Using fMRI to quantify the time dependence of remifentanil an algesia in the human brain

被引:88
作者
Wise, RG [1 ]
Williams, P
Tracey, I
机构
[1] Univ Oxford, John Radcliffe Hosp, Ctr Funct Magnet Resonance Imaging Brain, Dept Clin Neurol, Oxford OX3 9DU, England
[2] Univ Oxford, Dept Human Anat & Genet, Oxford, England
[3] GlaxoSmithKline, Harlow, Essex, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
pain; analgesia; fMRI; remifentanil; pharmacokinetics; pharmacodynamics;
D O I
10.1038/sj.npp.1300364
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
To understand and exploit centrally acting drugs requires reliable measures of their time course of action in the human brain. Functional magnetic resonance imaging (fMRl) is able to measure noninvasively, drug-induced changes in task-related brain activity. Here, we have characterized, in a specific region of the brain, the time of onset of action and the half-life of action of a clinically relevant dose of a potent opioid analgesic agent, remifentanil, These times were established from the temporal variation of the amplitude of the blood oxygen level-dependent response in the insular cortex contralateral to a painfully hot thermal stimulus, in volunteers receiving a remifentanil infusion. The insular cortex has repeatedly been reported as activated by noxious thermal stimulation. The times of onset and offset of drug action were each characterized by a half-life for changes in fMRI signal from within the insula. These characteristic times agreed with the observed drug-induced analgesia and previous pharmacokinetic-pharmacodynamic measurements for remifentanil. We have successfully measured, for the first time using fMRI, temporal pharmacological parameters for a CNS-active drug based on its effect on task-related activity in a specific brain region. Comparison of the time course of regional brain activity with pain perception could reveal those regions engaged in drug-induced analgesia.
引用
收藏
页码:626 / 635
页数:10
相关论文
共 60 条
[1]   The pharmacodynamic effect of a remifentanil bolus on ventilatory control [J].
Babenco, HD ;
Conard, PF ;
Gross, JB .
ANESTHESIOLOGY, 2000, 92 (02) :393-398
[2]  
Bannister PR, 2001, NEUROIMAGE, V13, pS70
[3]  
Becerra LR, 1999, MAGN RESON MED, V41, P1044, DOI 10.1002/(SICI)1522-2594(199905)41:5<1044::AID-MRM25>3.0.CO
[4]  
2-M
[5]  
Bloom AS, 1999, HUM BRAIN MAPP, V8, P235, DOI 10.1002/(SICI)1097-0193(1999)8:4<235::AID-HBM7>3.0.CO
[6]  
2-3
[7]   Acute effects of cocaine on human brain activity and emotion [J].
Breiter, HC ;
Gollub, RL ;
Weisskoff, RM ;
Kennedy, DN ;
Makris, N ;
Berke, JD ;
Goodman, JM ;
Kantor, HL ;
Gastfriend, DR ;
Riorden, JP ;
Mathew, RT ;
Rosen, BR ;
Hyman, SE .
NEURON, 1997, 19 (03) :591-611
[8]   TACTILE-VIBRATION-ACTIVATED FOCI IN INSULAR AND PARIETAL-OPERCULAR CORTEX STUDIED WITH POSITRON EMISSION TOMOGRAPHY - MAPPING THE 2ND SOMATOSENSORY AREA IN HUMANS [J].
BURTON, H ;
VIDEEN, TO ;
RAICHLE, ME .
SOMATOSENSORY AND MOTOR RESEARCH, 1993, 10 (03) :297-308
[9]   The noradrenergic α2 agonist clonidine modulates behavioural and neuroanatomical correlates of human attentional orienting and alerting [J].
Coull, JT ;
Nobre, AC ;
Frith, CD .
CEREBRAL CORTEX, 2001, 11 (01) :73-84
[10]   Thermosensory activation of insular cortex [J].
Craig, AD ;
Chen, K ;
Bandy, D ;
Reiman, EM .
NATURE NEUROSCIENCE, 2000, 3 (02) :184-190