Experiments have been carried out in order to study which ascending spinal pathways are utilized by peripherally-originated impulses and activating callosal fibres. In chloralose-anaesthetized cats stim uli of graded intensities were applied to the superficial (SRN) and deep (DRN) radial nerves. Mass potentials were recorded simultaneously from the cerebral cortex (SI, SII and 3a areas, according to the experiment), from the somesthetic callosal region (SCR) and, on some occasions, from the distal end of a cut dorsal rootlet (C7-C8; electroneurogram). The amplitude curves of cortical and callosal responses (averagings of 50 responses) were plotted as a function of stimulus intensities. In a first series of experiments (preparations with SCT intact) the dorsal columns (DC) were transected. After this section, the cortical and callosal responses elicited upon SRN stimulation were clearly reduced (60-75% in the cortex and 80-85% in the SCR) and their thresholds were slightly raised. The latency of the cortical responses was slightly increased (about 0.5 msec), whereas that of the callosal ones exhibited a greater increase (1.73 msec). In the cortical responses (3a) elicited upon DRN stimulation DC transection provoked amplitude reductions of 80-85% in respect of controls, and an increase of threshold up to about 2 cT (cortical threshold) whereas the callosal responses exhibited amplitude reductions of 55-65% and but a slight increase in their threshold. The latency of the cortical responses increased by 2.83 msec and that of the callosal ones by 2.73 msec. In a second series of experiments (preparations with DC intact) the spino-cervico-thalamic tract (SCT) was transected. After this section, the cortical potentials which were elicited upon SRN stimulation exhibited amplitude reductions of 15-45% when stimulus strengths lower than 2.6-2.8 cT were applied, whereas no amplitude change was observed when stronger stimuli were utilized. The impairment in the amplitude of callosal potentials was observed not only in the responses evoked by weaker stimuli but, usually, in all responses evoked over the entire strength range tested. No significant change was seen in the latency of both cortical and callosal responses. Upon DRN stimulation the cortical mass potentials exhibited a change in amplitude, threshold and latency. On the contrary, the callosal responses showed an amplitude reduction of about 50% and a slight increase in threshold, whereas no change was observed in their latency. The differential effects exerted by the sections on some parameters of the cortical and callosal mass potentials can be discussed with reference to the “filtering action” exerted by the somatosensory cortex on its callosal output.
@article{RLINA_1976_8_60_5_673_0, author = {Roberto Caminiti and Tullio Manzoni and Sandro Michelini and Giuseppe Spidalieri}, title = {Ruolo delle colonne dorsali e del tratto spino-cervico-talamico nella ritrasmissione di informazioni somestesiche al corpo calloso}, journal = {Atti della Accademia Nazionale dei Lincei. Classe di Scienze Fisiche, Matematiche e Naturali. Rendiconti}, volume = {60}, year = {1976}, pages = {673-679}, language = {it}, url = {http://dml.mathdoc.fr/item/RLINA_1976_8_60_5_673_0} }
Caminiti, Roberto; Manzoni, Tullio; Michelini, Sandro; Spidalieri, Giuseppe. Ruolo delle colonne dorsali e del tratto spino-cervico-talamico nella ritrasmissione di informazioni somestesiche al corpo calloso. Atti della Accademia Nazionale dei Lincei. Classe di Scienze Fisiche, Matematiche e Naturali. Rendiconti, Tome 60 (1976) pp. 673-679. http://gdmltest.u-ga.fr/item/RLINA_1976_8_60_5_673_0/
[1] Some properties of the thalamic relay cells in the spino-cervico-lemniscal path, «Acta Physiol. Scand.», 68, 72.
, e (1966) -[2] Does the spinocervical pathway exist?, «Brain Res.», 98, 359.
e (1975) -[3] Callosal transfer of impulses originating from superficial and deep nerves of the cat forelimb, «Arch. ital. Biol.», 114, 155.
, , e (1976) -[4] Central pathway for cutaneous impulses in the cat., «Am. J. Physiol.», 189, 141.
e (1957) -[5] Differential contributions of spinal pathways to body representation in postcentral gyrus of macaca mulatta, «J. Neurophysiol.», 37, 119.
, , e (1974) -[6] Response of somatosensory cerebral neurones to stimulation of dorsal and dorsolateral spinal funiculi, «Exp. Neurol.», 43, 124.
e (1974) -[7] Patterns of the somesthetic messages transferred through the corpus callosum, «Exp. Brain Res.», 19, 447.
, e (1974) -[8] The location of the thalamic relay in the spino-cervico-lemniscal path, «Acta Physiol. Scand.», 65, 164.
, (1965) -[9] Cortical projection of impulses in myelinated cutaneous afferent nerve fibers of the cat, «J. Physiol.», 142, 544.
e (1958) -[10] Tactile pathways from the hindlimb to the cerebral cortex in cat, «Acta Physiol. Scand.», 54, 9.
e (1962) -[11] An evoked potential study of different pathways from the hindlimb to the somatosensory areas in the cat, «Acta Physiol. Scand.», 66, 19.
(1966) -[12] Projection to cerebral cortex of large muscle-spindle afferents in forelimb nerves of the cat, «J. Physiol.», 169, 924.
e (1963) -[13] Short-latency projections to the cat's cerebral cortex from skin and muscle afferents in the contralateral forelimb, «J. Physiol.», 182, 164.
e (1966) -[14] Action of graded cutaneous and muscular afferent volleys on brain stem units in the decerebrate, cerebellectomized cat, «Arch. ital. Biol.», 101, 552.
e (1963) -[15] The sensory and motor role of impulses traveling in the dorsal columns towards cerebral cortex, «Brain», 93, 505.
(1970) -[16] Role of spinocervical tract in production of the primary cortical response evoked by forepaw stimulation, «Exp. Neurol.», 25, 349.
, e (1969) -