Key result
Vascular COX-2-derived prostacyclin balances platelet thromboxane to protect against atherothrombosis.
Answers are grounded in this paper and cite their sources.
Prostacyclin (PGI(2)) is one of the important vascular prostanoids, the effects of which counteract those of thromboxane (TXA(2)), and these 2 prostanoids provide an important balance in cardiovascular homeostasis. The clinical experience of COX-2 selective inhibitors having unexpected adverse effects in patients with cardiovascular risk has opened up a debate about the role of COX-2-derived prostanoids in vascular pathophysiology. PGI(2) is a major anti-atherogenic prostanoid produced by COX-2 in vascular cells, including endothelial and vascular smooth muscle cells. The balance between COX-2-derived PGI(2), COX-1-derived TXA(2), and other COX-2-mediated atherogenic prostanoids is a crucial factor in determining pathophysiological outcomes. Recent studies using stable PGI(2) analogs and genetically deficient mice have revealed novel effects of PGI(2) on its target cells, such as endothelial and endothelial progenitor cells. The role PGI(2) in the physiology and pathophysiology of vascular diseases is reviewed and the recent findings linking PGI(2), COX-2 and atherothrombosis are summarized.
No takes yet. Share an insight, caveat, or question.
Kawabe et al. (2010) conducted a review in Vascular diseases and atherothrombosis. Prostacyclin (PGI2) and COX-2 selective inhibitors vs. Thromboxane (TXA2) was evaluated. Prostacyclin (PGI2) produced by COX-2 in vascular cells counteracts COX-1-derived thromboxane (TXA2) to maintain cardiovascular homeostasis and prevent atherothrombosis.
Synapse has enriched 10 related papers. Consider them for comparative context: