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Ecstasy_-drug-

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MDMA

MDMA
Pregnancy cat. Legal status C[1] Prohibited (S9)(AU) Schedule III(CA) Class A(UK) Schedule I(US) Oral, Sublingual, Inhalation, Injection[2]

Routes

MDMA Systematic (IUPAC) name 1-(benzo[d][1,3]dioxol-5-yl)-Nmethylpropan-2-amine Identifiers CAS number ATC code PubChem ChemSpider Formula Mol. mass SMILES Bioavailability Metabolism Half life 69610-10-2 ? 1615 1556 C11H15NO2 193.25 g/mol eMolecules & PubChem ? Hepatic, CYP extensively involved, especially CYP2D6 The half-life of MDMA is dose dependent, increasing with higher doses, but is around 6–10 hours at doses of 40–125 mg Renal

Chemical data

Pharmacokinetic data

MDMA (3,4-methylenedioxymethamphetamine, also known as Ecstasy) is a semisynthetic member of the amphetamine class of psychoactive drugs. It is considered unusual for its tendency to produce a sense of intimacy with others and diminished feelings of fear and anxiety. These effects have led some to suggest it might have therapeutic benefits to some individuals. Before it was made a controlled substance, MDMA was used to aid psychotherapy, often couples therapy, the results of which are poorly documented. Studies have also recently been initiated to examine the therapeutic potential of MDMA for post-traumatic stress disorder and anxiety associated with cancer. MDMA is criminalized in most countries in the world under a UN agreement,[3] and its possession, manufacture, or sale may result in criminal prosecution, although some limited exceptions exist for scientific and medical research. MDMA is one of the most widely used illicit drugs in the world[4] and is taken in a variety of contexts far removed from its roots in psychotherapeutic settings. It is commonly associated with the rave culture and its related genres of music. There have been debates within science, health care, and drug policy circles about the risks of MDMA, specifically the possibility of neurotoxic damage to the central nervous system. Regulatory authorities in several locations around the world have approved studies administering MDMA to humans to examine either its therapeutic potential or, more commonly, its basic effects.[5]

Excretion

Therapeutic considerations

History
MDMA was first prepared in 1912 by Merck chemist Anton Köllisch. At the time, Merck

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was interested in developing substances that stopped abnormal bleeding. Merck wanted to evade an existing patent for one such compound hydrastinine, which was held by Bayer. At the behest of his superiors, Walther Beckh and Otto Wolfes, Köllisch developed a preparation of a hydrastinine analogue, methylhydrastinine. MDMA was only an intermediate compound on the route to methylhydrastinine, and Merck was not interested in its properties.[6] On December 24, 1912 Merck filed two patent applications that described the synthesis of MDMA[7] and its subsequent conversion to methylhydrastinine.[8] Over the following 65 years, MDMA was largely forgotten. Merck records indicate that its researchers would return to the compound sporadically. In 1927, Max Oberlin studied the pharmacology of MDMA and observed that its effects on the blood sugar and smooth muscles were similar to ephedrine’s but MDMA did not produce pupil dilation. Some experiments with MDMA were also conducted at Merck KGaA in 1952 and 1959.[6] In 1953–54, the United States Army commissioned a study of toxicity and behavioral effects of injected mescaline and several analogues including MDMA in animals. These classified investigations were declassified and published in 1973.[9] The first scientific paper on MDMA appeared in 1958 in Yakugaku Zasshi, the Journal of the Pharmaceutical Society of Japan. In this paper, Yutaka Kasuya desribed the synthesis of MDMA, which was a part of his research on antispasmodics.[10]

