2014
DOI: 10.1016/j.exger.2014.01.015
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Long-term atorvastatin improves age-related endothelial dysfunction by ameliorating oxidative stress and normalizing eNOS/iNOS imbalance in rat aorta

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Cited by 56 publications
(39 citation statements)
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“…In fact, previous reports have demonstrated that atorvastatin treatment reduces the endothelial dysfunction by increasing the release of NO [34][35][36] besides reducing the nitroxidative stress [35] and oxidative stress [36]. Corroborating these studies, our findings suggest that NO participation, in response to phenylephrine was increased by atorvastatin treatment in diabetic rats.…”
Section: Discussionsupporting
confidence: 83%
“…In fact, previous reports have demonstrated that atorvastatin treatment reduces the endothelial dysfunction by increasing the release of NO [34][35][36] besides reducing the nitroxidative stress [35] and oxidative stress [36]. Corroborating these studies, our findings suggest that NO participation, in response to phenylephrine was increased by atorvastatin treatment in diabetic rats.…”
Section: Discussionsupporting
confidence: 83%
“…For example, Wagner et al report that atorvastatin reduces inducible nitric oxide synthase expression in native endothelial cells in situ and the underlying mechanism is associated with inhibition of tumor necrosis factor‐α and interferon‐γ expressions . Furthermore, through normalization of eNOS/inducible nitric oxide synthase ratio, atorvastatin improves age‐related endothelial dysfunction as reported by Gong and colleagues …”
Section: Rho‐gtpase and Endothelium: Effects Of Statinsmentioning
confidence: 83%
“…NO plays a key signal molecule in regulating vascular function; it is generated by NO synthases (NOSs), which comprise endothelial NOS (eNOS), inducible NOS (iNOS), and neuronal NOS [46]. Intimal eNOS-derived NO is transported to the vascular smooth muscle cells of the vascular media and regulates vascular tension mainly by relaxing the vessels, thereby maintaining vascular function [47]. In our study, we showed that eNOS expression was upregulated in response to 3-day IH but significantly decreased at 8 weeks of IH.…”
Section: Discussionmentioning
confidence: 99%