依达拉奉通过改变炎症途径和肠道微生物群改善维生素 D3 和高脂饮食诱导的大鼠动脉粥样硬化中的炎症反应

IF 3.2 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Lingjuan Du, Jia Wan, Guokai Yang, Zhenhuan Ma, Zhaoxiang Li, Guojian Li
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引用次数: 0

摘要

心血管疾病是指影响心脏和血管的一组疾病,包括冠状动脉疾病、心力衰竭和中风等。依达拉奉(ED)可抑制氧化应激和自由基损伤,而氧化应激和自由基损伤被认为是导致各种疾病恶化的原因。因此,本研究旨在探讨 ED 对维生素 D3 和高脂肪诱导的大鼠动脉粥样硬化的心脏保护作用。本研究采用 Sprague Dawley(SD)大鼠。大鼠被分成几组,喂食高脂肪食物和维生素 D3 以诱发动脉粥样硬化。给动物口服不同剂量的依达拉奉,持续 30 天。给药后,依达拉奉能有效降低动物体重的增加以及水和食物的过量消耗。治疗组的血糖水平、瘦素和脂蛋白-B均有所下降。服用 ED 还能改善胆固醇参数、冠状动脉指数、致动脉粥样硬化指数和抗氧化参数。它还降低了升高的心率、收缩压、平均血压和舒张压。接受 ED 治疗组的炎症细胞因子水平有所下降。ED 明显(p
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Edaravone Ameliorate Inflammation in Vitamin D3 and High Fat Diet Induced Atherosclerosis in Rat via Alteration of Inflammatory Pathway and Gut Microbiota

Edaravone Ameliorate Inflammation in Vitamin D3 and High Fat Diet Induced Atherosclerosis in Rat via Alteration of Inflammatory Pathway and Gut Microbiota

Cardiovascular disease refers to a group of conditions that affect the heart and blood vessels, including coronary artery disease, heart failure, and stroke, among others. Edaravone (ED) inhibits oxidative stress and free radical damage, which are thought to contribute to the progression of various diseases. Thus, the purpose of the study is to examine the cardioprotective effect of ED against vitamin D3 and high fat-induced atherosclerosis in rats. In this study, Sprague Dawley (SD) rats were utilized. The rats were separated into several groups and fed a high-fat diet along with vitamin D3 to induce atherosclerosis. Various doses of ED were orally administered to the animals for 30 days. The administration of Edaravone effectively reduced the elevated body weight, as well as the excessive water and food consumption. The treated groups exhibited a decrease in glucose level, leptin, and apolipoprotein-B. Administration of ED also modified the cholesterol parameters, coronary artery index, atherogenic index, and antioxidant parameters. It also reduced the elevated heart rate, systolic blood pressure (BP), mean BP, and diastolic BP. The group treated with ED exhibited a decrease in the level of inflammatory cytokines. The ED significantly (p < 0.001) reduced the levels of MMP-2, MMP-3, and MMP-9. Furthermore, it induced significant (p < 0.001) adjustments in the abundance of Firmicutes, Bacteroidetes, Proteobacteria, Verrucomicrobia, and F/B ratio. Edaravone exhibited the cardio protection against HFD induced atherosclerosis in rats via alteration of gut microbiota.

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来源期刊
Chemical Biology & Drug Design
Chemical Biology & Drug Design 医学-生化与分子生物学
CiteScore
5.10
自引率
3.30%
发文量
164
审稿时长
4.4 months
期刊介绍: Chemical Biology & Drug Design is a peer-reviewed scientific journal that is dedicated to the advancement of innovative science, technology and medicine with a focus on the multidisciplinary fields of chemical biology and drug design. It is the aim of Chemical Biology & Drug Design to capture significant research and drug discovery that highlights new concepts, insight and new findings within the scope of chemical biology and drug design.
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