Cardiovascular effects of flavonoids are not caused only by direct antioxidant activity
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
20542108
DOI
10.1016/j.freeradbiomed.2010.06.010
PII: S0891-5849(10)00362-X
Knihovny.cz E-resources
- MeSH
- Platelet Activation drug effects MeSH
- Antioxidants pharmacology therapeutic use MeSH
- Cell Adhesion drug effects MeSH
- Enzyme Induction drug effects MeSH
- Flavonoids chemistry pharmacology therapeutic use MeSH
- Cardiovascular Diseases drug therapy physiopathology MeSH
- Humans MeSH
- Vasodilation drug effects MeSH
- Structure-Activity Relationship MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- Antioxidants MeSH
- Flavonoids MeSH
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.
References provided by Crossref.org
Sulfation of Phenolic Acids: Chemoenzymatic vs. Chemical Synthesis
3-Hydroxyphenylacetic Acid: A Blood Pressure-Reducing Flavonoid Metabolite
Inhibitory Effects of Quercetin and Its Human and Microbial Metabolites on Xanthine Oxidase Enzyme