Prefabricated nerve conduits advance histomorphological and functional outcomes in nerve regeneration of the sciatic nerve of the rat.

Bridging a nerve defect is sometimes necessary to achieve nerve regeneration after injury. Different methods and conduit designs have been considered, but only isograft transplants or prefabricated conduits are available. This study presents a comparison of prefabricated conduits and isograft transplants in rats, with the aim of making suggestions for clinical settings. In rats of inbred strains LEW and DA, a 1.5cm defect of the sciatic nerve was reconstructed by isograft (n=10) or conduit (n=10). Untreated rats (n=10), sham-operated rats (n=10) and nerves of the non-operated contralateral limb served as controls. Regeneration was evaluated by histomorphological examination and with walking track analysis of the ankle stance angle (ASA) and the sciatic functional index (SFI). After 16 weeks, myelinization and ASA in the conduit group were significantly superior to that in the isograft group. There was no significant difference in SFI between the groups. Reconstruction in the isograft group showed a negative impact on the non-operated side. Conduits and isografts did not reach the morphological or functional levels of untreated or sham-operated animals. The results suggest preferential conduits should be used for nerve reconstruction.

Dynamic response properties of visual neurons and context-dependent surround effects on receptive fields in the tectum of the salamander Plethodon shermani.

Neuronal responses to complex prey-like stimuli and rectangles were investigated in the tectum of the salamander Plethodon shermani using extracellular single-cell recording. Cricket dummies differing in size, contrast or movement pattern or a rectangle were moved singly through the excitatory receptive field of a neuron. Paired presentations were performed, in which a reference stimulus was moved inside and the different cricket dummies or the rectangle outside the excitatory receptive field. Visual object recognition involves much more complex spatial and temporal processing than previously assumed in amphibians. This concerns significant changes in absolute number of spikes, temporal discharge pattern, and receptive field size. At single presentation of stimuli, the number of discharges was significantly changed compared with the reference stimulus, and in the majority of neurons the temporal pattern of discharges was changed in addition. At paired presentation of stimuli, neurons mainly revealed a significant decrease in average spike number and a reduction of excitatory receptive field size to presentation of the reference stimulus inside the excitatory receptive field, when a large-sized cricket stimulus or the rectangle was located outside the excitatory receptive field. This inhibition was significantly greater for the large-sized cricket stimulus than for the rectangle, and indicates the biological relevance of the prey-like stimulus in object selection. The response properties of tectal neurons at single or paired presentation of stimuli indicate that tectal neurons integrate information across a much larger part of visual space than covered by the excitatory receptive field. The spike number of a tectal neuron and the spatio-temporal extent of its excitatory receptive field are not fixed but depend on the context, i.e. the stimulus type and combination. This dynamic processing corresponds with the selection of the stimuli in the visual orienting behavior of Plethodon investigated in a previous study, and we assume that tectal processing is modulated by top down processes as well as feedback circuitries.

Motor control of tongue movement during prey capture in plethodontid salamanders

Four species of salamander of the family Plethodontidae were examined using electromyographic (EMG) recording during prey-capture behavior to test the hypotheses that the tongue retractor, tongue protractor and jaw depressor muscles are activated simultaneously and in a stereotyped pattern, as was found in other salamanders, and to determine whether species with different tongue morphologies and tongue protraction abilities exhibit different motor control strategies. The results show that sequential activation was observed far more frequently than simultaneous activation; the jaw depressor muscle was activated first, followed by the tongue protractor and then the tongue retractor. Species with short, attached tongues (Desmognathus quadramaculatus and Plethodon jordani) showed simultaneous activation more often than species with long, free tongues (Pseudotriton ruber and Hydromantes supramontis), which showed strongly non-simultaneous activation. Most EMG variables showed no effect of prey-capture success, suggesting that sensory feedback is not involved in modulating the motor pattern during the prey-capture strike. Hydromantes supramontis was examined for modulation of its motor pattern in response to prey distance, and several EMG variables were found to be positively correlated with tongue protraction distance. The motor pattern of strongly non-simultaneous activation of antagonistic tongue muscles has evolved along with the evolution of long, free tongues in plethodontids. The variable motor patterns observed provide further evidence that amphibian feeding in general is not as highly stereotyped as has been previously thought.

