Mechanisms of flavonoid protection against myocardial ischemia-reperfusion injury |
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Authors: | Masoumeh Akhlaghi |
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Affiliation: | College of Pharmacy and Nutrition, University of Saskatchewan, Saskatoon, SK, Canada S7N 5C9 |
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Abstract: | Flavonoids have long been acknowledged for their unique antioxidant properties, and possess other activities that may be relevant to heart ischemia-reperfusion. They may prevent production of oxidants (e.g. by inhibition of xanthine oxidase and chelation of transition metals), inhibit oxidants from attacking cellular targets (e.g. by electron donation and scavenging activities), block propagation of oxidative reactions (by chain-breaking antioxidant activity), and reinforce cellular antioxidant capacity (through sparing effects on other antioxidants and inducing expression of endogenous antioxidants). Flavonoids also possess anti-inflammatory and anti-platelet aggregation effects through inhibiting relevant enzymes and signaling pathways, resulting ultimately in lower oxidant production and better re-establishment of blood in the ischemic zone. Finally, flavonoids are vasodilatory through a variety of mechanisms, one of which is likely interaction with ion channels. These multifaceted activities of flavonoids raise their utility as possible therapeutic interventions to ameliorate ischemia-reperfusion injury. |
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Keywords: | AP-1, activator protein-1 eNOS, endothelial nitric oxide synthase ICAM, intercellular adhesion molecules IL, interleukin MMP, matrix metalloproteinases NF-κB, nuclear factor-kappa B NO 0" alt=" radical dot" src=" http://cdn.els-cdn.com/sd/entities/rad" class=" glyphImg" >, nitric oxide NOS, nitric oxide synthase O2 0" alt=" radical dot" src=" http://cdn.els-cdn.com/sd/entities/rad" class=" glyphImg" >&minus , superoxide ROS, reactive oxygen species TNF-α, tumor necrosis factor VCAM, vascular cell adhesion molecules |
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