首页> 外文期刊>Free Radical Biology and Medicine: The Official Journal of the Oxygen Society >Cardiovascular effects of flavonoids are not caused only by direct antioxidant activity.
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Cardiovascular effects of flavonoids are not caused only by direct antioxidant activity.

机译:类黄酮的心血管作用不仅由直接的抗氧化剂活性引起。

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摘要

Epidemiological, as well as most in vivo, studies suggest that flavonoids have a positive influence on various cardiovascular diseases. Traditionally, these effects were only attributed to their antioxidant activity, which has been extensively studied. Apart from the direct antioxidant properties, which include direct reactive oxygen species scavenging activity and transient metal chelation, this review reports on many other effects that in pharmacologically achievable concentrations may also be responsible for their positive cardiovascular influence. These include direct inhibition of some radical-forming enzymes (xanthine oxidase, NADPH oxidase, and lipoxygenases), decreased platelet aggregation and leukocyte adhesion, and vasodilatory properties. For each of the aforementioned effects different structural features are necessary. Briefly, a catecholic B-ring is necessary for scavenging activity; hydroxyl groups in an ortho position, the 3-hydroxy-4-keto group, or the 5-hydroxy-4-keto group enable iron chelation; planar conformation with the 4-keto group and 2,3-double bond is essential for inhibition of leukocyte adhesion and platelet aggregation; specific hydroxy-methoxy ortho conformation in ring B is necessary for the inhibition of NADPH oxidase; and the 4-keto group is a requisite for vasodilatory action. This review shows that positive cardiovascular effects of flavonoids are achieved by various flavonoids via the interaction with different targets.
机译:流行病学以及大多数体内研究表明,类黄酮对各种心血管疾病具有积极影响。传统上,这些作用仅归因于其抗氧化活性,对此已进行了广泛研究。除了直接的抗氧化剂特性(包括直接的活性氧清除能力和短暂的金属螯合)外,本综述还报告了许多其他影响,即药理学上可达到的浓度也可能对其积极的心血管影响负责。这些措施包括直接抑制某些自由基形成酶(黄嘌呤氧化酶,NADPH氧化酶和脂氧合酶),减少的血小板聚集和白细胞粘附以及血管舒张特性。对于每个上述效果,需要不同的结构特征。简而言之,要清除活性,必须要有一个蜡烛形的B环。在邻位的羟基,3-羟基-4-酮基或5-羟基-4-酮基使铁螯合;具有4-酮基和2,3-双键的平面构象对于抑制白细胞粘附和血小板聚集至关重要。 B环中特定的羟基-甲氧基邻位构象对于抑制NADPH氧化酶是必需的;而4-酮基是血管舒张作用的必要条件。该综述表明,通过与不同靶标的相互作用,各种类黄酮可实现类黄酮的积极心血管作用。

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