Biology:Para-Methoxyamphetamine

From HandWiki
Revision as of 08:59, 9 March 2024 by Carolyn (talk | contribs) (url)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Short description: Chemical compound


para-Methoxyamphetamine
PMA.svg
4-Methoxyamphetamine molecule ball.png
Clinical data
Trade namesDr.Death
Routes of
administration		Oral
ATC code
  • none
Legal status
Legal status
Identifiers
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
Chemical and physical data
FormulaC10H15NO
Molar mass165.236 g·mol−1
3D model (JSmol)
 ☒N☑Y (what is this?)  (verify)

para-Methoxyamphetamine (PMA), also known as 4-methoxyamphetamine (4-MA), is a designer drug of the amphetamine class with serotonergic effects.[1][2][3] Unlike other similar drugs of this family, PMA does not produce stimulant, euphoriant, or entactogen effects,[4] and behaves more like an antidepressant in comparison,[5] though it does have some psychedelic properties.[6][7]

PMA has been found in tablets touted as MDMA (ecstasy)[8][9][10][11] although its effects are markedly different compared to those of MDMA. The consequences of such deception have often included hospitalization and death for unwitting users. PMA is commonly synthesized from anethole, the flavor compound of anise and fennel, mainly because the starting material for MDMA, safrole, has become less available due to law enforcement action, causing illicit drug manufacturers to use anethole as an alternative.[12]

Adverse effects

PMA has been associated with numerous adverse reactions including death.[13][14] Effects of PMA ingestion include many effects of the hallucinogenic amphetamines including accelerated and irregular heartbeat, blurred vision, and a strong feeling of intoxication that is often unpleasant. At high doses unpleasant effects such as nausea and vomiting, severe hyperthermia and hallucinations may occur. The effects of PMA also seem to be much more unpredictable and variable between individuals than those of MDMA, and sensitive individuals may die from a dose of PMA by which a less susceptible person might only be mildly affected.[15] While PMA alone may cause significant toxicity, the combination of PMA with MDMA has a synergistic effect that seems to be particularly hazardous.[16] Since PMA has a slow onset of effects, several deaths have occurred where individuals have taken a pill containing PMA, followed by a pill containing MDMA some time afterwards due to thinking that the first pill was not active.[17]

Overdose

PMA overdose can be a serious medical emergency that may occur at only slightly above the usual recreational dose range, especially if PMA is mixed with other stimulant drugs such as cocaine or MDMA. Characteristic symptoms are pronounced hyperthermia, tachycardia, and hypertension, along with agitation, confusion, and convulsions. PMA overdose also tends to cause hypoglycaemia and hyperkalaemia, which can help to distinguish it from MDMA overdose. Complications can sometimes include more serious symptoms such as rhabdomyolysis and cerebral hemorrhage, requiring emergency surgery. There is no specific antidote, so treatment is symptomatic, and usually includes both external cooling, and internal cooling via IV infusion of cooled saline. Benzodiazepines are used initially to control convulsions, with stronger anticonvulsants such as phenytoin or thiopental used if convulsions continue. Blood pressure can be lowered either with a combination of alpha blockers and beta blockers (or a mixed alpha/beta blocker), or with other drugs such as nifedipine or nitroprusside. Serotonin antagonists and dantrolene may be used as required. Despite the seriousness of the condition, the majority of patients survive if treatment is given in time, however, patients with a core body temperature over 40 °C at presentation tend to have a poor prognosis.[18]

Pharmacology

PMA acts as a selective serotonin releasing agent (SSRA) with weak effects on dopamine and norepinephrine transporters.[19][20][21] However, relative to MDMA, it is considerably less effective as a releaser of serotonin with properties more akin to a reuptake inhibitor in comparison.[22] It evokes robust hyperthermia in rodents while producing only modest hyperactivity and serotonergic neurotoxicity, substantially lower than that caused by MDMA, and only at very high doses.[20][21][22] Accordingly, it is not self-administered by rodents unlike amphetamine and MDMA,[4] and anecdotal reports by humans suggest it is not particularly euphoric at all, perhaps even dysphoric in contrast.[citation needed] PMA has also been shown to act as a potent, reversible inhibitor of the enzyme MAO-A with no significant effects on MAO-B,[23][24] and the combination of this property and serotonin release is likely responsible for its high lethality potential.[22]

