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Clinical Textbook of Addictive Disorders 3rd ed - R. Frances, S. Miller, A. Mack (Guilford, 2005) WW

Clinical Textbook of Addictive Disorders 3rd ed - R. Frances, S. Miller, A. Mack (Guilford, 2005) WW

Clinical Textbook of Addictive Disorders 3rd ed - R. Frances, S. Miller, A. Mack (Guilford, 2005) WW

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8. Marijuana, Hallucinogens, and Club Drugs 163MDMAMDMA has many names, but is perhaps best known as Ecstasy. It is sometimesclassifi<strong>ed</strong> as a stimulant and does have similar properties to the amphetamines,although it also has some unique effects that distinguish it (Hermle et al., 1993;Shulgin, 1986). MDMA was legal in this country until 1985, when it was madea Sch<strong>ed</strong>ule I drug. Prior to that, its use was unregulat<strong>ed</strong> and therefore legal.The primary appeal <strong>of</strong> MDMA is its psychological effect, a dramatic andconsistent ability to induce a pr<strong>of</strong>ound feeling <strong>of</strong> attachment and connection inthe user. The compound’s street name is perhaps a misnomer; the Los Angelesdrug dealer who coin<strong>ed</strong> the term “Ecstasy” originally want<strong>ed</strong> to call the drug“Empathy,” but ask<strong>ed</strong>, “Who would know what that means?” (Eisner, 1968).MDMA has long been known to damage brain serotonin (5-HT) neuronsin laboratory animals (McCann & Ricaurte, 1993; Montoya, Sorrentino, Lucas,& Price, 2002). Although a minority <strong>of</strong> researchers disagree with the conclusion,it has become increasingly apparent over the past decade that MDMA isneurotoxic to humans. Furthermore, the neurotoxicity has real and functionalimplications (McCann, Eligulashvili, & Ricaurte, 2000; Montoya et al., 2002;Morgan, 2000; Sprague, Everman, & Nichols, 1998). Ecstasy use is associat<strong>ed</strong>with sleep, mood, and anxiety disturbances, elevat<strong>ed</strong> impulsiveness, memorydeficits, and attention problems. Many <strong>of</strong> these disturbances appear to be permanentand seem likely to depend on the overall amount <strong>of</strong> MDMA consum<strong>ed</strong>over time, but may be caus<strong>ed</strong> by as little as a single dose (Rodgers, 2000; Turner& Parrott, 2000).HistoryA synthetic process for the creation <strong>of</strong> MDMA was patent<strong>ed</strong> in 1914 by Merckin Darmstadt, Germany (Shulgin, 1990). MDMA was not, as is sometimesthought, intend<strong>ed</strong> as an appetite suppressant. It was most likely develop<strong>ed</strong> as anexperimental compound. Except for a minor chemical modification mention<strong>ed</strong>in a patent in 1919, there is no other known historical record <strong>of</strong> MDMA untilthe 1950s. At that time, the Unit<strong>ed</strong> States Army experiment<strong>ed</strong> with MDMA.The resulting information was declassifi<strong>ed</strong> and became available to the generalpublic in the early 1970s. These findings consist<strong>ed</strong> primarily <strong>of</strong> a number <strong>of</strong>LD 50(m<strong>ed</strong>ian lethal dose) determinations for a variety <strong>of</strong> laboratory animals.Humans probably first us<strong>ed</strong> MDMA in the late 1960s. It was discover<strong>ed</strong> asa recreational drug by free-thinking individualists (New Age seekers), peoplewho lik<strong>ed</strong> its properties <strong>of</strong> inducing feelings <strong>of</strong> well-being and connection(Watson & Beck, 1986). MDMA does induce feelings <strong>of</strong> warmth and connect<strong>ed</strong>ness,and using this rationale, its use was promulgat<strong>ed</strong> by therapists in the1970s (Shulgin, 1990). Before the compound became illegal in 1985, it wasus<strong>ed</strong> extensively for this purpose (Beck, 1990).

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