Topographical organization of the tecto-olivo-cerebellar projection in the cat.

The superior colliculus sends a climbing fiber output to cerebellar vermal lobules VI-VII through the inferior olive. The present study in cats morphologically clarified the existence of a topographical organization in the tecto-olivo-cerebellar projection. A horseradish peroxidase study on the tecto-olivary projection showed that the rostral and caudal superior colliculus projected mostly contralaterally to the caudal and rostral areas of the caudomedial part of the medial accessory olive, respectively. The lateral superior colliculus was found to project more laterally than was the medial superior colliculus. Investigation on the olivocerebellar projection demonstrated that the rostral and caudal areas of the caudomedial part of the medial accessory olive sent climbing fiber terminals contralaterally to the lateral and medial parts of vermal lobules VI-VII, respectively. Thus, it was revealed that the rostral superior colliculus projected mostly to the medial part of ipsilateral vermal lobules VI-VII while the caudal superior colliculus projected mostly to the lateral part of ipsilateral vermal lobules VI-VII.     

Olivary branching projections to the flocculus,nodulus and uvula in the rabbit

Summary Olivocerebellar branching projections to the flocculus, nodulus and uvula were studied electrophysiologically in pigmented rabbits anesthetized with pentobarbital and halothane. Neurons in the dorsal cap of the inferior olive were antidromically activated by stimulation of the contralateral flocculus, nodulus and uvula. The antidromic responses in the dorsal cap from the flocculus, nodulus and uvula partially occluded with each other. Electrical stimulation of the nodulus (or uvula) evoked early and late climbing fiber responses in the flocculus with latencies of 4.0 ms and 10.0 ms, respectively. The early response was resistant to repetitive stimulation and not affected by interruption of the olivocerebellar fibers at the lower medulla, while the late response was abolished by these two procedures. This indicated that the early response was evoked through climbing fiber branches to the flocculus and nodulus (or uvula) as an axon reflex, while the late response was evoked via the inferior olive. Of 76 Purkinje cells in the flocculus, 35.6% showed climbing fiber activation through branches to the nodulus and/or uvula, 70% of which were orthodromically activated through climbing fibers from the contralateral optic tract. Electrical stimulation of the flocculus or uvula evoked the early and late climbing fiber responses in the nodulus. Of 60 Purkinje cells in the nodulus, 63.4% showed axon reflex activation from the flocculus and/or uvula, 42% of which were activated through climbing fibers from the contralateral optic tract. These findings demonstrated that the flocculus, nodulus and uvula receive branching climbing fiber projection from the inferior olive, a part of which conveys visual information.     

Sensory responses of intralaminar thalamic neurons activated by the superior colliculus

Summary The intralaminar thalamus of anesthetized rats was explored for neurons activated by stimulation of the superior colliculus and responsive to sensory inputs. Neurons activated by stimulation of the intermediate and deep collicular layers were distributed throughout the intralaminar thalamus. Approximately one half of them responded to tectal as well as sensory inputs. The majority were nociceptive or had a more complex response pattern including responses to auditory stimulation. A smaller population of low threshold units had contralateral orofacial receptive fields and responded to light taps; these units were preferentially localized anteriorly in the central lateral and paracentral nuclei. Neurons responsive to tectal and sensory stimulation were randomly intermingled with other neurons which had no detectable sensory input. The results indicate that ascending projection neurons of the intermediate and deep layers of the superior colliculus provide an input to functionally diverse subpopulations of intralaminar thalamic neurons. In view of its projections to motor cortex and basal ganglia, the intralaminar thalamus appears directly implicated in basal ganglia and superior colliculus related mechanisms of attention, arousal and postural orienting.     

