Effects of Paricalcitol and Enalapril on Atherosclerotic Injury in Mouse Aortas

被引:64
作者
Husain, Kazim [1 ]
Suarez, Edu [2 ]
Isidro, Angel [1 ]
Ferder, Leon [1 ]
机构
[1] Ponce Sch Med, Dept Physiol Pharmacol & Toxicol, Ponce, PR 00732 USA
[2] Univ Puerto Rico, San Juan, PR 00936 USA
关键词
Monocyte chemoattractant protein-1; Glutathione; Renin-angiotensin system; NF-KAPPA-B; CONVERTING-ENZYME-INHIBITOR; RENIN-ANGIOTENSIN SYSTEM; VITAMIN-D DEFICIENCY; OXIDATIVE STRESS; CARDIOVASCULAR-DISEASE; SUPEROXIDE-DISMUTASE; HYPERTENSION; RISK; PATHOGENESIS;
D O I
10.1159/000319445
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Aims: This study investigated the protective effect of vitamin D analog paricalcitol combined with angiotensin-converting enzyme inhibitor (enalapril) on aortic oxidative injury in atherosclerotic mice. Methods: Female mice were treated for 16 weeks as follows: (1) ApoE deficient + vehicle, (2) ApoE deficient + paricalcitol (200 ng 3 times a week), (3) ApoE deficient + enalapril (30 mg/l in drinking water), (4) ApoE deficient + paricalcitol + enalapril, and (5) wild-type controls. Results: ApoE-deficient mice developed hypertension which was prevented by enalapril or enalapril + paricalcitol treatment but not by paricalcitol treatment. Histology showed atherosclerotic plaque in the aorta of ApoE-deficient mice which was prevented by paricalcitol, enalapril, and paricalcitol + enalapril treatments. Aortic malondialdehyde levels, NADPH oxidase subunit p22(phox), manganese-superoxide dismutase (Mn-SOD), inducible nitric oxide synthase, monocyte chemoattaractant protein-1, tumor necrosis factor (TNF)-alpha, and cyclooxygenase-2 protein expressions increased, whereas glutathione levels, CuZn-SOD, and endothelial protein expressions decreased in ApoE-deficient mice compared to controls. Treatment with paricalcitol and enalapril alone or in combination protected the inflammatory and oxidative endothelial injury of the aorta in atherosclerotic mice. Conclusion: Combination therapy affords greater protection against aortic inflammatory and oxidative injury in atherosclerosis than monotherapy. Copyright (C) 2010 S. Karger AG, Basel
引用
收藏
页码:296 / 304
页数:9
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