To investigate the excitability of Adelta nociceptive pathways and the nature of the vertex laser evoked potentials (LEPs), we studied the recovery cycle of the P2-LEP component and compared it with that of the P200 of the somatosensory evoked potential (SEP). Using two identical CO(2)-laser stimulators, we delivered paired stimuli to two adjacent skin spots on the hand at interstimulus intervals ranging from 250 ms to 2 s. The test P2-LEP was strongly inhibited at the 250-ms interstimulus interval ( P<0.01) and progressively recovered by the 2-s interval. The P200-SEP, after paired stimuli to the median nerve, showed a time course even slower than the P2-LEP ( P<0.01). Besides providing the LEP recovery curve in normal subjects, our findings indicate that the P2-LEP relays through a number of synapses similar to (or even lower than) that for the P200-SEP, thus lending further support to the view that the nociceptive P2-LEP is not an endogenous potential equivalent to the P300.
Excitability of the Adelta nociceptive pathways as assessed by the recovery cycle of laser evoked potentials in humans / Truini, Andrea; P., Rossi; F., Galeotti; A., Romaniello; M., Virtuoso; DE LENA, Carlo; M., Leandri; Cruccu, Giorgio. - In: EXPERIMENTAL BRAIN RESEARCH. - ISSN 0014-4819. - 155:(2004), pp. 120-123. [10.1007/s00221-003-1785-x]
Excitability of the Adelta nociceptive pathways as assessed by the recovery cycle of laser evoked potentials in humans.
TRUINI, ANDREA;DE LENA, Carlo;CRUCCU, Giorgio
2004
Abstract
To investigate the excitability of Adelta nociceptive pathways and the nature of the vertex laser evoked potentials (LEPs), we studied the recovery cycle of the P2-LEP component and compared it with that of the P200 of the somatosensory evoked potential (SEP). Using two identical CO(2)-laser stimulators, we delivered paired stimuli to two adjacent skin spots on the hand at interstimulus intervals ranging from 250 ms to 2 s. The test P2-LEP was strongly inhibited at the 250-ms interstimulus interval ( P<0.01) and progressively recovered by the 2-s interval. The P200-SEP, after paired stimuli to the median nerve, showed a time course even slower than the P2-LEP ( P<0.01). Besides providing the LEP recovery curve in normal subjects, our findings indicate that the P2-LEP relays through a number of synapses similar to (or even lower than) that for the P200-SEP, thus lending further support to the view that the nociceptive P2-LEP is not an endogenous potential equivalent to the P300.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.