Identification of the midbrain locomotor nuclei and their descending pathways in the teleost carp, Cyprinus carpio

In order to identify the mesencephalic spinal pathways for initiation of swimming in the carp, we employed electrical and chemical microstimulation of the mesencephalic tegmentum. Electrical stimulation of the midbrain in decerebrate carp produced bilateral or unilateral rhythmic movements of the tail. Bilateral alternating movements were induced by stimulation with the lowest threshold currents to the brain region just beneath the third ventricle at the level of the mid mesencephalon. The region included the nucleus of medial longitudinal fasciculus (Nflm), the medial longitudinal fasciculus (flm), the red nucleus (Nrb). To specify the nuclei of the origin of the descending pathway, we microinjected 0.1 M

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-glutamic acid to the region. Both bilateral and unilateral tail movements were induced, the majority being the latter. The unilateral movements were accompanied with tail flips toward the ipsilateral side of stimulation sites. The smallest injection volume required for initiation of the movement was recorded at the Nflm. Bilateral tail movements were produced only by injections into the medial region between the nucleus of the both sides. The present results imply a crucial role of Nflm neurons in the initiation of swimming Nflm neurons on one side project through flm to the ipsilateral spinal cord along its entire length and regulate activities of the individual central pattern generators.     

Projections of the vestibular and cerebellar nuclei in Rana pipiens

The efferent projections and cytoarchitecture of the vestibulocerebellar region were examined to determine the nuclear boundaries and potential homologies. The anterior portion of the vestibular complex projects to the ipsilateral oculomotor and trochlear nuclei and is the major source of commissural fibers. Neurons in the rostromedial portions of the complex project to the contralateral trochlear nucleus. Large neurons in the ventrolateral portion of the complex give rise to a bilateral vestibulospinal pathway. Medium-sized neurons in the neuropil and small neurons in the central gray giving rise to bilateral projections to the spinal cord and oculomotor nuclei as well as commissural and ipsilateral cerebellar efferents. Projections from the nucleus of the cerebellum reach the contralateral spinal cord and cerebellar nucleus and there is also a bilateral projection to the ventral rhombencephalic and mesencephalic basal plates. The medial portion of the nucleus gives rise to commissural, ipsilateral mesencephalic and contralateral spinal projections. The lateral portion of the nucleus projects to the contralateral ventral mesencephalon. On the whole, the results of this investigation substantiate the division of the anuran vestibular complex in anurans into nuclei which may be homologous to the superior nucleus and nucleus of Deiters in mammals. The case for distinct descending and medial nuclei is less compelling. Further, it appears possible to divide the nucleus of the cerebellum into medial and lateral components whose connectivity is similar to that of reptiles and to a lesser extent mammals.     

On the organization of cerebellar efferent pathways in the nurse shark (Ginglymostoma cirratum)

The organization of the efferent fiber systems of the nurse shark cerebellum was studied with the Nauta and Fink-Heimer techniques. Lesions of the cerebellar cortex produce a pattern of terminal degeneration restricted to select regions of the cortex, as well as ipsi- and contralateral cerebellar nuclei. We found no evidence of cortical axons projecting beyond the nuclei, to the medulla and spinal cord as has often been reported. Lesions involving the cerebellar nucleus reveal three efferent pathways. The ipsilateral descending cerebello-bulbar (IDC) pathway extends as far caudal as the first spinal segment and issues fibers to the lateral parts of the reticular formation. The brachium conjunctivum splits into a larger ascending limb (BCA) and a smaller descending one (BCD). The latter descends to the caudal medulla terminating along its course in the medial reticular formation. The ascending limb provides an input to (1) a nucleus we have tentatively labelled the “red nucleus,” (2) the trochlear nucleus, (3) the oculomotor nuclei, (4) the midbrain central gray, and (5) a poorly differentiated nucleus in the dorsal thalamus.     