It appears that PMA elevates body temperatures dramatically; the cause of this property is suspected to be related to its ability to inhibit MAO-A and at the same time releasing large amounts of serotonin, effectively causing serotonin syndrome.[22][24] Amphetamines, especially serotonergic analogues such as MDMA, are strongly contraindicated to take with MAOIs. Many amphetamines and adrenergic compounds raise body temperatures, whereas some tend to produce more euphoric activity or peripheral vasoconstriction, and may tend to favor one effect over another. It appears that PMA activates the hypothalamus much more strongly than MDMA and other drugs like ephedrine, thereby causing rapid increases in body temperature (which is the major cause of death in PMA mortalities).[25][26][27] Many people taking PMA try to get rid of the heat by taking off their clothes, taking cold showers or wrapping themselves in wet towels, and even sometimes by shaving off their hair.[28]

History

PMA first came into circulation in the early 1970s, where it was used intentionally as a substitute for the hallucinogenic properties of LSD.[2] It went by the street names of "Chicken Powder" and "Chicken Yellow" and was found to be the cause of a number of drug overdose deaths (the dosages taken being in the range of hundreds of milligrams) in the United States and Canada from that time.[29] Between 1974 and the mid-1990s, there appear to have been no known fatalities from PMA.[30]

Several deaths reported as MDMA-induced in Australia in the mid-1990s are now considered to have been caused by PMA, the users unaware that they were ingesting PMA and not MDMA as they had intended.[11] There have been a number of PMA-induced deaths around the world since then.[31][32]

In July 2013, seven deaths in Scotland were linked to tablets containing PMA that had been mis-sold as ecstasy and which had the Rolex crown logo on them.[9] Several deaths in Northern Ireland, Particularly East Belfast were also linked to "Green Rolex" pills during that month.[33]

In 2014, 2015 and early 2016, PMA sold as ecstasy was attributed for more deaths in the United States, United Kingdom, Netherlands, and Argentina. The pills containing the drug were reported to be red triangular tablets with a "Superman" logo.[10][34][35][36]

The Red Ferarri pills are a new press of the Superman logo tablets that were reported to be found in Germany and Norway from 2016 to 2017.[37]

Society and culture

Legal status

International

PMA is a Schedule I drug under the Convention on Psychotropic Substances.[38]

Australia

PMA is considered a Schedule 9 prohibited substance in Australia under the Poisons Standard (October 2015).[39] A Schedule 9 substance is a substance which may be abused or misused, the manufacture, possession, sale or use of which should be prohibited by law except when required for medical or scientific research, or for analytical, teaching or training purposes with approval of Commonwealth and/or State or Territory Health Authorities.[39]

Finland

Substance is scheduled in decree of the government on amending the government decree on substances, preparations and plants considered to be narcotic drugs.[40][41]

Germany

PMA is part of the Appendix 1 of the Betäubungsmittelgesetz. Therefore, owning and distribution of PMA is illegal.

Netherlands

On 13 June 2012 Edith Schippers, Dutch Minister of Health, Welfare and Sport, revoked the legality of PMA in the Netherlands after five deaths were reported in that year.[42]

United Kingdom

PMA is a Class A drug in the UK.[citation needed]

United States

PMA is classified as a Schedule I hallucinogen under the Controlled Substances Act in the United States .[43]

Economics

Distribution

Because PMA is given out through the same venues and distribution channels that MDMA tablets are, the risk of being severely injured, hospitalized or even dying from use of ecstasy increases significantly when a batch of ecstasy pills containing PMA starts to be sold in a particular area.[44] PMA pills could be a variety of colours or imprints, and there is no way of knowing just from the appearance of a pill what drug(s) it might contain.[45][46] Notable batches of pills containing PMA have included Louis Vuitton,[47] Mitsubishi Turbo, Blue Transformers, Red/Blue Mitsubishi and Yellow Euro pills. Also PMA has been found in powder form.[48]

