首页> 美国卫生研究院文献>The Journal of Neuroscience >Inter-regional Contribution of Enhanced Activity of the Primary Somatosensory Cortex to the Anterior Cingulate Cortex Accelerates Chronic Pain Behavior
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Inter-regional Contribution of Enhanced Activity of the Primary Somatosensory Cortex to the Anterior Cingulate Cortex Accelerates Chronic Pain Behavior

机译:初级躯体感觉皮层对前扣带状皮层活动增强的区域间贡献加速了慢性疼痛行为。

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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.
机译:疼痛处理涉及多个皮质区域,包括主要的体感皮质(S1)和前扣带回皮质(ACC)。尽管有大量证据表明,S1活性在慢性疼痛条件下会增加,但尚不清楚S1内是否发生可塑性改变,以及可塑性改变是否以及如何促进慢性疼痛行为。在这里,我们提供了第一个证据,即通过调节ACC(慢​​性疼痛的重要皮质区域之一)中的神经元活动,小鼠S1内的区域内重塑可加速慢性疼痛行为。使用双光子Ca 2 + 成像,我们发现在慢性疼痛条件下,S1中第2/3层神经元的自发活动以及对感觉和第4层刺激的响应增加。此外,药理学衰减和促进S1活性分别减弱和促进了慢性疼痛行为。此外,ACC对周围刺激的电反应与S1神经元活性成功相关,并且抑制ACC活性可减轻机械性异常性疼痛。目前的结果将通过侧重于S1和ACC提供有效的治疗慢性疼痛的治疗策略。

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