Descending projections and excitation during fictive swimming in Xenopus embryos: neuroanatomy and lesion experiments

We describe the distribution of "descending" interneurons in late Xenopus laevis embryos after retrograde filling with horseradish peroxidaze via their ipsilateral, descending axons in the spinal cord. These multipolar neurons, with dendrites spread throughout the marginal zone, form a longitudinal column extending from midtrunk spinal cord into the brainstem to the level of the vagus. In the hindbrain these neurons are part of the uncrossed reticulospinal projection. They are most numerous in the caudal brainstem, their density falling by half at the eighth postotic segment. To examine their possible role in swimming we reduced the population of descending interneurons by making progressive transections of the brainstem or spinal cord at the first to fifth postotic segments. These led to progressive reduction in the initial frequency of fictive swimming in immobilized embryos, even when the brainstem was divided sagittally. Transecting the spinal cord at the fourth postotic segment did not reduce initial frequency rostral to the lesion. The effects of these lesions on the duration of fictive swimming episodes were similar. The results suggest that descending interneurons could provide excitatory drive during swimming and that some reticulospinal and spinal interneurons may form single homogeneous populations.     

Origin of excitatory drive to a spinal locomotor network

A long-standing hypotheses is that locomotion is turned on by descending excitatory synaptic drive. In young frog tadpoles, we show that prolonged swimming in response to a brief stimulus can be generated by a small region of caudal hindbrain and rostral spinal cord. Whole-cell patch recordings in this region identify hindbrain neurons that excite spinal neurons to drive swimming. Some of these hindbrain reticulospinal neurons excite each other. We consider how feedback excitation within the hindbrain may provide a mechanism to drive spinal locomotor networks.     

The control of locomotor frequency by excitation and inhibition

Every type of neural rhythm has its own operational range of frequency. Neuronal mechanisms underlying rhythms at different frequencies, however, are poorly understood. We use a simple aquatic vertebrate, the two-day-old Xenopus tadpole, to investigate how the brainstem and spinal circuits generate swimming rhythms of different speeds. We first determined that the basic motor output pattern was not altered with varying swimming frequencies. The firing reliability of different types of rhythmic neuron involved in swimming was then analyzed. The results showed that there was a drop in the firing reliability in some inhibitory interneurons when fictive swimming slowed. We have recently established that premotor excitatory interneurons [descending interneurons (dINs)] are critical in rhythmically driving activity in the swimming circuit. Voltage-clamp recordings from dINs showed higher frequency swimming correlated with stronger background excitation and phasic inhibition, but did not correlate with phasic excitation. Two parallel mechanisms have been proposed for tadpole swimming maintenance: postinhibition rebound firing and NMDAR-dependent pacemaker firing in dINs. Rebound tests in dINs in this study showed that greater background depolarization and phasic inhibition led to faster rebound firing. Higher depolarization was previously shown to accelerate dIN pacemaker firing in the presence of NMDA. Here we show that enhancing dIN background excitation during swimming speeds up fictive swimming frequency while weakening phasic inhibition without changing background excitation slows down swimming rhythms. We conclude that both strong background excitation and phasic inhibition can promote faster tadpole swimming.     

Expression of a serine protease (motopsin PRSS12) mRNA in the mouse brain: in situ hybridization histochemical study

Serine proteases are considered to play several important roles in the brain. In an attempt to find novel brain-specific serine proteases (BSSPs), motopsin (PRSS-12) was cloned from a mouse brain cDNA library by polymerase chain reaction (PCR). Northern blot analysis demonstrated that the postnatal 10-day mouse brain contained the most amount of motopsin mRNA. At this developmental stage, in situ hybridization histochemistry showed that motopsin mRNA was specifically expressed in the following regions: cerebral cortical layers II/III, V and VIb, endopiriform cortex and the limbic system, particularly in the CA1 region of the hippocampal formation. In addition, in the brainstem, the oculomotor nucleus, trochlear nucleus, mecencephalic and motor nuclei of trigeminal nerve (N), abducens nucleus, facial nucleus, nucleus of the raphe pontis, dorsoral motor nucleus of vagal N, hypoglossal nucleus and ambiguus nucleus showed motopsin mRNA expression. Expression was also found in the anterior horn of the spinal cord. The above findings strongly suggest that neurons in almost all motor nuclei, particularly in the brainstem and spinal cord, express motopsin mRNA, and that motopsin seems to have a close relation to the functional role of efferent neurons.     