Analogues

Four analogues of PMA have been reported to be sold on the black market, including PMMA, PMEA,[49] 4-ETA and 4-MTA. These are the N-methyl, N-ethyl, 4-ethoxy and 4-methylthio analogues of PMA, respectively. PMMA and PMEA are anecdotally weaker, more "ecstasy-like" and somewhat less dangerous than PMA itself, but can still produce nausea and hyperthermia similar to that produced by PMA, albeit at slightly higher doses. 4-EtOA was briefly sold in Canada in the 1970s, but little is known about it.[2] 4-MTA, however, is even more dangerous than PMA and produces strong serotonergic effects and intense hyperthermia, but with little to no euphoria, and was implicated in several deaths in the late 1990s.

See also

References

  1. ↑ Drug Enforcement Administration October 2000. The Hallucinogen PMA: Dancing With Death
  2. ↑ 2.0 2.1 2.2 "#97 4-MA". Pihkal: A Chemical Love Story. Transform Press. 1991. ISBN 978-0-9630096-0-9. http://www.erowid.org/library/books_online/pihkal/pihkal097.shtml. 
  3. ↑ "Warning of possible shift to killer drug". Sydney Morning Herald (Fairfax). 7 April 2008. http://news.smh.com.au/national/warning-of-possible-shift-to-killer-drug-20080407-2482.html. 
  4. ↑ 4.0 4.1 "The reinforcing and discriminative stimulus properties of para-ethoxy- and para-methoxyamphetamine". Pharmacology, Biochemistry, and Behavior 41 (1): 165–169. January 1992. doi:10.1016/0091-3057(92)90077-S. PMID 1539067. 
  5. ↑ "Paramethoxymethamphetamine (Mitsubishi turbo) abuse: Case report and literature review". European Psychiatry 41 (S1): s875. April 2017. doi:10.1016/j.eurpsy.2017.01.1762. 
  6. ↑ "Comparative behavioural and neurochemical studies with a psychomotor stimulant, an hallucinogen and 3,4-methylenedioxy analogues of amphetamine". Psychopharmacology 118 (3): 295–304. April 1995. doi:10.1007/BF02245958. PMID 7617822. 
  7. ↑ "The stimulus properties of para-methoxyamphetamine: a nonessential serotonergic component". Pharmacology, Biochemistry, and Behavior 20 (2): 201–203. February 1984. doi:10.1016/0091-3057(84)90242-9. PMID 6546992. 
  8. ↑ "EcstasyData.org: Results : Lab Test Results for Recreational Drugs". https://www.ecstasydata.org/results.php?start=0&search_field=all&s=pma. 
  9. ↑ 9.0 9.1 "Warning over fake ecstasy tablets after seven people die in Scotland". The Guardian. 10 July 2013. https://www.theguardian.com/society/2013/jul/10/fake-ecstasy-warning-die-scotland. 
  10. ↑ 10.0 10.1 "Four Dead Amid Fears Of Dodgy Batch Of 'Superman' Ecstasy Hitting The UK". HuffPost UK. 2 January 2015. https://www.huffingtonpost.co.uk/2015/01/02/pmma-pma-bad-batch-mdma_n_6405956.html. 
  11. ↑ 11.0 11.1 "Amphetamine derivative fatalities in South Australia--is "Ecstasy" the culprit?". The American Journal of Forensic Medicine and Pathology 19 (3): 261–265. September 1998. doi:10.1097/00000433-199809000-00013. PMID 9760094. 
  12. ↑ "Anise oil as para-methoxyamphetamine (PMA) precursor". Forensic Science International 133 (1–2): 159–170. April 2003. doi:10.1016/S0379-0738(03)00063-X. PMID 12742705. 
  13. ↑ "Three cases of fatal paramethoxyamphetamine overdose". Journal of Analytical Toxicology 25 (7): 649–651. October 2001. doi:10.1093/jat/25.7.649. PMID 11599618. 
  14. ↑ "A fatal paramethoxymethamphetamine intoxication". Legal Medicine 5 (Suppl 1): S138–S141. March 2003. doi:10.1016/s1344-6223(02)00096-2. PMID 12935573. 
