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首页> 外文期刊>Planta medica: Natural products and medicinal plant research >Phenolic Compounds as Arginase Inhibitors: New Insights Regarding Endothelial Dysfunction Treatment
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Phenolic Compounds as Arginase Inhibitors: New Insights Regarding Endothelial Dysfunction Treatment

机译:酚类化合物作为氨基酶抑制剂:关于内皮功能障碍治疗的新见解

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摘要

Endothelial dysfunction is characterised by the low bioavailability of nitric oxide with a relevant negative impact on the nitric oxide/cGMP pathway. The loss of nitric oxide/cGMP signaling may be caused by an increased arginase activity. Plant-derived substances, especially polyphenols, are compounds that have the potential to inhibit arginase activity and they may represent an attractive therapeutic option to combat clinical outcomes related to endothelial dysfunction. An extensive review was carried out using all available data published in English in the Pubmed database, and without restriction regarding the year of publication. Despite the increased number of new substances that have been tested as arginase inhibitors, it is rare to find a compound that satisfies all the toxicological criteria to be used in the development of a new drug. On the other hand, recent data have shown that substances from plants have great potential to be applied as arginase inhibitors, most of which are polyphenols. Of the relevant mechanisms in this process, the inhibition of arginase by natural products seems to act against endothelial dysfunction by reestablishing the vascular function and elevating nitric oxide levels (by increasing the amounts of substrate (L-arginine, and endothelial nitric oxide synthase activation and stabilisation) as well as decreasing the generation of reactive species (formed by uncoupledendothelial nitric oxide synthase). This review summarises several topics regarding arginase inhibition by natural substances as well as indicating this pathway as an emergent strategy to elevate nitric oxide levels in disorders involving endothelial dysfunction. In addition, some aspects regarding structural activity and future perspectives are discussed.
机译:内皮功能障碍的特征在于一氧化氮的低生物利用度,在一氧化氮/ CGMP途径上具有相关的负面影响。一氧化氮/ CGMP信号传导的损失可能是由增加的氨基酶活性引起的。植物衍生的物质,尤其是多酚,是具有抑制杀菌酶活性的潜力的化合物,它们可以代表一种有吸引力的治疗方法,以应对与内皮功能障碍有关的临床结果。使用PubMed数据库中的英语中发布的所有可用数据进行了广泛的审查,但不限于出版年份。尽管已被视为氨基酶抑制剂的新物质数量增加,但是罕见地找到一种满足新药开发中使用的毒理学标准的化合物。另一方面,最近的数据表明,来自植物的物质具有很大的潜力作为氨基酶抑制剂,其中大部分是多酚。在该过程中的相关机制中,通过重新建立血管功能和升高一氧化氮水平来抑制天然产物的氨基酶,似乎采用内皮功能障碍(通过增加底物的量(L-精氨酸和内皮内氧化物合酶活化和稳定化以及减少反应性物质的产生(由未耦合的一氧化氮合酶形成)。本综述总结了天然物质的杀虫酶抑制的若干主题,以及表明该途径作为促进涉及内皮疾病的一氧化氮水平的促进策略功能障碍。此外,还讨论了结构活动和未来观点的一些方面。

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