TY - JOUR
T1 - Imaging of central itch modulation in the human brain using positron emission tomography
AU - Mochizuki, Hideki
AU - Tashiro, Manabu
AU - Kano, Michiko
AU - Sakurada, Yumiko
AU - Itoh, Masatoshi
AU - Yanai, Kazuhiko
N1 - Funding Information:
This study was supported by Grants-in-Aid for Scientific Research (B) (No. 12557007, 14370027 and 14770489) from Japan Society for the Promotion of Science and a 21st century COE program (Bio-nano-technology) from the Ministry of Education, Science, Sports and Culture, Japan. We appreciate technical assistance of Mr M. Miyake, Y. Ishikawa and S. Watanuki in our PET studies.
PY - 2003/9
Y1 - 2003/9
N2 - The unpleasantness of itching is reduced by cooling. Although previous research suggests the presence of a central itch modulation system, there is little documentation about the modulation system in the brain. In the present study, we investigated the modulating system of the itching sensation in human brains using positron emission tomography and H2 15O. The significant increases of regional cerebral blood flow caused by histamine stimuli using iontophoresis were observed in the anterior cingulate cortex (BA24), the thalamus, the parietal cortex (BA40 and BA7), the dorsolateral prefrontal cortex (BA46) and the premotor cortex (BA6). We did not observe any changes in the secondary somatosensory cortex (S2) during the itching stimulus, corresponding to the previous imaging studies concerning itching. Activation in these areas related to itching stimuli was decreased by a simultaneous stimulation of itching and cold pain (the dual stimuli), as compared to itching alone. Interestingly, the midbrain, including periaqueductal gray matter (PAG), was only activated during the dual stimuli. PAG is well known to be a modulating noxious stimulus. Here we hypothesize that the activation of PAG may also be related to the itch modulation. These findings indicate that the modified brain activities in the PAG, the cingulate, the frontal and the parietal cortex might be associated with the itch modulation in the central nervous system and that the S2 might not be primarily involved in processing the itching perception in the brain since the activity of S2 was not observed in any concentration of itching stimuli.
AB - The unpleasantness of itching is reduced by cooling. Although previous research suggests the presence of a central itch modulation system, there is little documentation about the modulation system in the brain. In the present study, we investigated the modulating system of the itching sensation in human brains using positron emission tomography and H2 15O. The significant increases of regional cerebral blood flow caused by histamine stimuli using iontophoresis were observed in the anterior cingulate cortex (BA24), the thalamus, the parietal cortex (BA40 and BA7), the dorsolateral prefrontal cortex (BA46) and the premotor cortex (BA6). We did not observe any changes in the secondary somatosensory cortex (S2) during the itching stimulus, corresponding to the previous imaging studies concerning itching. Activation in these areas related to itching stimuli was decreased by a simultaneous stimulation of itching and cold pain (the dual stimuli), as compared to itching alone. Interestingly, the midbrain, including periaqueductal gray matter (PAG), was only activated during the dual stimuli. PAG is well known to be a modulating noxious stimulus. Here we hypothesize that the activation of PAG may also be related to the itch modulation. These findings indicate that the modified brain activities in the PAG, the cingulate, the frontal and the parietal cortex might be associated with the itch modulation in the central nervous system and that the S2 might not be primarily involved in processing the itching perception in the brain since the activity of S2 was not observed in any concentration of itching stimuli.
KW - Histamine
KW - Itch modulation
KW - Periaqueductal gray matter
KW - Positron emission tomography
KW - Secondary somatosensory cortex
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U2 - 10.1016/S0304-3959(03)00249-5
DO - 10.1016/S0304-3959(03)00249-5
M3 - Article
C2 - 14499452
AN - SCOPUS:0141515633
SN - 0304-3959
VL - 105
SP - 339
EP - 346
JO - Pain
JF - Pain
IS - 1-2
ER -