From Wikipedia, the free encyclopedia
Synthetic prostaglandin analogues are molecules which are manufactured to bind to a prostaglandin receptor.
Wider use of prostaglandin analogues is limited by unwanted side effects and their abortive potential.
- Prostaglandin analogues can also be used in the management of open-angle glaucoma. They reduce intra-ocular pressure by enhancing uveoscleral outflow and may also have some effect on the trabecular meshwork as well. Latanoprost, travoprost, unoprostone and bimatoprost are examples of prostaglandin analogues used in the management of open-angle glaucoma. In some countries such as Australia, they are now considered first line agents in open-angle glaucoma (rather than beta blockers)[1]
[edit] References
- ^ AMH 2008: Australian Medicines Handbook, 9th Edition Adelaide, S. Aust. : Australian Medicines Handbook, c2008.,
[edit] External links
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Antithrombotics (thrombolytics, anticoagulants and antiplatelet drugs) (B01) |
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Prostaglandin analogue ( PGI2)
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bronchoconstriction ( PGF2α, TXA2, LTC4, LTD4, LTE4)
vasoconstriction (PGF2α, TXA2, TXB2) · vasodilation (PGE2, PGI2, LTC4, LTD4, LTE4)
platelets: induce (TXA2) inhibit (PGD2, PGI2) · leukocytes: induce (TXA2, LTB4) inhibit (PGD2, PGE2)
labor stimulation: ( PGE2 (Dinoprostone), PGF2α (Dinoprost))
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