An HRP study in the monkey of olivary projections from the mesodiencephalic structures with particular reference to pretecto-olivary neurons

The cells of origin of the olivary projection from mesodiencephalic structures have been demonstrated in the Japanese monkey (Macaca fuscata) with the horseradish peroxidase (HRP) method. Particular attention has been paid to the pretecto-olivary projection which is entirely ipsilateral and originates from the nucleus of the optic tract (NOT), the posterior (or principal) pretectal nucleus (PPN), the sublentiform nucleus (SL), and the (pretectal) ventral lateral zone (VLZ). Pretecto-olivary cells are small-medium sizes of oval or fusiform types. To facilitate comparison among the findings of several experiments, a diagram of the macaque olive, as visualized unfolded, was constructed (Fig. 1). Although a topographic correlation has not emerged clearly from the present experiments, the pattern of the pretecto-olivary projection in the monkey appears to be similar to that found in the cat. Participation of some of the pretectal nuclei in the optokinetic nystagmus and the vestibulo-ocular reflex is discussed in connection with the pretecto-olivary and olivocerebellar projections.     

Ponto-medullary projections to the spinal cord: a quantitative study in the cat

The purpose of this research has been to study quantitatively the ponto-medullary projections to the lateral and ventral funiculi in both cervical (C3) and thoracic (Th8) levels. The method consisted in the partial interruption of the spinal cord, sparing one funiculus in which 5-30 microliter of HRP 30% solution was injected at about 1 cm caudally. 19 cats were utilized, 12 for cervical (6 for lateral and 6 for ventral funiculus) and 7 for lumbar injection (3 for lateral and 4 for ventral funiculus). The structures which project to both funiculi of spinal cord (RM, RL, Poo, PR at Th8 level; RM, RL, Poo at C3 level) could exert integrative effects on the proximal and distal segments of the limbs. The structures which project only to FV (VL and Poc at Th8 level; VL, VIN and Poc at C3 level) or to FL (LSC at Th8; PR at C3) could be implied in motor control of only the proximal or distal regions.     

Phrenic nerve afferents elicited cord dorsum potential in the cat cervical spinal cord

Background  

The diaphragm has sensory innervation from mechanoreceptors with myelinated axons entering the spinal cord via the phrenic nerve that project to the thalamus and somatosensory cortex. It was hypothesized that phrenic nerve afferent (PnA) projection to the central nervous system is via the spinal dorsal column pathway.     

Cortical neurons projecting to the posterior part of the superior temporal sulcus with particular reference to the posterior association area. An HRP study in the monkey

Corticocortical connections from the posterior association area to the posterior part of the superior temporal sulcal cortex (STs area) were studied in the monkey by means of retrograde axonal transport of horseradish peroxidase (HRP) or wheatgerm-agglutinin-conjugated HRP (WGA-HRP). After injecting 0.05-0.2 microliter of 50% HRP or 5% WGA-HRP into the STs area, labeled cells were examined in various cortical regions. The dorsal wall of the STs receives fibers mainly from the inferior parietal lobule (area 7) and superior temporal gyrus (area 22), whereas the ventral wall and floor part of the STs receive fibers from the posterior inferotemporal gyrus (area TEO) and prestriate cortex (areas 18 and 19). The deeper parts of the dorsal wall close to the floor region of the STs area also receive many fibers from the cortical walls surrounding the intraparietal, lunate and lateral sulci. Both the dorsal and ventral cortical walls of the intraparietal sulcus send fibers mainly to the deep dorsal wall of the STs. The ventral wall of the STs, on the other hand, receives fibers only from the ventral wall of the intraparietal sulcus. The medial surface of the prestriate cortex and the parahippocampal region send fibers to both walls of the STs. In the prestriate-STs projections originating from areas around the parieto-occipital sulcus, a topographic correlation is present; area 19 located anterior to the sulcus projects to the dorsal wall, whereas area 18 situated posterior to the sulcus projects to the ventral wall. Only the dorsal wall receives fibers from the cingulate (areas 23 and 24) and subparietal gyri (area 7). The deeper part of the dorsal wall and the ventral wall of the posterior STs area are interconnected with each other, while the upper part of the dorsal wall does not appear to receive fibers from the ventral wall.     

Afferent brainstem projections to the hypothalmic locomotor region of the cat brain

The location of sources of direct projections to the hypothalamic locomotor region, electrical stimulation of which in the lightly anesthetized animal induced stepping along a moving treadmill, was studied by the retrograde axonal transport of horseradish peroxidase method in the cat brain stem. Different formations in the brain stem were shown to have direct connections with hypothalamic locomotor regions on both sides. Most sources of these afferent projections were located at sites of catecholamine- (nucl. reticularis lateralis, locus coeruleus, nucl. tractus solitarii) and serotonin-containing (nucl. raphe and substantia grisea centralis) neurons, parabrachial nuclei, and various sensory nuclei. Hypothalamic locomotor regions of both sides form bilateral connections.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 16, No. 3, pp. 353–362, May–June, 1984.     

