Comparative dimensions of propriospinal neurons of different structural and functional groups in cats

A statistical comparison was made of geometric characteristics (area of cross section of the soma and proximal dendrites and d_con, the diameter of the circle of equivalent area to it) of propriospinal neurons of the cat spinal cord labeled with horseradish peroxidase. The linear dimensions of these cells differed by a factor of about seven. The mean d_con of propriospinal neurons in the cervical, thoracic, and lumbar divisions, whose axons reach level L6-7, was 39.9, 30.8, and 36.9 µm, respectively; direct correlation between the size of the neurons and the length of their axons was thus not observed. Characteristics of distribution of sizes of units in the cervical and thoracic divisions indicate the presence of two cell populations forming long propriospinal tracts; one consisting of a few, large neurons, concentrated in the cervical segments, the other consisting of small neurons, distributed among the cervical and thoracic segments. The mean d_con of neurons in the cervical division whose axons reach more caudal segments of the same cervical division was 44.2 µm (on account of a considerable number of large units in the ventral horn), evidence of the large relative size of the short-axon propriospinal neurons in this division of the spinal cord. Neurons located in the dorsal parts of the dorsal horn were the smallest in size, those located in the ventral horn were the largest. No significant differences were found in the dimensions of propriospinal neurons with uncrossed and crossed axons.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 16, No. 2, pp. 238–247, March–April, 1984.     

Lumbar collaterals of neurons of the C6 segment projecting to sacral segments of the cat spinal cord

Electrophysiological investigations of neurons of the C6 segment of the spinal cord were made in α-chloralose anesthetized animals. It was established in the experiments that a part of long descending propriospinal neurons originating in the sixth cervical segment (C6) that projected to sacral segments (S1/S2) gave off collateral branches at the level of the fourth lumbar segment (L4). Several types of neurons were distinguished according to the ipsilateral, contralateral or bilateral course of axons at the thoracic level as well as their lumbar or sacral projections. The cell bodies of 58 identified neurons were distributed in Rexed's laminae VII and VIII of the gray matter. Axons descended in lateral funiculi and their conduction velocities varied from 50 to 85 m/s. The existence of collaterals to various segments of the lumbosacral enlargement indicates that the same information conveyed by long descending propriospinal neurons can reach separate motor centers controlling various muscles of the hindlimbs.     

Synaptic links of propriospinal neurons of the lumbar section of the cat spinal cord

The distribution of propriospinal fiber terminals of the lateral funiculus in the lumbar segments of the cat spinal cord was examined by light and electron microscopy. For the selective demonstration of these terminals, preliminary hemisectioning of the brain at the boundary of the thoracic and lumbar segment, eliminating all the long descending pathways, and subsequent hemisectioning or sectioning of the lateral funiculus at the level of the third lumbar segment was carried out. It was established by staining the degenerating endings (by the Fink—Heimer method) that the terminals of the descending and ascending propriospinal fibers, which form part of the lateral and ventral funiculi, are located mainly in the lateral and medial parts of lamina VII and the dorsal section of lamina VIII, according to Rexed, as well as in the regions adjacent to the dorsolateral and ventromedial motor nuclei. A large number of these terminals is found in the corresponding regions of the gray matter on the contralateral side of the brain. Since, in the case of selective injury of the lateral funiculus the number of degenerating terminals in lamina VIII is noticeably decreased, it can be assumed that the propriospinal neuron terminals of the ventral funiculus are concentrated mainly in lamina VIII. The axons of the propriospinal neurons extend over several segments both in the ascending and in the descending directions. It was shown in an electron microscopic study of the regions in which most of the propriospinal terminals are located that these terminals are of an axo-dendritic nature and terminate in the dendrites of both inter- and motor neurons. Their degeneration can be of the "light" or "dark" type.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR. Translated from Neirofiziologiya, Vol. 3, No. 4, pp. 401–407, July–August, 1971.     

