Protective properties of nanoparticles green-synthesized by plant on myocardial ischemia

被引:0
|
作者
Liu, Yang [1 ]
Guo, Jun [2 ]
Zhou, Zhou [3 ]
Wu, Qingke [4 ]
Jin, Xin [4 ]
Wang, Tao [5 ]
机构
[1] Shandong Univ Tradit Chinese Med, Affiliated Hosp, Dept Cardiol, Jinan 250011, Peoples R China
[2] Jinan Fourth Peoples Hosp, Dept Pharm, Jinan 250000, Peoples R China
[3] Shandong Univ Tradit Chinese Med, Clin Med Coll 1, Jinan 250011, Peoples R China
[4] Anser Sci Joint Lab Platform, Jinan 250000, Peoples R China
[5] Shandong Univ, Shandong Prov Hosp 3, Dept Cardiol, Jinan 250031, Shandong, Peoples R China
关键词
Gold nanoparticles; Silybum marianum; Myocardial ischemia; PPAR-gamma; Anti-apoptosis; NF-kappa B; LIPID-PEROXIDATION; SILVER NANOPARTICLES; OPTICAL-PROPERTIES; LIVER-CIRRHOSIS; AU NPS; SILYMARIN; SILIBININ; ANTIBACTERIAL; CHEMOTHERAPY; ANTIOXIDANT;
D O I
10.1016/j.inoche.2023.110902
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The formulation and characterization of novel cardiovascular supplements and drugs without any side effects are in both developed and developing countries research priority. Myocardial ischemia-reperfusion causes to an inflammatory response that leads more damage to apoptosis. Chronic and acute immune responses elicited by myocardial ischemia is in the heart functional deterioration. In this study, we formulated a modern cardioprotective protective drug by gold nanoparticles containing Silybum marianum on isoproterenol-induced myocardial ischemia mice by investigating the PPAR-gamma/NF-kappa B pathway. Determining the antioxidant capacities of gold nanoparticles was done with the conventional free radical scavenging test, i.e., DPPH in the presence of butylated hydroxytoluene as the positive control. The gold nanoparticles were characterized by standard physicochemical techniques, including FT-IR, FE-SEM, UV-Vis, and TEM. The nanoparticles inhibited half of the DPPH molecules in the concentration of 72 mu g/mL. In the in vivo design, to induce myocardial ischemia in C57BL/6 mice, isoproterenol (40 mg/kg) was administered. The mice were randomly divided into five groups: (1) control; (2) isoproterenol; (3-5) isoproterenol + gold nanoparticles at different doses (10, 20 and 40 mu g/ml) and timings. After treatment, cardiac function was evaluated by histochemical and biochemical analysis. Gold nanoparticles treatment decreased the inflammatory milieu in the myocardial ischemia mice heart, thereby blocking the proinflammatory cytokines upregulation (IL-1 ss, TNF-alpha and IL-6). Also, gold nanoparticles treatment significantly ameliorate ventricular wall ischemia, reduces the mortality incidence, and inhibits the myocardial injury markers levels. In addition, gold nanoparticles administration significantly prevents the typical ST segment depression. Treatment with gold nanoparticles significantly suppresses the inflammation cytokines expression and decrease cell death. The gold nanoparticles beneficial effects is related to the normalization in PPAR-gamma and PPAR-gamma/NF-kappa B/I kappa B-alpha/IKK alpha/ss phosphorylation gene expression. Gold nanoparticles exert cardioprotective properties against isoproterenol-induced myocardial ischemia in mice, which may associated to the PPAR-gamma activation and NF-kappa B signaling inhibition.
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页数:9
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