Difference of climbing fiber input sources between the primate oculomotor-related cerebellar vermis and hemisphere revealed by a retrograde tracing study

The cerebellar flocculus–paraflocculus complex, vermal lobule VII (V-7) and hemispheric lobule VII (H-7) are involved in learning-dependent smooth pursuit eye movement control. To locate the sources of climbing fiber inputs to the H-7 and V-7, we injected retrograde tracers and examined the locations of retrogradely labeled neurons in the inferior olive in 4 monkeys. After the injection of cholera toxin B (CTB) into the H-7, retrogradely labeled neurons were observed abundantly in cell group d, i.e., dorsal cap, of the caudal medial accessory olive (MAO) and ventral lamella of principal olive (PO). After injections of fast blue (FB) into the V-7, retrogradely labeled neurons were observed mainly in cell group b of MAO, but rarely in cell group d or PO. Cell group d is known to receive inputs from the nucleus optic tract (NOT) and project climbing fibers to the flocculus and ventral paraflocculus, and cell group b is known to receive inputs from the superior colliculus. These results suggest that the three oculomotor cerebellar areas may use different visual signals for the control of smooth pursuit: the flocculus–paraflocculus complex and H-7 receive visual climbing fiber inputs derived mainly from the NOT via cell group d, while the V-7 receive visual climbing fiber inputs derived mainly from the superior colliculus via cell group b.     

Imaging parallel fiber and climbing fiber responses and their short-term interactions in the mouse cerebellar cortex in vivo

A major question in the study of cerebellar cortical function is how parallel fiber and climbing fiber inputs interact to shape information processing. Emphasis has been placed on the long-term effects due to conjunctive stimulation of climbing fibers and parallel fibers. Much less emphasis has been placed on short-term interactions and their spatial nature. To address this question the responses to parallel fiber and climbing fiber inputs and their short-term interaction were characterized using optical imaging with Neutral Red in the anesthetized mouse in vivo. Electrical stimulation of the cerebellar surface evoked an increase in fluorescence consisting of a transverse optical beam. The linear relationship between the optical responses and stimulus parameters, high spatial resolution and close coupling to the electrophysiological recordings show the utility of this imaging methodology. The majority of the optical response was due to activation of postsynaptic alpha-amino-3-hydroxyl-5-methyl-4-isoxazole propionate (AMPA) and metabotropic glutamate receptors with a minor contribution from the presynaptic parallel fibers. Stimulation of the inferior olive evoked parasagittal bands that were abolished by blocking AMPA glutamate receptors. Conjunctive stimulation of the cerebellar surface and inferior olive resulted in inhibition of the climbing fiber evoked optical responses. This lateral inhibition of the parasagittal bands extended out from both sides of an activated parallel fiber beam and was mediated by GABA(A) but not GABA(B) receptors. One hypothesized role for lateral inhibition of this type is to spatially focus the interactions between parallel fiber and climbing fiber input on Purkinje cells. In summary optical imaging with Neutral Red permitted visualization of cerebellar cortical responses to parallel fiber and climbing fiber activation. The GABA(A) dependent lateral inhibition of the climbing fiber evoked parasagittal bands by parallel fiber stimulation shows that cerebellar interneurons play a short-term role in shaping the responses of Purkinje cells to climbing fiber input.     

Relationship of parasagittal bands of acetylcholinesterase activity to the climbing fiber representation

The organization of the somatosensory representation by the climbing fiber system was correlated to parasagittal zones in the vermis, which were demarcated by the parasagittal banding pattern of acetylcholinesterase (AChE) activity. Extracellular recordings were made of climbing fiber responses that were elicited by tactile stimulation in anesthetized cats. After the climbing fiber representation was mapped physiologically, the cerebellum was histologically processed for AChE activity. The lateral edge of the lateral AChE banding coincided with the junction between a medial vermis (zones A and X) where 82% of the units were unresponsive and the lateral vermis (zone B) where 72% of the climbing fiber responses represented areas of the body surface.     

Inhibition of inferior olivary transmission by mesencephalic stimulation in the cat

Cerebellar climbing fiber responses (CFRs) evoked in anesthetized cats by stimulation of peripheral nerves, contralateral inferior olive and cerebellar white matter were investigated by recording unit activity and surface field responses in anterior lobe of cerebellar cortex. When nerve and olive stimulation was preceded at long intervals (greater than 35 ms) by weak electrical stimulation of an ipsilateral mesencephalic area close to the locus coeruleus and brachium conjunctivum, CFRs could be virtually abolished in the pars intermedia but not in the vermis. White-matter evoked CFRs were not affected; thus the site of the inhibition was the inferior olive.     