Laminar distribution of sources of ascending spinocerebral fiber systems in the cat spinal cord

The location of labeled neurons that are sources of ascending crossed and uncrossed supraspinal fiber systems was studied in the laminae of gray matter of the spinal cord in 18 cats by the retrograde axonal transport of horseradish peroxidase method. Neurons in the lateral zones of the dorsal horn were shown to make direct, and cells in neighboring regions indirect (through relay nuclei of the dorsal columns) connections with the contralateral thalamus. In the lower segments of the spinal cord sources of crossed spinoreticular and spinothalamic fiber systems are located in the medial regions of the ventral horn and lateral zones of the lateral basilar region. Some large neurons in the motor nuclei were shown to send their axons into the lateral reticular nucleus of the medulla. On the basis of the results a scheme of the laminar organization of sources of ascending fiber systems in the cat spinal cord is constructed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 11, No. 5, pp. 451–459, September–October, 1979.     

Tectal and Related Target Areas of Spinal and Dorsal Column Nuclear Projections in Hedgehog Tenrecs

The terminal distributions of spinal and dorsal column nuclear projections to tectum, pretectum, and central gray of hedgehog tenrecs (Echinops telfairi and Setifer setosus) were investigated using anterograde axonal flow and various tracer substances. In the inferior colliculus, the densest and most extensive mesencephalic projections were found within the pericentral regions. One target area, referred to as the external portion of the inferior colliculus, was represented as a semicircle of grain patches lateral and caudal to the central nucleus. This region received somesthetic afferents from the dorsal column nuclei and from spinal segments at various levels. In contrast, after high cervical injections, the pericentral portion dorsomedial to the rostral half of the central nucleus was labeled almost exclusively. This area of labeling was distinct from the labeling in the central gray and might be best compared with the intercollicular zone in other species. The superior colliculus received projections predominantly from the high cervical cord; minor projections also arose from lumbar spinal segments and the dorsal column nuclei. The terminal field covered roughly the caudal half of the colliculus and involved the stratum griseum intermediale in a patch-like fashion. Some labeling was also found in the stratum griseum profundum and in the stratum griseum superficiale. Other than in the colliculi, weak pretectal projections were observed following dorsal column nuclear injections, while the nucleus of Darkschewitsch was labeled best following lumbosacral injections. All mesencephalic target areas were labeled consistently on the contralateral side, while their ipsilateral side was involved to a varying degree: The relatively most prominent ipsilateral labeling was seen in the central gray, being roughly similar on both sides; scarcely any labeling was noted in the ipsilateral superior colliculus. Tectal injections of retrograde tracer, in addition, revealed a considerable number of labeled neurons in a relatively cell-poor region immediately ventral to the high cervial dorsal horn. This region might correspond to the lateral cervical nucleus, an aggregation of neurons that so far has only been demonstrated in higher mammals.     

Cauda equina syndrome and nitric oxide synthase immunoreactivity in the spinal cord of the dog

The development of the cauda equina syndrome in the dog and the involvement of spinal nitric oxide synthase immunoreactivity (NOS-IR) and catalytic nitric oxide synthase (cNOS) activity were studied in a pain model caused by multiple cauda equina constrictions. Increased NOS-IR was found two days post-constriction in neurons of the deep dorsal horn and in large, mostly bipolar neurons located in the internal basal nucleus of Cajal seen along the medial border of the dorsal horn. Concomitantly, NOS-IR was detected in small neurons close to the medioventral border of the ventral horn. High NOS-IR appeared in a dense sacral vascular body close to the Lissauer tract in S1-S3 segments. Somatic and fiber-like NOS-IR appeared at five days post-constriction in the Lissauer tract and in the lateral and medial collateral pathways arising from the Lissauer tract. Both pathways were accompanied by a dense punctate NOS immunopositive staining. Simultaneously, the internal basal nucleus of Cajal and neuropil of this nucleus exhibited high NOS-IR. A significant decrease in the number of small NOS immunoreactive somata was noted in laminae I-II of L6-S2 segments at five days post-constriction while, at the same time, the number of NOS immunoreactive neurons located in laminae VIII and IX was significantly increased. Moreover, high immunopositivity in the sacral vascular body persisted along with a highly expressed NOS-IR staining of vessels supplying the dorsal sacral gray commissure and dorsal horn in S1-S3 segments. cNOS activity, based on a radioassay of compartmentalized gray and white matter regions of lower lumbar segments and non-compartmentalized gray and white matter of S1-S3 segments, proved to be highly variable for both post-constriction periods.     

