 | |
 | |
| Clinical data | |
|---|---|
| Trade names | Flolan, Veletri |
| AHFS/Drugs.com | Monograph |
| License data | |
| Pregnancy category |
|
| ATC code | |
| Legal status | |
| Legal status | |
| Pharmacokinetic data | |
| Eliminationhalf-life | 42 seconds |
| Identifiers | |
| |
| CAS Number | |
| PubChemCID | |
| IUPHAR/BPS | |
| DrugBank |
|
| ChemSpider |
|
| UNII | |
| KEGG | |
| ChEMBL | |
| CompTox Dashboard(EPA) | |
| Chemical and physical data | |
| Formula | C20H32O5 |
| Molar mass | 352.471 g·mol−1 |
| 3D model (JSmol) | |
| |
| |
 N Y (what is this?) (verify) | |
Prostacyclin (also calledprostaglandin I2 orPGI2) is aprostaglandin member of theeicosanoid family oflipidmolecules. It inhibits platelet activation and is also an effective vasodilator.
When used as a drug, it is also known asepoprostenol.[1] The terms are sometimes used interchangeably.[2]
Prostacyclin chiefly prevents formation of theplatelet plug involved in primaryhemostasis (a part ofblood clot formation). It does this by inhibiting platelet activation.[3] It is also an effectivevasodilator. Prostacyclin's interactions contrast with those ofthromboxane (TXA2), another eicosanoid. Both molecules are derived fromarachidonic acid, and work together with opposite platelet aggregatory effects. These strongly suggest a mechanism of cardiovascularhomeostasis between these two hormones in relation tovascular damage.
It is used to treatpulmonary arterial hypertension (PAH),[4][5][6]pulmonary fibrosis,[7] as well asatherosclerosis.[7] Prostacyclins are given to people with class III or class IV PAH.[8]
Prostacyclin, which has ahalf-life of 42 seconds,[9] is broken down into 6-keto-PGF1, which is a much weaker vasodilator. A way to stabilize prostacyclin in its active form, especially during drug delivery, is to prepare prostacyclin in alkaline buffer. Even at physiological pH, prostacyclin can rapidly form the inactive hydration product6-keto-prostaglandin F1α.[10]
| Prostacyclin effect | Mechanism | Cellular response | |
|---|---|---|---|
| Classical functions | Vessel tone | ↑cAMP, ↓ET-1 ↓Ca2+, ↑K+ | ↓SMC proliferation ↑Vasodilation |
| Antiproliferative | ↑cAMP ↑PPARgamma | ↓Fibroblast growth ↑Apoptosis | |
| Antithrombotic | ↓Thromboxane-A2 ↓PDGF | ↓Platelet aggregation ↓Platelet adherence to vessel wall | |
| Novel functions | Antiinflammatory | ↓IL-1, IL-6 ↑IL-10 | ↓Proinflammatory cytokines ↑Antiinflammatory cytokines |
| Antimitogenic | ↓VEGF ↓TGF-β | ↓Angiogenesis ↑ECM remodeling | |
As mentioned above, prostacyclin (PGI2) is released by healthy endothelial cells and performs its function through aparacrine signaling cascade that involvesG protein-coupled receptors on nearby platelets and endothelial cells. The platelet Gs protein-coupled receptor (prostacyclin receptor) is activated when it binds to PGI2. This activation, in turn, signals adenylyl cyclase to producecAMP. cAMP goes on to inhibit any undue platelet activation (in order to promote circulation) and also counteracts any increase in cytosolic calcium levels that would result fromthromboxane A2 (TXA2) binding (leading to platelet activation and subsequentcoagulation). PGI2 also binds to endothelialprostacyclin receptors, and in the same manner, raises cAMP levels in the cytosol. This cAMP then goes on to activateprotein kinase A (PKA). PKA then continues the cascade by promoting the phosphorylation of themyosin light chain kinase, which inhibits it and leads tosmooth muscle relaxation andvasodilation. It can be noted that PGI2 and TXA2 work as physiological antagonists.
