The somatosensory intercollicular nucleus of the cat's mesencephalon (original) (raw)
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Journal of Comparative Neurology, 2004
Experiments were carried out on the second somatic sensory area (SII) of cats to study (1) the laminar distribution of axon terminals from the ipsilateral first somatic sensory cortex (SI); and (2) the topographical relations between their terminal field and the callosal neurons projecting to the contralateral homotopic cortex. To label simultaneously in SII both ipsilateral cortical afferents and callosal cells, cats were given iontophoretic injections of Phaseolus vulgaris-leucoagglutinin (PHA-L) in the forepaw zone of ipsilateral SI, and pressure injections of horseradish peroxidase (HRP) in the same zone of contralateral SII. The possibility that ipsilateral cortical axon terminals synape callosal neurons was investigated with the electron microscope by combining lesion-induced degeneration with retrograde HRP labelling.Fibers and terminations immunolabelled with PHA-L from ipsilateral SI were distributed in SII in a typical patchy pattern and were mostly concentrated in supragranular layers. Labelled fibers formed a very dense plexus in layer III and ramified densely also in layers I and II. Labelled axon terminals were both en passant and single-stalked boutons. Counts of 8,303 PHA-L-labelled terminals of either type showed that 82.40% were in supragranular layers. The highest concentration was in layer III (43.99%), followed by layers II (30.22%) and I (8.09%). The remaining terminals were distributed among layers IV (6.96%), V (4.93%), and VI (5.68%). The same region of SII containing anterogradely labelled axons and terminals also contained numerous neurons retrogradely labelled with HRP from contralateral SII. Callosal projection neurons were pyramidal, dwelt mainly in layer III, and were distributed tangentially in periodic patches. Patches of anterograde and retrograde labelling either interdigitated or overlapped both areally and laminarly. In the zones of overlap, numerous PHA-L-labelled axon terminals were seen in close apposition to HRP-labelled pyramidal cell dendrites. Combined HRP-electron microscopic degeneration experiments showed that in SII axon terminals from ipsilateral SI form asymmetric synapses with HRP-labelled dendrites and dendriticc spines pertaining to callosal projection neurons.These results are discussed in relation to the layering and function of the SI to SII projection, and to the evidence that SII neurons projecting to the homotopic area of the contralateral hemisphere have direct access to the sensory information transmitted from ipsilateral SI. © 1994 Wiley-Liss, Inc.
The Journal of Physiology, 1984
1. Previous studies of input on to spinocervical tract neurones have been extended by investigating the post-synaptic actions of non-cutaneous afferent fibres and of descending tracts on to these neurones, using intracellular recording. In particular, actions of group II muscle, joint and Pacinian afferent fibres and rubro-and corticospinal tract fibres were investigated. 2. Group II muscle afferent fibres evoked excitation and inhibition at a minimal latency compatible with a disynaptic linkage. Increasing the stimulus strength to include group III afferent fibres enhanced these post-synaptic actions only modestly. Inhibition was evoked less frequently and/or required trains of stimuli. 3. Weak stimulation of the interosseous nerve evoked short latency (disynaptic) inhibition or excitation, the latter less frequently. Post-synaptic potentials evoked below threshold for group III afferent fibres of the interosseous nerve are attributed to the actions of Pacinian corpuscles. 4. Low threshold joint afferent fibres evoked excitation at short latency. Higher threshold joint afferent fibres usually evoked inhibition at longer latency, although high threshold excitation was sometimes observed. 5. Stimulation of the pyramidal tract evoked constant latency, unitary e.p.s.p.s which followed high frequencies. The evidence suggests that such e.p.s.p.s are evoked monosynaptically. Polysynaptic excitation and inhibition were also observed. 6. No convincing evidence could be found of actions evoked directly by the rubrospinal tract, although actions mediated via other descending systems could be induced from the red nucleus. 7. A large degree of convergence was seen from different peripheral and descending systems on to individual neurones.
