Nur transcription factors in stress and addiction

被引:57
作者
Campos-Melo, Danae [1 ]
Galleguillos, Danny [1 ]
Sanchez, Natalia [1 ]
Gysling, Katia [1 ]
Andres, Maria E. [1 ]
机构
[1] Pontificia Univ Catolica Chile, Dept Cellular & Mol Biol, Fac Biol Sci, Santiago 8331150, Chile
来源
FRONTIERS IN MOLECULAR NEUROSCIENCE | 2013年 / 6卷
关键词
Nurr1; Nur77; Nor1; corticotropin releasing factor; addiction; stress; nuclear receptors; gene expression regulation; CORTICOTROPIN-RELEASING-FACTOR; ORPHAN NUCLEAR RECEPTOR; IMMEDIATE-EARLY GENES; MESSENGER-RNA EXPRESSION; FACTOR-INDUCIBLE-B; TYROSINE-HYDROXYLASE GENE; VENTRAL TEGMENTAL AREA; RETINOID-X-RECEPTORS; SERUM GROWTH-FACTORS; PROTEIN-KINASE-A;
D O I
10.3389/fnmol.2013.00044
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The Nur transcription factors Nur77 (NGFI-B, NR4A1), Nurr1 (NR4A2), and Nor-1 (NR4A3) are a sub-family of orphan members of the nuclear receptor superfamily. These transcription factors are products of immediate early genes, whose expression is rapidly and transiently induced in the central nervous system by several types of stimuli. Nur factors are present throughout the hypothalamus-pituitary-adrenal (HPA) axis where are prominently induced in response to stress. Drugs of abuse and stress also induce the expression of Nur factors in nuclei of the motivation/reward circuit of the brain, indicating their participation in the process of drug addiction and in non-hypothalamic responses to stress. Repeated use of addictive drugs and chronic stress induce long-lasting dysregulation of the brain motivation/reward circuit due to reprogramming of gene expression and enduring alterations in neuronal function. Here, we review the data supporting that Nur transcription factors are key players in the molecular basis of the dysregulation of neuronal circuits involved in chronic stress and addiction.
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页数:13
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共 173 条
  • [1] Corticotropin releasing hormone, receptor regulation and the stress response
    Aguilera, G
    [J]. TRENDS IN ENDOCRINOLOGY AND METABOLISM, 1998, 9 (08) : 329 - 336
  • [2] mRNA expression of the Nurr1 and NGFI-B nuclear receptor families following acute and chronic administration of methamphetamine
    Akiyama, Kazufumi
    Isao, Taketo
    Ide, Soichiro
    Ishikawa, Mikiko
    Saito, Atsushi
    [J]. PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2008, 32 (08) : 1957 - 1966
  • [3] The N-Terminal Region of Nurr1 (a.a 1-31) Is Essential for Its Efficient Degradation by the Ubiquitin Proteasome Pathway
    Alvarez-Castelao, Beatriz
    Losada, Fernando
    Ahicart, Patricia
    Castano, Jose G.
    [J]. PLOS ONE, 2013, 8 (02):
  • [5] Dual Control of Dopamine Synthesis and Release by Presynaptic and Postsynaptic Dopamine D2 Receptors
    Anzalone, Andrea
    Lizardi-Ortiz, Jose E.
    Ramos, Maria
    De Mei, Claudia
    Hopf, F. Woodward
    Iaccarino, Ciro
    Halbout, Briac
    Jacobsen, Jacob
    Kinoshita, Chisato
    Welter, Marc
    Caron, Marc G.
    Bonci, Antonello
    Sulzer, David
    Borrelli, Emiliana
    [J]. JOURNAL OF NEUROSCIENCE, 2012, 32 (26) : 9023 - 9034
  • [6] PIASγ Enhanced SUMO-2 Modification of Nurr1 Activation-Function-1 Domain Limits Nurr1 Transcriptional Synergy
    Arredondo, Cristian
    Orellana, Marcelo
    Vecchiola, Andrea
    Alberto Pereira, Luis
    Galdames, Leopoldo
    Estela Andres, Maria
    [J]. PLOS ONE, 2013, 8 (01):
  • [7] Elevated locomotor activity without altered striatal dopamine contents in Nurr1 heterozygous mice after acute exposure to methamphetamine
    Bäckman, C
    You, ZB
    Perlmann, T
    Hoffer, BJ
    [J]. BEHAVIOURAL BRAIN RESEARCH, 2003, 143 (01) : 95 - 100
  • [8] A selective group of dopaminergic neurons express Nurr1 in the adult mouse brain
    Bäckman, C
    Perlmann, T
    Wallén, Å
    Hoffer, BJ
    Morales, M
    [J]. BRAIN RESEARCH, 1999, 851 (1-2) : 125 - 132
  • [9] Gestational Restraint Stress and the Developing Dopaminergic System: An Overview
    Baier, Carlos J.
    Katunar, Maria R.
    Adrover, Ezequiela
    Eugenia Pallares, Maria
    Antonelli, Marta C.
    [J]. NEUROTOXICITY RESEARCH, 2012, 22 (01) : 16 - 32
  • [10] Transcription factors specifying dopamine phenotype are decreased in cocaine users
    Bannon, MJ
    Pruetz, B
    Barfield, E
    Schmidt, CJ
    [J]. NEUROREPORT, 2004, 15 (03) : 401 - 404