MDMA
California, heard from his students about unusual effects of MDMA. The drug even helped one of them to overcome his stutter. Intrigued, Shulgin synthesized MDMA and tried it himself in 1976.[12] Two years later, he and David Nichols published the first report on the drug’s psychotropic effect in humans. They described "altered state of consciousness with emotional and sensual overtones" that can be compared "to marijuana, to psilocybin devoid of the hallucinatory component".[13] Shulgin had taken to using MDMA occasionally, for relaxation, referring to it as "my low-calorie martini" and giving the drug to his friends, researchers and other people who he had thought could benefit from it. One such person was psychotherapist Leo Zeff who had been known to use psychedelics in his practice. Zeff was so impressed with the action of MDMA that he came out of his semi-retirement to proselytize for it. Over the following years, Zeff traveled around the US and occasionally to Europe training other psychotherapists in the use of MDMA.[12][14][15] Among the underground psychotherapists, MDMA developed a reputation for enhancing communication during clinical sessions, reducing patients’ psychological defenses, and increasing capacity for therapeutic introspection. Although some therapists continued to conduct therapy illegally, MDMA was not legally given to humans until Charles Grob initiated an ascending-dose safety study in healthy volunteers. Subsequent legally approved MDMA studies in humans have taken place in the U.S. in Detroit (Wayne State University), Chicago (University of Chicago), San Francisco (UCSF and California Pacific Medical Center), Baltimore (NIDA-NIH Intramural Program), and South Carolina, as well as in Switzerland (University Hospital of Psychiatry, Zürich), the Netherlands (Maastricht University), and Spain (Universitat Autònoma de Barcelona).[16] Due to the wording of the United Kingdom’s existing Misuse of Drugs Act of 1971, MDMA was automatically classified as a Class A drug in 1977. In the early 1980s in the United States, MDMA rose to prominence as "Adam" in trendy nightclubs in the Dallas area, then in gay dance clubs.[17] From there, use spread to rave clubs in major cities around the country, and then to mainstream society. The

MDMA first appeared as a street drug in the early 1970s after its counterculture analogue, MDA, became criminalized in the United States in 1970.[11] In the mid-1970s, Alexander Shulgin, then at University of

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drug was first proposed for scheduling by the DEA in July 1984,[18] and was classified as a Schedule I controlled substance in the United States from May 31, 1985.[19] In the late 1980s MDMA as "ecstasy" began to be widely used in the United Kingdom and other parts of Europe, becoming an integral element of rave culture and other psychedelic/dancefloor-influenced music scenes, such as Madchester and Acid House. Spreading along with rave culture, illicit MDMA use became increasingly widespread among young adults in universities and later in high schools. MDMA became one of the four most widely used illicit drugs in the United States, along with cocaine, heroin and marijuana. Today in the US, according to some estimates, only marijuana will attract more first-time users.[20]

MDMA
in the US and other countries are evaluating the efficacy of MDMA-assisted psychotherapy for treating those diagnosed with posttraumatic stress disorder (PTSD) or anxiety related to cancer. In a newspaper interview, the researchers from the South Carolina PTSD study report tendencies for some participants to have reduced disease severity after MDMA psychotherapy.[26] However, these reports focus on individual participants. Statistical results from the entire study will need to be published and, ultimately, results will need to be confirmed in studies by other scientists to demonstrate the efficacy of MDMA as a psychotherapeutic agent.

Mechanism of action
For more details on this topic, see Effects of MDMA on the human body. The mechanism of MDMA’s unusual effects has yet to be fully understood, although it is generally thought that the primary relevant pharmacological characteristic of the drug is its affinity for SERTs. SERTs are the part of the serotonergic neuron which remove serotonin from the synapse to be recycled or stored for later use. Not only does MDMA inhibit the reuptake of serotonin into this pump, but it reverses the action of the transporter so that it begins pumping serotonin into the synapse from inside the cell.[27] In addition, MDMA induces the release of norepinephrine and dopamine.[28] MDMA’s unusual empathic/entactogenic effects have been hypothesized to be at least partly the result of the release of oxytocin,[29] a hormone usually released following such events as orgasm and childbirth, which is thought to facilitate bonding and the establishment of trust. MDMA is thought to cause this release by indirectly stimulating 5-HT1A receptors. However, the evidence that oxytocin is involved in the effects of MDMA is derived from studies conducted on rats where the emotional effects can only be indirectly measured, in this case by the time animals spend in close proximity to one another. Controlled human studies have not yet been carried out, and it is not known conclusively if MDMA has oxytocinergic action in humans. The question of why other serotonergic drugs do not produce a similarly profound emotional state like MDMA does also remains unanswered.

Therapeutic uses
There have long been suggestions that MDMA might be useful in psychotherapy, facilitating self-examination with reduced fear.[21][22][23] Indeed, some therapists, including Leo Zeff, Claudio Naranjo, George Greer, Peter Mandelson, Joseph Downing, and Philip Wolfson, used MDMA in their practices until it was made illegal. George Greer synthesized MDMA in the lab of Alexander Shulgin and administered it to about 80 of his clients over the course of the remaining years preceding MDMA’s Schedule I placement in 1985. In a published summary of the effects,[24] the authors reported patients felt improved in various, mild psychiatric disorders and other personal benefits, especially improved intimate communication with their significant others. In a subsequent publication on the treatment method, the authors reported that one patient with severe pain from terminal cancer experienced lasting pain relief and improved quality of life.[25] However, few of the results in this early MDMA psychotherapy were measured using methods considered reliable or convincing in scientific practice. For example, the questionnaires used might not have been sensitive to negative changes and it is not known to what extent similar patients might improve from chance or from psychotherapy. The therapeutic potential of MDMA is currently being tested in several ongoing studies, some sponsored by the Multidisciplinary Association for Psychedelic Studies. Studies

