Papaverine: Difference between revisions

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{{Short description|Chemical compound}}
{{Short description|Chemical compound}}
{{Drugbox
{{Infobox drug
| Verifiedfields = changed
| Verifiedfields = changed
| Watchedfields = changed
| Watchedfields = changed
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| IUPAC_name = 1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxyisoquinoline
| IUPAC_name = 1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxyisoquinoline
| image = Papaverine.svg
| image = Papaverine.svg
| image_class = skin-invert-image
| image2 = Papaverine-from-xtal-3D-balls-B.png
| image2 = Papaverine-from-xtal-3D-balls-B.png
| image_class2 = bg-transparent


<!--Clinical data-->
<!--Clinical data-->| pronounce = {{IPAc-en|p|ə|ˈ|p|æ|v|ər|iː|n}}
| pronounce = {{IPAc-en|p|ə|ˈ|p|æ|v|ər|iː|n}}
| tradename = Pavabid, others
| tradename = Pavabid, others
| Drugs.com = {{drugs.com|monograph|papaverine-hydrochloride}}
| Drugs.com = {{drugs.com|monograph|papaverine-hydrochloride}}
Line 17: Line 18:
| legal_AU = S4
| legal_AU = S4
| legal_US = Rx-only
| legal_US = Rx-only
| routes_of_administration = Oral, [[intravenous]], [[intramuscular]], rectal, [[intracavernosal]]
| routes_of_administration = [[By mouth]], [[intravenous therapy|intravenous]], [[intramuscular injection|intramuscular]], [[rectal administration|rectal]], [[intracavernosal injection|intracavernosal]]


<!--Pharmacokinetic data-->
<!--Pharmacokinetic data-->| bioavailability = 80%
| bioavailability = 80%
| protein_bound = ~90%
| protein_bound = ~90%
| metabolism = [[Hepatic]]
| metabolism = [[Hepatic]]
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| excretion = [[Renal]]
| excretion = [[Renal]]


<!--Identifiers-->
<!--Identifiers-->| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 58-74-2
| CAS_number = 58-74-2
| CAS_supplemental = <br/>61-25-6 (hydrochloride) <!-- Also CAS verified -->
| CAS_supplemental = <br/>61-25-6 (hydrochloride) <!-- Also CAS verified -->
Line 42: Line 41:
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = D07425
| KEGG = D07425
| ChEBI_Ref = {{ebicite|changed|EBI}}  
| ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 28241
| ChEBI = 28241
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 19224
| ChEMBL = 19224


<!--Chemical data-->
<!--Chemical data-->| C = 20
| C=20 | H=21 | N=1 | O=4
| H = 21
| N = 1
| O = 4
| smiles = COc1ccc(cc1OC)Cc2c3cc(c(cc3ccn2)OC)OC
| smiles = COc1ccc(cc1OC)Cc2c3cc(c(cc3ccn2)OC)OC
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
Line 74: Line 75:
Papaverine is also being investigated as a topical growth factor in [[tissue expansion]] with some success.<ref>{{cite journal | vauthors = Tang Y, Luan J, Zhang X | title = Accelerating tissue expansion by application of topical papaverine cream | journal = Plastic and Reconstructive Surgery | volume = 114 | issue = 5 | pages = 1166–1169 | date = October 2004 | pmid = 15457029 | doi = 10.1097/01.PRS.0000135854.48570.76 }}</ref>
Papaverine is also being investigated as a topical growth factor in [[tissue expansion]] with some success.<ref>{{cite journal | vauthors = Tang Y, Luan J, Zhang X | title = Accelerating tissue expansion by application of topical papaverine cream | journal = Plastic and Reconstructive Surgery | volume = 114 | issue = 5 | pages = 1166–1169 | date = October 2004 | pmid = 15457029 | doi = 10.1097/01.PRS.0000135854.48570.76 }}</ref>


