Nox-2 up-regulation and platelet activation: Novel insights

• Platelet Nox-related O2− formation enhances platelet activation and aggregation.
• Nox2 activation has a major role in the formation of platelet 8-iso-PGF2α.
• Nox2 is up-regulated in patients with atherosclerotic diseases.
• Atorvastatin reduces Nox2 activation and 8-iso-PGF2α formation.
• Extra virgin olive oil blunts post-prandial Nox2-related oxidative stress.

Platelet activation is a key step in the onset of cardiovascular complications in patients affected by systemic atherosclerosis. Among other mechanisms, oxidative stress seems to play a crucial role in platelet activation. Reactive Oxidant Species (ROS) including O2−, OH− or H2O2 act as second messenger to activate platelets via (1) calcium mobilization, (2) nitric oxide inactivation and (3) through the interaction with arachidonic acid to give formation of isoprostanes. One important source of ROS is represented by platelet NADPH oxidase. Growing data from experimental and clinical studies provide evidence that Nox2, the catalytic core of the NADPH oxidase system, is implicated in platelet activation. Accordingly, an impaired platelet activation has been described in patients with genetically determined Nox2 deficiency. Moreover, platelets added with specific inhibitors of Nox2 revealed impaired platelet activation, along with ROS down-production. Similar results were seen in animals treated with apocynin, a Nox inhibitor, showed reduced platelet adhesion and atherosclerotic plaque. A significant association between Nox2 and platelet activation has been detected in patients with atherosclerotic diseases. The observed up-regulation of Nox2 with subsequent isoprostanes over-production in patients with cardiovascular diseases suggests the need to explore the potential benefit of targeting Nox2 as part of a holist anti-atherothrombotic strategy in patients with systemic atherosclerosis.