The climbing fibers of the cerebellar cortex,their origin and pathways in cat

Summary The sources and pathways of the climbing fibers to the cerebellar posterior vermis were studied with combined electrophysiological and anatomical methods in cats.Recording from identified cerebellar Purkinje cells, monosynaptic climbing fiber (CF) responses have been obtained both for stimulation of the inferior olive (IO) and various parts of the brain stem (BS). CF responses were found to be of three types, IO only, BS only or both IO and BS. However the responses to BS stimulation were very few in number in comparison with IO or IO and BS types of responses. The latencies of the responses were shorter for the BS cases consistent with their distance from the cerebellum.A comparison of latencies and the relative responsiveness of the different area of the brain stem which were studied, indicate that part of the CF ascend through the pontine region and enter the cerebellum by way of the medium and superior peduncles. This finding is confirmed by the results of anatomical studies in which degenerating fibers were found in the molecular layer (using the Nauta technique) after lesion of the brachium pontis but not after lesions of the medial portion of the pons. Similarly, injection of radioactive leucine into the pontine nuclei failed to show any labeled fibers in the molecular layer.Horseradish peroxidase (HRP) was injected into localized regions of the posterior vermis after total bilateral destruction of the inferior peduncles. Large numbers of positive, marked cells were still found in the inferior olive.It is concluded that nearly all, if not all, the climbing fibers originate in the inferior olive and that they ascend to the cerebellum by way of all the peduncles.     

Termination and functional organization of the dorsolateral spino-olivocerebellar path

1. Pathways ascending in the lateral funiculus of the spinal cord and terminating as climbing fibres in the anterior lobe of the cerebellum have been investigated in decerebrate cats with the cord partially transected in the third cervical segment, sparing only part of the left lateral funiculus. The climbing fibre responses evoked in Purkinje cells by electrical stimulation of peripheral nerves were studied by recording from single cells and by recording the mass activity at the cerebellar surface.2. Two pathways have been distinguished. One ascends through the dorsal part of the lateral funiculus and relays in the inferior olive. It is denoted the dorsolateral spino-olivocerebellar path (DLF-SOCP) and forms the subject of this paper. The other path occupies in part a more ventral position in the lateral funiculus and it is not known if it relays in the inferior olive. It is denoted the LF-CF-SCP (lateral funiculus-climbing fibre-spinocerebellar path).3. The DLF-SOCP is activated predominantly by cutaneous afferents from restricted areas in the ipsilateral paws. The relay in the spinal cord is almost certainly monosynaptic, but a long delay in the brain stem suggests that the path is interrupted by several synapses at this level. The pathway terminates in the pars intermedia in sagittal zones with a somatotopical organization (Fig. 12).4. Components of the DLF-SOCP and the dorsal spino-olivocerebellar path converge onto the same olivary neurones which project to the pars intermedia and it is concluded on this evidence that the DLF-SOCP also relays in the inferior olive.5. The DLF-SOCP is compared with the other known spinocerebellar paths terminating as climbing fibres in the anterior lobe. The functional role of these paths and the general significance of the sagittal projection patterns are discussed.     

Sagittal zonal organization of climbing fibre input to the cerebellar anterior lobe of the ferret

The organization of climbing fibre input to the cerebellar anterior lobe of the ferret was investigated in barbiturate-anaesthetized animals. Climbing fibre field potentials evoked on electrical stimulation of forelimb and hindlimb nerves were recorded at the cerebellar surface. Based on characteristic latencies of climbing fibre responses and their relative localization along the longitudinal axis of the folia, nine sagittally oriented zones could be distinguished and were tentatively named, from medial to lateral, A, X, B, C1, Cx, C2, C3, D1 and D2. Within the C1, C2 and C3 zones, climbing fibre input from the ipsilateral forelimb was found caudally and from the hindlimb rostrally, while the corresponding topographical representation in the B and D2 zones was medial to lateral. The X, Cx and D1 zones did not receive input from the hindlimb, while input from the forelimb to the A zone was weak. Overall, the sagittal zonal organization of climbing fibre input appears to conform with the compartmentalization of the ferret cerebellum based on the myeloarchitecture of corticonuclear fibres, although the X and Cx zones have not been previously identified. In terms of both general electrophysiological characteristics of input to different zones and intrazonal topographical representation, the organization of climbing fibre input to the ferret cerebellum seems to strongly resemble that in the cat. The findings thus provide evidence of cross-species generality of cerebellar sagittal organization. Received: 31 January 1997/Accepted: 30 April 1997     

