Reward circuitry activation by noxious thermal stimuli

被引:409
作者
Becerra, L
Breiter, HC
Wise, R
Gonzalez, RG
Borsook, D [1 ]
机构
[1] Massachusetts Gen Hosp, Ctr Funct Pain Neuroimaging & Therapy Res, Boston, MA 02129 USA
[2] Massachusetts Gen Hosp, Motivat & Emot Neurosci Ctr, Boston, MA 02129 USA
[3] Massachusetts Gen Hosp, Athinoula A Martinos Ctr Biomed Imaging, Boston, MA 02129 USA
[4] Massachusetts Gen Hosp, Dept Radiol, Boston, MA 02129 USA
[5] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02129 USA
[6] Massachusetts Gen Hosp, Dept Psychiat, Boston, MA 02129 USA
[7] Harvard Univ, Sch Med, Program Neurosci, Boston, MA 02129 USA
[8] NIDA, NIH, Baltimore, MD 21224 USA
关键词
D O I
10.1016/S0896-6273(01)00533-5
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Using functional magnetic resonance imaging (fMRI), we observed that noxious thermal stimuli (46 degreesC) produce significant signal change in putative reward circuitry as well as in classic pain circuitry. Increases in signal were observed in the sublenticular extended amygdala of the basal forebrain (SLEA) and the ventral tegmentum/periaqueductal gray (VT/PAG), while foci of increased signal and decreased signal were observed in the ventral striatum and nucleus accumbens (NAc). Early and late phases were observed for signals in most brain regions, with early activation in reward related regions such as the SLEA, VT/PAG, and ventral striatum, In contrast, structures associated with somatosensory perception, including SI somatosensory cortex, thalamus, and insula, showed delayed activation. These data support the notion that there may be a shared neural system for evaluation of aversive and rewarding stimuli.
引用
收藏
页码:927 / 946
页数:20
相关论文
共 124 条
[1]
ALTIER N, 1997, BEHAV BRAIN RES, V89, P161
[2]
Differentiating cortical areas related to pain perception from stimulus identification: Temporal analysis of fMRI activity [J].
Apkarian, AV ;
Darbar, A ;
Krauss, BR ;
Gelnar, PA ;
Szeverenyi, NM .
JOURNAL OF NEUROPHYSIOLOGY, 1999, 81 (06) :2956-2963
[3]
Effects of excitotoxic lesions of the basal forebrain on MFB self-stimulation [J].
Arvanitogiannis, A ;
Waraczynski, M ;
Shizgal, P .
PHYSIOLOGY & BEHAVIOR, 1996, 59 (4-5) :795-806
[4]
Barbas H, 2000, ADV NEUROL, V84, P87
[5]
ENDOGENOUS PAIN CONTROL-SYSTEMS - BRAIN-STEM SPINAL PATHWAYS AND ENDORPHIN CIRCUITRY [J].
BASBAUM, AI ;
FIELDS, HL .
ANNUAL REVIEW OF NEUROSCIENCE, 1984, 7 :309-338
[6]
Becerra LR, 1999, MAGN RESON MED, V41, P1044, DOI 10.1002/(SICI)1522-2594(199905)41:5<1044::AID-MRM25>3.0.CO
[7]
2-M
[8]
Bechara A, 1998, J NEUROSCI, V18, P428
[9]
BERNARD JF, 1992, J NEUROPHYSIOL, V68, P551
[10]
THE SPINO(TRIGEMINO)PONTOAMYGDALOID PATHWAY - ELECTROPHYSIOLOGICAL EVIDENCE FOR AN INVOLVEMENT IN PAIN PROCESSES [J].
BERNARD, JF ;
BESSON, JM .
JOURNAL OF NEUROPHYSIOLOGY, 1990, 63 (03) :473-490