Activation of afferents to the ventral tegmental area in response to acute amphetamine:: a double-labelling study

被引:51
作者
Colussi-Mas, Joyce
Geisler, Stefanie
Zimmer, Luc
Zahm, Daniel S.
Berod, Anne [1 ]
机构
[1] Univ Lyon 1, Neuropharmacol Lab, CNRS, FRE 3006, F-69373 Lyon 08, France
[2] St Louis Univ, Sch Med, Dept Pharmacol & Physiol Sci, St Louis, MO 63104 USA
关键词
cholera toxin; Fos; psychostimulant; rat; retrograde transport;
D O I
10.1111/j.1460-9568.2007.05738.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The ventral tegmental area (VTA), primary source of the mesocorticolimbic dopaminergic system, is regarded as a critical site for initiation of behavioural sensitization to psychostimulants. The present study was undertaken to identify the neural pathways converging on the VTA that are potentially implicated in this process. Rats were sensitized by a single exposure to amphetamine (5 mg/kg, s.c.). The distribution of VTA-projecting neurons activated by amphetamine was examined by combining retrograde transport of the cholera toxin beta subunit (CTb), injected into the VTA, with immunodetection of Fos. The quantitative analysis of CTb-Fos double labelling demonstrates that amphetamine induced a rapid activation of Fos in a large number of brain areas projecting to the VTA. More than half of the CTb-Fos double-labelled neurons were located in the prefrontal cortex, lateral preoptic area-lateral hypothalamus, pontomesencephalic tegmentum, dorsal raphe nucleus, ventral pallidum and nucleus accumbens. In addition, scattered CTb-Fos double-labelled cells were observed in many other VTA afferent structures, such as claustrum, lateral septum, diagonal band-magnocellular preoptic nucleus, deep mesencephalic nucleus, oral part of pontine reticular nucleus and dorsomedial tegmental area. This suggests that systemic amphetamine activates a wide population of neurons projecting to the VTA that may be important for the modulation of neurobehavioural plasticity produced by this psychostimulant.
引用
收藏
页码:1011 / 1025
页数:15
相关论文
共 84 条
[1]   Behavioural sensitisation to repeated d-amphetamine:: Effects of excitotoxic lesions of the pedunculopontine tegmental nucleus [J].
Alderson, HL ;
Faulconbridge, LFH ;
Gregory, LP ;
Latimer, MP ;
Winn, P .
NEUROSCIENCE, 2003, 118 (02) :311-315
[2]  
Arana FS, 2003, J NEUROSCI, V23, P9632
[3]   Drug-induced neurobehavioral plasticity: the role of environmental context [J].
Badiani, A ;
Robinson, TE .
BEHAVIOURAL PHARMACOLOGY, 2004, 15 (5-6) :327-339
[4]  
Badiani A, 1998, J NEUROSCI, V18, P10579
[5]  
Bjijou Y, 1996, J PHARMACOL EXP THER, V277, P1177
[6]   D-amphetamine-induced behavioral sensitization: Effect of lesioning dopaminergic terminals in the medial prefrontal cortex, the amygdala and the entorhinal cortex [J].
Bjijou, Y ;
De Deurwaerdere, P ;
Spampinato, U ;
Stinus, L ;
Cador, M .
NEUROSCIENCE, 2002, 109 (03) :499-516
[7]   Orexin A in the VTA is critical for the induction of synaptic plasticity and Behavioral Sensitization to cocaine [J].
Borgland, SL ;
Taha, SA ;
Sarti, F ;
Fields, HL ;
Bonci, A .
NEURON, 2006, 49 (04) :589-601
[8]   Acute and chronic cocaine-induced potentiation of synaptic strength in the ventral tegmental area: Electrophysiological and behavioral correlates in individual rats [J].
Borgland, SL ;
Malenka, RC ;
Bonci, A .
JOURNAL OF NEUROSCIENCE, 2004, 24 (34) :7482-7490
[9]   D-amphetamine-induced behavioral sensitization: Implication of a glutamatergic medial prefrontal cortex-ventral tegmental area innervation [J].
Cador, M ;
Bjijou, Y ;
Cailhol, S ;
Stinus, L .
NEUROSCIENCE, 1999, 94 (03) :705-721
[10]   EVIDENCE OF A COMPLETE INDEPENDENCE OF THE NEUROBIOLOGICAL SUBSTRATES FOR THE INDUCTION AND EXPRESSION OF BEHAVIORAL SENSITIZATION TO AMPHETAMINE [J].
CADOR, M ;
BJIJOU, Y ;
STINUS, L .
NEUROSCIENCE, 1995, 65 (02) :385-395