Homotypical ipsilateral cortical projections between somatosensory areas I and II in the cat
Neuroscience, 1985
In 11 cats, small quantities of horseradish peroxidase conjugated to wheat germ agglutinin were placed into cortical zones of somatosensory area I representing the distal digits (n = 3), distal toes (n = 2), toes and digits (n = 1), proximal forelimb (n = 1), proximal hindlimb (n = 1), trunk (n = 2), and the face and nose (n = 1). Reconstruction of the pattern of retrograde labeling in somatosensory area II revealed dense, heavily labeled patches of cells in regions that were precisely homotypical to the injection site as determined by electrophysiological recordings. This dense, homotypical patch of labeled cells was usually surrounded by a less densely populated fringe of labeled cells that bordered, but did not appear to enter, heterotypical zones. In two animals, however, some retrogradely labeled cells were found in the cortex representing somatotopic zones adjacent to the sites injected with horseradish peroxidase. These results indicated that somatosensory area II primarily sends homotypical projections to somatosensory area I. In a few cases, however, some retrogradely labeled cells may represent either homo-or heterotypical projections depending on how receptive field sizes and the areal extent of labeling in somatosensory areas I and II are interpreted.
Brain Research, 1986
The terminal areas and the cells of origin of the projection from the sensory trigeminal nuclei to the mesencephalon were investigated, using the method of anterograde and retrograde transport of horseradish peroxidase or wheat germ agglutinin-horseradish peroxidase conjugate. Injection of tracer into the nucleus interpolaris or nucleus oralis (in the latter cases with involvement of the nucleus principalis) resulted in dense anterograde labeling in the deep and intermediate gray layers of the contralateral superior colliculus, extending throughout the rostrocaudal extent of the colliculus with the exception of its caudalmost part, which was not labeled. Minor projections to the intercollicular nucleus, posterior pretectal nucleus and nucleus of Darkschewitsch were found. Injection of tracer into the nucleus caudalis yielded a completely different result; terminal labeling in the midbrain was now present only in the periaqueductal gray matter, in its rostral and middle parts. The retrograde labeling observed after injection of tracer into the midbrain terminal areas showed that the cells of origin were located mainly in the alaminar spinal trigeminal nucleus, and the highest density of labeled neurons was found in the rostral part (subnucleus y) of the nucleus oralis. The retrograde labeling in the nucleus principalis was very sparse and almost exclusively involved peripherally located neurons. In the nucleus caudalis the overwhelming majority of the retrogradely labeled neurons were situated in its marginal layer. The functional implications of the above observations are discussed in relation to the findings in previous studies of the projections from the dorsal column nuclei and spinal cord to the midbrain. The combined results suggest that the trigeminal projections to the superior colliculus may be involved in the mechanisms of orientational behavior. The observation that the projection to the periaqueductal gray matter originates in the marginal layer suggests that it transmits information related to noxious stimuli.
Pyramidal excitation in long propriospinal neurones in the cervical segments of the cat
Experimental Brain Research, 1991
1. The effect of stimulating the contralateral pyramid has been investigated with intracellular recording from 128 long propriospinal neurones (long PNs) in the C3-Th1 segments of the cat. Long PNs were identified by the antidromic activation from the Th13 segment. They were located in laminae VII-VIII of Rexed. Single pyramidal stimulation evoked monosynaptic EPSPs in 15/40 of the long PNs in cats with intact pyramid. In 15 other long PNs, a train of three to four pyramidal stimuli evoked EPSPs with latencies indicating a minimal disynaptic linkage. The remaining 25% of the long PNs lacked mono- or disynaptic pyramidal EPSPs. In a few cases longer latency excitation was observed. 