Structural and functional properties of reticulospinal neurons in the early-swimming stage Xenopus embryo

This study presents direct evidence that in Xenopus laevis embryos ipsi- and contralaterally descending reticulospinal fibers from the caudal brain stem project to the spinal cord, where they directly contact primary motoneurons. At stage 30, occasional contacts between primary motoneurons and descending axons are present. These contacts are possibly already functional since presynaptic vesicles were sometimes observed. Furthermore, the physiological data obtained in this study suggest that reticulospinal neurons in the caudal brain stem are involved in the central generation of early swimming. The first ingrowth of reticulospinal axons was observed in the rostral spinal cord after application of HRP to the caudal brain stem of stage 27/28 embryos. By stage 32, many supraspinal axons could be found in the spinal cord at the level of the 12/13th myotome, near the time of the first rhythmic swimming. Both lamellipodial and varicose growth cones were found. Intracellular recordings from the brain stem and extracellular recordings from the myotomal muscles in curarized embryos around stage 30 revealed neurons in the caudal brain stem which were active during early fictive swimming. After intracellular staining with Lucifer yellow neurons with descending axons were found in the brain-stem reticular formation. These reticulospinal neurons showed "motoneuron-like" phasic activity, producing one spike each swimming cycle. Rhythmically occurring spikes with swimming periodicity were superimposed on a sustained depolarization level of some 5-30 mV. Reticulospinal neurons in the brain stem resemble descending interneurons in the spinal cord by their morphology, projection pattern, and activity during early swimming. Reticulospinal neurons and descending interneurons might therefore form one continuous population of projecting interneurons with a different location but a similar function. In support of this we propose that the embryonic brain-stem reticular formation forms part of the swimming pattern generator.     

Central nervous system distribution of the transcription factor Phox2b in the adult rat

Phox2b is required for development of the peripheral autonomic nervous system and a subset of cranial nerves and lower brainstem nuclei. Phox2b mutations in man cause diffuse autonomic dysfunction and deficits in the automatic control of breathing. Here we study the distribution of Phox2b in the adult rat hindbrain to determine whether this protein is selectively expressed by neurons involved in respiratory and autonomic control. In the medulla oblongata, Phox2b-immunoreactive nuclei were present in the dorsal vagal complex, intermediate reticular nucleus, dorsomedial spinal trigeminal nucleus, nucleus ambiguus, catecholaminergic neurons, and retrotrapezoid nucleus (RTN). Phox2b was expressed by both central excitatory relays of the sympathetic baroreflex (nucleus of the solitary tract and C1 neurons) but not by the inhibitory relay of this reflex. Phox2b was absent from the ventral respiratory column (VRC) caudal to RTN and rare within the parabrachial nuclei. In the pons, Phox2b was confined to cholinergic efferent neurons (salivary, vestibulocochlear) and noncholinergic peritrigeminal neurons. Rostral to the pons, Phox2b was detected only in the oculomotor complex. In adult rats, Phox2b is neither a comprehensive nor a selective marker of hindbrain autonomic pathways. This marker identifies a subset of hindbrain neurons that control orofacial movements (dorsomedial spinal trigeminal nucleus, pontine peritrigeminal neurons), balance and auditory function (vestibulocochlear efferents), the eyes, and both divisions of the autonomic efferent system. Phox2b is virtually absent from the respiratory rhythm and pattern generator (VRC and dorsolateral pons) but is highly expressed by neurons involved in the chemical drive and reflex regulation of this oscillator.     

Cystathionine β-synthase in the CNS of masu salmon <Emphasis Type="Italic">Oncorhynchus masou</Emphasis> (Salmonidae) and carp <Emphasis Type="Italic">Cyprinus carpio</Emphasis> (Cyprinidae)

Immunohistochemical labeling showed the presence of cystathionine β-synthase in neurons of the ventral spinal column, medulla oblongata, the cells and fibers of the cerebellum, optic tectum, and telencephalon of the masu salmon Oncorhynus masou and the carp Cyprinus carpio. We found considerable interspecies differences in the localization and optical density of immunoreactive structures in brain areas of masu salmon and carp which are presumably related to the specificities of the feeding and behavior of these fishes. In carp, the medulla oblongata and spinal cord had intensely labeled vessels, which were absent in masu salmon. The periventricular area of the medulla oblongata and ventral and lateral areas of the cerebellum of the carp had strongly CBS-positive cells without outgrowths. The sizes of cells and their location in the brain and interrelations with H2S-producing neurons suggest that periventricular area of the carp brain has H2S-producing glia.     

