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Am J Physiol Renal Physiol 289: F235-F246, 2005; doi:10.1152/ajprenal.00454.2004
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INVITED REVIEW

Prostacyclin signaling in the kidney: implications for health and disease

Rania Nasrallah and Richard L. Hébert

Department of Cellular and Molecular Medicine and Kidney Research Centre, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada

The balance between vasodilator and vasoconstrictor pathways is key to the maintenance of homeostasis and the outcome of disease. In the kidney, prostaglandins (PGs) uphold this balance and regulate renal function: hemodynamics, renin secretion, growth responses, tubular transport processes, and cell fate. With the advent of cyclooxygenase (COX)-2-selective inhibitors, targeted deletions in mice (COX knockouts, PG receptor knockouts), and the discovery of intracrine signaling options for PGs (peroxisome proliferator-activated receptors and perinuclear PGE2 receptors: EP1,3,4), many advances have been made in the study of arachidonic acid metabolites. Although prostacyclin (PGI2) is a major product of the COX pathway, there is very little emphasis on its importance to the kidney. This review will discuss PGI2 biology and its relevance to different aspects of renal disease (growth, fibrosis, apoptosis), highlighting the most significant research from the past decade of PGI2 literature, what we have learned from other organ systems, while stressing the significance of cross talk between various PGI2 signaling pathways and its implications for renal health and disease.

prostaglandin I2; IP receptors; peroxisome proliferator-activated receptor-{delta}



Address for reprint requests and other correspondence: R. L. Hébert, Dept. of Cellular and Molecular Medicine, Kidney Research Ctr., Faculty of Medicine, Univ. of Ottawa, 451 Smyth Rd., Rm. 1337, Ottawa, ON, Canada K1H 8M5 (E-mail: rlhebert{at}uottawa.ca)




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