Organization of somatic nerve projections in various cortical areas of the cat cerebellum

We conducted a layer analysis of evoked potentials arising in various cortical cerebellar areas (vermis and intermediate zones of the anterior lobe, and the ansiform lobe) of non-anesthetized cats upon stimulation of nerves in fore- and hindlimbs. This analysis yielded the conclusion on the arrival of stimuli at the cerebellar cortex over two types of moss fibers innervating two types of granule cells which we described earlier. Impulses transmitted over type I moss fibers stimulate Purkinje cells. The activation of type II moss fibers has no immediate effect on these cells. Type I moss fibers terminate in the vermis and the intermediate zone of the hemispheres and do not terminate in the lateral hemispheric region. While projections of type I moss fibers are somatotopically organized in the intermediate zone they are diffuse in the vermis. Type II moss fibers terminate in all the regions of the crebellar cortex under study, but their projections show no somatotopic organization. The question of the afferent pathways terminating as type I and II moss fibers is discussed.Institute of Problems of Information Transmission, Academy of Sciences of the USSR, Moscow. M. V. Lomonosov Moscow State University. Translated from Neirofiziologiya, Vol. 3, No. 2, pp. 166–174, March–April, 1971.     

Autoradiographic evidence of visual cortical projections to the frontal cortex in the cat

In II adult cats, areas 17, 18, 19 as well as the lateral suprasylvian area were separately injected with L-[5-3H] proline and their efferent projections to the frontal cortex were autoradiographically searched. Only area 19 and lateral suprasylvian area showed such projections; terminal sites were localized in the ventral and dorsal banks of the cruciate sulcus and in the adjacent mesial surface of the brain. The possibility that these labeled regions may correspond to the monkey's frontal eye field is discussed.     

Spinal, thalamic and cortical levels of splanchno-splanchnic interactions]

Using the occlusion method, we have shown splanchno splanchnic interactions on spinal, thalamic and cortical cells in cat. 1. At the first level, splanchno splanchnic interactions concern only the cells located in the Rexed V layer. The splanchnic fibres involved are small sized ones (Agammadelta, B and C types). 2. At the second level, splanchno splanchnic interactions have been observed in the VPL nucleus. The latencies of responses suggest that only large fibres are concerned. 3. At the third level, cortical cells of SI and SII areas have been studied. Splanchno splanchnic interactions have been elicited by different afferent splanchnic fibres (medullated and non medullated ones).     

Striatal projections from the lateral and posterior thalamic complexes. An anterograde tracer study in the cat

Striatal projections from the lateral intermediate (LI) and posterior (Po) thalamic complexes were studied with the anterograde tracers wheat germ agglutinin-horseradish peroxidase and Phaseolus vulgaris leucoagglutinin. Projections to the lateral part of the head and body of the caudate nucleus (CN) and to the putamen (Pu) were found to arise from the ventral parts of the caudal subdivision of the LI besides the well established sources in the intralaminar and ventral thalamic nuclei. No projections to the CN and only a few to the Pu were found to arise from the medial division of the Po. The presence of terminal and intercalated varicosities in the thalamostriatal fibers suggests that they form both terminal and en passant synapses. Thalamostriatal fibers from these thalamic sectors were unevenly distributed within the CN, with patches of either low-density innervation or with no projections at all interspersed within irregular, more densely innervated areas. The former coincided with the acetylcholinesterase-poor striosomes and the latter areas of dense projection with the extrastriosomal matrix.     

Direct projections of the thalamic centrum medianum in the cerebral cortex of the cat (radioautographic studies)

After injection of radioactive amino acids into the cat thalamic centrum medianum, its projections have been revealed in the ipsilateral hemisphere in the frontal, motor, limbic, orbital and basal temporal cortex, in the parasubiculum and striatum. The anterograde tracing of the fibers and terminals reveals the centrum medianum projections in the layers VI-V and I of the frontal and limbic cortex and in the layers VI-V, IV or III (or in both) and in I of the motor and orbital cortex.     

Rubrocaudate projections in the cat

Small numbers of neurons projecting to the caudate nucleus were found in the cat red nucleus using horseradish peroxidase retrograde axonal transport techniques. Rubrocaudate neurons were found in both the parvo- and magnocellular sections of the red nucleus. Organization of reciprocal connections between the red nucleus and the striopallidal system is discussed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 20, No. 1, pp. 28–32, January–February, 1988.     