Cholecystokinin-induced excitation in the substantia nigra: evidence for peripheral and central components

Cholecystokinin (CCK), one of the most common brain peptides, coexists with dopamine (DA) in neurons of the medial substantia nigra (SN). CCK has been shown to excite these neurons following either direct iontophoretic or systemic administration suggesting that peripherally administered CCK may cross the blood brain barrier to act directly on nigral DA cells. However, biochemical evidence suggests that CCK does not cross the blood brain barrier, and several studies have shown that the behavioral and the satiety-inducing effects of peripherally administered CCK are abolished by vagotomy. In order to test for vagal mediation of the nigral response to systemically administered CCK, we examined the effects of a series of lesions to the vagal pathways on CCK-induced excitation in the SN. Neither acute thoracic nor chronic subdiaphragmatic vagotomies had any effect on the excitatory response of nigral DA neurons to systemically administered CCK. High cervical spinal cord transections were similarly without effect. In contrast, lesions of either vagal fibers in the medulla or of the efferent pathways from the nucleus tractus solitarii, the primary sensory nucleus of the vagus, produced significant attenuations of the nigral effects of systemically administered CCK. However, neither lesion blocked effects of CCK completely. We suggest that peripherally administered CCK has two components to its excitatory action in the SN; a component probably mediated through CCK receptors in the nucleus tractus solitarii and a direct action on DA neurons.     

Connections of the auditory midbrain in a teleost fish, Cyprinus carpio

Central auditory pathways were traced in Japanese carp, Cyprinus carpio, using electrophysiological mapping and HRP tract-tracing methods. Multiunit recordings made from the carp torus semicircularis, the major midbrain area for processing octavolateralis information, revealed a mediolateral segregation of auditory and lateral line sensory modalities. Iontophoretic injections of HRP were made into the medial torus to trace afferent and efferent projections of the carp auditory midbrain. Following unilateral HRP injections into the medial torus, retrogradely labeled neurons were observed within six nuclei of the carp medulla. Two octaval nuclei, the anterior octavus nucleus and descending octavus nucleus, contained HRP-filled neurons. Labeled neurons were also observed within the ipsilateral superior olive, scattered among fibers of both lateral lemnisci, and bilaterally within the medullary reticular formation. In addition, bilateral retrograde cell labeling was found within a group of Purkinje-like cells located adjacent to the IVth ventricle, just rostral to the level of the VIIIth nerve. Few labeled neurons were found within the nucleus medialis, a principal target for lateral line afferents within the medulla. At midbrain levels, retrogradely labeled neurons were observed within the contralateral torus semicircularis and the ipsilateral optic tectum. Three forebrain nuclei project to the carp auditory midbrain. Within the diencephalon, descending projections originate from the anterior tuberal nucleus, bilaterally, and from the ipsilateral central posterior thalamic nucleus. The ipsilateral caudal telencephalon also projects to the carp auditory midbrain via large multipolar neurons within area dorsalis pars centralis. Anterograde labeling of fibers and terminals revealed efferent projections of the carp auditory midbrain to the following targets: the ipsilateral superior olive, the ipsilateral medullary reticular formation, the deep layers of the optic tectum, the contralateral torus semicircularis, the anterior tuberal nucleus, and the central posterior thalamic nucleus. These results, together with recent studies of lateral line pathways in teleosts (Finger, '80, '82a), demonstrate that central auditory and lateral line pathways are anatomically distinct in the carp, at least from medullary to diencephalic levels. Furthermore, there are striking similarities in the organization of the central auditory pathways of the carp and those of amphibians and land vertebrates.     

Spinal projections from the midbrain in monkey.

