Information About

Prostacyclin







Prostacyclin is a member of the family of Lipid Molecule s known as Eicosanoids . When given as a drug it is known as '''epoprostenol'''. (Dorlands)  It is produced in Endothelial Cell s from Prostaglandin H2 (PGH2) by the action of the Enzyme Prostacyclin Synthase . Although prostacyclin is considered an independent mediator, it is called '''PGI2''' (prostaglandin I2) in eicosanoid nomenclature, and is a member of the Prostanoid s (together with the Prostaglandin s and Thromboxane ).

The series-3 prostaglandin PGH3 also follows the prostacyclin synthase pathway, yeilding another prostacyclin, PGI3.(Fischer, 1985)  The unqualified term 'prostacyclin' usually refers to PGI2. PGI2 is derived from the ω-6 Arachidonic Acid . PGI3 is derived from the ω-3 EPA .


MODE OF ACTION

Prostacyclin acts chiefly to prevent Platelet formation and clumping involved in Blood Clot ting. It is also an effective Vasodilator . Prostacyclin's interactions in contrast to Thromboxane , another eicosanoid, strongly suggest a mechanism of cardiovascular Homeostasis between the two hormones in relation to Vascular damage.


PHARMACOLOGY

Synthetic prostacyclin analogues ( Iloprost , cisaprost) are used intravenously, subcutaneously or by inhalation:

Its production is inhibited indirectly by NSAIDs , which inhibit the Cyclooxygenase enzymes COX1 and COX2. These convert arachidonic acid to PGH2, the immediate precursor of prostacyclin.


REFERENCES




SEE ALSO

Essential Fatty Acid