Cortico-nigral projections in the cat

Using the methods of retrograde axonal transport of horseradish peroxidase and silver impregnation of degenerating axons, certain data have been obtained demonstrating that frontal, motor, orbital, insular and limbic fields of the cortex serve as sources of afferent fibers for the compact zone of the substantia nigra. The lateral zone gets projections from the same cortical areas (besides the limbic one) as the compact part and, in addition, from the parietal associative, acoustic and visual areas.     

Unit responses of the cat caudate nucleus to cortical stimulation before and after destruction of nonspecific thalamic nuclei

Responses of caudate neurons to stimulation of the anterior sigmoid and various parts of the suprasylvian gyrus were studied in acute experiments on cats. The experiments consisted of two series: on animals with an intact thalamus and on animals after preliminary destruction of the nonspecific thalamic nuclei. Stimulation of all cortical areas tested in intact animals evoked complex multicomponent responses in caudate neurons with (or without) initial excitation, followed by a phase of inhibition and late activation. The latent periods of the initial responses to stimulation of all parts of the cortex were long and averaged 14.5–25.5 msec. Quantitative and qualitative differences were established in responses of the caudate neurons to stimulation of different parts of the cortex. Considerable convergence of cortical influences on neurons of the caudate nucleus was found. After destruction of the nonspecific thalamic nuclei all components of the complex response of the caudate neurons to cortical stimulation were preserved, and only the time course of late activation was modified.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 12, No. 5, pp. 464–471, September–October, 1980.     

Postnatal development of thalamic reticular nucleus projections to the anterior thalamic nuclei in rats

The thalamic reticular nucleus (TRN) projects inhibitory signals to the thalamus, thereby controlling thalamocortical connections. Few studies have examined the development of TRN projections to the anterior thalamic nuclei with regard to axon course and the axon terminal distributions. In the present study, we used parvalbumin (PV) immunostaining to investigate inhibitory projections from the TRN to the thalamus in postnatal (P) 2- to 5-week-old rats (P14–35). The distribution of PV-positive (+) nerve fibers and nerve terminals markedly differed among the anterior thalamic nuclei at P14. Small, beaded nerve terminals were more distributed throughout the anterodorsal nucleus (AD) than in the anteroventral nucleus (AV) and anteromedial nucleus (AM). PV+ fibers traveling from the TRN to the AD were observed in the AV and AM. Nodular nerve terminals, spindle or en passant terminals, were identified on the axons passing through the AV and AM. At P21, axon bundles traveling without nodular terminals were observed, and nerve terminals were distributed throughout the AV and AM similar to the AD. At P28 and P35, the nerve terminals were evenly distributed throughout each nucleus. In addition, DiI tracer injections into the retrosplenial cortex revealed retrogradely-labeled projection neurons in the 3 nuclei at P14. At P14, the AD received abundant projections from the TRN and then projected to the retrosplenial cortex. The AV and AM seem to receive projections with distinct nodular nerve terminals from the TRN and project to the retrosplenial cortex. The projections from TRN to the AV and AM with nodular nerve terminals at P14 are probably developmental-period specific. In comparison, the TRN projections to the AD at P14 might be related to the development of spatial navigation as part of the head orientation system.Key words: Thalamic reticular nucleus, parvalbumin, axon terminal, development, anterior thalamic nucleus, rat     

The initiation of bursts in thalamic neurons and the cortical control of thalamic sensitivity

Thalamic neurons generate high-frequency bursts of action potentials when a low-threshold (T-type) calcium current, located in soma and dendrites, becomes activated. Computational models were used to investigate the bursting properties of thalamic relay and reticular neurons. These two types of thalamic cells differ fundamentally in their ability to generate bursts following either excitatory or inhibitory events. Bursts generated with excitatory inputs in relay cells required a high degree of convergence from excitatory inputs, whereas moderate excitation drove burst discharges in reticular neurons from hyperpolarized levels. The opposite holds for inhibitory rebound bursts, which are more difficult to evoke in reticular neurons than in relay cells. The differences between the reticular neurons and thalamocortical neurons were due to different kinetics of the T-current, different electrotonic properties and different distribution patterns of the T-current in the two cell types. These properties enable the cortex to control the sensitivity of the thalamus to inputs and are also important for understanding states such as absence seizures.