菠菜提取物绿色合成氧化铁纳米颗粒对Triton x -100诱导大鼠动脉粥样硬化的影响。

IF 3.4 Q2 BIOCHEMICAL RESEARCH METHODS
Biochemistry Research International Pub Date : 2022-10-07 eCollection Date: 2022-01-01 DOI:10.1155/2022/9311227
Habila Obidah Abert, Hauwa Umaru Aduwamai, Saminu Shehu Adamu
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引用次数: 0

摘要

采用马齿苋叶提取物合成氧化铁纳米颗粒(FeONPs),观察其对Triton x -100诱导的Wistar大鼠动脉粥样硬化的影响。对FeONPs进行了表征,确定了它们的大小、结构、组成和形状。测定FeONPs对2,2 -二苯基-1-苦基-水合肼(DPPH)的体外抗氧化活性。腹腔注射5% Triton X-100 (100 mg/kg体重)诱导动脉粥样硬化14天。第1组给予标准鼠粮和水。第2组给予Triton X-100 100 mg/kg体重,饲喂标准日粮。第3组给予Triton X-100 100 mg/kg体重,随后给予阿托伐他汀20 mg/kg体重,疗程21 d。第4组、第5组和第6组分别给予100 mg/kg体重Triton X-100,随后分别给予100、300和500µg/kg体重不同浓度的FeONPs,持续21 d。对血液样本进行脂质、肝脏、抗氧化剂和心血管标志物的分析。同时进行心脏组织病理学检查。表征揭示了FeONPs的无定形性质、官能团和簇状形貌。FeONPs的抗氧化活性呈剂量依赖性上调。Triton X-100的使用表明,除高密度脂蛋白(HDL)外,脂质生物标志物水平升高,与1组相比,2组的高密度脂蛋白(HDL)降低。肝脏、抗氧化剂和心血管生物标志物均显著升高。组织病理学检查发现心脏组织结构改变。给药FeONPs显著降低所有生物标志物,升高HDL水平。同时,组织结构也得到了恢复。我们的研究结果表明,FeONPs可以有效改善Triton x -100诱导的大鼠动脉粥样硬化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effect of Green Synthesized Iron Oxide Nanoparticles Using Spinach Extract on Triton X-100-Induced Atherosclerosis in Rats.

Effect of Green Synthesized Iron Oxide Nanoparticles Using Spinach Extract on Triton X-100-Induced Atherosclerosis in Rats.

Effect of Green Synthesized Iron Oxide Nanoparticles Using Spinach Extract on Triton X-100-Induced Atherosclerosis in Rats.

Effect of Green Synthesized Iron Oxide Nanoparticles Using Spinach Extract on Triton X-100-Induced Atherosclerosis in Rats.

The effect of iron oxide nanoparticles (FeONPs) synthesized using Spinacia oleracea leaf extract on Triton X-100-induced atherosclerosis in white Wistar rats was determined. FeONPs were characterized to determine their size, structure, composition, and shape. In vitro antioxidant activity of FeONPs against 2, 2-diphenyl-1-picryl-hydrazyl-hydrate (DPPH) was determined. Atherosclerosis was induced by intraperitoneal administration of 5% Triton X-100 (100 mg/kg body weight) for 14 days. Group 1 received standard rat chow and water. Group 2 received 100 mg/kg body weight of Triton X-100 and a standard diet. Group 3 received 100 mg/kg body weight of Triton X-100 followed by 20 mg/kg body weight of atorvastatin for 21 days. Groups 4, 5, and 6 received 100 mg/kg body weight Triton X-100 was followed by variable concentrations of 100, 300, and 500 µg/kg body weight FeONPs, respectively, for 21 days. Blood samples were analyzed for lipid, liver, antioxidant, and cardiovascular markers. Histopathology of the heart was also examined. Characterization revealed the amorphous nature, functional groups, and clustered topography of FeONPs. An upregulated antioxidant activity of FeONPs was observed in a dose-dependent manner. Administration of Triton X-100 showed elevated levels of lipid biomarkers except for high-density lipoprotein (HDL), which decreased in group 2 in comparison to group 1. Liver, antioxidant, and cardiovascular biomarkers all significantly increased. The structural alteration was observed in the heart tissue following histopathology examination. Administration of FeONPs significantly decreased all biomarkers and increased the level of HDL. Also, tissue architecture was restored. Our findings demonstrated that FeONPs were effective in ameliorating Triton X-100-induced atherosclerosis in rats.

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来源期刊
Biochemistry Research International
Biochemistry Research International BIOCHEMICAL RESEARCH METHODS-
CiteScore
6.30
自引率
0.00%
发文量
27
审稿时长
14 weeks
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