Localization and distribution patterns of nicotinamide adenine dinucleotide phosphate diaphorase exhibiting axons in the white matter of the spinal cord of the rabbit

The funicular distribution of nicotinamide adenine dinucleotide phosphate diaphorase (NADPHd)-exhibiting axons was examined in the white matter of the rabbit spinal cord by using horizontal, parasaggital, and transverse sections. Four morphologically distinct kinds of NADPHd-exhibiting axons (2.5–3.5 m in diameter) were identified in the sulcomarginal fasciculus as a part of the ventral column in the cervical and upper thoracic segments and in the long propriospinal bundle of the ventral column in Th3–L3 segments. Varicose NADPHd-exhibiting axons of the sympathetic preganglionic neurons, characterized by widely spaced varicosities, were found in the ventral column of Th2–L3 segments. A third kind of NADPHd-positive ultrafine axons, 0.3–0.5 m in diameter with numerous varicosities mostly spherical in shape, was identified in large number within Lissauer's tract. The last group of NADPHd-exhibiting axons (1.0–1.5 m in diameter) occurred in the Lissauer tract. Most of these axons were traceable for considerable distances and generated varicosities varying in shape from spherical to elliptical forms. The majority of NADPHd-exhibiting axons identified in the cuneate and gracile fascicles were concentrated in the deep portion of the dorsal column. An extremely reduced number of NADPHd-exhibiting axons, confirmed by a computer-assisted image-processing system, was found in the dorsal half of the gracile fascicle. Axonal NADPHd positivity could not be detected in a wide area of the lateral column consistent with the location of the dorsal spinocerebellar tract. Numerous, mostly thin NADPHd-positive axonal profiles were detected in the dorsolateral funiculus in all the segments studied and in a juxtagriseal portion of the lateral column as far as the cervical and lumbar enlargements. A massive occurrence of axonal NADPHd positivity was detected in the juxtagriseal layer of the ventral column all along the rostrocaudal axis of the spinal cord. The prominent NADPHd-exhibiting bundles containing thick, smooth, nonvaricose axons were identified in the mediobasal and central portion of the ventral column. First, the sulcomarginal fasciculus was found in the basal and medial portion of the ventral column in all cervical and upper thoracic segments. Second, more caudally, a long propriospinal bundle displaying prominent NADPHd positivity was localized in the central portion of the ventral column throughout the Th3–L3 segments.     

Experimental morphological study of endings of propriospinal fibers of the lateral funiculus in the cat cervical spinal cord

The distribution and ultrastructure of terminals of the propriospinal fibers of the lateral funiculus in the cervical segments of the cat spinal cord were studied by the experimental degeneration method. A preliminary lateral hemisection of the spinal cord was carried out 5–6 months earlier at the level of segments C2 or C3 to destroy all the long descending pathways; the lateral funiculus was then divided at the level of C4 or C5. It was shown by the method of Fink and Heimer that terminals of descending and ascending propriospinal pathways damaged by the second division are distributed in the gray matter ipsilaterally in the lateral zones of Rexed's laminase V–VII and also in the dorsolateral motor nuclei. An electron-microscopic study showed that the synapses of the degenerating terminals are mainly axo-dendritic in type and account for 14.5% of the total number of terminals counted. Residual synaptic vesicles in these terminals were spherical in shape. The mean diameter of the degenerating myelinated propriospinal fibers in the lateral funiculus was 10±3 µ. The results of this investigation were compared with those of electrophysiological investigations of the function of propriospinal neurons.     

Descending neuronal projections to the lumbar segment of the spinal cord of cats

In the experiments, performed on cats by means of retrograde axonal horseradish peroxidase transport, localization of the sources of descending supra- and propriospinal projections to the area of the lumbar parts of the spinal cord, where the generator of locomotor movements is located. After local administration of horseradish peroxidase into the spinal cord, the greatest amount of the labelled neurons is observed in the ipsilateral reticular formation and in the Koelliker-Fuse nucleus. Comparison of the number of neurons, forming the descending projections from the I cervical up to the IV lumbar segments demonstrates an essential predominance of short propriospinal connections over the long, as well as over the supraspinal ones.     

