首页> 外文期刊>Molecular pharmacology. >Modulation of expression of endothelial nitric oxide synthase by nordihydroguaiaretic acid, a phenolic antioxidant in cultured endothelial cells.
【24h】

Modulation of expression of endothelial nitric oxide synthase by nordihydroguaiaretic acid, a phenolic antioxidant in cultured endothelial cells.

机译:去甲二氢愈创木酸,一种酚类抗氧化剂,在培养的内皮细胞中对内皮型一氧化氮合酶表达的调节。

获取原文
获取原文并翻译 | 示例

摘要

Retrospective epidemiological studies have suggested that antioxidant therapy may decrease cardiovascular morbidity and mortality rates, although the mechanisms for this effect remain unclear. In the present study, we demonstrate that selective antioxidants can enhance expression of endothelial nitric oxide synthase (eNOS). We found that the antioxidants nordihydroguaiaretic acid (NDGA), catechol, glutaryl probucol, and N-acetylcysteine increased eNOS expression in cultured bovine aortic endothelial cells (BAECs). NDGA seemed to be the most potent of the phenolic antioxidants, producing a 3-fold increase in eNOS mRNA. This effect of NDGA was enhanced by nonphenolic antioxidants such as N-acetylcysteine and ascorbic acid. Nuclear run-on studies indicated that NDGA increased eNOS transcription. A similar increase in eNOS protein content was observed with Western blot analysis after treating BAECs or human aortic endothelial cells with NDGA. Exposure of BAECs to NDGA enhanced NO production, as measured by electron paramagnetic resonance spin trapping and eNOS activity, as measured by [14C]arginine-to-[14C]citrulline assay. Methylation of the phenolic hydroxyl groups completely inhibited the NDGA effect on eNOS mRNA levels. This effect of NDGA was not due to inhibition of lipoxygenase because cis-5,8,11,14-eicosatetraynoic acid did not alter eNOS expression. We conclude that antioxidants may not only increase the bioactivity of nitric oxide but also enhance expression of the eNOS enzyme. Such an effect may prove useful in conditions such as hypertension and atherosclerosis, in which nitric oxide production and/or biological activity is impaired.
机译:回顾性流行病学研究表明,抗氧化剂治疗可能会降低心血管疾病的发病率和死亡率,尽管这种作用的机制尚不清楚。在本研究中,我们证明了选择性抗氧化剂可以增强内皮型一氧化氮合酶(eNOS)的表达。我们发现抗氧化剂nordihydroguaiaretic酸(NDGA),儿茶酚,戊二酰普罗布考和N-乙酰半胱氨酸增加了培养的牛主动脉内皮细胞(BAECs)中的eNOS表达。 NDGA似乎是最有效的酚类抗氧化剂,可使eNOS mRNA增加3倍。非酚类抗氧化剂(例如N-乙酰半胱氨酸和抗坏血酸)增强了NDGA的这种作用。核试验研究表明,NDGA可增加eNOS转录。用NDGA处理BAEC或人主动脉内皮细胞后,用Western blot分析观察到eNOS蛋白含量有类似的增加。通过电子顺磁共振自旋阱测量和通过[14C]精氨酸对[14C]瓜氨酸测定法测量的eNOS活性,将BAEC暴露于NDGA会增强NO的产生。酚羟基的甲基化完全抑制了NDGA对eNOS mRNA水平的影响。 NDGA的这种作用不是由于抑制脂加氧酶,因为顺式5、8、11、14-二十碳四丁酸不会改变eNOS的表达。我们得出的结论是,抗氧化剂不仅可以增加一氧化氮的生物活性,而且可以增强eNOS酶的表达。在诸如高血压和动脉粥样硬化的情况下,一氧化氮的产生和/或生物活性受到损害,这种作用可能被证明是有用的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号