Faculty of Human Life and Environment, Nara Women's University, Japan.
Department of Integrative Physiology, National Institute for Physiological Sciences, Okazaki, Japan.
Eur J Pain. 2018 Nov;22(10):1791-1799. doi: 10.1002/ejp.1275. Epub 2018 Jul 16.
This study investigated the characteristics of temperature-related evoked neural activities to baseline skin temperatures on target and adjacent sites using contact heat evoked potentials (CHEPs).
Contact heat evoked potentials were recorded from 12 normal subjects during three stimuli: target temperatures for "warm", "hot" and "pain" were set at 41, 46 and 51 °C, respectively. The baseline temperature was separately set at 30, 35 and 40 °C under all conditions, and a heat pulse was delivered over the right forearm at 41 °C under the warm condition, at 46 °C under the hot condition and at 51 °C under the pain condition.
The N2-P2 amplitude was significantly larger at the 40 °C baseline than at the 30 and 35 °C baselines during the pain condition, whereas no significant differences were observed during the hot and warm conditions. In addition, the effects of an interference warm stimulation to adjacent sites were examined; however, no significant effects were observed.
These results suggest that the priming effects of temperature on CHEPs were only observed under the pain condition, indicating the specificity of thermal pain, as well as a difference in the neural mechanisms responsible for thermal noxious and innocuous processing in human brains.
This study using CHEPs shows the importance of baseline and target skin temperatures to investigate the characteristics of temperature-related neural activities. This measure may contribute to understanding of warm-, hot-, and pain-related neural activities in human brains.
本研究采用接触热诱发电位(CHEPs),研究了与基线皮肤温度相关的温度诱发神经活动的特点。
在三种刺激条件下,对 12 名正常受试者的接触热诱发电位进行了记录:“温暖”、“热”和“疼痛”的目标温度分别设定为 41、46 和 51°C;在所有条件下,基线温度分别设定为 30、35 和 40°C,在温暖条件下,41°C 时,在热条件下 46°C 时,在疼痛条件下 51°C 时,在右前臂上施加热脉冲。
在疼痛条件下,40°C 基线时的 N2-P2 振幅明显大于 30°C 和 35°C 基线时的振幅,而在热和温暖条件下则没有观察到明显差异。此外,还检查了相邻部位干扰性热刺激的影响,但没有观察到显著影响。
这些结果表明,CHEPs 中温度的启动效应仅在疼痛条件下观察到,表明热痛的特异性以及人类大脑中负责热伤害性和无害性处理的神经机制的差异。
本研究使用 CHEPs 表明,基线和目标皮肤温度对研究与温度相关的神经活动特征非常重要。这种测量方法可能有助于理解人类大脑中与温暖、热和疼痛相关的神经活动。