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From Wikipedia, the free encyclopedia

MDMA
Serious complications increasing in likelihood with dose, environmental severity, degree of physical activity, and/or certain drug interactions include: • Hyperthermia (due to an intemperate environment and/or lack of hydration and/ or rest from physical activity, usually dancing) • Dehydration (due to an intemperate environment and/or rest from physical activity, usually dancing) • Hyponatremia (due to drug induced antidiuretic hormone release and/or excess compensatory intake of fluids, a rare complication) • Serotonin syndrome (believed to be due to excess release of serotonin, sometimes triggered by coadministration of other serotonergic drugs)

Effects
Acute effects
For more details on this topic, see Effects of MDMA on the human body. The primary effects attributable to MDMA consumption are predictable and fairly consistent amongst users. Generally, users report feeling effects with 30–60 minutes of consumption, reaching a plateau that lasts about 4–6 hours, followed by a "comedown" period of a few hours which may be accompanied by fatigue and minor effects lasting for anywhere from a few hours to a few days.[30][31][32] The most common subjective effects reported by users include: • Euphoria • Decreased hostility and insecurity • Increased feelings of intimacy with others • Feelings of empathy towards others • Ability to discuss anxiety-provoking topics with markedly increased ease • A strong sense of inner peace and selfacceptance • Feelings of insightfulness and mental clarity • Intensification of sensory experience, particularly proprioception, hearing and touch • Decreased appetite • Short-term memory lapses The most common physical side effects reported by users include: • Urinary retention (also see hyponatremia) • Mydriasis (abnormal pupil dilation) • Increased physical energy • Increased heart rate and blood pressure • Increased mean body temperature • Trisma (lockjaw) • Bruxia (involuntary teeth grinding) • Gurning (projecting the lower jaw forward. Usually caused by higher doses) • Nystagmus (rapid, uncontrollable eye movements) The most common lingering side effects (i.e., following primary subjective effects) reported by users include: • Several hours of restlessness, sometimes accompanied by residual euphoria • Fatigue • A period of general malaise, normally resolving within a few days • Mildly blurred vision, gradually resolving over a period of up to several days

Effects of chronic use
For more details on this topic, see Effects of MDMA on the human body. Some further studies have also shown that this damage causes increased rates of depression and anxiety, even after quitting the drug.[33][34] In addition to this, some studies have indicated that MDMA may cause longterm memory[35] and cognition impairment.[36] Many factors, including total lifetime MDMA consumption, the duration of abstinence between uses, the environment of use, poly-drug use/abuse, quality of mental health, various lifestyle choices, and predispositions to develop clinical depression and other disorders may contribute to various possible health consequences. MDMA use has been occasionally associated with liver damage,[37] excessive wear of teeth,[38] and (very rarely) Hallucinogen persisting perception disorder.[39]

Recreational use
The European Monitoring Centre for Drugs and Drug Addiction notes that although there are some reports of tablets being sold for as little as €1, most countries in Europe now report typical retail prices in the range of €3 to €9 per tablet.[40] The United Nations Office on Drugs and Crime claimed in its 2008 World Drug Report that typical US retail prices are higher, at 15 to 20 dollars per tablet, or can be from 5 to 10 dollars per tablet if bought in stacks of 10 or more.[41]

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MDMA
status, there is limited risk of prosecution if caught. BZP possession does entail a greater risk.

Chemistry
Safrole, a colorless or slightly yellow oil, extracted from the root-bark or the fruit of sassafras plants is the primary precursor for all manufacture of MDMA. There are numerous synthetic methods available in the literature to convert safrole into MDMA via different intermediates.[46][47][48][49] One common route is via the MDP2P (3,4-methylenedioxyphenyl-2-propanone, also known as piperonyl acetone) intermediate. This intermediate can be produced in at least two different ways. One method is to isomerize safrole in the presence of a strong base to isosafrole and then oxidize isosafrole to MDP2P. Another, reportedly better method, is to make use of the Wacker process to oxidize safrole directly to the MDP2P (3,4-methylenedioxy phenyl-2-propanone) intermediate. This can be done with a palladium catalyst. Once the MDP2P intermediate has been produced it is then consumed via a reductive amination to form MDMA as the product.

MDMA, which has been made criminally illegal worldwide, is taken most commonly in pill form.

