Abstract
Primary cold and warm afferent fibers show a robust overshoot in their firing during periods of temperature change, which subsides during tonic thermal stimulation. Our objective was to analyze cortical activation, on a scale of hundreds of milliseconds, occurring during the process of dynamic cooling and warming, based on an evaluation of the amplitude changes seen in 10 Hz electroencephalographic oscillations.
Eleven right-handed subjects were exposed to innocuous cold ramp stimuli (from 32 degrees C to 22 degrees C, 10 degrees C/s) and warm ramp stimuli (32 degrees C to 42 degrees C, 10 degrees C/s) on the thenar region of their right palm, using a contact thermode. EEG was recorded from 111 scalp sites, and the 10 Hz current source densities were modeled using low-resolution electromagnetic tomography.
During cooling, the earliest amplitude decreases of 10 Hz oscillations were seen in the contralateral posterior insula and secondary somatosensory cortex (SII), and the premotor cortex (PMC). During warming, the earliest events were only observed in the PMC and occurred approximately 0.7 s later than during cooling.
Linear regression analysis between 10 Hz current source densities and temperature variations revealed cooling-sensitive activation in the bilateral posterior insula, PMC and the anterior cingulate cortex. During warming, the amplitude of 10 Hz oscillations in the PMC and posterior insula correlated with stimulus temperature.
Dynamic thermal stimulation activates, in addition to the posterior insula and parietal operculum, the lateral PMC. The activation of the anterior cingulate cortex during cooling may aid in the anticipation of the cold temperature end-point and provide continuous evaluation of the thermal stimulus.