  15. ↑ "Amphetamine toxicity in the emergency department". European Journal of Emergency Medicine 12 (4): 193–197. August 2005. doi:10.1097/00063110-200508000-00010. PMID 16034267. 
  16. ↑ "The designer drug situation in Ibiza". Forensic Science International 140 (2–3): 195–206. March 2004. doi:10.1016/j.forsciint.2003.11.021. PMID 15036441. 
  17. ↑ "Fatality due to combined use of the designer drugs MDMA and PMA: a distribution study". Journal of Analytical Toxicology 27 (5): 318–322. 1 July 2003. doi:10.1093/jat/27.5.318. PMID 12908947. 
  18. ↑ "Dancing with "death": p-methoxyamphetamine overdose and its acute management". Journal of Toxicology. Clinical Toxicology 41 (2): 143–154. 2003. doi:10.1081/CLT-120019130. PMID 12733852. 
  19. ↑ "Pharmacological evidence for the central serotonergic effects of monomethoxyamphetamines". The Journal of Pharmacology and Experimental Therapeutics 197 (2): 272–279. May 1976. PMID 946817. http://jpet.aspetjournals.org/cgi/pmidlookup?view=long&pmid=946817. 
  20. ↑ 20.0 20.1 "Effect of para-methoxyamphetamine on catecholamine metabolism in the mouse brain". Life Sciences. Pt. 1 10 (19): 1087–1095. October 1971. doi:10.1016/0024-3205(71)90227-x. PMID 5132700. 
  21. ↑ 21.0 21.1 "Comparative actions of monomethoxyamphetamines on the release and uptake of biogenic amines in brain tissue". The Journal of Pharmacology and Experimental Therapeutics 197 (2): 263–271. May 1976. PMID 1271280. http://jpet.aspetjournals.org/cgi/pmidlookup?view=long&pmid=1271280. 
  22. ↑ 22.0 22.1 22.2 22.3 "Differential behavioural and neurochemical effects of para-methoxyamphetamine and 3,4-methylenedioxymethamphetamine in the rat". Progress in Neuro-Psychopharmacology & Biological Psychiatry 24 (6): 955–977. August 2000. doi:10.1016/S0278-5846(00)00113-5. PMID 11041537. 
  23. ↑ "p-Methoxyamphetamine, a potent reversible inhibitor of type-A monoamine oxidase in vitro and in vivo". The Journal of Pharmacy and Pharmacology 32 (4): 262–266. April 1980. doi:10.1111/j.2042-7158.1980.tb12909.x. PMID 6103055. 
  24. ↑ 24.0 24.1 "Selective inhibition of monoamine oxidase in monoaminergic neurons in the rat brain". Naunyn-Schmiedeberg's Archives of Pharmacology 324 (2): 79–87. September 1983. doi:10.1007/BF00497011. PMID 6646243. 
  25. ↑ "Effects of 3,4-methylenedioxymethamphetamine and related amphetamines on autonomic and behavioral thermoregulation". Pharmacology, Biochemistry, and Behavior 81 (3): 485–496. July 2005. doi:10.1016/j.pbb.2005.04.005. PMID 15904952. 
  26. ↑ "Differences in the in vivo dynamics of neurotransmitter release and serotonin uptake after acute para-methoxyamphetamine and 3,4-methylenedioxymethamphetamine revealed by chronoamperometry". Neurochemistry International 47 (5): 350–361. October 2005. doi:10.1016/j.neuint.2005.04.026. PMID 15979209. 
  27. ↑ "Pharmacological and behavioral determinants of cocaine, methamphetamine, 3,4-methylenedioxymethamphetamine, and para-methoxyamphetamine-induced hyperthermia". Psychopharmacology 194 (1): 41–52. September 2007. doi:10.1007/s00213-007-0825-9. PMID 17530474. 
  28. ↑ "Paramethoxyamphetamine (PMA) poisoning; a 'party drug' with lethal effects". Acta Anaesthesiologica Scandinavica 47 (10): 1298–1299. November 2003. doi:10.1046/j.1399-6576.2003.00245.x. PMID 14616331. 