Papaverine is used as an [[off-label_use|off-label]] [[prophylaxis]] (preventative) of [[migraine headaches]].<ref>{{cite journal | vauthors = Sillanpää M, Koponen M | title = Papaverine in the prophylaxis of migraine and other vascular headache in children | journal = Acta Paediatrica Scandinavica | volume = 67 | issue = 2 | pages = 209–212 | date = March 1978 | pmid = 343489 | doi = 10.1111/j.1651-2227.1978.tb16304.x | s2cid = 28817628 }}</ref><ref>{{cite journal | vauthors = Vijayan N | title = Brief therapeutic report: papaverine prophylaxis of complicated migraine | journal = Headache | volume = 17 | issue = 4 | pages = 159–162 | date = September 1977 | pmid = 893088 | doi = 10.1111/j.1526-4610.1977.hed1704159.x | s2cid = 36626189 }}</ref><ref>{{cite journal | vauthors = Poser CM | title = Letter: Papaverine in prophylactic treatment of migraine | journal = Lancet | volume = 1 | issue = 7869 | pages = 1290 | date = June 1974 | pmid = 4134173 | doi = 10.1016/S0140-6736(74)90045-2 }}</ref>  It is not a first line drug such as a few [[beta blockers]], [[calcium channel blockers]], [[tricyclic antidepressants]], and some [[anticonvulsants]] such as [[divalproex]], but rather when these first line drugs and secondary drugs such as [[SSRIs]], [[angiotensin II receptor antagonist]]s, etc. fail in the prophylaxis of migraines, have intolerable side effects or are contraindicated.
Papaverine is used as an [[off-label_use|off-label]] [[prophylaxis]] (preventative) of [[migraine headaches]].<ref>{{cite journal | vauthors = Sillanpää M, Koponen M | title = Papaverine in the prophylaxis of migraine and other vascular headache in children | journal = Acta Paediatrica Scandinavica | volume = 67 | issue = 2 | pages = 209–212 | date = March 1978 | pmid = 343489 | doi = 10.1111/j.1651-2227.1978.tb16304.x | s2cid = 28817628 }}</ref><ref>{{cite journal | vauthors = Vijayan N | title = Brief therapeutic report: papaverine prophylaxis of complicated migraine | journal = Headache | volume = 17 | issue = 4 | pages = 159–162 | date = September 1977 | pmid = 893088 | doi = 10.1111/j.1526-4610.1977.hed1704159.x | s2cid = 36626189 }}</ref><ref>{{cite journal | vauthors = Poser CM | title = Letter: Papaverine in prophylactic treatment of migraine | journal = Lancet | volume = 1 | issue = 7869 | page = 1290 | date = June 1974 | pmid = 4134173 | doi = 10.1016/S0140-6736(74)90045-2 }}</ref>  It is not a first line drug such as a few [[beta blockers]], [[calcium channel blockers]], [[tricyclic antidepressants]], and some [[anticonvulsants]] such as [[divalproex]], but rather when these first line drugs and secondary drugs such as [[SSRIs]], [[angiotensin II receptor antagonist]]s, 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 [[papaveretum]] ([[Omnopon]], [[Pantopon]]) and others, along with [[morphine]], [[codeine]], and in some cases [[noscapine]] and others in a percentage similar to that in opium, or modified for a given application.
Papaverine is also present in combinations of opium alkaloid salts such as [[papaveretum]] ([[Omnopon]], [[Pantopon]]) and others, along with [[morphine]], [[codeine]], and in some cases [[noscapine]] and others in a percentage similar to that in opium, or modified for a given application.


