Geha P Y, Baliki M N, Wang X, Harden R N, Paice J A, Apkarian A V
Department of Physiology, Northwestern University, Feinberg School of Medicine, 5-120 Ward Building, 303 East Chicago Avenue, Chicago, IL 60611, USA Rehabilitation Institute of Chicago, Northwestern University, Feinberg School of Medicine, 303 East Chicago Avenue, Chicago, IL 60611, USA Department of Medicine, Northwestern University, Feinberg School of Medicine, 303 East Chicago Avenue, Chicago, IL 60611, USA Departments of Anesthesia, Surgery, and Lurie Cancer Center, Northwestern University, Feinberg School of Medicine, 303 East Chicago Avenue, Chicago, IL 60611, USA.
Pain. 2008 Sep 15;138(3):641-656. doi: 10.1016/j.pain.2008.02.021. Epub 2008 Apr 1.
Postherpetic neuralgia (PHN) is a debilitating chronic pain condition often accompanied by a sensation of pain when the affected region is touched (tactile allodynia). Here we identify brain regions involved in stimulus-induced touch-evoked pain (dynamical mechanical allodynia, DMA), compare brain activity between DMA and spontaneous pain (described earlier for the same patients in [Geha PY, Baliki MN, Chialvo DR, Harden RN, Paice JA, Apkarian AV. Brain activity for spontaneous pain of postherpetic neuralgia and its modulation by lidocaine patch therapy. Pain 2007;128:88-100]), delineate regions that specifically code the magnitude of perceived allodynia, and show the transformation of allodynia-related information in the brain as a time-evolving network. Eleven PHN patients were studied for DMA and its modulation with Lidoderm therapy (patches of 5% lidocaine applied to the PHN affected body part). Continuous ratings of pain while the affected body part was brushed during fMRI were contrasted with non-painful touch when brushing was applied to an equivalent opposite body site, and with fluctuations of a bar observed during scanning, at three sessions relative to Lidoderm treatment. Lidoderm treatment did not decrease DMA ratings but did decrease spontaneous pain. Multiple brain areas showed preferential activity for allodynia. However, mainly responses in the bilateral putamen and left medial temporal gyrus were related to the magnitude of allodynia. Both DMA and spontaneous pain perceptions were best represented within the same sub-cortical structures but with minimal overlap, implying that PHN pain modulates behavioral learning and hedonics. These results have important clinical implications regarding adequate therapy.
带状疱疹后神经痛(PHN)是一种使人衰弱的慢性疼痛病症,常在受影响区域被触碰时伴有疼痛感觉(触觉异常性疼痛)。在此,我们确定了与刺激诱发的触摸诱发疼痛(动态机械性异常性疼痛,DMA)相关的脑区,比较了DMA与自发痛之间的脑活动([Geha PY、Baliki MN、Chialvo DR、Harden RN、Paice JA、Apkarian AV. 带状疱疹后神经痛自发痛的脑活动及其利多卡因贴片治疗的调节作用。疼痛2007;128:88 - 100]中对同一患者先前已有描述),描绘了专门编码所感知异常性疼痛程度的区域,并展示了作为一个随时间演变的网络的脑内异常性疼痛相关信息的转化。对11名PHN患者进行了DMA及其利多卡因贴剂治疗(将5%利多卡因贴片应用于PHN受累身体部位)调节作用的研究。在功能磁共振成像(fMRI)期间对受累身体部位进行刷擦时的连续疼痛评分,与在等效对侧身体部位进行刷擦时的非疼痛性触摸以及扫描期间观察到的横条波动进行对比,这是相对于利多卡因贴剂治疗的三个阶段。利多卡因贴剂治疗并未降低DMA评分,但确实降低了自发痛。多个脑区对异常性疼痛表现出优先活动。然而,主要是双侧壳核和左侧颞中回的反应与异常性疼痛的程度相关。DMA和自发痛感知在同一皮质下结构中表现最佳,但重叠最小,这意味着PHN疼痛调节行为学习和享乐感受。这些结果对于适当治疗具有重要的临床意义。