Now or Later? An fMRI study of the effects of endogenous opioid blockade on a decision-making network

被引:54
作者
Boettiger, Charlotte A. [1 ,5 ]
Kelley, Elizabeth A. [2 ]
Mitchell, Jennifer M. [2 ,3 ]
D'Esposito, Mark [4 ,6 ]
Fields, Howard L. [2 ,3 ]
机构
[1] Univ N Carolina, Dept Psychol, Biomed Res Imaging Ctr, Chapel Hill, NC 27599 USA
[2] Ernest Gallo Clin & Res Ctr, Emeryville, CA USA
[3] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[4] Univ Calif Berkeley, Dept Psychol, Helen Wills Neurosci Inst, Berkeley, CA 94720 USA
[5] Univ N Carolina, Curriculum Neurobiol, Chapel Hill, NC 27599 USA
[6] Univ Calif Berkeley, Henry J Wheeler Brain Imaging Ctr, Berkeley, CA 94720 USA
关键词
Alcoholism; Executive function; Human; Naltrexone; Orbitofrontal; ORBITAL PREFRONTAL CORTEX; MESSENGER-RNA EXPRESSION; ORBITOFRONTAL CORTEX; BETA-ENDORPHIN; HUMAN-BRAIN; ALCOHOL DEPENDENCE; RECEPTOR GENE; PLASMA-CONCENTRATIONS; ETHANOL INTOXICATION; NALTREXONE TREATMENT;
D O I
10.1016/j.pbb.2009.02.008
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Previously, we found that distinct brain areas predict individual selection bias in decisions between small immediate ("Now") and larger delayed rewards ("Later"). Furthermore, such selection bias can be manipulated by endogenous opioid blockade. To test whether blocking endogenous opioids with naltrexone (NTX) alters brain activity during decision-making in areas predicting individual bias, we compared fMRI BOLD signal correlated with Now versus Later decision-making after acute administration of NTX (50 mg) or placebo. We tested abstinent alcoholics and control subjects in a double-blind two-session design. We defined regions of interest (ROIs) centered on activation peaks predicting Now versus Later selection bias. NTX administration significantly increased BOLD signal during decision-making in the right lateral orbital gyrus ROI, an area where enhanced activity during decision-making predicts Later bias. Exploratory analyses identified additional loci where BOLD signal during decision-making was enhanced (left orbitofrontal cortex, left inferior temporal gyrus, and cerebellum) or reduced (right superior temporal pole) by NTX. Additional analyses identified sites, including the right lateral orbital gyrus, in which NTX effects on BOLD signal predicted NTX effects on selection bias. These data agree with opioid receptor expression in human frontal and temporal cortices, and suggest possible mechanisms of NTX's therapeutic effects. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:291 / 299
页数:9
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