Fluctuation of extracellular potassium and calcium in the cerebellar cortex related to climbing fiber activity

It is known that repetitive stimulation of spino- and cortico-olivary pathways can lead to waxing and waning of the evoked climbing fiber responses of cerebellar Purkinje cells. Extracellular recordings performed with ion-selective microelectrodes showed that the amplitude fluctuations of climbing fiber-related field potentials were accompanied by corresponding changes in ion-activity levels. When the amplitude of the field potentials increased, potassium activity rose by up to 0.7 mmol.l^?1 and calcium activity fell by up to 0.3 mmol.l^?1. Ion activities returned to baseline values when climbing fiber responses failed.The rhythmic fluctuations in ion activities have cycle lengths of 10–20 s, or multiples of it. Presumably they are secondary consequences of slow variations of synaptic transmission in the inferior olive. The generator for the slow fluctuations of olivary synaptic transmission and the consequent variations in ion activities within the cerebellum is probably located within the inferior olive. The ionic modulations could have functional implications for cerebellar information processing. Possible mechanisms of the rhythmogenesis are discussed.     

The excitatory synaptic action of climbing fibres on the Purkinje cells of the cerebellum

1. A single climbing fibre makes an extraordinarily extensive synaptic contact with the dendrites of a Purkinje cell. Investigation of this synaptic mechanism in the cerebellum of the cat has been based on the discovery by Szentagothai & Rajkovits (1959) that the climbing fibres have their cells of origin in the contralateral inferior olive.2. Stimulation in the accessory olive selectively excites fibres that have a powerful synaptic excitatory action on Purkinje cells in the contralateral vermis, evoking a repetitive spike discharge of 5-7 msec duration. Almost invariably this response had an all-or-nothing character. In every respect it corresponds with the synaptic action that is to be expected from climbing fibres.3. Intracellular recording from Purkinje cells reveals that this climbing fibre stimulation evokes a large unitary depolarization with an initial spike and later partial spike responses superimposed on a sustained depolarization.4. Typical climbing fibre responses can be excited, but in a much less selective manner, by stimulation of the olive-cerebellar pathway in the region of the fastigial nucleus, there being often a preceding antidromic spike potential of the Purkinje cell under observation.5. Impaled Purkinje cells rapidly deteriorate with loss of all spike discharge, the climbing fibre response being then reduced to an excitatory post-synaptic potential. This potential shows that stimulation of the inferior olive may evoke two or more discharges at about 2 msec intervals in the same climbing fibre. The complexity of neuronal connexions in the inferior olive is also indicated by the considerable latency range in responses.6. A further complication is that, with stimulation in the region of the fastigial nucleus, the initial direct climbing fibre response is often followed by a reflex discharge, presumably from the inferior olive, which resembles the responses produced by inferior olive stimulation in being often repetitive.7. Typical climbing fibre responses have been evoked by peripheral nerve stimulation and frequently occur spontaneously.8. An account is given of the way in which the responses evoked by climbing fibres in the individual Purkinje cells can account for the potential fields that an inferior olive stimulus evokes on the surface and through the depth of the cerebellar cortex.9. By the application of currents through the recording intracellular electrode it has been possible to effect large changes in the excitatory post-synaptic potential produced by a climbing fibre, it being diminished and even reversed with depolarizing currents and greatly increased by hyperpolarizing currents.     

Non-reciprocal connections between the vestibular nuclei and the cerebellar paramedian lobule, with special reference to the climbing fiber zones: an analysis in the rabbit using the retrograde horseradish peroxidase method.

