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Synergistic effect of amlodipine and atorvastatin in reversing LDL-induced endothelial dysfunction

Mason, R. Preston and Kubant, Ruslan and Heeba, Gehan and Jacob, Robert F. and Day, Charles A. and Medlin, Yehudi S. and Funovics, Philipp and Malinski, Tadeusz (2008) Synergistic effect of amlodipine and atorvastatin in reversing LDL-induced endothelial dysfunction. PHARMACEUTICAL RESEARCH, 25 (8). pp. 1798-1806.

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Official URL: http://www.springerlink.com/content/72mu10280648n1...

Abstract

Purpose. Statins and certain calcium channel blockers may improve nitric oxide (NO) release and endothelial function through various mechanisms, but their combined effects are not well understood. Methods. The separate versus combined effects of amlodipine (AML) and atorvastatin (AT) on NO and peroxynitrite (ONOO-) were measured in human umbilical vein endothelial cells (HUVEC) in the presence and absence of low-density lipoprotein (LDL) using electrochemical nanosensors. Results. The combination of AML (5 mu mol/l) and AT (3-6 mu mol/l) directly stimulated NO release that was about twofold greater than the sum of their separate effects (p < 0.05). This synergistic activity is attributed to enhanced endothelial NO synthase (eNOS) function and decreased cytotoxic ONOO-. LDL (100 mg/dl) caused a dysfunction of HUVEC manifested by a 60% reduction in NO and an almost twofold increase in ONOO-. Treatment with AML/AT partially reversed the effects of LDL on endothelial function, including a 90% increase in NO and 50% reduction in ONOO-. Small-angle X-ray diffraction analysis indicates that AML and AT are lipophilic and share an overlapping molecular location in the cell membrane that could facilitate electron transfer for antioxidant mechanisms. Conclusion. These findings indicate a synergistic effect of AML and AT on an increase in NO concentration, reduction of nitroxidative stress. Also, AML/AT partially restored the NO level of LDL-induced dysfunctional endothelium. Their combined effects may be enhanced by antioxidant properties related to their intermolecular actions in the cell membrane and an increase in the expression and coupling of endothelial nitric oxide synthase.

Item Type:Article
Uncontrolled Keywords:endothelium; LDL; nitric oxide; oxidative stress
Subjects:Analytical Science > Nanotechnology for sensing and actuating
Biomedical Science > Nanotechnology for human health
Biomedical Science > Nanomedicine
ID Code:1223
Deposited By:Anuj Seth
Deposited On:16 Dec 2008 11:05
Last Modified:19 Jan 2009 11:39

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