Morphine tolerance and transcription factor expression in mouse spinal cord tissue

被引:31
作者
Li, XQ
Clark, JD
机构
[1] Stanford Univ, Dept Anesthesiol, Palo Alto, CA 94304 USA
[2] Vet Adm Palo Alto Hlth Care Syst, Palo Alto, CA 94304 USA
关键词
c-Fos; Fos B; Delta Fos B; CREB; morphine; tolerance; spinal cord;
D O I
10.1016/S0304-3940(99)00559-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Little is known about changes in gene expression responsible for the acquisition and maintenance of tolerance to the analgesic effects of opioids. In these studies we examine changes in the expression of several transcription factors in the spinal cords of morphine tolerant C57BL/6 mice. Western blots demonstrate a 1.9-fold increase in cyclic AMP response element binding protein (CREB) and a 2.4-fold increase phospho-CREB immunoreactivities in spinal cord homogenates from morphine tolerant animals. Likewise, Fos B and Delta Fos B immunoreactivities were increased 2.2 and 2.3-fold, respectively. The expression of c-Fos remained unchanged. Immunohistological analysis showed the increase of phospho-CREB and Fos B/Delta Fos B to be primarily in the dorsal horn region of the spinal cord. We conclude that chronic exposure to opioids causes changes in gene expression in sensory processing areas of the spinal cord. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:79 / 82
页数:4
相关论文
共 20 条
[1]   Competitive and non-competitive NMDA antagonists block the development of antinociceptive tolerance to morphine, but not to selective mu or delta opioid agonists in mice [J].
Bilsky, EJ ;
Inturrisi, CE ;
Sadee, W ;
Hruby, VJ ;
Porreca, F .
PAIN, 1996, 68 (2-3) :229-237
[2]  
Chen JS, 1997, J NEUROSCI, V17, P4933
[3]   Hyperalgesia in mice lacking the Kv1.1 potassium channel gene [J].
Clark, JD ;
Tempel, BL .
NEUROSCIENCE LETTERS, 1998, 251 (02) :121-124
[4]   Psychomotor stimulant- and opiate-induced c-fos mRNA expression patterns in the rat forebrain: Comparisons between acute drug treatment and a drug challenge in sensitized animals [J].
Curran, EJ ;
Akil, H ;
Watson, SJ .
NEUROCHEMICAL RESEARCH, 1996, 21 (11) :1425-1435
[5]   CYCLIC-AMP STIMULATES SOMATOSTATIN GENE-TRANSCRIPTION BY PHOSPHORYLATION OF CREB AT SERINE-133 [J].
GONZALEZ, GA ;
MONTMINY, MR .
CELL, 1989, 59 (04) :675-680
[6]   REGULATION OF CYCLIC-AMP RESPONSE ELEMENT-BINDING PROTEIN (CREB) PHOSPHORYLATION BY ACUTE AND CHRONIC MORPHINE IN THE RAT LOCUS-CERULEUS [J].
GUITART, X ;
THOMPSON, MA ;
MIRANTE, CK ;
GREENBERG, ME ;
NESTLER, EJ .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (03) :1168-1171
[7]  
LaneLadd SB, 1997, J NEUROSCI, V17, P7890
[8]   MORPHINE INDUCES C-FOS AND JUNB IN STRIATUM AND NUCLEUS-ACCUMBENS VIA D-1 AND N-METHYL-D-ASPARTATE RECEPTORS [J].
LIU, JL ;
NICKOLENKO, J ;
SHARP, FR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (18) :8537-8541
[9]   Antinociceptive tolerance to the mu-opioid agonist DAMGO is dose-dependently reduced by MK-801 in rats [J].
Mao, JR ;
Price, DD ;
Lu, J ;
Mayer, DJ .
NEUROSCIENCE LETTERS, 1998, 250 (03) :193-196
[10]   Chronic morphine administration enhances the expression of Kv1.5 and Kv1.6 voltage-gated K+ channels in rat spinal cord [J].
MatusLeibovitch, N ;
Vogel, Z ;
EzraMacabee, V ;
Etkin, S ;
Nevo, I ;
Attali, B .
MOLECULAR BRAIN RESEARCH, 1996, 40 (02) :261-270