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      Inter-regional Contribution of Enhanced Activity of the Primary Somatosensory Cortex to the Anterior Cingulate Cortex Accelerates Chronic Pain Behavior

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          Abstract

          Multiple cortical areas are involved in pain processing, including the primary somatosensory cortex (S1) and the anterior cingulate cortex (ACC). Although accumulations of evidence suggest that the S1 activity increases under chronic pain conditions, whether plastic change occurs or not within the S1, and whether and how the plastic change contributes to chronic pain behavior, is unknown. Here, we provide the first evidence that intra-regional remodeling within the mouse S1 accelerates chronic pain behavior by modulating neuronal activity in the ACC, one of the important cortical areas for chronic pain. Using two-photon Ca 2+ imaging, we found that the spontaneous activity of layer 2/3 neurons in the S1 and then response to sensory and layer 4 stimulations increased under chronic pain conditions. In addition, pharmacological attenuation and facilitation of S1 activity attenuated and facilitated the chronic pain behavior, respectively. Furthermore, electrical response of the ACC to peripheral stimulation successfully correlated with S1 neuronal activity, and inhibition of ACC activity alleviated the mechanical allodynia. The present results will provide development of efficient therapeutic strategies against chronic pain by focusing on the S1 and ACC.

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          Author and article information

          Journal
          J Neurosci
          J. Neurosci
          jneuro
          jneurosci
          J. Neurosci
          The Journal of Neuroscience
          Society for Neuroscience
          0270-6474
          1529-2401
          25 May 2011
          : 31
          : 21
          : 7631-7636
          Affiliations
          [1] 1Department of Developmental Physiology, Division of Homeostatic Development, National Institute for Physiological Sciences, Okazaki 444-8585, Japan,
          [2] 2Laboratory of Pathophysiology, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka 812-8582, Japan,
          [3] 3Department of Genetic and Behavioral Neuroscience, Gunma University Graduate School of Medicine, Maebashi 371-8511, Japan, and
          [4] 4Department of Physiological Sciences, The Graduate University for Advanced Studies (SOKENDAI), Okazaki 444-8585, Japan
          Author notes
          Correspondence should be addressed to Dr. Junichi Nabekura, Division of Homeostatic Development, Department of Developmental Physiology, National Institute for Physiological Sciences, 38 Nishigonaka, Myodaiji, Okazaki 444-8585, Japan. nabekura@ 123456nips.ac.jp

          Author contributions: K.E., H.W., M.W., H.I., M.N., Y.Y., and J.N. designed research; K.E. performed research; K.E. analyzed data; K.E. and J.N. wrote the paper.

          Article
          PMC6633125 PMC6633125 6633125 3697432
          10.1523/JNEUROSCI.0946-11.2011
          6633125
          21613476
          a6f63863-b512-416c-90b4-aac0027af22f
          Copyright © 2011 the authors 0270-6474/11/317631-06$15.00/0
          History
          : 22 February 2011
          : 31 March 2011
          : 9 April 2011
          Categories
          Brief Communication

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