O. Galal, Ahmed Mostafa, Haytham Mohamed, A-Halim R. Ahmed, Marwa Hashim, Nagwa Abd Mohamed
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引用次数: 0
摘要
背景:心血管疾病(CVD)是一个公共卫生问题,2019年全球有1790万人死亡。维生素D是一种脂溶性维生素,具有多种心脏保护作用,缺乏维生素D与多种心血管疾病有关。纳米维生素D系统可以克服口服维生素D的可变生物利用度、水溶性差和化学降解等问题。目的:在异丙肾上腺素诱导心肌梗死(MI)大鼠模型上评价口服维生素D和纳米维生素D的潜在心脏保护作用。材料和方法:本研究评估了维生素D和维生素D纳米颗粒对心肌梗死率模型的影响。异丙肾上腺素100 mg/ kg在30天治疗期的最后2天诱发心肌梗死。我们分析了心脏损伤、脂质过氧化标志物和脂质谱。结果:异丙肾上腺素处理大鼠心肌肌钙蛋白- i (cTn-I)、丙二醛(MDA)明显升高(p值<0.0001)。口服维生素D可降低ctn - 1和MDA水平,改善血脂。结论:与口服常规维生素D相比,维生素D纳米颗粒对异丙肾上腺素诱导的心肌梗死具有更有效的心脏保护作用。
Cardioprotective Effects of Nano-Vitamin D on Isoprenaline-Induced Myocardial Infarction Rat Model
Background : Cardiovascular disease (CVD) is a public health problem accounting for 17.9 million deaths worldwide in 2019. Vitamin D is a fat-soluble vitamin that has various cardioprotective actions and its deficiency is associated with a variety of CVDs. Nano systems for vitamin D may overcome the variable oral bioavailability, poor water solubility and chemical degradation of vitamin D. Objectives : The potential cardioprotective effect of oral vitamin D and vitamin D nanoparticles was evaluated on isoprenaline induced myocardial infarction (MI) rat model. Materials and method : the study evaluated the effect of vitamin D and vitamin D nanoparticles on MI rate models. MI induced by isoprenaline 100 mg/ kg on the last two days of the 30 day treatment period. We analyzed cardiac injury, lipid peroxidation markers and lipid profile. Results : isoprenaline treated rats show marked elevation in cardiac troponin-I (cTn-I), and malondialdehyde (MDA), (p value <0.0001). Oral vitamin D reduced cTn-I and MDA levels and improved lipid profile. Vitamin D nanoparticles enhance the cardioprotective effect of conventional vitamin D. Conclusion : vitamin D nanoparticles have a more efficient cardioprotective effect against isoprenaline induced MI in rats compared to oral conventional vitamin D.