Genetic deficiency of inducible nitric oxide synthase reduces atherosclerosis and lowers plasma lipid peroxides in apolipoprotein E-knockout mice

Article

关键词: LOW-DENSITY-LIPOPROTEIN;    IN-VITRO;    SUPEROXIDE;    PEROXYNITRITE;    ATHEROGENESIS;    MACROPHAGES;    OXIDATION;    MONOCYTE;    RELEASE;    LESIONS;   

DOI  :  10.1161/01.CIR.103.25.3099

来源: SCIE

【 摘 要 】

Background-inducible nitric oxide synthase (iNOS) is expressed by leukocytes and smooth muscle cells in atherosclerotic lesions. To test whether NO produced by INOS deficiency affects atherosclerosis, we studied apoE/iNOS-double knockout (dKO) and apoE-knockout (KO) control animals fed a Western-type diet. Methods and Results-After 16 weeks of Western-type diet, the aortic lesion area in apoE/iNOS-dKO males and females was significantly reduced, by 228 and 21%, respectively, compared with apoE-KO males and females. This effect was more pronounced after 24 weeks of Western-type diet, after which lesion formation in male and female dKO mice was reduced by 38% and 40%. respectively. Plasma levels of lipoperoxides in apoE/iNOS-dKO mice (2.0 +/-0.23 mu mol/L) were significantly lower than in apoE-KO control animals (3.2 +/-0.14 mu mol/L; P=0.02), To test whether substrate deficiency plays a role in the proatherogenic actions of INOS, we administered L-arginine to apoE-KO animals for 16 and 24 weeks. L-Arginine treatment did not affect lesion formation in apoE-KO animals fed a Western-type diet. Conclusions-Genetic deficiency of INOS decreases diet-induced atherosclerosis and lowers plasma levels of lipoperoxides, a marker for oxidative stress, in apoE-KO animals. Reduction in iNOS-mediated oxidative stress could partly explain protection from lesion formation in dKO animals. L-Arginine supplementation did not change lesion area in apoE-KO mice, indicating that substrate deficiency is not a likely cause for iNOS-mediated injury in this model of atherosclerosis.

【 授权许可】

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