Effect of native and oxidized low-density lipoprotein on endothelial nitric oxide and superoxide production - Key role of L-arginine availability

Article

关键词: RELAXING FACTOR;    DEPENDENT RELAXATION;    RABBIT AORTA;    ATHEROSCLEROSIS;    INCREASES;    SYNTHASE;    RELEASE;    ANION;    LDL;    PEROXYNITRITE;   

DOI  :  10.1161/01.CIR.101.11.1261

来源: SCIE

【 摘 要 】

Background-Native and oxidized LDLs (n-LDL and ox-LDL) are involved in the atherogenic process and affect endothelium-dependent vascular tone through their interaction with nitric oxide (NO). Methods and Results-In this study we evaluated directly, by using a porphyrinic microsensor, the effect of increasing lipoprotein concentrations on endothelial NO and superoxide (O-2(-)) production. We investigated where lipoproteins may affect the L-arginine-NO pathway by pretreating cells with L-arginine, L-N-arginine methyl ester (L-NAME), and superoxide dismutase, Bovine aortic endothelial cells were exposed for 1 hour to increasing concentrations of n-LDL (from 0 to 240 mg cholesterol/dL) and ox-LDL (from 0 to 140 mg cholesterol/dL). A stimulated (calcium ionophore) NO concentration decreased to 29% of the control at n-LDL concentration of 80 mg cholesterol/dL and to 15% of the control at 20 mg cholesterol/dL of ox-LDL. L-Arginine partially neutralized the inhibitory effect of n-LDL and ox-LDL on the NO generation. Superoxide dismutase pretreatment did not modify NO production, whereas L-NAME blunted NO generation at all LDL concentrations. O-2(-) production was increased at low n-LDL and very low ox-LDL concentrations; this was reversed by L-arginine. Conclusions-These findings confirm the inhibitory role of n-LDL and ox-LDL on NO generation and suggest that lipoproteins may induce a decreased uptake of L-arginine. The local depletion of the L-arginine substrate may derange the NO synthase, leading to overproduction of O-2(-) from oxygen, the other substrate of NO synthase.

【 授权许可】

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