Neurons descending from the midbrain to the spinal cord in the monkey were identified with the retrograde horseradish peroxidase technique. Beginning in the caudal midbrain and extending anteriorly beneath the superior colliculus, large numbers of neurons of the nucleus cuneiformis and lateral central gray were found to project ipsilaterally to the spinal cord. In the posterolateral superior colliculus, neurons of the intermediate and deep layers, stratum griseum intermediale and stratum griseum profundum, were found to give rise to contralateral projections to the upper cervical spinal segments. An ipsilateral tectospinal projection from the anteromedial part of the collicus may also exist. In the red nucleus, neurons of the magnocellular division were shown to give rise to a somatotopically organized projection to the upper cervical cord and spinal enlargements. No neurons of the parvocellular red nucleus were labeled from the spinal cord. In the anterior midbrain, neurons of the interstitial nucleus of Cajal, nucleus of Darkschewitsch, and the adjacent dorsomedial and ventromedial midbrain tegmentum were found to give rise to an extensive ipsilateral descending spinal projection. Neurons located in various midline nuclei including the supratrochlear nucleus, oculomotor nucleus, Edinger-Westphal nucleus, and the ventral part of the central gray were also labeled from the spinal cord. These findings indicate that the primate midbrain is the origin of an extensive system of descending spinal pathways, some of which are likely to be involved in mediating descending influences involved in complex motor and sensory behavior.     

Morphology and distribution of the projection neurons in the cerebellum in a teleost, Sebastiscus marmoratus

Cerebellar efferent neurons in a teleost, Sebastiscus marmoratus, were studied by means of the horseradish peroxidase (HRP) tracing and Golgi impregnation methods. The cerebellar efferents or eurydendroid neurons are classified into two types (A and B) on the basis of the morphology of the dendrites, intracerebellar distribution, and other afferent connections. Type A neurons form a cell cluster in the lobus caudalis and have one thick primary dendrite from which several branches with sparse but long spines extend into the molecular layer of the lobus caudalis. Type B neurons, observed in both the valvula and corpus cerebelli, have two or three primary dendrites running along the ganglion cell layer, and the distal dendritic branches are distributed in molecular layer perpendicularly to the cerebellar surface. Small spines are densely studded on the dendrites of type B neurons. Somata of type A and B neurons are located in and just beneath the ganglion cell layer. The cerebellum projects to the ipsilateral nucleus lateralis valvulae and torus longitudinalis and bilaterally, but mostly contralaterally to the nucleus ventromedialis thalami of Schnitzlein ('62), nucleus ruber, the vicinity of the oculomotor complex, torus semicircularis, and brainstem reticular formation. Type A neurons send axons primarily to the vicinity of the oculomotor complex and partly to the nucleus ventromedialis thalami and the nucleus ruber, whereas type B cells project to all main cerebellar targets. In addition, type B cells are organized topographically in the cerebellum in relation to the efferent targets in the brainstem.     

Cerebellar efferents in the lizard Varanus exanthematicus. II. Projections of the cerebellar nuclei

The projections of the cerebellar nuclei have been studied in the lizard Varanus exanthematicus with various experimental anatomical techniques. In anterograde degeneration experiments (lesions of the cerebellar peduncle) both ascending and decending contralateral projections were found. Ascending fibers which could be traced from the cerebellar commissure ventralward decussated at the level of the trochlear and oculomotor nuclei. These fibers coursed rostralward to the mesodiencephalic junction. With anterograde tracing techniques (3H-leucine and HRP) this tract was found to terminate in the nucleus ruber and the interstitial nucleus of the fasciculus longitudinalis medialis. Moreover, retrograde tracer studies (HRP, "Fast Blue") showed that this tract appeared to arise mainly in the lateral cerebellar nucleus. With both anterograde degeneration and tracing techniques (3H-leucine and HRP) a bundle of fibers could be followed, which decussates in the basal part of the cerebellum and passes dorsally around the contralateral medial cerebellar nucleus to the lateral side of the brainstem. This contralaterally descending projection system was found, lateral to the vestibular nuclear complex, and as far caudally as the descending vestibular nucleus, to terminate on various vestibular nuclei. Horseradish peroxidase studies showed that this contralaterally descending projection system originates mainly in the medial cerebellar nucleus, but ipsilaterally descending projections were also found. With the fluorescent double labeling technique ("Fast Blue" and "Nuclear Yellow") the projections of the cerebellar nuclei described above were confirmed. Furthermore, double labeling revealed neurons in both cerebellar nuclei (especially the medial nucleus) that project to both the mesencephalon and the cervical spinal cord. The present results indicate that the efferent connections of the cerebellar nuclei in the lizard Varanus exanthematicus are organized as two main projections, an ascending projection comparable to the mammalian brachium conjunctivum arising in the lateral cerebellar nucleus, and a descending projection comparable to the mammalian hook bundle (fasciculus uncinatus), originating mainly in the medial cerebellar nucleus. Such projections are common for terrestrial vertebrates.     