The Effect of Cauda Equina Constriction on Nitric Oxide Synthase Activity

Nitric oxide synthase (NOS) activity was studied in the gray and white matter regions of the spinal cord 2 and 5 days after multiple cauda equina constrictions of the central processes of L7-Co5 dorsal root ganglia neurons. The results show considerable differences in enzyme activity in the thoracic, upper lumbar, lower lumbar, and sacral segments. Increased NOS activity was observed at 2 days after multiple cauda equina constrictions in the dorsal, lateral, and ventral columns of the lower lumbar segments and in the ventral column of the upper lumbar segments. The values returned to control levels within 5 postconstriction days. In the lateral columns of thoracic segments taken 2 and 5 days after surgery, NOS activity was enhanced by 54% and 55% and in the upper lumbar segments by 130% and 163%, respectively. Multiple cauda equina constrictions performed surgically for 2 and 5 days caused a significant increase in NOS activity predominantly in the gray matter regions of thoracic segments. A quite different response was found 5 days postconstriction in the upper lumbar segments, where the enzyme activity was significantly decreased in the dorsal horn, intermediate zone, and ventral horn. No such extreme differences could be seen in the lower lumbar segments, where NOS activity was significantly enhanced only in the ventral horn. The data correspond with a higher number of NOS immunoreactive somata, quantitatively evaluated in the ventral horn of the lower lumbar segments at 5 days after multiple cauda equina constrictions. While the great region-dependent heterogeneity in NOS activity seen 2 and 5 days after multiple cauda equina constrictions is quite apparent and suggestive of an active role played by nitric oxide in neuroprotective or neurotoxic processes occurring in the gray and white matter of the spinal cord, the extent of damage or the degree of neuroprotection caused by nitric oxide in compartmentalized gray and white matter in this experimental paradigm would be possible only using longer postconstriction periods.     

The dorsomedial nuclear group of cranial nerves in the frog.

The dorsomedial motor nuclei were demonstrated by the cobalt-labeling technique applied to the so-called somatic motor cranial nerves. The motoneurons constituting these nuclei are oval-shaped and smaller than the motoneurons in the ventrolateral motor nuclei. They give rise to ventral and dorsal dendrite groups which have extensive arborization areas. A dorsolateral cell group in the rostral three quarters of the oculomotorius nucleus innervates ipsilateral eye muscles (m.obl.inf., m.rect.inf., m.rect.med.) and a ventromedial cell group innervates the contralateral m. rectus superior. Ipsilateral axons originate from ventral dendrites, contralateral axons emerge from the medial aspect of cell bodies, or from dorsal dendrites, and form a "knee" as they turn around the nucleus on their way to join the ipsilateral axons. A few labeled small cells found dorsal and lateral to the main nucleus in the central gray matter are regarded as representing the nucleus of Edinger-Westphal. The trochlearis nucleus is continuous with the ventromedial cell group of the oculomotorius nucleus. The axons originate in dorsal dendrites, run dorsally along the border of the gray matter and pierce the velum medullare on the contralateral side. A compact dendritic bundle of oculomotorius neurons traverse the nucleus, and side branches appear to be in close apposition to the trochlearis neurons. A dorsomedial and a ventrolateral cell group becomes labeled via the abducens nerve. The former supplies the m. rectus lateralis, while the latter corresponds to the accessorius abducens nucleus which innervates the mm. rectractores. Neurons in this latter nucleus are large and multipolar, resembling the neurons in the ventrolateral motor nuclei. Their axons originate from dorsal dendrites and form a "knee" around the dorsomedial aspect of the abducens nucleus. Cobalt applied to the hypoglossus nerve reaches a dorsomedial cell group (the nucleus proper), spinal motoneurons and sympathetic preganglionic neurons. Of the dorsomedial motor cells, the hypoglossus neurons are the largest, and a branch of their ventral dendrites terminates on the contralateral side. Some functional and developmental biological aspects of the morphological findings, such as the crossing axons and the peculiar morphology of the accessory abducens nucleus, are discussed.     

