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

被引:117
作者
Eto, Kei [1 ]
Wake, Hiroaki [1 ]
Watanabe, Miho [1 ]
Ishibashi, Hitoshi [1 ]
Noda, Mami [2 ]
Yanagawa, Yuchio [3 ]
Nabekura, Junichi [1 ,4 ]
机构
[1] Natl Inst Physiol Sci, Div Homeostat Dev, Dept Dev Physiol, Okazaki, Aichi 4448585, Japan
[2] Kyushu Univ, Lab Pathophysiol, Grad Sch Pharmaceut Sci, Fukuoka 8128582, Japan
[3] Gunma Univ, Dept Genet & Behav Neurosci, Grad Sch Med, Maebashi, Gunma 3718511, Japan
[4] Grad Univ Adv Studies SOKENDAI, Dept Physiol Sci, Okazaki, Aichi 4448585, Japan
关键词
LONG-TERM POTENTIATION; NEUROPATHIC PAIN; PLASTICITY; ALLODYNIA; CONNECTIVITY; NEUROSCIENCE;
D O I
10.1523/JNEUROSCI.0946-11.2011
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
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 Ca2+ 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.
引用
收藏
页码:7631 / 7636
页数:6
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