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Papaverine ( , "poppy") is an drug, used primarily in the treatment of visceral and (especially those involving the intestines, heart, or brain), occasionally in the treatment of erectile dysfunction and acute mesenteric ischemia. While it is found in the opium poppy, papaverine differs in both structure and pharmacological action from the analgesic and its derivatives (such as ).

In addition to opium, papaverine is purported to be present in high concentrations in star gooseberry.


History
Papaverine was discovered in 1848 by Georg Merck (1825–1873). Merck was a student of the German chemists Justus von Liebig and August Hofmann, and he was the son of Emanuel Merck (1794–1855), founder of the corporation, a major German chemical and pharmaceutical company.
(2002). 9780521524735, Cambridge University Press. .


Uses
Papaverine is approved to treat spasms of the gastrointestinal tract, and and for use as a and coronary in subarachnoid hemorrhage (combined with balloon angioplasty) and coronary artery bypass surgery. Papaverine may also be used as a smooth muscle relaxant in where it is applied directly to blood vessels.

Papaverine is used as an erectile dysfunction drug, alone or sometimes in combination. Papaverine, when injected in penile tissue, causes direct relaxation and consequent filling of the corpus cavernosum with blood resulting in . A is also available for ED treatment.

It is also commonly used in of along with the other glycosaminoglycans and protein suspensions. Functions as a during cryopreservation when used in conjunction with , , , or .

Papaverine is also being investigated as a topical growth factor in with some success.

Papaverine is used as an off-label (preventative) of migraine headaches. It is not a first line drug such as a few , calcium channel blockers, tricyclic antidepressants, and some such as , but rather when these first line drugs and secondary drugs such as , angiotensin II receptor antagonists, etc. fail in the prophylaxis of migraines, have intolerable side effects or are contraindicated.

Papaverine is also present in combinations of opium alkaloid salts such as (, ) and others, along with , , and in some cases and others in a percentage similar to that in opium, or modified for a given application.

Papaverine is found as a contaminant in some and can be used by forensic laboratories in heroin profiling to identify its source. The metabolites can also be found in the urine of heroin users, allowing street heroin to be distinguished from pharmaceutical .


Mechanism
The in vivo mechanism of action is not entirely clear, but an inhibition of the phosphodiesterase causing elevation of cyclic AMP and cyclic GMP levels is significant. It may also alter respiration.

Papaverine has also been demonstrated to be a selective phosphodiesterase inhibitor for the PDE10A subtype found mainly in the of the brain. When administered chronically to mice, it produced motor and cognitive deficits and , but conversely may produce an effect, although not all studies support this view.


Side effects
Frequent side effects of papaverine treatment include polymorphic ventricular tachycardia, constipation, interference with sulphobromophthalein retention test (used to determine hepatic function), increased levels, increased alkaline phosphatase levels, , and vertigo.

Rare side effects include flushing of the face, (excessive sweating), , arterial , , loss of appetite, , , , mixed , headache, allergic reaction, chronic active hepatitis, and paradoxical aggravation of cerebral vasospasm.

Papaverine in the plant Sauropus androgynus is linked to bronchiolitis obliterans.


Formulations and trade names
Papaverine is available in its salt form as the , codecarboxylate, adenylate, and teprosylate. It was also once available as a salt of , camsylate, cromesilate, , and . The hydrochloride salt is available for intramuscular, intravenous, rectal and oral administration. The teprosylate is available in intravenous, intramuscular, and orally administered formulations. The codecarboxylate is available in oral form, only, as is the adenylate.

The codecarboxylate is sold under the name Albatran, the adenylate as Dicertan, and the hydrochloride salt is sold variously as Artegodan (Germany), Cardioverina (countries outside Europe and the United States), Dispamil (countries outside Europe and the United States), Opdensit (Germany), Panergon (Germany), Paverina Houde (Italy, Belgium), Pavacap (United States), Pavadyl (United States), Papaverine (Israel), Papaverin-Hamelin (Germany), Paveron (Germany), Spasmo-Nit (Germany), Cardiospan, Papaversan, Cepaverin, Cerespan, Drapavel, Forpaven, Papalease, Pavatest, Paverolan, Therapav (Canada CSST - Service du répertoire toxicologique. (French)), Vasospan, Cerebid, Delapav, Dilaves, Durapav, Dynovas, Optenyl, Pameion, Papacon, Pavabid, Pavacen, Pavakey, Pavased, Pavnell, Alapav, Myobid, Vasal, Pamelon, Pavadel, Pavagen, Ro-Papav, Vaso-Pav, Papanerin-hcl, Qua bid, Papital T.R., Paptial T.R., Pap-Kaps-150. In , papaverine and homatropine methylbromide are used in mild drugs that help "flush" the .

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