Anatomical Studies of the Spinocervical Tract of the Rat

The retrograde transport of horseradish peroxidase (HRP) was used to identify and examine the cells of origin of the spinocervical tract (SCt) in the rat. Initially, precise data on the boundaries of the rat lateral cervical nucleus (LCn) were gathered after injecting HRP into the ventrobasal thalamus. These data indicated that the LCn of the rat is restricted to a region on the extreme lateral edge of the dorsalmost portion of the lateral funiculus (DLf) within spinal segment C₂ Following small iontophoretic injections of HRP that were restricted to this area, labeled SCt neurons were found in the ipsilateral nucleus proprius at all levels of the spinal cord but were most numerous in the cervical enlargement. Lesion studies indicated that the overwhelming majority of SCt axons ascend to the LCn within the DLf. In an attempt to determine whether our injection techniques labeled a significant number of cells through axons of passage, HRP injections were made in the DLf ventral to the LCn. Such injections labeled, presumably through axons of passage, cells in several areas of the spinal cord gray matter, including a large number in the contralateral marginal zone Injections in areas immediately rostral to the LCn labeled 20% or less of the total number of cells within the enlargements that were labeled by injections into the LCn. Thus, the majority of cells labeled by injections of HRP into the LCn were labeled through preterminal fibers or terminals themselves. The cells of origin of the SCt in the rat are similar in location to those in the cat but far fewer in number.     

Neuronal types in the spinal dorsal gray of the turtle Chrysemys d'orbigny: a Golgi study

At thoracic and lumbar levels the spinal dorsal gray of young specimens of the turtle Chrysemys d'orbigny consists of a cell-free neuropil and an aggregation of perikarya termed here the lateral column of the dorsal horn (LCDH). Nerve cell clusters also occur in the dorsal commissure. The main neuropil area can be divided into a thin superficial layer containing some myelinated fibers (neuropil area Ib) and a compact core composed of unmyelinated axon terminals, dendritic branches, and thin glial processes (neuropil area II). A looser neuropil area is located at the horn base (neuropil area III). The so-called marginal zone of de Lange represents a fourth synaptic field termed here neuropil area Ia. The LCDH consists of neurons of different size and shape. Two peculiar nerve cell types have been recognized in the dorsal horn: giant and bitufted neurons. The former exhibits a large dendritic arbor, which after passing through neuropil areas II and Ib projects into neuropil area Ia and the adjacent white matter. Most frequently Golgi-stained giant neurons have perikarya and dendritic domains on the same side (ipsilateral giant neurons). There are also heterolateral giant neurons whose dendritic branches invade the opposite horn. Bitufted neurons are characterized by the presence of two main dendritic shafts connecting neuropil area II of both dorsal horns. At neuropil levels the major dendritic branches ramify profusely giving rise to short tortuous terminal processes. Perikarya of bitufted neurons occur in the dorsal commissure. The LCDH also contains many small and medium-sized neurons. These are oriented in two main directions: parallel or radial with respect to the dorsal horn surface. The population of horizontally oriented neurons comprises two subtypes termed here alpha and beta. Radially oriented neurons are pleomorphic, defying precise, unequivocal classification.     

Horseradish peroxidase-labeled cells as sources of the spinoreticular and spinothalamic systems of the brain]

The cells of spinoreticular and spinothalamic fibrous systems of the cat brain were studied by the method of axone transmission of horse-radish peroxidase (HP). A dense accumulation of HP-labeled neurons establishing direct relations with the reticular formation and thalamus was seen in the upper segments of the spinal cord. In the lower segments these zones were confined to the medial part of the ventral horn and the intermediate zone of the gray matter. The neurons established direct connections with contralateral nuclei of the reticular formation as well as with the thalamus ipsi- and contralateral nuclei. Possible pathways of transmitting somatic and pain sensitivity are discussed.     

Polysynaptic components of the early somato-sympathetic reflex response in lumbar white rami

The second and third components of the somato-sympathetic reflex discharge in the lumbar white rami were investigated in anesthetized cats. Both components, under different experimental conditions, may undergo changes that are: parallel, not parallel, or actually opposite in direction to those in components of the propriospinal wave of the somato-somatic reflex. This suggests that the interneuronal apparatus of both types of reflexes may include common and separate components. It is postulated that the separate components of the somato-sympathetic reflex may be formed by discharges of sympathetic preganglionic neurons whose axons conduct at different velocities. On the basis of calculations of the central delay time it is concluded that the second component is formed by discharges of lateral horn neurons and the third component by neurons with axons conducting excitation at less than 1.5 m/sec, found in the lateral part of the intermediate zone.     

