TY - JOUR
T1 - Stimulus site and modality dependence of functional activity within the human spinal cord
AU - Brooks, Jonathan C.W.
AU - Kong, Yazhuo
AU - Lee, Michael C.
AU - Warnaby, Catherine E.
AU - Wanigasekera, Vishvarani
AU - Jenkinson, Mark
AU - Tracey, Irene
N1 - Funding Information:
This paper reports on part of the activities of the Grupo de Radiacidn Solar de Valencia and project CTIDIB/2002/113 funded by the regional government, the Generalitat Valenciana. We would like to thank the R+D+i Linguistic Assistance Office at the Universidad Politecnica of Valencia for their help in revising this paper.
PY - 2012/5/2
Y1 - 2012/5/2
N2 - Chronic pain is thought to arise because of maladaptive changes occurring within the peripheral nervous system and CNS. The transition from acute to chronic pain is known to involve the spinal cord (Woolf and Salter, 2000). Therefore, to investigate altered human spinal cord function and translate results obtained from other species, anoninvasive neuro imaging techniqueis desirable. We have investigated the functional response in the cervical spinal cord of 18 healthy human subjects (aged 22-40years) to noxious thermal and non-noxious tactile stimulation of the left and right forearms. Physiological noise, which is a significant source of signal variability in the spinal cord, was accounted for in the general linear model. Group analysis, performed using a mixed-effects model, revealed distinct regions of activity that were dependent on both the side and the type of stimulation. In particular, thermal stimulation on the medial aspect of the wrist produced activity within the C6/C5 segment ipsilateral to the side of stimulation. Similar to data recorded in animals (Fitzgerald, 1982), painful thermal stimuli produced increased ipsilateral and decreased contralateral blood flow, which may reflect, respectively, excitatory and inhibitory processes. Non painful punctate stimulation of the thenar eminence provoked more diffuse activity but was still ipsilateral to the side of stimulation. These results present the first noninvasive evidence for a lateralized response to noxious and non-noxious stimuli in the human spinal cord. The development of these techniques opens the path to understanding, at a subject-specific level, central sensitization processes that contribute to chronic pain states.
AB - Chronic pain is thought to arise because of maladaptive changes occurring within the peripheral nervous system and CNS. The transition from acute to chronic pain is known to involve the spinal cord (Woolf and Salter, 2000). Therefore, to investigate altered human spinal cord function and translate results obtained from other species, anoninvasive neuro imaging techniqueis desirable. We have investigated the functional response in the cervical spinal cord of 18 healthy human subjects (aged 22-40years) to noxious thermal and non-noxious tactile stimulation of the left and right forearms. Physiological noise, which is a significant source of signal variability in the spinal cord, was accounted for in the general linear model. Group analysis, performed using a mixed-effects model, revealed distinct regions of activity that were dependent on both the side and the type of stimulation. In particular, thermal stimulation on the medial aspect of the wrist produced activity within the C6/C5 segment ipsilateral to the side of stimulation. Similar to data recorded in animals (Fitzgerald, 1982), painful thermal stimuli produced increased ipsilateral and decreased contralateral blood flow, which may reflect, respectively, excitatory and inhibitory processes. Non painful punctate stimulation of the thenar eminence provoked more diffuse activity but was still ipsilateral to the side of stimulation. These results present the first noninvasive evidence for a lateralized response to noxious and non-noxious stimuli in the human spinal cord. The development of these techniques opens the path to understanding, at a subject-specific level, central sensitization processes that contribute to chronic pain states.
UR - http://www.scopus.com/inward/record.url?scp=84860324918&partnerID=8YFLogxK
U2 - 10.1523/JNEUROSCI.2543-11.2012
DO - 10.1523/JNEUROSCI.2543-11.2012
M3 - Article
C2 - 22553029
AN - SCOPUS:84860324918
VL - 32
SP - 6231
EP - 6239
JO - Journal of Neuroscience
JF - Journal of Neuroscience
SN - 0270-6474
IS - 18
ER -