Descending brain neurons in larval lamprey: Spinal projection patterns and initiation of locomotion

In larval lamprey, partial lesions were made in the rostral spinal cord to determine which spinal tracts are important for descending activation of locomotion and to identify descending brain neurons that project in these tracts. In whole animals and in vitro brain/spinal cord preparations, brain-initiated spinal locomotor activity was present when the lateral or intermediate spinal tracts were spared but usually was abolished when the medial tracts were spared. We previously showed that descending brain neurons are located in eleven cell groups, including reticulospinal (RS) neurons in the mesenecephalic reticular nucleus (MRN) as well as the anterior (ARRN), middle (MRRN), and posterior (PRRN) rhombencephalic reticular nuclei. Other descending brain neurons are located in the diencephalic (Di) as well as the anterolateral (ALV), dorsolateral (DLV), and posterolateral (PLV) vagal groups. In the present study, the Mauthner and auxillary Mauthner cells, most neurons in the Di, ALV, DLV, and PLV cell groups, and some neurons in the ARRN and PRRN had crossed descending axons. The majority of neurons projecting in medial spinal tracts included large identified Müller cells and neurons in the Di, MRN, ALV, and DLV. Axons of individual descending brain neurons usually did not switch spinal tracts, have branches in multiple tracts, or cross the midline within the rostral cord. Most neurons that projected in the lateral/intermediate spinal tracts were in the ARRN, MRRN, and PRRN. Thus, output neurons of the locomotor command system are distributed in several reticular nuclei, whose neurons project in relatively wide areas of the cord.     

Distribution of the vestibular neurons projecting to the oculomotor and trochlear nuclei in rabbits

Horseradish peroxidase and Fast Blue were injected into the oculomotor and trochlear nuclei of rabbits so as to study the distribution of vestibular neurons that project to these nuclei. After the oculomotor nucleus was injected, labelled neurons were found in the superior, medial, and descending vestibular nuclei as well as in cell group Y. In the superior nucleus, most of the neurons (510 +/- 46) were ipsilateral to the injection, although contralaterally labelled neurons were also observed (104 +/- 19) more peripherally. In cell group Y, 186 +/- 24 contralaterally labelled neurons were observed, whereas hardly any (8 +/- 3) were found on the ipsilateral side. The largest group of labelled neurons (811 +/- 65) constituted a neuronal band located contralaterally in the medial nucleus and rostral part of the descending nucleus. This band rostromedially continued with the caudal part of the group of internuclear neurons of the abducens nucleus. Only 190 +/- 31 neurons were labelled in the medial and descending nucleus ipsilateral to the injected oculomotor nucleus. After injection of the trochlear nucleus, labelled neurons were found in the ipsilateral superior nucleus and contralateral medial and descending nuclei: a few labelled cells were also observed in the ipsilateral medial and descending nuclei as well as in the contralateral cell group Y.     

The ascending projection of the nucleus of the lateral descending trigeminal tract: A nucleus in the infrared system of the rattlesnake,Crotalus viridis

The efferent projections of the nucleus of the lateral descending trigeminal tract (LTTD) in the rattlesnake (Crotalus viridis) were studied by anterograde tracing techniques. The LTTD, a brainstem trigeminal nucleus, is the sole projection site of the infrared-sensitive trigeminal fibers that innervate the pit organs in these snakes. The efferent fibers exit from the ventromedial edge of the LTTD and course medially and caudally toward the central grey area of the medulla. Upon reaching the central region of the medulla these fibers turn and move laterally and rostrally, eventually forming a tract on the ventrolateral surface of the brainstem. Embedded in this tract and slightly overlapping the LTTD in the rostrocaudal axis, is a population of large (20–45 μm) multipolar neurons that forms the nucleus reticularis caloris. Heavy terminal and preterminal degeneration in this area indicates that many of the efferent fibers of the LTTD terminate in this nucleus. A small bundle of degenerating fibers turn dorsally from the ventrolateral tract and ascend to terminate in a nucleus associated with the cerebellum, the lateral tegmental nucleus. No projection was found to any other nuclei or areas in the brain. This study demonstrates that the infrared-sensitive snakes, along with developing peripheral specializations (the pit organs), have developed specialized nuclei to handle this additional sensory information. The direct projection from the LTTD to the nucleus reticularis caloris provides a pathway linking the infrared sensitive neurons of the LTTD with neurons of the same modality in the optic tectum. The second LTTD projection, to the lateral tegmental nucleus, suggests a connection between the infrared system and the cerebellum in these animals.     