The organization of the secondary vestibular projections onto the cerebellar paramedian lobule (PML) and possible reciprocal corticovestibular connections were investigated by the retrograde horseradish (HRP) technique in the rabbit. Following injections of the tracer into the vestibular nuclear complex (VNC), an ill-defined, sagittal band composed of numerous labelled Purkinje cells was found ipsilaterally throughout the length of the lateral portion of the vermis, the ventral paraflocculus and the flocculus. However, no labelled Purkinje cells were found in the cortex of the PML. The results indicate that zone B, considered to give rise to cerebellar corticovestibular projections, is not present in the rabbit PML. After injections of HRP into the PML, the retrograde labelling pattern in the VNC was analyzed, in relation to the climbing fiber zones identified by retrograde labelling in the inferior olive. No clear-cut correspondence could be found between the vestibular subdivisions and climbing fiber zones in the PML, except that only the interstitial nucleus of the vestibular nerve projects into zone D1 in sublobules e and d. There were no vestibular projections to zone D2. The only salient feature was that cells projecting onto zones C2, C1 and C3 of the PML were arranged rostrocaudally in the inferior vestibular nucleus and the caudal portion of the medial vestibular nucleus. In addition, a topical relationship was found between parts of the VNC and sublobules of the PML.     

Projections of extraocular, neck muscle, and retinal afferents to superior colliculus in the cat: their connections to cells of origin of tectospinal tract.

Unit recordings were made in the superior colliculus of cats anesthetized with chloralose and with Pentothal. Electrical stimulation of extraocular muscle afferents and neck muscle afferents excited more units in the superior colliculus than did a variety of moving and stationary visual stimuli. Units responding to neck muscle afferent stimulation fell into three populations; one population firing with a short latency and following stimulus presentation up to 1/s, a second population with a long latency and following stimulus presentation at frequencies lower than 15/min, and a third population exhibiting paired firing. The latencies and firing patterns of the third population combined the characteristics of each of the first two patterns. It is suggested that these characteristics of unit discharges stem from the existence of two pathways from neck muscle afferents to the superior colliculus. The projection is predominantly bilateral. Units responding to neck muscle afferent stimulation are distributed throughout the superior colliculus on the basis of their latencies. Long-latency responses predominate in the superficial layers of the superior colliculus and short-latency responses, while more common in the intermediate and deep layers, predominate in the tegmentum. Extraocular muscle afferent projections to the superior colliculus constitute the single richest projection found in these experiments. While the response patterns and latencies are similar to those of the neck muscle afferents, long-latency responses are the most common and dominate in all collicular regions. Few units in the tegmentum could be excited by extraocular muscle afferents. Both extraocular muscle and neck muscle afferents show considerable convergence with one another and with retinal afferents within the superior colliculus. Cells of origin of the tectospinal tract were identified within the superior colliculus and tegmentum by antidromic excitation from the upper cervical cord. These cells were distributed predominantly within the intermediate and deep layers of the superior colliculus, and sparsely in the superficial layers and tegmentum. Almost 50% of the cells of origin of the tectospinal tract receive a convergent input from extraocular muscle and neck muscle afferents and from the retina. About 30% of the cells were inexcitable to the stimuli employed in these experiments. The significance of these projections is discussed with respect to superior collicular function in the cat and i     

Functional properties of pulvinar-lateral posterior neurons which receive input from the superior colliculus

Summary Focal electrical stimulation of the superior colliculus induced short latency responses and/or a long duration suppression of spontaneous activity in single cells isolated in the pulvinar and lateral posterior (LP) nuclei of the cat. Cells which responded with one or more spikes at short latencies were relatively few in number, and these tended to be encountered in or near the principal tectorecipient zone of LP. In contrast, a suppression response was observed in many more cells which were widely distributed throughout the pulvinar-LP complex. Stimulation of the superficial layers of the colliculus was more effective in driving or suppressing pulvinar-LP cells than that of intermediate and deep layers. There was also an indication of a coarse topograhy in this projection. On the basis of their sensory response properties the cells responsive to tectal stimulation, at short latency or with a suppression, could not be differentiated from the overall sample of pulvinar-LP neurons.Supported in part by NIMH MH31947     

