Transcript Slide 1

Early involvement of right operculo-insular cortex in processing pain
unpleasantness: evidence from laser evoked potentials
139784
488-P94
Deborah E. Bentley1, Ulf Baumgärtner2, Alison Watson1, Geoff Barrett3, Bhavna Kulkarni1, Paula D. Youell1,
Anthony K. P. Jones1, Rolf-Detlef Treede2
1
Univ. of Manchester Human Pain Research Group, Hope Hospital, Salford, UK; 2 Institute for Physiology & Pathophysiology,
Johannes Gutenberg Univ., Mainz, Germany; 3 Human Sciences Team, Defence Science and Technology Laboratory, Fareham, UK
N300-T7 and -FCz sub-groups
LEPs, global field power (GFP) and scalp
topography
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Amplitude (µV)
Right (ipsilateral) operculo-insular
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-4
-3
-2
-1
0
1
2
Left (contra) operculo-insular
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-6
FCz
T8
Electrode
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-3
-2
T7
FCz
T8
Electrode
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GFP peaks: 308 and 470 ms
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2
0
-500
0
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1000
1500
FCz
Latency (ms)
T7
Cz
T7
Pz
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The 21 volunteers differed in the scalp distribution of
the N300 peak; 10 showed a contralateral maximum at
electrode T7 while the other 11 showed a midline
maximum at FCz.
Amplitude (µV)
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-500
0
500
1000
1500
0
Latency (ms)
5
10
Source analysis
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N300
20
FCz
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500
1000
Amplitude (µV)
Amplitude (µV)
0
1500
0
Latency (ms)
5
10
4
0
0
Latency (ms)
430-440 ms
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15
30
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300
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500
600
Ipsilateral (right)
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0
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-30
P600-800
(P3e)
Amplitude (µV)
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500
1000
1500
600-800 ms
0
5
0
Control
Loc
Unpl
Unpl. > Control
FCz group
P<0.05 T7 group
Control
Loc
Unpl
The right (ipsilateral) source was significantly more
active during the Unpleasantness rating task than
during the Control task across the whole group
(strongest for T7 sub-group). There were no task
effects on other source activities or peak latencies.
Latency (ms)
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50
0
Greater activity in right operculo-insular
cortex during Unpleasantness task
suggests early processing of affective
component of pain in this area.
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-150
-200
15
P800-1000
20
(P3l)
Acknowledgements
60
800-1000 ms
Source activity (nAm)
Pz
Source activity (nAm)
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0
10
0
700
20
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-500
20
10
40
1500
Source activity (nAm)
Amplitude (µV)
1000
0
-10
30
20
Contralateral (left)
P450
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40
30
Latency (ms)
-10
500
50
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Conclusions
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Cz
0
60
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2
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-500
60
3
20
• 21 healthy right-handed volunteers randomly
received moderately painful CO2 laser stimuli to
2 adjacent sites on right forearm. Volunteers
performed 3 tasks:
• Attend to pain location - report pain location
(medial/lateral)
• Attend to pain unpleasantness - report
unpleasantness on 0-10 scale
• Control - report whether painful or not
• LEPs recorded from 61 electrodes (bandpass:
0.15-70 Hz, A/D rate: 500 Hz).
• 4-dipole model of Schlereth et al. (2003) fitted
to data using BESA: sources in bilateral
operculo-insular cortices, posterior midcingulate
and contralateral postcentral gyrus.
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Control task
n=21
GFP
290-300 ms
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-500
70
-5
0
T7
Right (ipsi) operculo-insular
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3
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-10
Methods
N300-FCz sub-group
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-5
LEPs (n=21)
Control task
GFP
N300-T7 sub-group
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Task and sub-group differences in
operculo-insular source activities
Source activity (nAm)
• Pain has sensory-discriminative, affectivemotivational & cognitive-evaluative components
(Melzack & Casey, 1968).
• The functional brain anatomy underlying these
components remains under investigation.
• We used source analysis of laser evoked
potentials (LEPs) to compare the temporal
sequence of brain activation when volunteers
selectively attended to either the
unpleasantness (affective component) or the
localisation (sensory component) of pain,
compared to a control task that was matched
for generalised attention.
• The results of the peak analyses of these data
were reported in Bentley et al. (2004).
Mean amplitude (µV)
Results
Mean amplitude (µV)
Introduction
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20
0
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LEPs consisted of 2 main components, N300
(maximal at T7 and FCz) and P450 (maximal at Cz),
with some late positivity evident at parietal sites (early
& late P3, P3e & P3l).
Latency (ms)
LEP data were well-explained by the source model
(mean goodness-of-fit = 83.5 ± 7.7%). The sources
were activated in the order: contralateral (left)
operculo-insular (opi) (blue, 280 ms), ipsilateral (right)
opi (red, 288 ms), early cingulate (green, 291 ms),
postcentral gyrus (magenta, 297 ms), late cingulate
(green, 450 ms).
Supported by the Arthritis Research Campaign, Dr
Hadwen Trust for Humane Research, Deutsche
Forschungsgemeinschaft & Human Sciences Domain
of the UK Ministry of Defence Scientific Research
Programme.