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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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208 III. SUBSTANCES OF ABUSEnin, and their precursor enzymes tyrosine hydroxylase, and tryptophan hydroxylase,are deplet<strong>ed</strong>, which in turn affects levels <strong>of</strong> the major metabolites <strong>of</strong>these transmitters, their receptors, and their reuptake transporters. Methamphetaminealso affects serotonergic, noradrenergic, and glutamatergic systemsthrough interactions with dopamine transporters, monoamine transporters, andN-methyl-D-aspartate (NMDA) receptors. Nitric oxide may have a role inmethamphetamine-induc<strong>ed</strong> behavioral sensitization and neurotoxicity.Chronic methamphetamine abuse can lead to psychotic behavior (particularlyparanoia), visual and auditory hallucinations, and violent behavior.Chronic methamphetamine users also demonstrate deficits in attention, verbalmemory, abstract reasoning, task shifting, and spatial abilities (Simon etal., 2000). Animal studies have demonstrat<strong>ed</strong> that chronic administration <strong>of</strong>methamphetamine decreases striatal concentrations <strong>of</strong> dopamine and dopaminemetabolites in several regions <strong>of</strong> the brain (Nordahl, Salo, & Leamon,2003).Other than symptomatic treatment <strong>of</strong> drug-induc<strong>ed</strong> sequelae, there are nospecific pharmacological treatments for methamphetamine addiction (Lukas,1997). Continu<strong>ed</strong> progress in understanding the neurobiological basis for methamphetamineaddiction, as well as m<strong>ed</strong>ication development initiatives aim<strong>ed</strong> atcocaine and other drugs, may benefit methamphetamine pharmacotherapy inthe future. Nonpharmacological therapies for methamphetamine addiction aresimilar to those for other chemical dependencies but ne<strong>ed</strong> to take into accountmethamphetamine’s longer duration <strong>of</strong> action, withdrawal period, and potentiallylonger recovery phase. In addition, methamphetamine users may experienceparanoia, psychotic symptoms, and protract<strong>ed</strong> depression and anh<strong>ed</strong>onia,making them more difficult to treat than the standard drug treatment population.Regarding nonpharmacological treatment, methamphetamine usersand cocaine users respond similarly to manualiz<strong>ed</strong> behavioral and cognitivebehavioraltreatment strategies (Shoptaw, Rawson, McCann, & Obert, 1994).In addition, new behavioral treatments under development show promise. TheMatrix Program, a multisite, Center for Substance Abuse Treatment (CSAT)–fund<strong>ed</strong> drug treatment program, demonstrat<strong>ed</strong> significantly r<strong>ed</strong>uc<strong>ed</strong> methamphetamineuse from pretreatment levels in a follow-up sample 2–5 yearsposttreatment (Rawson et al., 2002). However, continuing high rates <strong>of</strong> dropoutand relapse in this population indicate a ne<strong>ed</strong> for further treatment researchfor this difficult population.CONCLUSIONOver the past 15 years, much has chang<strong>ed</strong> with regard to the use and our understanding<strong>of</strong> both amphetamines and cocaine. Most notably, cocaine depend-

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