Cerebellar and olivary projections of the external and rostral internal cuneate nuclei in the cat

Summary The cerebellar projection of the external cuneate nucleus and the adjoining rostral part of the internal cuneate nucleus were investigated by means of anterograde transport of tritiated leucine. The cuneocerebellar tract terminates as mossy fiber rosettes in the granular layer. The termination area has a more or less spherical form with its centre at the ipsilateral side. It comprises the anterior and posterior vermes bilaterally and the ipsilateral hemispheral parts of the anterior and simple lobules, the medial aspect of the ansiform lobule and the paramedian lobule. Within this area the mossy fiber terminals are arranged in continuous sagittal strips, some of them clearly separated from one another. The strips were found in the cerebellar modules A-D. Concomitant bilateral projections to several subdivisions of the inferior olive were found. Some of these provide the anatomical substrate for the simultaneous activation of a number of mossy and climbing fiber zones observed in the anterior lobe following stimulation of different forelimb nerves. No evidence was found for a termination of mossy fiber collaterals in the central cerebellar nuclei.Abbreviations subnucleus - bp brachium pontis - CCT cuneocerebellar tract - CE nucleus cuneatus externus - cf climbing fiber - CI nucleus cuneatus internus - cr corpus restiforme - DAO dorsal accessory olive - DCN dorsal column nuclei - DF-SOCP dorsal funiculus spino-olivocerebellar pathway - dl dorsal lamina of the PO - dmcc dorso-medial cell column - DV nucleus vestibularis descendens - E-CCP exteroceptive cuneocerebellar pathway - F nucleus fastigii - FL flocculus - flm fasciculus longitudinalis medialis - G nucleus gracilis - HRP horseradish peroxidase - HVI hemisphere of lobule VI (Roman numerals) - IA nucleus interpositus anterior - IP nucleus interpositus posterior - L nucleus lateralis - MAO medial accessory olive - mf mossy filber - mft mossy fiber terminal - MV nucleus vestibularis medialis - PAR lobus paramedianus - PFLD dorsal paraflocculus - PFLV ventral paraflocculus - PH nucleus prepositus hypoglossi - PO principal olive - P-CCP proprioceptive cuneocerebellar pathway - rV ramus descendens of the nucleus trigeminus - TS nucleus solitarius - Vi pars interpolaris of the nucleus trigeminus - vl ventral lamina of the PO - I-X lobules I to X (Roman numerals) - XII nucleus hypoglossi (Roman numerals)     

Maturation of evoked climbing fiber input to rat cerebellar Purkinje cells (I.)

Summary An analysis of evoked responses of Purkinje cells in developing rat cerebellum to climbing fiber input was conducted to determine which identifying properties of this afferent system are established early in development and which specific features mature with age. Rat pups at various ages were anesthetized with 0.5% halothane and unit recordings made with glass micropipettes. By the third postnatal day, electrical stimulation of the sensorimotor cortex and limbs at low stimulation rates (<1/sec) could elicit distinct burst responses appearing at long latencies (180 msec), indicating that pathways of both ascending and descending climbing fiber systems are intact early in cerebellar cortical development. A distinctive feature maturing over the first 1–1.5 weeks was the characteristic of the all-or-none burst response since before about day 11 the interspike interval, amount of inactivation, and number of spikes in evoked burst responses all varied from stimulation to stimulation. Mean latencies decreased from 180 msec at day 3 to 50 msec by day 10, but did not achieve the adult value of 20 msec until the fourth week. Typically, climbing fiber responses could only follow at stimulation rates of less than 0.2/sec at day 3, but by day 12 could follow up to 10/sec, which is the same as in the adult. The data indicate that the climbing fiber system establishes connectivity from diverse sources and exhibits identifying characteristics similar to the adult early in cerebellar development. Most aspects of the maturation of transmission can be explained if there were a decrease in the time scale of function of the synapses involved, mainly those in the inferior olive.Supported by N.I.H. Grant 5-R01-6M00133 and N.S.F. Grant GB 43301     

