首页> 美国卫生研究院文献>American Journal of Physiology - Regulatory Integrative and Comparative Physiology >10th Annual Meeting for New Research in Cardiovascular and Kidney Diseases: Asymmetric dimethylarginine oxidative stress and vascular nitric oxide synthase in essential hypertension
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10th Annual Meeting for New Research in Cardiovascular and Kidney Diseases: Asymmetric dimethylarginine oxidative stress and vascular nitric oxide synthase in essential hypertension

机译:第十届心血管和肾脏疾病新研究年会:原发性高血压中的不对称二甲基精氨酸氧化应激和血管一氧化氮合酶

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摘要

We reported impaired endothelium-derived relaxation factoritric oxide (EDRF/NO) responses and constitutive nitric oxide synthase (cNOS) activity in subcutaneous vessels dissected from patients with essential hypertension (n = 9) compared with normal controls (n = 10). We now test the hypothesis that the patients in this study have increased circulating levels of the cNOS inhibitor, asymmetric dimethylarginine (ADMA), or the lipid peroxidation product of linoleic acid, 13-hydroxyoctadecadienoic acid (HODE), which is a marker of reactive oxygen species. Patients had significantly (P < 0.001) elevated (means ± SD) plasma levels of ADMA (PADMA, 766 ± 217 vs. 393 ± 57 nmol/l) and symmetric dimethylarginine (PSDMA: 644 ± 140 vs. 399 ± 70 nmol/l) but similar levels of l-arginine accompanied by significantly (P < 0.015) increased rates of renal ADMA excretion (21 ± 9 vs. 14 ± 5 nmol/μmol creatinine) and decreased rates of renal ADMA clearance (18 ± 3 vs. 28 ± 5 ml/min). They had significantly increased plasma levels of HODE (PHODE: 309 ± 30 vs. 226 ± 24 nmol/l) and renal HODE excretion (433 ± 93 vs. 299 ± 67 nmol/μmol creatinine). For the combined group of normal and hypertensive subjects, the individual values for plasma levels of ADMA and HODE were both significantly (P < 0.001) and inversely correlated with microvascular EDRF/NO and positively correlated with mean blood pressure. In conclusion, elevated levels of ADMA and oxidative stress in a group of hypertensive patients could contribute to the associated microvascular endothelial dysfunction and elevated blood pressure.
机译:我们报告从原发性高血压患者(n = 9)与正常对照组(n = 10)相比,皮下血管中内皮源性舒张因子/一氧化氮(EDRF / NO)反应和本构一氧化氮合酶(cNOS)活性受损。现在,我们检验以下假设:本研究中的患者的循环水平升高了cNOS抑制剂,不对称二甲基精氨酸(ADMA)或亚油酸13-羟基十八碳二烯酸(HODE)的脂质过氧化产物,后者是活性氧的标志物种类。患者的ADMA(PADMA,766±217 vs.393±57 nmol / l)和对称二甲基精氨酸(PSDMA:644±140 vs. 399±70 nmol / l)的血浆水平显着(P <0.001)升高(平均值±SD) ),但左旋精氨酸水平相似(P <0.015),肾ADMA排泄率显着提高(21±9 vs.14±5 nmol /μmol肌酐),肾ADMA清除率降低(18±3 vs.28) ±5毫升/分钟)。他们的血浆HODE水平显着升高(PHODE:309±30 vs. 226±24 nmol / l)和肾脏HODE排泄(433±93 vs. 299±67 nmol /μmol肌酐)。对于正常和高血压受试者的组合组,血浆ADMA和HODE的各个值均显着(P <0.001),与微血管EDRF / NO呈负相关,与平均血压呈正相关。总之,一组高血压患者的ADMA水平升高和氧化应激可能导致相关的微血管内皮功能障碍和血压升高。

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