  29. ↑ DEA. "The Hallucinogen PMA: Dancing With Death". http://www.erowid.org/chemicals/pma/pma_dea_intellbrief.pdf. 
  30. ↑ "Recent paramethoxyamphetamine deaths". Journal of Analytical Toxicology 22 (2): 169–172. 1 March 1998. doi:10.1093/jat/22.2.169. PMID 9547415. 
  31. ↑ "Caveat Emptor: Death involving the use of 4-methoxyamphetamine". Journal of Clinical Forensic Medicine 9 (3): 160. September 2002. doi:10.1016/S1353-1131(02)00043-3. PMID 15274949. 
  32. ↑ "Fatal paramethoxy-amphetamine (PMA) poisoning in the Australian Capital Territory". The Medical Journal of Australia 188 (7): 426. April 2008. doi:10.5694/j.1326-5377.2008.tb01695.x. PMID 18393753. 
  33. ↑ "Renewed warning over 'Rolex' pills". BBC News. 24 July 2013. https://www.bbc.com/news/uk-northern-ireland-23440537. 
  34. ↑ "WATCH OUT FOR DANGEROUS SUPERMAN PILL - News - Deep House Amsterdam". 30 January 2014. http://www.deephouseamsterdam.com/watch-out-for-dangerous-superman-pill/. 
  35. ↑ "¿Qué es Superman, la droga que ya ha cobrado varias vidas en el mundo?" (in Spanish). ElPais. 18 April 2016. http://www.elpais.com.uy/mundo/superman-droga-que-mezcla-metanfetamina-extasis.html. 
  36. ↑ "Las claves para entender qué pasó". La Nación. 2016-04-17. http://www.lanacion.com.ar/1890180-las-claves-para-entender-que-paso. 
  37. ↑ "Drug Warning – Reagent Tests UK". https://www.reagent-tests.uk/blog/category/drug-warning/. 
  38. ↑ "Annual Estimates Of Requirements Of Narcotic Drugs, Manufacture Of Synthetic Drugs, Opium Production And Cultivation Of The…". http://www.incb.org/pdf/e/list/green.pdf. 
  39. ↑ 39.0 39.1 Poisons Standard October 2015 https://www.comlaw.gov.au/Details/F2015L01534
  40. ↑ "Valtioneuvoston asetus huumausaineina pidettävistä aineista, valmisteista ja kasveista annetun valtioneuvoston asetuksen muuttamisesta" (in Finnish). Finlex. Helsinki: Finland's Ministry of Justice. 25 October 2018. https://www.finlex.fi/fi/laki/alkup/2018/20180839. 
  41. ↑ "Valtioneuvoston asetus huumausaineina pidettävistä aineista, valmisteista ja kasveista annetun valtioneuvoston asetuksen muuttamisesta" (in Finnish). Finlex. Helsinki: Finland's Ministry of Justice. 13 January 2022. https://www.finlex.fi/fi/laki/alkup/2022/20220013. 
  42. ↑ "Doden na gebruik speed met 4-MA" (in nl). 13 June 2012. http://nos.nl/artikel/383346-schippers-verbiedt-dodelijk-4ma.html. 
  43. ↑ 21 CFR 1308.11
  44. ↑ "Caveat Emptor: Death involving the use of 4-methoxyamphetamine". Journal of Clinical Forensic Medicine 9 (3): 160. September 2002. doi:10.1016/s1353-1131(02)00043-3. PMID 15274949. 
  45. ↑ "Drug Info". http://dancesafe.org/documents/druginfo/pma_faq.php. 
  46. ↑ "Warning: pills sold as ecstasy found to contain PMA". http://ecstasy.org/testing/pma.html. 
  47. ↑ Chamberlin T, Murray D. NET Syndicated QLD News 'Louis Vuitton' designer death drug hits the streets
  48. ↑ "Fatalities caused by the MDMA-related drug paramethoxyamphetamine (PMA)". Journal of Analytical Toxicology 25 (7): 645–648. October 2001. doi:10.1093/jat/25.7.645. PMID 11599617. 
  49. ↑ "The Characterization of 4-Methoxy-N-ethylamphetamine Hydrochloride". Microgram Journal 4 (1–4): 42–46. 2006. 

External links



Retrieved from "https://handwiki.org/wiki/index.php?title=Biology:Para-Methoxyamphetamine&oldid=3714038"