Papaverine is found as a contaminant in some [[heroin]]<ref>{{cite journal | vauthors = Paterson S, Cordero R | title = Comparison of the various opiate alkaloid contaminants and their metabolites found in illicit heroin with 6-monoacetyl morphine as indicators of heroin ingestion | journal = Journal of Analytical Toxicology | volume = 30 | issue = 4 | pages = 267–273 | date = May 2006 | pmid = 16803666 | doi = 10.1093/jat/30.4.267 | quote = In addition to morphine, street heroin contains various alkaloids extracted from the opium poppy, Papaversomniferum, including codeine, thebaine, noscapine, and papaverine | doi-access = free }}</ref> and can be used by forensic laboratories in heroin profiling to identify its source.<ref>{{cite journal | vauthors = Seetohul LN, Maskell PD, De Paoli G, Pounder DJ | title = Biomarkers for illicit heroin: a previously unrecognized origin of papaverine | journal = Journal of Analytical Toxicology | volume = 37 | issue = 2 | pages = 133 | date = March 2013 | pmid = 23316026 | doi = 10.1093/jat/bks099 | doi-access = free }}</ref> The metabolites can also be found in the urine of heroin users, allowing street heroin to be distinguished from pharmaceutical [[diacetylmorphine]].<ref>{{cite journal | vauthors = Strang J, Metrebian N, Lintzeris N, Potts L, Carnwath T, Mayet S, Williams H, Zador D, Evers R, Groshkova T, Charles V, Martin A, Forzisi L | display-authors = 6 | title = Supervised injectable heroin or injectable methadone versus optimised oral methadone as treatment for chronic heroin addicts in England after persistent failure in orthodox treatment (RIOTT): a randomised trial | journal = Lancet | volume = 375 | issue = 9729 | pages = 1885–1895 | date = May 2010 | pmid = 20511018 | doi = 10.1016/s0140-6736(10)60349-2 | s2cid = 205958031 }}</ref>
Papaverine is found as a contaminant in some [[heroin]]<ref>{{cite journal | vauthors = Paterson S, Cordero R | title = Comparison of the various opiate alkaloid contaminants and their metabolites found in illicit heroin with 6-monoacetyl morphine as indicators of heroin ingestion | journal = Journal of Analytical Toxicology | volume = 30 | issue = 4 | pages = 267–273 | date = May 2006 | pmid = 16803666 | doi = 10.1093/jat/30.4.267 | quote = In addition to morphine, street heroin contains various alkaloids extracted from the opium poppy, Papaversomniferum, including codeine, thebaine, noscapine, and papaverine | doi-access = free }}</ref> and can be used by forensic laboratories in heroin profiling to identify its source.<ref>{{cite journal | vauthors = Seetohul LN, Maskell PD, De Paoli G, Pounder DJ | title = Biomarkers for illicit heroin: a previously unrecognized origin of papaverine | journal = Journal of Analytical Toxicology | volume = 37 | issue = 2 | page = 133 | date = March 2013 | pmid = 23316026 | doi = 10.1093/jat/bks099 | doi-access = free }}</ref> The metabolites can also be found in the urine of heroin users, allowing street heroin to be distinguished from pharmaceutical [[diacetylmorphine]].<ref>{{cite journal | vauthors = Strang J, Metrebian N, Lintzeris N, Potts L, Carnwath T, Mayet S, Williams H, Zador D, Evers R, Groshkova T, Charles V, Martin A, Forzisi L | display-authors = 6 | title = Supervised injectable heroin or injectable methadone versus optimised oral methadone as treatment for chronic heroin addicts in England after persistent failure in orthodox treatment (RIOTT): a randomised trial | journal = Lancet | volume = 375 | issue = 9729 | pages = 1885–1895 | date = May 2010 | pmid = 20511018 | doi = 10.1016/s0140-6736(10)60349-2 | s2cid = 205958031 }}</ref>