Projections of neurons of the hypothalamic locomotor region to some brainstem and spinal cord structures in the cat

Efferent projections of the thalamic locomotor region were investigated using the horseradish peroxidase technique of retrograde axonal transport. This enzyme was injected into different brain structures. Function was monitored during a micro-injection into the locomotor areas. It was found that direct descending projections from the hypothalamic locomotor region lead mainly to ipsilateral structures and reach the lumbar sections of the spinal cord. Neurons of the locomotor area of the hypothalamus make their major connections with thelocus coeruleus area and the medial brainstem reticular formation. Projections were observed from the hypothalamic locomotor region to the mesencephalic locomotor area and the locomotor strip.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 17, No. 6, pp. 817–23, November–December, 1985.     

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.     

Corticocortical projections to the monkey temporal lobe with particular reference to the visual processing pathways

Cortico-cortical connections occurring within the temporal lobe and afferent projections to the temporal cortex particularly from the prefrontal and parahippocampal areas were studied in the monkey by means of retrograde axonal transport of horseradish peroxidase (HRP) or wheat-germ-agglutinin-conjugated HRP (WGA-HRP). In particular, 0.1-0.3 microliter of 50% HRP or 5% WGA-HRP was injected into various parts of the temporal cortex, i.e. the rostral (TEr), the caudal (TEc), and the most caudal (TEO) parts of the inferotemporal cortex, the superior temporal gyrus, and the temporal pole (TG), and in the upper bank of the inferior arcuate sulcus in the frontal lobe. Labeled cells, which represent cells of origin of association fibers projecting to the injection site, appeared in various cortical regions. The main findings of the present study are the following. The temporal pole (TG) receives fibers almost exclusively from the most rostral part of the TE. The rostral part of the TE receives many fibers from both the caudal part of the TE and the TEO. The caudal part of the TE receives fibers from the TEO, and the TEO from the prestriate cortex (OA and OB). Taking these findings together, the morphological basis of the "step-wise" progression of visual impulses from the prestriate cortex to the TEO, TE and finally to the TG is clearly presented. The superior temporal gyrus (TA or area 22) receives most fibers from the dorsolateral frontal gyrus, while the inferotemporal cortex (TE or areas 21 and 20) receives most fibers from the ventrolateral frontal gyrus (inferior frontal convexity). Both the temporal pole (TG) and the inferotemporal cortex (TE) receives a fair number of fibers from the parahippocampal region (TH and TF).     

Afferent projections from the brainstem to the area hypothalamica dorsalis: a horseradish peroxidase study in the cat

Experiments using the retrograde transport of horseradish peroxidase were performed in order to identify the cells of origin the ascending projections from different brainstem regions to the area hypothalamica dorsalis (aHd) in the cat. The afferent inputs to this area originate mainly from the midbrain and medulla oblongata regions. The main afferent source of the area hypothalamica dorsalis arises from the substantia grisea centralis, where a large number of labeled cells were observed bilaterally, although more abundant on the ipsilateral side. Substantial afferents reach the aHd from the nuclei vestibularis medialis and inferior and the formatio reticularis mesencephali. A modest number of peroxidase-labeled neurons were observed in the nuclei ruber, interpeduncularis, substantia nigra, reticularis gigantocellularis, vestibularis lateralis, cuneatus and gracilis. From the pons, the nucleus raphe magnus sends a weak projection to the aHd. These anatomical data suggest that such area could be involved in visceral, sexual, nociceptive somatosensorial, sleep-waking and motor mechanisms.     

Motor cortex projections to the thalamus. An autoradiographic study in the cat

Adult cats received tritiated proline-leucine injections into the pericruciate cortex (areas 4 gamma and 3a) unilaterally and the projections to the thalamus were analyzed. Ipsilateral projections were found in the following nuclei, from rostral to caudal: ventral anterior, reticular, ventral lateral, central medial, paracentral, central lateral, ventral medial, mediodorsal, ventral posterolateral, ventral posteroinferior, centre median, parafascicular and posterior complex. In the contralateral hemithalamus sparse projections were found within the paracentral, central lateral and ventral medial nuclei.     

The effects of long-standing limb loss on anatomical reorganization of the somatosensory afferents in the brainstem and spinal cord

We examined the terminations of sensory afferents in the brainstem and spinal cord of squirrel monkeys and prosimian galagos 4-8 years after a therapeutic forelimb or hindlimb amputation within 2 months of birth. In each animal, the distributions of labeled sensory afferent terminations from remaining body parts proximal to the limb stump were much more extensive than in normal animals. These sprouted afferents extended into the portions of the dorsal horn of the spinal cord as well as the cuneate and external cuneate nuclei of the brainstem (forelimb amputees) or spinal Clarke's column (hindlimb amputee) related to the amputated limb. Such reorganization in sensory afferents along with reorganization of the motor efferents to muscles (Wu and Kaas, J Neurosci 19 : 7679-7697, 1999, Neuron 28 : 967-978, 2000) may provide a basis for mislocated phantom sensations of missing forelimb movements accompanying actual shoulder movements during cortical stimulation or movement imagery in patients with amputations.     