MDMA hydrochloride is used to manufacture ecstasy pills. Some users take this powdered form for recreation.

Legal alternatives
A substantial number of "ecstasy" tablets sold for recreational use (in the UK especially]) are actually piperazine (mCPP or BZP) pills.[42] These substances crudely mimic some of the positive effects of ecstasy, yet feature far greater negative side-effects (insomnia, migraines, nausea etc). mCPP is known to induce headaches in humans,[43][44] and has been used for testing potential anti-migraine medications.[45] These "legal highs" represent a considerable profit for the dealer; they are cheaply acquired online (with custom logos to mimic known "good" pills) and, given mCPP’s legal

Industrial scale methamphetamine/MDMA factory in Cikande, Indonesia Relatively small quantities of essential oil are required to make large numbers of MDMA pills. The essential oil of Ocotea

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cymbarum typically contains between 80 and 94 percent safrole. This would allow 500mL of the oil, which retails at between $20 and $100, to be used to produce an estimated 1,300 to 2,800 tablets containing 120mg of MDMA.[50]

MDMA
While the Expert Committee found the reports intriguing, it felt that the studies lacked the appropriate methodological design necessary to ascertain the reliability of the observations. There was, however, sufficient interest expressed to recommend that investigations be encouraged to follow up these preliminary findings. To that end, the Expert Committee urged countries to use the provisions of article 7 of the Convention on Psychotropic Substances to facilitate research on this interesting substance. In the United Kingdom, MDMA is a Class A drug under the Misuse of Drugs Act 1971, making it illegal to sell, buy, or possess without a license. Penalties include a maximum of seven years and/or unlimited fine for possession; life and/or unlimited fine for production or trafficking.

Legal issues
MDMA is legally controlled in most of the world under the UN Convention on Psychotropic Substances and other international agreements, although exceptions exist for research. Generally, the unlicensed use, sale or manufacture of MDMA are all criminal offenses. In the United States, MDMA was legal and unregulated until May 31, 1985, at which time it was emergency scheduled to DEA Schedule I, for drugs deemed to have no medical uses and a high potential for abuse. During DEA hearings to schedule MDMA, most experts recommended DEA Schedule III prescription status for the drug, due to beneficial usage of MDMA in psychotherapy. The judge overseeing the hearings, Francis Young, also recommended that MDMA be placed in Schedule III. Nonetheless, the DEA chose to ignore the ruling of its own Administrative Law Judge and unilaterally classified MDMA as Schedule I.[51] In 2001, responding to a mandate from the U.S. Congress, the U.S. Sentencing Commission, resulted in an increase in the penalties for MDMA by nearly 3,000%,[52] despite scientific protest calling for a decrease in the penalties for MDMA possession and distribution.[53] The increase makes 1 gram of MDMA (four pills at 250 mg per pill’s total weight regardless of purity, standard for Federal charges) equivalent to 1 gram of heroin (approximately fifty doses) or 2.2 pounds (1 kg) of marijuana for sentencing purposes at the federal level.[54] That same year, 1985, the World Health Organization’s Expert Committee on Drug Dependence recommended that MDMA be placed in Schedule I of the Convention on Psychotropic Substances. The Convention has a provision in Article 7(a) that allows use of Schedule I drugs for "scientific and very limited medical purposes." The committee’s report stated:[55] The Expert Committee held extensive discussions concerning therapeutic usefulness of 3,4 Methylenedioxymethamphetamine.

Health concerns
While the short-term adverse effects and contraindications of MDMA are fairly well known, there is significant debate within the scientific and medical communities possible regarding long-term physical and psychological effects of MDMA. Short-term physical health risks of MDMA consumption include hyperthermia,[56][57] and hyponatremia.[58] Continuous activity without sufficient rest or rehydration may cause body temperature to rise to dangerous levels, and loss of fluid via excessive perspiration puts the body at further risk as the stimulatory and euphoric qualities of the drug may render the user oblivious to their energy expenditure for quite some time. Diuretics such as alcohol may exacerbate these risks further. MDMA causes a reduction in the concentration of serotonin transporters (SERTs) in the brain. The rate at which the brain recovers from serotonergic changes is unclear. A number of studies [59] have demonstrated lasting serotonergic changes occurring due to MDMA exposure. Other studies[60][61] have suggested that the brain may recover from serotonergic damage; however, damage caused by heavy, prolonged use of MDMA may be long lasting. Some studies show that MDMA may be neurotoxic in humans.[62][63] Other studies, however, suggest that any potential brain