2. The location of the intercalated neurones which mediate the disynaptic pyramidal EPSPs was investigated by making four different lesions of the corticofugal fibres: 1) at the border of the C5 and C6 segments, 2) at the border of the C2 and C3 segments, 3) at the caudal part of the pyramid; three mm rostral to the decussation and 4) at the level of the trapezoid body. Stimulation of the corticofugal fibres was made either rostral to lesion 3 (rPyr) in order to activate neurones in a cortico-bulbospinal pathway or caudal to lesion 3 (cPyr) to activate neurones in a corticospinal pathway. In the former case, in one experiment, stimulation was made in the pyramid between lesions 3 and 4 (double pyramidal lesion). In case of cPyr stimulation, lesions 1 and 2 were added sequentially in order to investigate if the corticospinal excitation was mediated via C3-C4 PNs. All lesions were made mechanically, except lesion 2 which in some of the experiments was performed by reversible cooling. 3. Stimulation in the pyramid rostral to lesion 3 and in between lesions 3 and 4 evoked disynaptic EPSPs in the long PNs, which shows that they were mediated via reticulospinal neurones. Stimulation in cPyr after lesion 3 elicited disynaptic EPSPs, which remained after lesion 1 but were abolished after adding lesion 2. It is concluded that the disynaptic cPyr EPSPs were mediated via intercalated neurones in the C3-C4 segments. 4. When the disynaptic cPyr EPSP was conditioned with a single volley in nucleus ruber and/or in tectum, it was markedly facilitated, especially when the conditioned volley was applied simultaneously with the effective cPyr volley. The results show that the intercalated neurones in the C3-C4 segments receive monosynaptic convergence from cortico-, rubro- and tectospinal fibres. Stimulation in the lateral reticular nucleus (LRN) evoked monosynaptic EPSPs.(ABSTRACT TRUNCATED AT 400 WORDS)
Ipsilateral Area 3b Responses to Median Nerve Somatosensory Stimulation
NeuroImage, 2003
Magnetoencephalography investigation of the somatosensory evoked fields for median nerve stimulation detected ipsilateral area 3b responses in 18 hemispheres of 14 (1 normal subject and 13 patients with brain diseases) among 482 consecutive subjects. The major three peaks in the ipsilateral response were named iP50m, iN75m, and iP100m, based on the current orientation in the posterior, anterior, and posterior directions and the latency of 52.7 ؎ 6.2, 74.1 ؎ 9.4, and 100.2 ؎ 15.8 ms (mean ؎ standard deviation), respectively. The moment of the iP50m dipole (9.4 ؎ 5.7 nAm) was significantly smaller than that of the N20m dipole of the contralateral response (cN20m, 27.5 ؎ 10.5 nAm, P < 0.0001). Dipoles of iP50m and cN20m were similarly localized on the posterior bank of the central sulcus. iP50m in the present study had the same current orientation as and peak latency similar to that of the first ipsilateral primary somatosensory response to lip stimulation in our previous report. Therefore, the somatosensory afferent pathway from the hand may reach directly to the ipsilateral area 3b at least in part of the human population. © 2002 Elsevier Science (USA)
Brain Research, 1989
Experiments were carried out on adult anesthetized cats in which the effects of nucleus raphe magnus (NRM) conditioning stimulation (20 ms) were tested on the responses evoked by orofacial stimuli in single brainstem neurons of trigeminal (V) subnucleus oralis. The NRM stimulation induced inhibition of the responses of 57 of 77 low-threshold mechanoreceptive (LTM) neurons and the one wide-dynamic range (WDR) neuron tested. The duration of the neuronal inhibition ranged from 300-600 ms and the mean threshold for inhibition ranged from 47.8 + 4.8 to 102.7 + 15 gA depending on the orofacial stimulation site (skin or tooth pulp) and form (mechanical or electrical) of cutaneous stimuli used to evoke neuronal responses. In 20 LTM neurons showing NRM-induced inhibition that were specifically examined for the effects of NRM stimulation on the mechanoreceptive field, one population (n = I1) showed shrinkage (mean 55 + 4.4% from control area) of the mechanoreceptive field while the remaining neurons (n = 9) showed no change in mechanoreceptive field size during NRM stimulation. The former group of neurons were also distinguished from the latter neurons by their significantly larger mechanoreceptive field and the activation of the majority of them by electrical stimuli applied outside their mechanoreeeptive field. The responses of these neurons evoked by low-threshold inputs from the edge of the mechanoreceptive field were more sensitive to NRM conditioning stimulation than responses evoked from the mechanoreceptive field center, as judged by threshold, magnitude and duration of the NRM-induced inhibition. These findings underscore the sensitivity of LTM neurons to NRM influences. They also reveal a particular population of oralis neurons which have a differential sensitivity of low-threshold inputs evoked from the edge compared to the center of the mechanoreceptive field.