The effects of long-standing limb loss on anatomical reorganization of the somatosensory afferents in the brainstem and spinal cord

We examined the terminations of sensory afferents in the brainstem and spinal cord of squirrel monkeys and prosimian galagos 4-8 years after a therapeutic forelimb or hindlimb amputation within 2 months of birth. In each animal, the distributions of labeled sensory afferent terminations from remaining body parts proximal to the limb stump were much more extensive than in normal animals. These sprouted afferents extended into the portions of the dorsal horn of the spinal cord as well as the cuneate and external cuneate nuclei of the brainstem (forelimb amputees) or spinal Clarke's column (hindlimb amputee) related to the amputated limb. Such reorganization in sensory afferents along with reorganization of the motor efferents to muscles (Wu and Kaas, J Neurosci 19: 7679-7697, 1999, Neuron 28: 967-978, 2000) may provide a basis for mislocated phantom sensations of missing forelimb movements accompanying actual shoulder movements during cortical stimulation or movement imagery in patients with amputations.     

An ecological study of a small New Zealand stream with particular reference to the Oligochaeta

The composition, temporal and spatial distribution, and productivity of profundal benthos were investigated in a Colorado Front Range reservoir which impounds water diverted from the Western Slope of the Rocky Mountains. Horsetooth Reservoir, 10.6 km × 1.0 km, consists of three basins with depths greater than 50 m connected by two equalizing channels ca. 30 m deep. Water quality parameters did not vary significantly between sites, but temperature, pH, and dissolved oxygen varied seasonally. The composition and organic content of sediment exhibited a gradient from inlet to outlet which significantly influenced faunal density and distribution patterns. Although 28 genera of macroinvertebrates were collected, the oligochaetes Tubifex tubifex (Müller) and Limnodrilus hoffmeisteri Claparède comprised 97.6% of the total organisms. Chironomids comprised 2.2%. The relative contribution of chironomids to total biomass decreased with increasing depth; the reverse was true for oligochaetes. Mean annual density ranged from 3,827 to 51,901 total organisms/m² for six sampling sites. Mean annual biomass varied from 0.16 to 2.3 g ash-free dry wt/m². Annual turnover ratios ranged from 3.6 to 4.5. Annual production estimates varied from 7.2 to 82.8 kg/ha ash-free dry weight, averaging 39.3 kg/ha or 26.9 kcal/m².     

Ventral migration of early-born neurons requires Dcc and is essential for the projections of primary afferents in the spinal cord

Neuronal migration and lamina-specific primary afferent projections are crucial for establishing spinal cord circuits, but the underlying mechanisms are poorly understood. Here, we report that in mice lacking Dcc (deleted in colorectal cancer), some early-born neurons could not migrate ventrally in the spinal cord. Conversely, forced expression of Dcc caused ventral migration and prevented dorsolateral migration of late-born spinal neurons. In the superficial layer of the spinal cord of Dcc-/- mutants, mislocalized neurons are followed by proprioceptive afferents, while their presence repels nociceptive afferents through Sema3a. Thus, our study has shown that Dcc is a key molecule required for ventral migration of early-born neurons, and that appropriate neuronal migration is a prerequisite for, and coupled to, normal projections of primary afferents in the developing spinal cord.     

Trigeminal primary afferent projections to the spinal cord of the frog,Rana ridibunda

The distribution in the spinal cord of the trigeminal primary projections in the frog Rana ridibunda was studied by means of the anterograde transport of horseradish peroxidase (HRP). Upon entering the medulla via the single trigeminal root, a conspicuous descending tract that reaches the cervical spinal cord segments is established. This projection arises in the ophthalmic (V1), maxillary (V2), and mandibular (V3) trigeminal nerve subdivisions. In the spinal cord, only a minor somatotopic arrangement of the trigeminal fibers was observed, with the fibers arising in V3 terminating somewhat more medially than those from V1 and V2. A dense projection to the medial aspect of the spinal cord, above the central canal, primarily involves V3. Each trigeminal branch sends projections at cervical levels to the contralateral dorsal field, and those from V2 are most abundant. Bilateral experiments with HRP application show convergence of primary trigeminal and spinal afferents within the dorsal field of the spinal cord. The pattern of arrangement of the trigeminal primary afferent fibers in the spinal cord of this frog largely resembles that of amniotes. However, the organization seems simpler and the slight somatotopic distribution of V1, V2, and V3 fibers is similar to the condition in other anamniotes. © 1993 Wiley-Liss, Inc.