Morphology, axonal projection pattern, and response types of tectal neurons in plethodontid salamanders. I: tracer study of projection neurons and their pathways.

In three salamander species (Hydromantes italicus, H. genei, Plethodon jordani), the tectobulbospinal and tectothalamic pathways and their cells of origin were studied by means of anterograde and retrograde biocytin and tetramethylrhodamine tracing. In plethodontid salamanders, five types of tectal projection neurons were identified. TO1 neurons have widefield dendritic trees that arborize in the layers of retinal afferents and form a neuropil in the superficial layer; axons constitute the crossed tectospinal tract. Dendrites of TO2 cells have the largest dendritic trees that arborize in the intermediate and deep layers of retinal afferents; axons constitute a lateral uncrossed tectospinal tract. TO3 cells have widefield dendritic trees that arborize in the deep layer of retinal afferents and in the layer of tectal efferents; axons constitute a superficial uncrossed tectospinal tract. TO4 cells have slender primary dendrites and small-field dendritic trees that arborize in the intermediate layers of retinal afferents; axons constitute another lateral uncrossed tectospinal tract. TO2, TO3, and TO4 cells also have ascending axons that run to the ventral and dorsal thalamus. TO5 cells have slender primary dendrites and small-field dendritic trees that extend into the superficial layers of retinal afferents; their fine axons constitute the bulk of the pathways ascending to the ipsilateral and contralateral thalamus. These morphological types of projection neurons and their ascending and descending axonal pathways closely resemble those found in frogs, reptiles, and birds. Their role in visual and visuomotor functions is discussed.

Morphology, axonal projection pattern, and response types of tectal neurons in plethodontid salamanders. II: intracellular recording and labeling experiments.

In the plethodontid salamanders Plethodon jordani and P. glutinosus, the morphology and axonal projections of 140 tectal neurons and their responses to electrical optic nerve stimulation were determined by intracellular recording and biocytin labeling. Six types of neurons are distinguished morphologically. TO1 neurons have wide dendritic trees that arborize mainly in tectal layers 1 and 3; they project bilaterally to the tegmentum and contralaterally to the medulla oblongata. TO2 neurons have very wide dendritic trees that arborize mainly in layers 2 and 3; axons project bilaterally or unilaterally to the pretectum and thalamus and ipsilaterally to the medulla oblongata. TO3 neurons have very wide and flat dendritic trees confined to layers 3-5; some have the same axonal projection as TO2 neurons, whereas others have descending axons that reach only the level of the cerebellum. TO4 neurons have narrower dendritic trees that arborize in layers 2 and 3; they project to the ipsilateral pretectum, thalamus, and medulla oblongata. TO5 neurons have dendritic trees that arborize in layers 1 and 2 or 1-3 and project bilaterally or unilaterally to the pretectum and thalamus. TO-IN are interneurons, with a number of subtypes with respect to variations in dendritic arborization pattern. TO1-TO5 neurons generally have short latencies of 2-16 ms (average = 8.4 ms) at electrical optic nerve stimulation; first responses are always excitatory, often followed by inhibition. They are likely to be mono- or oligosynaptically driven by retinal afferents. TO-IN interneurons have long latencies of 20-80 ms (average = 38.6 ms) and appear to receive no direct retinal input. With their specific dendritic arborization, consequent dominant retinal input, specific axonal projections, the different types of tectal projection neurons constitute separate ascending and descending visual pathways. Hypotheses are presented regarding the nature of the information processed by these pathways.

Primary and secondary somatosensory projections in direct-developing plethodontid salamanders.

