以前,我们发现肠乳铁蛋白(ELF)可以减少已知的内脏脂肪积累,以强烈地赋予代谢综合征症状,并且因此随着动脉粥样硬化的风险增加。在这项研究中,使用MicroMinipig在高脂肪和高胆固醇饮食(HFCD)诱导的高胆固醇血症和动脉粥样硬化模型中评估LF的动脉粥样硬化潜力。八周口服给药ELF显着降低了HFCD诱导的血清总和低密度脂蛋白胆固醇水平,但不高密度脂蛋白胆固醇水平。 15个动脉的组织学分析显示ELF系统性地抑制动脉粥样硬化病变的发育。使用鉴定基因的途径分析肝脏中的ELF给药揭示了类固醇生物合成途径(SSC00100)的显着变化,并且上调了该途径中的所有受影响的基因,表明通过ELF回收HFCD抑制的胆固醇合成。总之,ELF可能通过保护胆固醇代谢功能障碍的肺部诱导功能障碍来防止高胆固醇血症和动脉粥样硬化。

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