Pan Xiaoyu, Zhang Xueqing, Ban Jiangli, Yue Lin, Ren Lin, Chen Shuchun
Department of Internal Medicine, Hebei Medical University, Shijiazhuang, Hebei, People's Republic of China.
Department of Endocrinology, Hebei General Hospital, Shijiazhuang, Hebei, People's Republic of China.
Diabetes Metab Syndr Obes. 2023 Mar 28;16:873-882. doi: 10.2147/DMSO.S405327. eCollection 2023.
To investigate the effect of high-fat diet on protein expression in mouse heart and aorta using proteomic techniques.
A high-fat diet was used to construct an obese mouse model, and body weight was checked regularly. After the experiment, serum lipid and oxidative stress levels were measured. Proteomic detection of cardiac and aortic protein expression. Cardiac and aortic common differentially expressed proteins (Co-DEPs) were screened based on proteomic results. Subsequently, functional enrichment analysis and screening of key proteins were performed.
A high-fat diet significantly increased body weight in mice. Obese mice had considerably higher levels of TC, TG, LDL-C, ROS, and MDA. In the heart and aorta, 17 Co-DEPs were discovered. The results of functional analysis of these proteins indicated that they were mainly related to lipid metabolism. Ech1, Decr1, Hsd17b4, Hsdl2 and Acadvl were screened as key proteins. In mice, a high-fat diet causes lipid metabolism to become disrupted, resulting in higher levels of oxidative stress and lipid peroxidation products.
Ech1, Decr1, Hsd17b4, Hsdl2 and Acadvl as cardiac and aortic Co-DEPs are closely related to lipid metabolism and may serve as potential diagnostic and therapeutic targets for obesity-induced cardiovascular disease.
运用蛋白质组学技术研究高脂饮食对小鼠心脏和主动脉中蛋白质表达的影响。
采用高脂饮食构建肥胖小鼠模型,并定期检查体重。实验结束后,测定血清脂质和氧化应激水平。对心脏和主动脉蛋白质表达进行蛋白质组学检测。根据蛋白质组学结果筛选心脏和主动脉共同差异表达蛋白(Co-DEPs)。随后进行功能富集分析和关键蛋白筛选。
高脂饮食显著增加小鼠体重。肥胖小鼠的总胆固醇(TC)、甘油三酯(TG)、低密度脂蛋白胆固醇(LDL-C)、活性氧(ROS)和丙二醛(MDA)水平显著更高。在心脏和主动脉中,发现了17种Co-DEPs。这些蛋白质的功能分析结果表明它们主要与脂质代谢有关。筛选出Ech1、Decr1、Hsd17b4、Hsdl2和Acadvl作为关键蛋白。在小鼠中,高脂饮食导致脂质代谢紊乱,从而导致氧化应激和脂质过氧化产物水平升高。
Ech1、Decr1、Hsd17b4、Hsdl2和Acadvl作为心脏和主动脉的Co-DEPs与脂质代谢密切相关,可能成为肥胖诱导的心血管疾病潜在的诊断和治疗靶点。