==Mechanism==
==Mechanism==
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Rare side effects include flushing of the face, [[hyperhidrosis]] (excessive sweating), [[drug eruption|cutaneous eruption]], arterial [[hypotension]], [[tachycardia]], loss of appetite, [[jaundice]], [[eosinophilia]], [[thrombopenia]], mixed [[hepatitis]], headache, allergic reaction, chronic active hepatitis, and paradoxical aggravation of cerebral vasospasm.<ref>{{cite journal | vauthors = Clyde BL, Firlik AD, Kaufmann AM, Spearman MP, Yonas H | title = Paradoxical aggravation of vasospasm with papaverine infusion following aneurysmal subarachnoid hemorrhage. Case report | journal = Journal of Neurosurgery | volume = 84 | issue = 4 | pages = 690–695 | date = April 1996 | pmid = 8613866 | doi = 10.3171/jns.1996.84.4.0690 | s2cid = 1172874 }}</ref>
Rare side effects include flushing of the face, [[hyperhidrosis]] (excessive sweating), [[drug eruption|cutaneous eruption]], arterial [[hypotension]], [[tachycardia]], loss of appetite, [[jaundice]], [[eosinophilia]], [[thrombopenia]], mixed [[hepatitis]], headache, allergic reaction, chronic active hepatitis, and paradoxical aggravation of cerebral vasospasm.<ref>{{cite journal | vauthors = Clyde BL, Firlik AD, Kaufmann AM, Spearman MP, Yonas H | title = Paradoxical aggravation of vasospasm with papaverine infusion following aneurysmal subarachnoid hemorrhage. Case report | journal = Journal of Neurosurgery | volume = 84 | issue = 4 | pages = 690–695 | date = April 1996 | pmid = 8613866 | doi = 10.3171/jns.1996.84.4.0690 | s2cid = 1172874 }}</ref>


Papaverine in the plant [[Sauropus androgynus]] is linked to [[bronchiolitis obliterans]].<ref name="pmid26413127">{{cite journal | vauthors = Bunawan H, Bunawan SN, Baharum SN, Noor NM | title = Sauropus androgynus (L.) Merr. Induced Bronchiolitis Obliterans: From Botanical Studies to Toxicology | journal = Evidence-Based Complementary and Alternative Medicine | volume = 2015 | pages = 714158 | year = 2015 | pmid = 26413127 | pmc = 4564651 | doi = 10.1155/2015/714158 | doi-access = free }}</ref>
Papaverine in the plant [[Sauropus androgynus]] is linked to [[bronchiolitis obliterans]].<ref name="pmid26413127">{{cite journal | vauthors = Bunawan H, Bunawan SN, Baharum SN, Noor NM | title = Sauropus androgynus (L.) Merr. Induced Bronchiolitis Obliterans: From Botanical Studies to Toxicology | journal = Evidence-Based Complementary and Alternative Medicine | volume = 2015 | article-number = 714158 | year = 2015 | pmid = 26413127 | pmc = 4564651 | doi = 10.1155/2015/714158 | doi-access = free }}</ref>


== Formulations and trade names==
== Formulations and trade names==
Papaverine is available in its salt form as the [[hydrochloride]], [[pyridoxal phosphate|codecarboxylate]], [[adenosine monophosphate|adenylate]], and teprosylate. It was also once available as a salt of [[hydrobromide]], [[camphorsulfonic acid|camsylate]], cromesilate, [[nicotinic acid|nicotinate]], and [[Mandelic acid|phenylglycolate]]. 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.
Papaverine is available in its salt form as the [[hydrochloride]], [[pyridoxal phosphate|codecarboxylate]], [[adenosine monophosphate|adenylate]], and teprosylate. It was also once available as a salt of [[hydrobromide]], [[camphorsulfonic acid|camsylate]], cromesilate, [[nicotinic acid|nicotinate]], and [[Mandelic acid|phenylglycolate]]. 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,{{cn|date=June 2023}} the adenylate as Dicertan,{{cn|date=June 2023}} 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<ref>{{cite web | url=http://www.reptox.csst.qc.ca/Produit.asp?no_produit=108688&nom=THERAPAV+(PRODUIT+PUR)&incr=0 | title=THERAPAV (PRODUIT PUR) - Détail | access-date=26 September 2005  }} CSST - Service du répertoire toxicologique. (French)</ref>), 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.{{cn|date=June 2023}} In [[Hungary]], papaverine and [[homatropine methylbromide]] are used in mild drugs that help "flush" the [[bile]].<ref>{{cite web|url=http://www.ogyi.hu/drug_database/index.php?action=show_details&item=21736|title=Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézet|website=www.ogyi.hu|access-date=2008-10-14|archive-url=https://web.archive.org/web/20150123100209/http://www.ogyi.hu/drug_database/index.php?action=show_details&item=21736|archive-date=2015-01-23|url-status=dead}}</ref>
The codecarboxylate is sold under the name Albatran,{{cn|date=June 2023}} the adenylate as Dicertan,{{cn|date=June 2023}} 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<ref>{{cite web | url=http://www.reptox.csst.qc.ca/Produit.asp?no_produit=108688&nom=THERAPAV+(PRODUIT+PUR)&incr=0 | title=THERAPAV (PRODUIT PUR) - Détail | access-date=26 September 2005  }} CSST - Service du répertoire toxicologique. (French)</ref>), 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.{{cn|date=June 2023}} In [[Hungary]], papaverine and [[homatropine methylbromide]] are used in mild drugs that help "flush" the [[bile]].<ref>{{cite web|url=http://www.ogyi.hu/drug_database/index.php?action=show_details&item=21736|title=Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézet|website=www.ogyi.hu|access-date=2008-10-14|archive-url=https://web.archive.org/web/20150123100209/http://www.ogyi.hu/drug_database/index.php?action=show_details&item=21736|archive-date=2015-01-23}}</ref>