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damage may be at least partially reversible following prolonged abstinence from [61][64] However, other studies sugMDMA. gest that SERT-depletion arises from longterm MDMA use due to receptor down-regulation, rather than true neurotoxicity.[65] Depression and deficits in memory have been shown to occur more frequently in long-term MDMA users.[66][67] However, some recent studies have suggested that MDMA use may not be associated with chronic depression.[68][69] One now infamous study on MDMA toxicity, by George A. Ricaurte of Johns Hopkins School of Medicine, which claimed that a single recreational dose of MDMA could cause Parkinson’s Disease in later life due to severe dopaminergic stress, was actually retracted by Ricaurte himself after he discovered his lab had administered not MDMA but methamphetamine, which is known to cause dopaminergic changes similar to the serotonergic changes caused by MDMA.[70] Ricaurte blamed this mistake on the chemical supply company that sold the material to his lab. Most studies have found that levels of the dopamine transporter (or other markers of dopamine function) in MDMA users deserve further study or are normal.[71][72][73][74][75][76][77] Another concern associated with MDMA use is toxicity from chemicals other than MDMA in ecstasy tablets. Due to its near-universal illegality, the purity of a substance sold as ecstasy is unknown to the typical user. The MDMA content of tablets varies widely between regions and different brands of pills and fluctuates somewhat each year. Pills may contain other active substances meant to stimulate in a way similar to MDMA, such as amphetamine, methamphetamine, ephedrine, or caffeine, all of which may be comparatively cheap to produce and can help to boost profit overall. In some cases, tablets sold as ecstasy do not even contain any MDMA. Instead they may contain an assortment of presumably undesirable drugs such as paracetamol, ibuprofen, etc.[78] There have been a number of deaths attributed to PMA, a potent and highly neurotoxic hallucinogenic amphetamine, being sold as Ecstasy. PMA is unique in its ability to quickly elevate body temperature and heart rate at relatively low doses, especially in comparison to MDMA.[79] Hence, a user who

MDMA
believes he is consuming two 120 mg pills of MDMA could actually be consuming a dose of PMA that is potentially lethal, depending on the purity of the pill. Not only does PMA cause the release of serotonin, but also acts as an MAO-A inhibitor. When combined with an ecstasy-like substance, serotonin syndrome can result.

UK government assessment of overall harm
The chief executive of the UK Medical Research Council stated that MDMA is "on the bottom of the scale of harm," and was rated to be of lesser concern than alcohol, tobacco, and cannabis, as well as several classes of prescription medications, when examining the harmfulness of twenty popular recreational drugs. The UK study placed great weight on the risk for acute physical harm, the propensity for physical and psychological dependency on the drug, and the negative familial and societal impacts of the drug. Based on these factors, the study placed MDMA at number 18 in the list.[80] David Nutt, chairman of the UK Advisory Council on the Misuse of Drugs, stated in the Journal of Psychopharmacology in January 2009 that ecstasy use compared favorably with horse riding in terms of risk, leading to around 50 deaths a year compared to about 100 from horse riding. The ACMD subsequently made clear that Professor Nutt’s comments were not made on behalf of the ACMD.[81] An investigation is also currently being run to reclassify ecstasy as a class B drug in the United Kingdom. It is currently a class A drug, the same class as heroin.[1]

Drug interactions
Individuals who have stopped taking any type of SSRI after prolonged medication may not be able to experience the desired effects of MDMA for as long as several months following discontinuation of the medication. This is due to the fact that SSRIs decrease the brain’s sensitivity to the presence of serotonin as the brain seeks to reestablish a normalized neuro-electrical balance. Most people who die while under the influence of MDMA have also consumed significant quantities of at least one other drug. The

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risk of MDMA-induced death overall is minimal.[82] The use of MDMA can be dangerous when combined with other drugs (particularly monoamine oxidase inhibitors (MAOIs) and antiretroviral drugs, in particular ritonavir). Combining MDMA with MAOIs can precipitate hypertensive crisis, as well as serotonin syndrome which can be fatal.[83] MAO-B inhibitors such as deprenyl do not seem to carry these risks when taken at selective doses, and have been used to completely block neurotoxicity in rats.[84]