Correlations among climbing fiber responses of nearby cerebellar Purkinje cells in the immature rat

Summary Correlations between pairs of spontaneous climbing fiber responses (CFRs) recorded from couples of nearby Purkinje cells (PCs) were studied in immature rats by using cross-correlograms between CFR pairs, and compared to those in adult animals. Correlations were found as early as day 3. Some days later, on PN days 7–9, these correlations were higher than in the adult. In most cases, this was apparently not due to the multiple innervation of PC by climbing fibers (CFs) which normally occurs during this immature stage since: 1) temporal relationships between the paired CFRs varied by more than 30 ms and 2) thresholds for pairs of graded CFRs and additional components of the responses evoked in the 2 PCs by juxtafastigial or olivary stimulation were different. Synchronizing mechanisms were therefore likely to be already located at the olivary level. However, in 3 couples of multiply innervated PCs whose spontaneous CF activities were highly correlated, stimulation experiments revealed a common innervation of the 2 cells by branches of the same CF. In multiply innervated cells, spontaneous responses mediated through distinct CFs were also synchronized, suggesting that these fibers originate from neighboring neurons of the inferior olive. Finally, in 7 to 9-day-old rats, correlations among CFR pairs were much more restricted in the longitudinal axis of the folium than in the transverse one. On the whole, the present study indicates that correlations among CFRs of nearby PCs exist as soon as CF-PC synapses are established and the latter are already organized in sagittal strips at early stages of development.This work was supported by INSERM (C.R.L. Nr. 78.1.003.6)     

Influence of the superior colliculus on visual responses of cells in the rabbit's lateral posterior nucleus

Summary The lateral posterior-pulvinar (LP-P) complex of mammals receives a major input from the superior colliculus (SC). We have studied the response properties of LP cells and investigated the effects of reversible inactivation of the colliculus on the visual responses of LP units in anesthetized and paralyzed rabbits. Cells in LP had large receptive fields responsive to either stationary or moving stimuli. One third of the motion-sensitive cells were direction selective. The size of the receptive fields increased with eccentricity and there was a retinotopic organization along the dorso-ventral axis. Comparison of the LP and superior colliculus properties revealed substantial differences in visual response characteristics of these two structures such as the size of the receptive fields and the number of direction-selective cells. Electrical stimulation of the LP evoked antidromic action potentials in tectal cells that were motion sensitive. We found a dorsoventral gradient in the projections of collicular cells. Units located more dorsally in the colliculus sent their axons to LP while cells lying more ventrally sent axons toward the region lying posterior to LP. A micropipette filled with lidocaine hydrochloride was lowered into the superficial layers of the superior colliculus in order to reversibly inactivate a small population of collicular cells. Rendering the superior colliculus inactive produced a sharp attenuation of visual responses in the majority of LP cells. Some neurons ceased all stimulus-driven activity after collicular blockade while a few cells exhibited increased excitability following collicular inactivation. These experiments also indicate that the tecto-LP path is topographically organized. An injection in the colliculus failed to influence the thalamic response when it was not in retinotopic register with the LP cells being recorded. Our results demonstrate that the superior colliculus input to LP is mainly excitatory in nature.     

Vagal representation in the cerebellum of the cat

The cervical vagus nerve (VN) was electrically stimulated in Nembutal-anaesthetized cats. The responses recorded from the cerebellar surface were found in lob. V and VI in a bilateral sagittal strip perpendicular to the longitudinal axis of the folia. At a longer latency, potentials were also found in the paramedian lobule. Field potential analysis confirmed the existence of a sagittal strip in the deep parts of the lobules. The distribution of these potentials and their field potential profiles indicate that they are transmitted through the climbing fiber (CF) system. Experiments with local anaesthetics and deafferentation support our view that the potentials described in the vermis by Dell and Olson (1951) could be originated extracerebellarly. A strong parallelism was found between the amplitude of the cerebellar responses and the amplitude of the group B₁ component of the vagal afferent potentials, having a conduction velocity between 4 and 20 m/s. The pathway by which the vagal afferents reach the inferior olive and the functional significance of these afferents are discussed.