== References ==
== References ==

Latest revision as of 07:03, 23 December 2025

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| _has_physiological_data= | _has_gene_therapy=

| vaccine_type= | mab_type= | _number_of_combo_chemicals=Script error: No such module "ParameterCount". | _vaccine_data= | _mab_data= | _mab_vaccine_data= | _mab_other_data=202114COc1ccc(cc1OC)Cc2c3cc(c(cc3ccn2)OC)OC1S/C20H21NO4/c1-22-17-6-5-13(10-18(17)23-2)9-16-15-12-20(25-4)19(24-3)11-14(15)7-8-21-16/h5-8,10-12H,9H2,1-4H3XQYZDYMELSJDRZ-UHFFFAOYSA-NTemplate:StdinchiciteTemplate:Stdinchicite | _combo_data= | _physiological_data= | _clinical_data=Template:Drugs.coma682707 ABy mouth, intravenous, intramuscular, rectal, intracavernosalPavabid, othersA03Template:ATC | _legal_data=S4Rx-only

| _other_data=1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxyisoquinoline

| _image_0_or_2 = Papaverine.svgPapaverine-from-xtal-3D-balls-B.png | _image_LR =

| _datapage = Papaverine (data page) | _vaccine_target=_type_not_vaccine | _legal_all=S4Rx-only | _ATC_prefix_supplemental=A03Template:ATC | _has_EMA_link = | CAS_number=58-74-2 | PubChem=4680 | ChemSpiderID=4518 | ChEBI=28241 | ChEMBL=19224 | DrugBank=DB01113 | KEGG=D07425 | _hasInChI_or_Key=yes | UNII=DAA13NKG2Q | _hasJmol02 = |_hasMultipleCASnumbers = |_hasMultiplePubChemCIDs = |_hasMultipleChEBIs =

| _countSecondIDs=Script error: No such module "ParameterCount". | _countIndexlabels=Script error: No such module "ParameterCount". | _trackListSortletter= |QID = |QID2 = |Verifiedfields=changed |Watchedfields=changed |verifiedrevid=464197236}}

Papaverine (Latin papaver, "poppy") is an opium alkaloid antispasmodic drug, used primarily in the treatment of visceral spasms and vasospasms (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 morphine and its derivatives (such as codeine).

In addition to opium, papaverine is purported to be present in high concentrations in star gooseberry.[1]

History

File:Opium pod cut to demonstrate fluid extraction1.jpg
Capsule of Papaver somniferum showing latex (opium) exuding from incision. Papaverine occurs naturally in opium.

Papaverine was discovered in 1848 by Georg Merck (1825–1873).[2] 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 Merck corporation, a major German chemical and pharmaceutical company.[3]

Uses

Papaverine is approved to treat spasms of the gastrointestinal tract, bile ducts and ureter and for use as a cerebral and coronary vasodilator in subarachnoid hemorrhage (combined with balloon angioplasty)[4] and coronary artery bypass surgery.[5] Papaverine may also be used as a smooth muscle relaxant in microsurgery where it is applied directly to blood vessels.

