Why the study?
Silver nanoparticles are widely used in medicine, including the cardiovascular field, but limited research has investigated their effect on protection against myocardial infarction.
Do silver nanoparticles protect against isoproterenol-induced myocardial infarction in rats?
Do silver nanoparticles protect against isoproterenol-induced myocardial infarction in rats?
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Silver nanoparticles demonstrate superior cardioprotective effects compared to silver ions against isoproterenol-induced myocardial infarction in rats, likely through amelioration of oxidative stress and NF-κB expression.
Background Silver nanoparticles (AgNPs) are widely used in the medical field, including cardiovascular. However, limited research has investigated the effect of AgNPs on the protection of myocardial infarction (MI). Objectives Isoproterenol (Iso)-induced MI and the cardiac protection offered by AgNPs were investigated in the present study. Additionally, we characterized the profile of Ag in the form of nanoparticles. Methods Twenty-four male Wistar rats were randomly divided into four groups as follows: normal, Iso, Iso + AgNO 3 , and Iso + AgNP groups. AgNPs and silver ion (AgNO 3 ) were administered intraperitoneally at 2.5 mg/kg BW for 14 days. Iso induction was performed using two doses of 85 mg/kg BW given subcutaneously on days 13 and 14. Blood and cardiac tissue samples were taken 24 h after the last dose of Iso and checked for Creatine Kinase-MB (CK-MB), lactate dehydrogenase in plasma along with oxidative stress parameters, mitochondria biogenesis markers, and inflammation representative genes in cardiac tissue. Additionally, we analyzed the histopathological features in cardiac tissue. Results The silver was confirmed in the form of nanoparticles by its size at intervals of 8.72–37.84 nm. Both AgNO 3 and AgNPs showed similar cardioprotective effects, as shown by the decrease in biochemical markers of cardiac toxicity, namely, CK-MB. Additionally, AgNPs group have better efficacy compared with AgNO 3 group in ameliorating Iso-mediated oxidative stress production, as evidenced by the significant decrease in malondialdehyde level and increased superoxide dismutase activity ( P < 0.0001 and P < 0.01, respectively) in cardiac tissue compared with the Iso group. Mechanistically, AgNPs, but not AgNO 3 , enhanced the expression levels of mitochondrial transcription factor A and peroxisome proliferator-activated receptor-gamma coactivator 1-alpha in post-MI heart and reduced the protein expression of nuclear factor-kappa B (NF-κB) assessed by western blot analysis. Furthermore, these results were confirmed with the histopathological evaluation of cardiac tissue. Nevertheless, pretreatment with either AgNO 3 or AgNPs improved the aspartate aminotransferase level. Conclusion These results suggested that AgNPs have more superior cardioprotective effect compared with AgNO 3 against Iso-induced MI, at least in part through amelioration of NF-κB expression level induced by oxidative stress overproduction.
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Arozal et al. (2022) studied this question.
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