MDMA
pharmacokinetics arise via autoinhibition of CYP2D6 and CYP2D8, resulting in zeroth order kinetics at higher doses. It is thought that this can result in sustained and higher drug concentrations if the user takes consecutive doses of the drug. Because the enzyme CYP2D6 is deficient or totally absent in some people[86], it was once hypothesized that these people might have elevated risk when taking MDMA. However, there is still no evidence for this theory and available evidence argues against it.[87] It is now thought that the contribution of CYP2D6 to MDMA metabolism in humans is less than 30% of the metabolism. Indeed, an individual lacking CYP2D6 was given MDMA in a controlled clinical setting and a larger study gave MDMA to healthy volunteers after inhibiting CYP2D6 with paroxetine. Lack of the enzyme caused a modest increase in drug exposure and decreases in some metabolites, but physical effects did not appear appreciably elevated. While there is little or no evidence that low CYP2D6 activity increases risks from MDMA, it is likely that MDMA-induced CYP2D inhibition will increase risk of those prescription drugs that are metabolized by this enzyme. MDMA-induced CYP2D inhibition appears to last for up to a week after MDMA exposure. There are a number of reported potentially dangerous possible interactions between MDMA and other drugs. Several cases have been reported of death in individuals who ingested MDMA while taking ritonavir, which inhibits multiple CYP450 enzymes. Toxicity or death has also been reported in people who took MDMA in combination with monoamine oxidase inhibitors, such as phenelzine or moclobemide. MDMA and metabolites are primarily excreted as conjugates, such as sulfates and glucuronides.[88] MDMA is a chiral compound and has been almost exclusively administered as a racemate. However, an early uncontrolled report suggests that the S-enantiomer is significantly more potent in humans than the Renantiomer (Anderson et al. 1978). Studies in humans[89][90] indicate that the disposition of MDMA is stereoselective, with the S-enantiomer having a shorter elimination half-life and greater excretion than the R-enantiomer. For example, Fallon et al.[89] reported that the area under the blood plasma concentration versus time curve (AUC) was two to four

Pharmacokinetics
MDMA reaches maximal concentrations in the blood between 1.5 and 3 hours after ingestion. It is then slowly metabolized and excreted, with levels decreasing to half their peak concentration over approximately 8 hrs. Thus, there are still high MDMA levels in the body when the experiential effects have mostly ended, indicating that the brain has developed short-term tolerance to the presence of MDMA. Taking additional MDMA at this point therefore produces higher concentrations of MDMA in the blood and brain than might be expected based on the perceived effects. Metabolites of MDMA that have been identified in humans include 3,4-methylenedioxyamphetamine (MDA), 4-hydroxy-3-methoxy-methamphetamine (HMMA), 4-hydroxy-3-methoxyamphetamine (HMA), 3,4-dihydroxyamphetamine (DHA, also called alpha-methyldopamine), 3,4-methylenedioxyphenylacetone (MDP2P), and N-hydroxy-3,4-methylenedioxyamphetamine (MDOH). The contributions of these metabolites to the psychoactive and toxic effects of MDMA are an area of active research. 65% of MDMA is excreted unchanged in the urine (additionally 7% is metabolised into MDA) during 24 hours after usage.[85] MDMA is known to be metabolized by two main metabolic pathways: (1) O-demethylenation followed by catechol-O-methyltransferase (COMT)-catalyzed methylation and/or glucuronide/sulfate conjugation; and (2) Ndealkylation, deamination, and oxidation to the corresponding benzoic acid derivatives conjugated with glycine. The metabolism may be primarily by cytochrome P450 enzymes (CYP2D6 (in humans, but CYP2D1 in mice), and CYP3A4) and COMT. Complex, nonlinear

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times higher for the R-enantiomer than the Senantiomer after a 40 mg oral dose in human volunteers. Similarly, the plasma half-life of (R)-MDMA was significantly longer than that of the S-enantiomer (5.8 ± 2.2 hours vs 3.6 ± 0.9 hours). However, because MDMA has dose dependent kinetics, it is likely that these half lives would be higher at more typical doses (100 mg is sometimes considered a typical dose). Given as the racemate, MDMA has a half-life of around 8 hours.

MDMA

Poly substance use
MDMA is occasionally known for being taken in conjunction with psychedelic drugs, such as LSD or psilocybin mushrooms. As this practice has become more prevalent, most of the more common combinations have been given nicknames, such as "candy flipping", for MDMA combined with LSD,[91] and "hippie flipping" when combined with psilocybin mushrooms. Such combinations have the ability to produce an extremely powerful experience and may carry an increased risk of neurotoxicity, complications and/or injury when compared to any individual substance. Many users use mentholated products while taking MDMA for its cooling sensation while experiencing the drug’s effects. Examples include menthol cigarettes, Vicks[92] and lozenges. This sometimes has deleterious results on the upper respiratory tract.[93]