Distribution of acidic fibroblast growth factor mRNA-expressing neurons in the adult mouse central nervous system

The distribution of acidic fibroblast growth factor (aFGF) mRNA-expressing neurons was studied throughout the adult mouse central nervous system (CNS) with in situ hybridization histochemistry using a radiolabelled synthetic oligodeoxynucleotide probe complementary to the mRNA of human aFGF. We report here a widespread distribution of aFGF mRNA in several defined functional systems of the adult mouse brain, whereby the highest levels of aFGF mRNA were found in large somatomotor neurons in the nuclei of the oculomotor, trochlear, abducens, and hypoglossal nerves; in the motoneurons of the ventral spinal cord and the special visceromotor neurons in the motor nucleus of the trigeminal nerve; and in the facial and ambigaus nuclei. Labelled perikarya were also detected in all central structures of the auditory pathway including the level of the inferior colliculus, i.e., the lateral and medial superior nuclei; the trapezoid, cochlear, and lateral lemniscal nuclei; and parts of the anterior colliculus. Furthermore, many aFGF-positive cell bodies were found in the vestibular system and other structures projecting to the cerebellum, in the deep cerebellar nuclei, in somatosensory structures of the medulla (i.e., in the gracile, cuneate, and external cuneate nuclei), as well as in the spinal nucleus of the trigeminal nerve. The findings that aFGF mRNA is expressed in all components of several well-defined systems (i.e., in sensory structures) as Well as in central neurons that process sensory information and, finally, in some efferent projections point towards a concept of aFGF expression primarily within certain neuronal circuitries. © 1995 Wiley-Liss, Inc.     

Somatomotor connectivity in the midbrain of Rana pipiens

The mesencephalic oculomotor nuclei of Rana pipiens and their surrounding cell groups were investigated using the anterograde and retrograde transport of horseradish peroxidase and Golgi techniques. The cell groups surrounding the oculomotor and trochlear nuclei were divided into the nucleus interstitialis (nInt) groups A, B, and C, the basal optic nucleus, and the nucleus reticularis tegmenti. Afferents to the ventral mesencephalon originate from the retina and from vestibular, cerebellar, visual, and accessory oculomotor nuclei. These afferents produce a sequence of terminal arborizations in which visual afferents are found in the outer neuropil, and accessory oculomotor, vestibular, and cerebellar afferents are found along the inner neuropil and central gray. The oculomotor neurons in anurans have extensive dendritic fields, extending to the outer margins of the neuropils, as do many large cells along the margin of nInt. Other neurons in nInt have dendritic fields restricted to the proximal portions of the neuropil. Efferents from nInt area A project to the cerebellum and bilaterally to the spinal cord. Area B nInt projects to the ipsilateral spinal cord, contralateral nInt, pretectal nucleus lentiformis mesencephali, and ipsilateral trochlear nucleus. Efferents from area C nInt reach the deep tectal layers and ipsilateral spinal cord. The outer portions of the neuropil contain the nucleus of the basal optic root which comprises ganglionic elongate and stellate neurons and projects to the pretectum. In the center of the neuropil peri-nBOR neurons have dendrites directed towards the visual terminal fields and axons towards the central gray and oculomotor neurons. The nucleus reticularis tegmenti receives afferents from the tectum and lateral forebrain bundle and projects to the deep tectal layers. In anurans, the oculomotor neurons receive a variety of visual, somatic, and vestibular afferents and appear relatively undifferentiated, whereas the nInt appears more developed.