Papaverine is used as an erectile dysfunction drug, alone or sometimes in combination.[6][7] Papaverine, when injected in penile tissue, causes direct smooth muscle relaxation and consequent filling of the corpus cavernosum with blood resulting in erection. A topical gel is also available for ED treatment.[8]

It is also commonly used in cryopreservation of blood vessels along with the other glycosaminoglycans and protein suspensions.[9][10] Functions as a vasodilator during cryopreservation when used in conjunction with verapamil, phentolamine, nifedipine, tolazoline or nitroprusside.[11][12]

Papaverine is also being investigated as a topical growth factor in tissue expansion with some success.[13]

Papaverine is used as an off-label prophylaxis (preventative) of migraine headaches.[14][15][16] It is not a first line drug such as a few beta blockers, calcium channel blockers, tricyclic antidepressants, and some anticonvulsants such as divalproex, but rather when these first line drugs and secondary drugs such as SSRIs, 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 papaveretum (Omnopon, Pantopon) and others, along with morphine, codeine, and in some cases noscapine and others in a percentage similar to that in opium, or modified for a given application.

Papaverine is found as a contaminant in some heroin[17] and can be used by forensic laboratories in heroin profiling to identify its source.[18] The metabolites can also be found in the urine of heroin users, allowing street heroin to be distinguished from pharmaceutical diacetylmorphine.[19]

Mechanism

The in vivo mechanism of action is not entirely clear, but an inhibition of the enzyme phosphodiesterase causing elevation of cyclic AMP and cyclic GMPScript error: No such module "Unsubst". levels is significant. It may also alter mitochondrial respiration.

Papaverine has also been demonstrated to be a selective phosphodiesterase inhibitor for the PDE10A subtype found mainly in the striatum of the brain. When administered chronically to mice, it produced motor and cognitive deficits and increased anxiety, but conversely may produce an antipsychotic effect,[20][21] although not all studies support this view.[22]

Side effects

Frequent side effects of papaverine treatment include polymorphic ventricular tachycardia, constipation, interference with sulphobromophthaleinScript error: No such module "Unsubst". retention test (used to determine hepatic function), increased transaminase levels, increased alkaline phosphatase levels, somnolence, and vertigo.

Rare side effects include flushing of the face, hyperhidrosis (excessive sweating), cutaneous eruption, arterial hypotension, tachycardia, loss of appetite, jaundice, eosinophilia, thrombopenia, mixed hepatitis, headache, allergic reaction, chronic active hepatitis, and paradoxical aggravation of cerebral vasospasm.[23]

Papaverine in the plant Sauropus androgynus is linked to bronchiolitis obliterans.[24]

Formulations and trade names

Papaverine is available in its salt form as the hydrochloride, codecarboxylate, adenylate, and teprosylate. It was also once available as a salt of hydrobromide, camsylate, cromesilate, nicotinate, and phenylglycolate. 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,Script error: No such module "Unsubst". the adenylate as Dicertan,Script error: No such module "Unsubst". 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[25]), 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.Script error: No such module "Unsubst". In Hungary, papaverine and homatropine methylbromide are used in mild drugs that help "flush" the bile.[26]

References

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  13. Script error: No such module "Citation/CS1".
  14. Script error: No such module "Citation/CS1".
  15. Script error: No such module "Citation/CS1".
  16. Script error: No such module "Citation/CS1".
  17. Script error: No such module "Citation/CS1".
  18. Script error: No such module "Citation/CS1".
  19. Script error: No such module "Citation/CS1".
  20. Script error: No such module "Citation/CS1".
  21. Script error: No such module "Citation/CS1".
  22. Script error: No such module "Citation/CS1".
  23. Script error: No such module "Citation/CS1".
  24. Script error: No such module "Citation/CS1".
  25. Script error: No such module "citation/CS1". CSST - Service du répertoire toxicologique. (French)
  26. Script error: No such module "citation/CS1".

Script error: No such module "Check for unknown parameters".

Template:Components of Opium Script error: No such module "Navbox". Template:Drugs for erectile dysfunction and PE Script error: No such module "Navbox".