References
[1] Stimulants, narcotics, hallucinogens Drugs, Pregnancy, and Lactation, Gerald G. Briggs, OB/GYN News, June 1, 2003. [2] "Methylenedioxymethamphetamine (MDMA, Ecstasy)". Drugs and Human Performance Fact Sheets. National Highway Traffic Safety Administration. http://www.nhtsa.dot.gov/people/injury/ research/job185drugs/ methylenedioxymethamphetamine.htm. Retrieved on 30 April 2009. [3] "Where is Ecstasy Legal?" [4] Ecstasy Abuse Information [5] MAPS: Psychedelic Research Worldwide [6] ^ Bernschneider-Reif S, Oxler F, Freudenmann RW (November 2006). "The origin of MDMA ("ecstasy")-separating the facts from the myth". Pharmazie 61 (11): 966–72. doi:10.1111/ j.1360-0443.2006.01511.x. PMID

17152992. http://www.erowid.org/ references/ refs_view.php?A=ShowDoc1&ID=6707. [7] Firma E. Merck in Darmstadt (1914-05-16). "German Patent 274350: Verfahren zur Darstellung von Alkyloxyaryl-, Dialkyloxyaryl- und Alkylendioxyarylaminopropanen bzw. deren am Stickstoff monoalkylierten Derivaten". Kaiserliches Patentamt. http://v3.espacenet.com/ publicationDetails/ originalDocument?CC=DE&NR=274350C&KC=C&F Retrieved on 2009-04-12. [8] Firma E. Merck in Darmstadt (1914-10-15). "German Patent 279194: Verfahren zur Darstellung von Hydrastinin Derivaten". Kaiserliches Patentamt. http://v3.espacenet.com/ publicationDetails/ originalDocument?CC=DE&NR=279194C&KC=C&F Retrieved on 2009-04-12. [9] Hardman HF, Haavik CO, Seevers MH (June 1973). "Relationship of the structure of mescaline and seven analogs to toxicity and behavior in five species of laboratory animals". Toxicol. Appl. Pharmacol. 25 (2): 299–309. PMID 4197635. http://www.erowid.org/ references/ refs_view.php?A=ShowDoc1&ID=639. [10] Quoted from Chemical Abstracts, 1958, 97822Kasuya Y (1958). "Antispasmodics. XI. Synthesis of aralkylamines and their quarternary ammonium derivatives". Yakugaku Zasshi 78: 509–511. [11] The first confirmed sample was seized and identified by Chicago Police in 1970, see Sreenivasan VR (1972). "Problems in Identification of Methylenediony and Methoxy Amphetamines". Journal of Criminal Law, Criminology & Police Science 63 (2): 304–312. http://www.erowid.org/references/ refs_view.php?A=ShowDoc1&ID=1149. [12] ^ Ann Shulgin; Alexander Shulgin (1991). Pihkal: A Chemical Love Story. Part I. Chapter 12. Transform Press. ISBN 0-9630096-0-5. [13] Shulgin AT; Nichols DE (1978). "CHARACTERIZATION OF THREE NEW PSYCHOTOMIMETICS". in Willette, Robert E.; Stillman, Richard Joseph. The Psychopharmacology of hallucinogens. New York: Pergamon Press. pp. 74–83. ISBN 0-08-021938-1.

