Evaluation of cardiovascular responses to silver nanoparticles (AgNPs) in spontaneously hypertensive rats
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Silver nanoparticles (AgNPs) are used in the medical, pharmaceutical and food industry. Adverse effects and toxicity induced by AgNPs upon cardiac function related to nitric oxide (NO) and oxidative stress (OS) are described. AgNPs-toxicity may be influenced by cardiovascular pathologies such as hypertension. However, the molecules involved under pathophysiological conditions are not well studied. The aim of this work was to evaluate perfusion pressure (PP) and left ventricle pressure (LVP) as physiological parameters of cardiovascular function in response to AgNPs, using isolated perfused hearts from spontaneously hypertensive rats (SHR), and identify the role of NO and OS. The results suggest that AgNPs reduced NO derived from endothelial/inducible NO-synthase and increased OS, leading to increased and sustained vasoconstriction and myocardial contractility. Additionally, the hypertension condition alters phenylephrine (Phe) and acetylcholine (ACh) classic effects. These data suggest that hypertension intensified AgNPs-cardiotoxicity. Nevertheless, the precise mechanism of action is still under elucidation. © 2017 Elsevier Inc.
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Nitric oxide; Oxidative stress; Silver nanoparticles; Spontaneously hypertensive rats Function evaluation; Metal nanoparticles; Nitric oxide; Oxidative stress; Physiological models; Rats; Silver nanoparticles; Toxicity; Cardiac functions; Cardiovascular function; Mechanism of action; Myocardial contractility; Pathophysiological; Physiological parameters; Silver nanoparticles (AgNps); Spontaneously hypertensive rats; Silver compounds; endothelial nitric oxide synthase; inducible nitric oxide synthase; nitric oxide; silver nanoparticle; endothelial nitric oxide synthase; inducible nitric oxide synthase; metal nanoparticle; nitric oxide; Nos2 protein, rat; Nos3 protein, rat; silver; animal cell; animal tissue; Article; cardiac muscle; cardiotoxicity; cardiovascular function; cardiovascular response; controlled study; drug synthesis; heart left ventricle pressure; heart muscle contractility; hypertension; in vitro study; isolated heart; lipid peroxidation; male; nonhuman; oxidative stress; pathophysiology; perfusion pressure; photon correlation spectroscopy; protein expression; rat; scanning electron microscopy; spontaneously hypertensive rat; systolic blood pressure; transmission electron microscopy; vasoconstriction; X ray photoelectron spectroscopy; zeta potential; animal; chemistry; drug effect; evaluation study; gene expression regulation; genetics; hypertension; metabolism; pathophysiology; Animals; Gene Expression Regulation; Hypertension; Male; Metal Nanoparticles; Nitric Oxide; Nitric Oxide Synthase Type II; Nitric Oxide Synthase Type III; Oxidative Stress; Rats; Rats, Inbred SHR; Silver; Vasoconstriction
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