Journal of Neurophysiology, 2002
Nudo. An index of topographic normality in rat somatosensory cortex: application to a sciatic nerve crush model. J Neurophysiol 88: 1339 -1351, 2002; 10.1152/jn.00019.2002. Previous studies have demonstrated that peripheral denervation of the skin is reflected in the CNS as a reorganization of somatotopic representations. In cases in which peripheral nerve regeneration occurs there is a gradual reactivation of cortex by novel receptive fields that is reversed as regenerated nerves reestablish connections with the original skin surface. Functional recovery appears to depend on the pattern in which somatotopic organization in the cortex is reestablished. The relationship between functional recovery and cortical topography is not precise, however, since the descriptions of postinjury representations in the cortex have been largely descriptive and not quantitative. The purpose of this study was to derive an index to quantify deviations from normal somatotopic organization in the somatosensory cortex. Multiunit recordings of cutaneous representations in the somatosensory cortex (S1) of the rat were defined using Semmes-Weinstein monofilaments to stimulate the skin over the distal hindlimb of the rat 2 and 4 months after a sciatic nerve crush. To derive a sensitive index of topography, the sciatic nerve crush was selected as the injury model since nerve regeneration following crush injuries has been reported to reinstate preinjury cortical topography. Group comparisons were made with an intact control group. The results show that there were subtle, but significant differences in topography between rats with a regenerated sciatic nerve and normal rats. In addition, average thresholds for evoking cortical responses were higher than normal (but within normal range) 2 and 4 months after the crush. These results demonstrate that the index of topography derived for this study can reveal deviations that may not be distinguishable from normal topography when based on qualitative descriptions.
Cerebral Cortex, 2005
Wang, Lei, Ronald Millecchia, and Paul B. Brown. Correlation petitive process such as Hebbian activity-dependent selfof peripheral innervation density and dorsal horn map scale. J. organization (Hebb 1949; Will-Neurophysiol. 78: 689-702, 1997. Dorsal horn map scale and peshaw and von der Malsburg 1976). ripheral innervation density were compared to test a hypothesized In our proposed sequence of developmental events linear relationship. In anesthetized cats, low-threshold mechanore- (Brown et al. 1997), hindlimb primary afferents establish ceptive peripheral nerve innervation fields (IFs) were measured mediolateral (ML) gradients of somatotopy at their level of by outlining areas of skin from which action potentials could be entry into the spinal cord by sorting their projections along elicited in cutaneous nerves. The same nerves were processed histothe ML axis of the dorsal horn in the order of the distoproxilogically and used to count myelinated axons. Innervation density mal locations of their RFs on the skin. The slope of the for each nerve was calculated as number of axons divided by IF area. Single units were recorded throughout the hindlimb represen-presynaptic somatotopic gradient at each rostrocaudal (RC) tation, in laminae III and IV. These data, combined with singlelevel would therefore be determined by the relative abununit data from other animals and with cell counts in laminae III dance of RFs at different distances from the tips of the toes. and IV, permitted estimation of numbers of cells whose receptive We suggest that this presynaptic somatotopy is reflected in field centers fell in contiguous 1-cm bands from tips of toes to postsynaptic somatotopy of dorsal horn cell RFs established proximal thigh. A similar estimate was performed with the use of by initial axonal contacts of locally ingrowing primary afferthe nerve innervation data, so that peripheral innervation densities ent axons with dorsal horn cell dendrites (prototype RFs). and map scales for the different 1-cm bands of skin could be Then primary afferents grow collaterals along an RC course, compared. Correlation between the two was quite high (r Å 0.8), connecting to cells within whose prototype RFs their own and highly significant (P Å 2.5 1 10 07 ). These results are consis-RFs are included. Finally, the RFs may be refined by a tent with a proposed developmental model in which map scale, peripheral innervation density, and reciprocal of dorsal horn cell competitive mechanism that leads to constant divergence receptive field size are mutually proportional, as a result of develand convergence. opmental mechanisms that produce constant divergence and con-One piece of evidence we used to justify this hypothesized vergence between primary afferent axons and dorsal horn cells.