Expression of Fos-related antigens in the nucleus accumbens during opiate withdrawal and their attenuation by a D2 dopamine receptor agonist

被引:24
|
作者
Walters, CL [1 ]
Aston-Jones, G [1 ]
Druhan, JP [1 ]
机构
[1] Univ Penn, Med Ctr, Ctr Neurobiol & Behav, Dept Psychiat, Philadelphia, PA 19104 USA
关键词
nucleus accumbens; Fos-related antigens; dopamine receptors; opiate withdrawal; morphine; drug abuse;
D O I
10.1016/S0893-133X(00)00113-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Previous studies from this laboratory indicated that D2 dopamine (DA) receptors within the nucleus accumbens (NAc) are important for regulating somatic signs of opiate withdrawal. The present study measured the expression of Fos-related antigens (FRAs) within the NAc during opiate withdrawal to determine whether decreases in somatic withdrawal signs produced by a D2 receptor agonist are accompanied by related changes in accumbens neuronal activity. In an initial experiment, quantitative analyses of FRA immunoreactivity revealed increases in the number of FRA-positive cells throughout the NAc of opiate dependent animals undergoing naltrexone-precipitated withdrawal relative to dependent or non-dependent animals that did not experience withdrawal. A second experiment showed that somatic signs and FRA expression within the NAc could each be attenuated when the D2 agonist propylnorapomorphine (NPA; 0.1 or 0.3 mg/kg, i.p.) was administered prior to naltrexone-precipitated withdrawal. These findings suggest that D2 regulation or neuronal activity within the NAc may be important for the expression of opiate withdrawal symptoms. (C) 2000 American College of Neuropsychopharmacology. Published by Elsevier Science Inc. All rights reserved.
引用
收藏
页码:307 / 315
页数:9
相关论文
共 50 条
  • [31] Effects of prolactin on expression of Fos-related antigens in tyrosine hydroxylase-immunoreactive neurons in subdivisions of the arcuate nucleus
    Hentschel, K
    Moore, KE
    Lookingland, KJ
    BRAIN RESEARCH, 2000, 857 (1-2) : 110 - 118
  • [32] Inputs from the basolateral amygdala to the nucleus accumbens shell control opiate reward magnitude via differential dopamine D1 or D2 receptor transmission
    Lintas, Alessandra
    Chi, Ning
    Lauzon, Nicole M.
    Bishop, Stephanie F.
    Sun, Ninglei
    Tan, Huibing
    Laviolette, Steven R.
    EUROPEAN JOURNAL OF NEUROSCIENCE, 2012, 35 (02) : 279 - 290
  • [33] STRIATAL FOS EXPRESSION IS INDICATIVE OF DOPAMINE D1/D2 SYNERGISM AND RECEPTOR SUPERSENSITIVITY
    LAHOSTE, GJ
    YU, J
    MARSHALL, JF
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (16) : 7451 - 7455
  • [34] Stimulation of dopamine D2 receptors in the nucleus accumbens inhibits inflammatory pain
    Taylor, BK
    Joshi, C
    Uppal, H
    BRAIN RESEARCH, 2003, 987 (02) : 135 - 143
  • [35] Dopamine D2/D3-receptor and transporter densities in nucleus accumbens and amygdala of type 1 and 2 alcoholics
    E Tupala
    H Hall
    K Bergström
    T Särkioja
    P Räsänen
    T Mantere
    J Callaway
    J Hiltunen
    J Tiihonen
    Molecular Psychiatry, 2001, 6 : 261 - 267
  • [36] Dopamine D2/D3-receptor and transporter densities in nucleus accumbens and amygdala of type 1 and 2 alcoholics
    Tupala, E
    Hall, H
    Bergström, K
    Särkioja, T
    Räsänen, P
    Mantere, T
    Callaway, J
    Hiltunen, J
    Tiihonen, J
    MOLECULAR PSYCHIATRY, 2001, 6 (03) : 261 - 267
  • [38] D1 and D2 dopamine receptor mediation of amphetamine-induced acetylcholine release in nucleus accumbens
    Keys, AS
    Mark, GP
    NEUROSCIENCE, 1998, 86 (02) : 521 - 531
  • [39] Effects of the D3/D2 dopamine receptor agonist 7-OH-DPAT on locomotor activin and extracellular dopamine and 5-HT release in the nucleus accumbens
    Choi, KH
    Zarandi, B
    Baker, GB
    Greenshaw, AJ
    JOURNAL OF NEUROCHEMISTRY, 1998, 70 : S36 - S36
  • [40] D2 DOPAMINE RECEPTOR ANTAGONISTS INDUCE FOS AND RELATED PROTEINS IN RAT STRIATAL NEURONS
    DRAGUNOW, M
    ROBERTSON, GS
    FAULL, RLM
    ROBERTSON, HA
    JANSEN, K
    NEUROSCIENCE, 1990, 37 (02) : 287 - 294