期刊
NEUROPSYCHOPHARMACOLOGY
卷 35, 期 1, 页码 217-238出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/npp.2009.110
关键词
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资金
- Pearson Center for Alcoholism and Addiction Research
- National Institutes of Health
- National Institute on Alcohol Abuse and Alcoholism [AA12602, AA08459, AA06420]
- National Institute on Drug Abuse [DA04043, DA04398, DA10072]
- National Institute of Diabetes and Digestive and Kidney Diseases [DK26741]
- Tobacco-Related Disease Research Program from the State of California [17RT-0095]
- NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [P01DK026741] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM [R01AA008459, R01AA012602, ZIAAA000550, P60AA006420, R37AA008459, P50AA006420] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE ON DRUG ABUSE [R01DA010072, R01DA004398, R01DA004043] Funding Source: NIH RePORTER
Drug addiction is a chronically relapsing disorder that has been characterized by (1) compulsion to seek and take the drug, (2) loss of control in limiting intake, and (3) emergence of a negative emotional state (eg, dysphoria, anxiety, irritability) reflecting a motivational withdrawal syndrome when access to the drug is prevented. Drug addiction has been conceptualized as a disorder that involves elements of both impulsivity and compulsivity that yield a composite addiction cycle composed of three stages: 'binge/intoxication', 'withdrawal/negative affect', and 'preoccupation/anticipation' (craving). Animal and human imaging studies have revealed discrete circuits that mediate the three stages of the addiction cycle with key elements of the ventral tegmental area and ventral striatum as a focal point for the binge/intoxication stage, a key role for the extended amygdala in the withdrawal/negative affect stage, and a key role in the preoccupation/anticipation stage for a widely distributed network involving the orbitofrontal cortex-dorsal striatum, prefrontal cortex, basolateral amygdala, hippocampus, and insula involved in craving and the cingulate gyrus, dorsolateral prefrontal, and inferior frontal cortices in disrupted inhibitory control. The transition to addiction involves neuroplasticity in all of these structures that may begin with changes in the mesolimbic dopamine system and a cascade of neuroadaptations from the ventral striatum to dorsal striatum and orbitofrontal cortex and eventually dysregulation of the prefrontal cortex, cingulate gyrus, and extended amygdala. The delineation of the neurocircuitry of the evolving stages of the addiction syndrome forms a heuristic basis for the search for the molecular, genetic, and neuropharmacological neuroadaptations that are key to vulnerability for developing and maintaining addiction. Neuropsychopharmacology Reviews (2010) 35, 217-238; doi:10.1038/npp.2009.110; published online 26 August 2009
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