Spatial distribution of descending propriospinal tract neurons in the cat spinal cord

Quantitative estimates of the density of distribution of interneurons forming descending intersegmental connections in the cat spinal cord were obtained. Neurons were labeled by retrograde axonal transport of horseradish peroxidase injected unilaterally at different segmental levels. The mean number of labeled units per section 50 µ thick, in a given zone, was used as the measure of density. The density of distribution of the propriospinal neurons forming the longest tracts between the cervical and lumbosacral regions of the cord was found to be about half the density of distribution of neurons with short (not more than two segments) axons, and to be several times less than the corresponding value for neurons with axons of intermediate length. No marked local peaks of density of distribution of long-axon neurons were found at the level of the brachial enlargement. The number of neurons with crossed axons in most segments was close to half of the total number of propriospinal units. Zones of transverse section of the spinal cord with maximal concentrations of neurons forming direct and crossed propriospinal tracts of different lengths were determined at different levels. Correlation between the quantitative composition of propriospinal neuron populations with characteristics of influences transmitted by these populations is examined.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 16, No. 1, pp. 96–105, January–February, 1984.     

Complete sciatic nerve transection induces increase of neuropeptide Y-like immunoreactivity in primary sensory neurons and spinal cord of frogs

Neuropeptide Y (NPY) was immunohistochemically investigated in the frog spinal cord and dorsal root ganglia after axotomy. In normal ganglia, moderate NPY-like immunoreactivity (NPY-IR) prevailed in large and medium cells. In the spinal cord, the NPY-IR was densest in the dorsal part of the lateral funiculus. Other fibers and neurons NPY-IR were observed in the dorsal and ventral terminal fields and mediolateral band. NPY-IR fibers were also found in the ventral horn and in the ventral and lateral funiculi. The sciatic nerve transection increased the NPY-IR in large and medium neurons of the ipsilateral and contralateral dorsal root ganglia at 3 and 7 days, but no clear change was found at 15 days. In the spinal cord, there was a bilateral increase in the NPY-IR of the dorsal part of the lateral funiculus. In the ipsilateral side, the NPY-IR was increased at 3 and 7 days but was decreased at 15 days. In the contralateral side, a significant reduction at 15 days occurred. These findings seem to favor the role of NPY in the modulation of pain-related information in frogs, suggesting that this role of NPY may have appeared early in vertebrate evolution.     

Organization of bilateral spinal projections to the lateral reticular nucleus of the rat

The present study was carried out to analyze the topography of bilateral spinal projections to the lateral reticular nucleus (LRN). We used retrograde transport of fluorescent tracers Fast Blue and Diamidino Yellow to identify spinal neurons projecting to the ipsilateral and/or contralateral LRN, as well as orthograde transport of Phaseolus vulgaris leucoagglutinin to identify the LRN areas where spinoreticular axons terminate. Orthograde labeling confirmed that bilateral spinoreticular projections coming from cervical and upper-thoracic segments terminate in the magnocellular division of LRN, while those coming from the lower-thoracic, lumbar and sacral segments end in the parvocellular division of the nucleus; only a sparse spinal input has been observed in the subtrigeminal division of LRN. Retrograde labeling showed that labeled neurons were present at all spinal levels and in particular large numbers in the cervical and lumbar enlargements. Retrogradely single-labeled cells were located, with contralateral predominance, in all segments of the spinal cord, within laminae IV, V, VI, VIII, and X, whereas in laminae III and VII labeled neurons were mainly observed ipsilaterally. Furthermore, a small fraction of double-labeled cells (7.4%) was observed throughout the spinal cord, mainly in laminae III, IV, VII and VIII.     

Synaptic organization of supraspinal control over propriospinal ventral horn interneurons in cat and monkey spinal cord

Synaptic responses evoked in propriospinal neurons of the upper lumbar segments (L₃–L₄) by reticulo-, vestibulo-, and corticospinal impulses were studied in experiments on cats and monkeys. Propriospinal cells, identified by antidromic stimulation, were stained with Procion red, so that they could be localized in the different zones of the ventral horn. Monosynaptic reticular and vestibular excitatory influences were discovered in cats; convergence of these influences on the same neurons was demonstrated. In monkeys bulbospinal monosynaptic effects were supplemented by monosynaptic influences arriving from the motor cortex; convergence of monosynaptic excitatory influences from all supraspinal sources studied was found on some propriospinal neurons. The propriospinal neurons studied also had synaptic inputs from primary afferents.I. M. Sechenov Institute of Evolutionary Physiology and Biochemistry, Academy of Sciences of the USSR, Leningrad. Translated from Neirofiziologiya, Vol. 9, No. 2, pp. 177–184, March–April, 1977.