In three species of plethodontid salamanders (Plethodon jordani, Hydromantes italicus, and Bolitoglossa subpalmata), primary and secondary somatosensory pathways were investigated by means of tract-tracing in vivo and in vitro using biocytin, horseradish peroxidase, and neurobiotin. Afferent sensory fibers of cranial nerves V, VII, and X and the brachial nerve run in the dorsal funiculus of the medulla oblongata and spinal cord. Fibers ascend to the level of, but do not enter, the cerebellum. In the caudal medulla oblongata, sensory tracts of the cranial nerves descend in a dorsal and a dorsolateral bundle and reach the level of the fourth spinal nerve. Two bundles are likewise formed by spinal afferent fibers, which descend to the level of the seventh spinal nerve. Secondary somatosensory projections ascend in contralateral ventral, contralateral lateral, and ipsilateral lateral tracts, the latter two corresponding to the spinal lemniscal tracts of Herrick. These tracts reach the cerebellum, mesencephalic, and diencephalic targets (tegmentum, torus, tectum, tuberculum posterius, pretectum, and ventral thalamus) ipsi- and contra-laterally. The projection to the tectum is confined to fiber layer 4. Fibers of the ascending tracts cross in the cerebellar and tectal commissure. Our study demonstrates that the ascending secondary somatosensory pathways of plethodontid salamanders differ remarkably from those of other amphibians.

Neural substrate for motor control of feeding in amphibians.

Descending pathways to premotor/motor centers and their cell groups of origin were studied by means of retrograde biocytin tracing experiments in the frog Discoglossus pictus and the plethodontid salamander Plethodon jordani, which differ remarkably in the structure and function of their feeding apparatus and their feeding strategy. Labeled neurons were found in 30 major cell groups located in the telencephalon, diencephalon, synencephalon, mesencephalon and rhombencephalon. The number and distribution of nuclei are very similar in both species. Furthermore, the descending pathways of these groups of neurons take the same courses inside the medulla oblongata. Axons of most nuclei descend either in the ventromedial or ventrolateral medulla oblongata, and it is concluded that the spatial arrangement of pathways is identical in the species studied. Bilateral electrical stimulation of the optic tectum of the plethodontid salamander Hydromantes italicus elicited strong discharges of short latencies in the hypoglossal nerve. In most hypoglossal motor neurons, excitatory postsynaptic potentials (EPSPs) of short latencies followed paired shocks applied at intervals as short as 3 ms, but showed temporal and spatial facilitation, suggesting that the EPSPs include mono- as well as polysynaptic components. In the ventral white matter, orthodromic single units were found that are candidates for excitatory reticular interneurons. These properties of tectal descending pathways in salamanders strongly differ from those found in toads. Differences in feeding behavior and its control by the premotor/motor networks between the species investigated do not appear to result from anatomically altered input or from a different organization of descending pathways to these premotor/motor centers, but rather from differences in local properties of reticular premotor networks as well as from different effects of neuromodulatory systems.

5-HT-like immunoreactivity in the brains of plethodontid and salamandrid salamanders (Hydromantes italicus, Hydromantes genei, Plethodon jordani, Desmognathus ochrophaeus, Pleurodeles waltl): an immunohistochemical and biocytin double-labelling study.

The distribution of 5-HT-like-immunoreactive cell bodies and fibres was studied in the brains of the salamanders Hydromantes italicus, H. genei, Plethodon jordani, Desmognathus ochrophaeus (family Plethodontidae), and Pleurodeles waltl (family Salamandridae). In addition, double-labelling experiments with biocytin were carried out to identify the relationship between serotonergic fibres and neurons involved in the processing of sensory and sensorimotor information. In all species, 5-HT-immunopositive somata are found in the ventral thalamus close to the ventricle forming the paraventricular organ. In the hypothalamus, cells are labelled in the ependymal layer around the infundibular recess and at the lateral edge of the periventricular grey. In the pretectum, a few immunoreactive cells are situated dorsolaterally in the grey matter. In the tegmentum and medulla oblongata, cells of the raphe nuclei are regularly distributed along the midline; labelled perikarya are occasionally found in the cervical spinal cord. 5-HT-like-immunoreactive fibres are widely distributed throughout the nervous system. Densely arborizing fibres are found in the olfactory bulb, striatum and amygdala. Distinct fibre projections extend in the ventral thalamus and tectum. Biocytin tracing of striatal and tectal projection neurons and ascending reticular neurons combined with the demonstration of 5-HT suggest that the striatum, the tectum and the ascending activating system are strongly influenced by 5-HT.

