LeBlanc Brian W, Lii Theresa R, Silverman Andrew E, Alleyne Robert T, Saab Carl Y
Department of Neurosurgery, Rhode Island Hospital, and Department of Neuroscience, Brown University, Providence, RI, USA.
Pain. 2014 Apr;155(4):773-782. doi: 10.1016/j.pain.2014.01.013. Epub 2014 Jan 20.
Thalamocortical oscillations are critical for sensory perception. Although pain is known to disrupt synchrony in thalamocortical oscillations, evidence in the literature is controversial. Thalamocortical coherence has been reported to be increased in patients with neurogenic pain but decreased in a rat model of central pain. Moreover, theta (4 to 8 Hz) oscillations in primary somatosensory (S1) cortex are speculated to predict pain in humans. To date, the link between pain and network oscillations in animal models has been understudied. Thus, we tested the hypothesis that pain disrupts thalamocortical coherence and S1 theta power in two rat models of pain. We recorded electrocorticography (ECoG) waveforms over S1 and local field potentials (LFP) within ventral posterolateral thalamus in freely behaving rats under spontaneous (stimulus-independent) pain conditions. Rats received intradermal capsaicin injection (Cap) in the hindpaw, followed hours later by chronic constriction injury (CCI) of the sciatic nerve lasting several days. Our results show that pain decreases coherence between LFP and ECoG waveforms in the 2- to 30-Hz range, and increases ECoG power in the theta range. These changes are short-lasting after Cap and longer-lasting after CCI. These data might be particularly relevant to preclinical correlates of spontaneous pain-like behavior, with potential implications to clinical biomarkers of ongoing pain.
丘脑皮质振荡对感觉感知至关重要。虽然已知疼痛会破坏丘脑皮质振荡的同步性,但文献中的证据存在争议。据报道,神经源性疼痛患者的丘脑皮质相干性增加,但在中枢性疼痛的大鼠模型中则降低。此外,推测初级体感(S1)皮层中的θ(4至8赫兹)振荡可预测人类的疼痛。迄今为止,动物模型中疼痛与网络振荡之间的联系尚未得到充分研究。因此,我们在两种疼痛大鼠模型中测试了疼痛会破坏丘脑皮质相干性和S1区θ功率的假设。我们在自由活动的大鼠处于自发(与刺激无关)疼痛状态下,记录了S1区上方的皮质电图(ECoG)波形以及腹后外侧丘脑内的局部场电位(LFP)。大鼠后爪接受皮内辣椒素注射(Cap),数小时后进行坐骨神经慢性压迫损伤(CCI),持续数天。我们的结果表明,疼痛会降低2至30赫兹范围内LFP与ECoG波形之间的相干性,并增加θ范围内的ECoG功率。这些变化在Cap注射后持续时间较短,而在CCI后持续时间较长。这些数据可能与自发性疼痛样行为的临床前相关性特别相关,对持续性疼痛的临床生物标志物具有潜在意义。