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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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13. Pathological Gambling and Other “Behavioral” Addictions 307lifetime prevalence <strong>of</strong> compulsive buying have rang<strong>ed</strong> from 1.1 to 5.9%(Christenson et al., 1994; McElroy, Keck, Pope, Smith, & Strakowski, 1994).ETIOLOGYA growing body <strong>of</strong> literature implicates multiple neurotransmitter systems (e.g.,serotonergic, dopaminergic, noradrenergic, opioidergic), as well as familial andinherit<strong>ed</strong> factors, in the pathophysiology <strong>of</strong> ICDs (Potenza & Hollander, 2002).The most consistent findings involve the serotonin (5-hydroxyindole or 5-HT) system, believ<strong>ed</strong> to underlie impulse control (Potenza & Hollander, 2002).Evidence for serotonergic involvement in ICDs comes in part from studies<strong>of</strong> platelet monoamine oxidase B (MAO-B) activity, which correlates withcerebrospinal fluid (CSF) levels <strong>of</strong> 5-hydroxyindoleacetic acid (5-HIAA, ametabolite <strong>of</strong> 5-HT) and is consider<strong>ed</strong> a peripheral marker <strong>of</strong> 5-HT function(Potenza & Hollander, 2002). Low CSF 5-HIAA levels have been found tocorrelate with high levels <strong>of</strong> impulsivity and sensation seeking (Potenza &Hollander, 2002). Pharmacological challenge studies that measure hormonalresponse after administration <strong>of</strong> serotonergic drugs also provide evidence for serotonergicdysfunction in ICDs (Potenza & Hollander, 2002).Dopaminergic systems influencing rewarding and reinforcing behaviorshave also been implicat<strong>ed</strong> in ICDs. “Reward deficiency syndrome,” a hypothesiz<strong>ed</strong>hypodopaminergic state involving multiple genes and environmentalstimuli that puts an individual at high risk for multiple addictive, impulsive,and compulsive behaviors, is one propos<strong>ed</strong> mechanism (Blum et al., 2000).Alterations in dopaminergic pathways have been propos<strong>ed</strong> as underlying theseeking <strong>of</strong> rewards (gambling, drugs) that trigger the release <strong>of</strong> dopamine andproduce feelings <strong>of</strong> pleasure (Blum et al., 2000).Noradrenergic systems, believ<strong>ed</strong> to underlie arousal, excitement, and sensationseeking, have been implicat<strong>ed</strong> in impulsive behaviors (Potenza & Hollander,2002). Anticipation <strong>of</strong> or engagement in seemingly impulsive behaviorscan activate the autonomic nervous system. Correlations between scores on theextroversion scale <strong>of</strong> the Eysenck Personality Questionnaire and markers <strong>of</strong>noradrenergic functioning (e.g., CSF or plasma 3-methoxy-4-hydroxyphenylglycol[MHPG] levels, urinary outputs <strong>of</strong> norepinephrine and its major metabolites)suggest a disturbance in central noradrenergic system functioning in PG(Roy, De Jong, & Linnoila, 1989).The mu opioid system is believ<strong>ed</strong> to underlie urge regulation through theprocessing <strong>of</strong> reward, pleasure, and pain, at least in part via modulation <strong>of</strong>dopamine neurons in mesolimbic pathway through gamma-aminobutyric acid(GABA) interneurons (Potenza & Hollander, 2002). Opioidergic involvementin ICDs comes from studies <strong>of</strong> naltrexone, a mu opioid receptor antagonist with

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