| PROSTACYCLINS[11] | |||
|---|---|---|---|
| Flolan (epoprostenol sodium) for Injection | Continuously infused | 2 ng/kg/min to start, increased by 2 ng/kg/min every 15 minutes or longer until suitable efficacy/tolerability balance is achieved | Class III Class IV |
| Veletri (epoprostenol) for Injection | Continuously infused | 2 ng/kg/min to start, increased by 2 ng/kg/min every 15 minutes or longer until suitable efficacy/tolerability balance is achieved | Class III Class IV |
| Remodulin SC§ (treprostinil sodium) Injection | Continuously infused | 1.25 ng/kg/min to start, increased by up to 1.25 ng/kg/min per week for 4 weeks, then up to 2.5 ng/kg/min per week until suitable efficacy/tolerability balance is achieved | Class II Class III Class IV |
| Ventavis (iloprost) Inhalation Solution | Inhaled 6–9 times daily | 2.5 μg 6–9 times daily to start, increased to 5.0 μg 6–9 times daily if well tolerated | Class III Class IV |
Synthetic prostacyclin analogues (iloprost, cisaprost) are used intravenously, subcutaneously or by inhalation:
The production of prostacyclin is inhibited by the action ofNSAIDs oncyclooxygenase enzymes COX1 and COX2. These convertarachidonic acid toprostaglandin H2 (PGH2), the immediate precursor of prostacyclin. Since thromboxane (aneicosanoid stimulator of platelet aggregation) is also downstream of COX enzymes, one might think that the effect of NSAIDs would act to balance. However, prostacyclin concentrations recover much faster than thromboxane levels, so aspirin administration initially has little to no effect but eventually prevents platelet aggregation (the effect of prostaglandins predominates as they are regenerated). This is explained by understanding the cells that produce each molecule, TXA2 and PGI2. Since PGI2 is primarily produced in a nucleated endothelial cell, the COX inhibition by NSAID can be overcome with time by increased COX gene activation and subsequent production of more COX enzymes tocatalyze the formation of PGI2. In contrast, TXA2 is released primarily by anucleated platelets, which are unable to respond to NSAID COX inhibition with additionaltranscription of the COX gene because they lackDNA material necessary to perform such a task. This allows NSAIDs to result in PGI2 dominance that promotes circulation and retardsthrombosis.
In patients withpulmonary hypertension, inhaled epoprostenol reduces pulmonary pressure, and improves right ventricularstroke volume in patients undergoing cardiac surgery. A dose of 60 μg is hemodynamically safe, and its effect is completely reversed after 25 minutes. No evidence ofplatelet dysfunction or an increase in surgical bleeding after administration of inhaled epoprostenol has been found.[12] The drug has been known to cause flushing, headaches and hypotension.[13]
Prostacyclin is produced inendothelialcells, which line the walls of arteries and veins,[14] fromprostaglandin H2 (PGH2) by the action of theenzymeprostacyclin synthase. Although prostacyclin is considered an independent mediator, it is calledPGI2 (prostaglandin I2) in eicosanoid nomenclature, and is a member of theprostanoids (together with theprostaglandins andthromboxane). PGI2, derived primarily from COX-2 in humans, is the major arachidonate metabolite released from the vascular endothelium. This is a controversial point, some assign COX 1 as the major prostacyclin producing cyclooxygenase in the endothelial cells of the blood vessels.[15]
The series-3 prostaglandin PGH3 also follows the prostacyclin synthase pathway, yielding another prostacyclin,PGI3.[16] The unqualified term 'prostacyclin' usually refers to PGI2. PGI2 is derived from the ω-6arachidonic acid. PGI3 is derived from the ω-3EPA.
Prostacyclin can besynthesized from themethylester ofprostaglandin F2α.[17] After its synthesis, the drug is reconstituted in saline and glycerin.[18]
Because prostacyclin is so chemically labile, quantitation of their inactive metabolites, rather than the active compounds, is used to assess their rate of synthesis.[19]
During the 1960s, a UK research team, headed by ProfessorJohn Vane, began to explore the role ofprostaglandins in anaphylaxis and respiratory diseases. Working with a team from theRoyal College of Surgeons, Vane discovered that aspirin and other oral anti-inflammatory drugs work by inhibiting the synthesis of prostaglandins. This critical finding opened the door to a broader understanding of the role of prostaglandins in the body.
A team at The Wellcome Foundation led by Salvador Moncada had identified a lipid mediator they called "PG-X," which inhibits platelet aggregation. PG-X, later known as prostacyclin, is 30 times more potent than any other then-known anti-aggregatory agent. They did this while searching for an enzyme that generates a fellow unstable prostanoid,Thromboxane A2[20]
In 1976, Vane and fellow researchersSalvador Moncada,Ryszard Gryglewski, andStuart Bunting published the first paper on prostacyclin inNature.[21] The collaboration produced a synthesized molecule, which was named epoprostenol. But, as with native prostacyclin, the epoprostenol molecule is unstable in solution and prone to rapid degradation.[citation needed] This presented a challenge for both in vitro experiments and clinical applications.
To overcome this challenge, the research team that discovered prostacyclin continued the research. The research team synthesized nearly 1,000 analogues.[citation needed]
| Subsidiaries |
| ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Predecessors, acquisitions | |||||||||
| Products |
| ||||||||
| People |
| ||||||||
| Litigation | |||||||||
| Other | |||||||||
