Rapid neuroadaptation in the nucleus accumbens and bed nucleus of the stria terminalis mediates suppression of operant responding during withdrawal from acute opioid dependence

被引:11
作者
Criner, S. H.
Liu, J.
Schulteis, G.
机构
[1] VA San Diego Healthcare Syst, Res Serv, La Jolla, CA 92161 USA
[2] Univ Calif San Diego, Dept Anesthesiol, Sch Med, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Biol, La Jolla, CA 92093 USA
关键词
amygdala; withdrawal; morphine; addiction; rat;
D O I
10.1016/j.neuroscience.2006.11.002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Single injections of morphine induce a state of acute opiold dependence in humans and animals, measured as precipitated withdrawal when an antagonist is administered 4-24 h after morphine. Additional morphine exposure at daily or weekly intervals results in further increases in withdrawal severity, suggesting that acute opioid dependence reflects the early stages in the development of a chronic state of dependence. The current study evaluated the role of the nucleus accumbens (NAC), bed nucleus of stria terminalis (BNST), interstitial nucleus of posterior limb of the anterior commissure (IPAC), and central amygdala (CeA) in the expression of antagonist-precipitated suppression of operant responding for food as a measure of withdrawal from acute opioid dependence. Rats trained on a fixed-ratio 15 schedule received one or four daily injections of morphine, with the lipophobic opioid antagonist methylnaloxonium (16-2000 ng) infused into one of the brain regions or the lateral ventricle (i.c.v.) 4 h after the final morphine injection. After acute morphine methylnaloxonium was more potent upon infusion into the NAC (17.9-fold potency shift), BNST (6.8-fold) and CeA (5.5-fold) than it was upon i.c.v. administration. Following repeat morphine the NAC and BNST but not CeA continued to show greater sensitivity relative to i.c.v. infusion (12.9-, 8.7-, and 3.2-fold potency shifts, respectively). The IPAC was insensitive to methyinaloxonium after acute or repeat morphine at doses that reliably suppressed responding upon i.c.v. infusion (125-500 ng). Thus, among the components of extended amygdala examined in this study, rapid neuroadaptation within the nucleus accumbens and bed nucleus of the stria terminalis appear to play the most prominent role in antagonist-precipitated suppression of operant responding during the early stages in the development of opioid dependence. (c) 2006 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1436 / 1446
页数:11
相关论文
共 64 条
[1]  
ADAMS JU, 1990, J PHARMACOL EXP THER, V253, P483
[2]   NALTREXONE-SENSITIZING EFFECTS OF CENTRALLY ADMINISTERED MORPHINE AND OPIOID-PEPTIDES [J].
ADAMS, JU ;
HOLTZMAN, SG .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1991, 193 (01) :67-73
[3]  
Alheid GF, 2003, ANN NY ACAD SCI, V985, P185
[4]  
[Anonymous], RAT BRAIN STEREOTAXI
[5]   Conditioned place aversion is a highly sensitive index of acute opioid dependence and withdrawal [J].
Azar, MR ;
Jones, BC ;
Schulteis, G .
PSYCHOPHARMACOLOGY, 2003, 170 (01) :42-50
[6]   OPIOID PHYSICAL-DEPENDENCE DEVELOPMENT - EFFECTS OF SINGLE VERSUS REPEATED MORPHINE PRETREATMENTS AND OF SUBJECTS OPIOID EXPOSURE HISTORY [J].
AZORLOSA, JL ;
STITZER, ML ;
GREENWALD, MK .
PSYCHOPHARMACOLOGY, 1994, 114 (01) :71-80
[7]  
BICKEL WK, 1988, J PHARMACOL EXP THER, V244, P126
[8]   Trends in abuse of OxyContin® and other opioid analgesics in the United States:: 2002-2004 [J].
Cicero, TJ ;
Inciardi, JA ;
Muñoz, A .
JOURNAL OF PAIN, 2005, 6 (10) :662-672
[9]   ANTAGONIST TREATMENT IN NUCLEUS ACCUMBENS OR PERIAQUEDUCTAL GREY AFFECTS HEROIN SELF-ADMINISTRATION [J].
CORRIGALL, WA ;
VACCARINO, FJ .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1988, 30 (02) :443-450
[10]   A COMPARATIVE-STUDY OF SELF-ADMINISTRATION OF MORPHINE INTO THE AMYGDALA AND THE VENTRAL TEGMENTAL AREA IN MICE [J].
DAVID, V ;
CAZALA, P .
BEHAVIOURAL BRAIN RESEARCH, 1994, 65 (02) :205-211