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[80] Scientists want new drug rankings, BBC (MDMA), and News, 23 March 2007 Methylenedioxyethylamphetamine [81] Ecstasy ’not worse than riding’, BBC (MDEA) Enantiomers by GC–MS" (PDF). News, 7 February 2009 Journal of Analytical Toxicology 23 (6): [82] Primetime video 518–523. http://www.maps.org/w3pb/ [83] Vuori E, Henry JA, Ojanperä I, et al. new/1999/1999_hensley_175_1.pdf. (March 2003). "Death following ingestion [91] UMD Center for Substance Abuse of MDMA (ecstasy) and moclobemide". Research. "Ecstasy:CESAR". Addiction 98 (3): 365–8. doi:10.1046/ http://www.cesar.umd.edu/cesar/drugs/ j.1360-0443.2003.00292.x. PMID ecstasy.asp. 12603236. http://www.mdma.net/ [92] "Director’s Report to the National toxicity/moclobemide.html. Advisory Council on Drug Abuse". [84] The Prozac Misunderstanding, at National Institute on Drug Abuse. May TheDEA.org 2000. http://search2.google.cit.nih.gov/ [85] Verebey K, Alrazi J, Jaffe JH (1988). "The search?q=cache:y3dIYYo3lKwJ:www.drugabuse.gov/ complications of ’ecstasy’ (MDMA)". DirReports/DirRep500/ DirectorReport5.html. JAMA 259 (11): 1649–50. doi:10.1001/ [93] Erowid Experience Vaults: Vicks used jama.259.11.1649. PMID 2893845. with Ecstasy - Important Warning About http://www.erowid.org/references/ Vicks on Ecstasy - 4287 refs_view.php?ID=1015. [86] eMedicine - Toxicity, MDMA : Article by David Yew [87] de la Torre R, Farré M, Roset PN, et al. • Julie Holland, Ecstasy: The Complete (April 2004). "Human pharmacology of Guide: a Comprehensive Look at the Risks MDMA: pharmacokinetics, metabolism, and Benefits of MDMA Park Street Press and disposition". Ther Drug Monit 26 (2001). (2): 137–44. doi:10.1097/ • Jerome Beck, Marsha Rosenbaum, Pursuit 00007691-200404000-00009. PMID of Ecstasy: The MDMA Experience SUNY 15228154. http://meta.wkhealth.com/pt/ Press (1994). pt-core/template-journal/lwwgateway/ • Leslie Iversen, Speed, Ecstasy, Ritalin: media/ The Science of Amphetamines Oxford landingpage.htm?issn=0163-4356&volume=26&issue=2&spage=137. University Press (2008). [88] Shima N, Kamata H, Katagi M, • David Pearce - "Utopian Pharmacology: Tsuchihashi H, Sakuma T, Nemoto N Mental Health in the Third Millenium: (September 2007). "Direct determination MDMA and Beyond." (2008). of glucuronide and sulfate of • Kobie Whetstone - "An Analysis of MDMA4-hydroxy-3-methoxymethamphetamine, induced Neurotoxicity." (2009). the main metabolite of MDMA, in human • Erowid, Earth. “Do Antioxidants Protect urine". J. Chromatogr. B Analyt. Technol. Against MDMA Hangover, Tolerance, and Biomed. Life Sci. 857 (1): 123–9. Neurotoxicity?” Erowid Extracts doi:10.1016/j.jchromb.2007.07.003. (December 2001). PMID 17643356. • NIDA InfoFacts: MDMA (Ecstasy) (August [89] ^ J. K. Fallon, A. T. Kicman, J. A. Henry, 2008). P. J. Milligan, D. A. Cowan, A. J. Hutt (01 • European Monitoring Centre for Drugs July 1999). "Stereospecific Analysis and and Drug Addiction (EMCDDA), Drug Enantiomeric Disposition of Profiles: 3,4-Methylenedioxymethamphetamine Methylenedioxymethamphetamine (Ecstasy) in Humans". Clinical Chemistry (MDMA). 45 (7): 1058–1069. • Nature News, Ecstasy could augment the http://www.clinchem.org/cgi/reprint/45/ benefits of psychotherapy (19 November 7/1058. 2008). [90] D. Hensley, J. T. Cody (1999). • Marsha Rosenbaum, Rick Doblin, Why "Simultaneous Determination of MDMA Should Not Have Been Made Amphetamine, Methamphetamine, Illegal. SAGE Publications (1991). Methylenedioxyamphetamine (MDA), Methylenedioxymethamphetamine

Further reading

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From Wikipedia, the free encyclopedia
• Reuters Health, Ecstasy may help PTSD victims get better (20 March 2009). • The Economist, Agony and ecstasy: Ecstasy may be good for those who can’t get over something truly horrible (18 December 2008). • New Scientist, Ecstasy’s long-term effects revealed (11 February 2009). • Advisory Council on the Misuse of Drugs, MDMA (‘ecstasy’): a review of its harms and classification under the Misuse of Drugs Act 1971 UK Home Office (2009).

MDMA
• MDMA PiHKAL • info entry • Erowid Vaults: MDMA • Jennings, Peter. "Primetime Special: Peter Jennings — Ecstasy Rising." ABC News, April 1, 2004. • Multidisciplinary Association for Psychedelic Studies MDMA Research Page - A regularly updated information source about MDMA research, including efforts to get MDMA approved as a prescription medicine. • EcstasyData.org A database of photos and lab-test results of over 1500 pills of "Ecstasy." • "Ecstasy" (MDMA) at DanceSafe.org

External links
• MDMA PiHKAL entry

Retrieved from "http://en.wikipedia.org/wiki/MDMA" Categories: Entactogens and Empathogens, Class A drugs, Psychedelic phenethylamines, Amphetamines This page was last modified on 23 May 2009, at 18:34 (UTC). All text is available under the terms of the GNU Free Documentation License. (See Copyrights for details.) Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a U.S. registered 501(c)(3) taxdeductible nonprofit charity. Privacy policy About Wikipedia Disclaimers

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