Similarities and differences in the cytoarchitecture of the tectum of frogs and salamanders.

Frogs exhibit a morphologically complex (multiply laminated) optic tectum, while salamanders have one of the morphologically simplest tecta among vertebrates. In a comparative approach, the morphology of tectal projection neurons is investigated in three salamander species, Hydromantes italicus, H. genei and Plethodon jordani, and two frog species, Discoglossus pictus and Eleutherodactylus coqui, by means of retrograde Biocytin labeling complemented by intracellular Biocytin staining of cells. Despite striking differences in the gross anatomy of the tectum, salamanders and frogs have the same types of tectal neurons with respect to their dendritic arborization and the pattern of ipsilaterally and bilaterally ascending (to praetectum and thalamus) and ipsilaterally or contralaterally descending projections (to nucleus isthmi, medulla oblongata and rostral spinal cord). In the light of these findings, the relationship between morphological complexity of the tectum and behavioral complexity (feeding behavior) is discussed.

Tectal activation of premotor and motor networks during feeding in salamanders.

In salamanders, three separate pathways, a crossed and two uncrossed ones, extend from the tectum mesencephali to the brain stem and spinal cord. These pathways arise from different types of tectal neurons; their dendrites arborize in different layers of retinal afferents and, thus, receive different types of retinal information. Collaterals of descending axons extend in regions, where motoneurons and interneurons related to prey capture are situated. The response properties of tectal neurons, interneurons and motoneurons related to prey capture were revealed by intracellular recording with subsequent dye (biocytin) injection. Most tectal neurons exhibit long latencies after optic-nerve stimulation, which indicates a complex processing of visual information inside the tectum. Our data show that no one-way connection exists between the tectum and motor nuclei; rather, these centres, together with a number of interneurons, exhibit a complex interaction during feeding.

Motor neurons and motor columns of the anterior spinal cord of salamanders: posthatching development and phylogenetic distribution.

The posthatching development of rostral (1st-4th) spinal motor neurons was studied in ten species of salamanders, using horseradish peroxidase and cobaltic lysine tracing techniques. Development of spinal motor neurons differs among species in association with differences in life history and general developmental patterns (i.e., between species with aquatic larvae versus those with direct development, with or without ontogenetic repatterning). In the plesiomorphic state, represented by species with aquatic larvae, five types of motor neurons are present: (1) large, multipolar neurons, believed to be primary motor neurons; (2) medial, pear-shaped neurons; (3) larger, spindle-shaped neurons, which increase in number during posthatching development; (4) cone-shaped neurons, and (5) bilaterally arborizing neurons (found only at the rostral pole of the first spinal nucleus). Direct-developing desmognathine salamanders have the plesiomorphic set of motor neurons, but appear to lack Mauthner neurons. Direct-developing plethodontine salamanders have cone-shaped, pear-shaped, and spindle-shaped neurons, but lack primary motor neurons and Mauthner neurons. Direct-developing bolitoglossine salamanders, which exhibit both pedomorphosis and ontogenetic repatterning, have only medial, pear-shaped neurons, and lack primary motor neurons, spindle-shaped neurons, cone-shaped and bilaterally arborizing neurons. At all developmental stages in all species studied, pear-shaped neurons are always found in medial positions and spindle-shaped neurons are always found in lateral positions. Spindle-shaped neurons are found more laterally as development proceeds. The medial and lateral motor columns of salamanders and amniotes differ in their connections with peripheral targets (i.e., axial muscles vs. limbs). This implies a lack of homology of neuron types in salamanders and amniotes, which has been obscured by the current terminology.

Topography and cytoarchitecture of the motor nuclei in the brainstem of salamanders.

The organization of the motor nuclei of cranial nerves V (including mesencephalic nucleus), VI, VII, IX, and X is described from HRP-stained material (whole mounts and sections) for 25 species representing five families of salamanders, and the general topology of the brainstem is considered. Location and organization of the motor nuclei, cytoarchitecture of each nucleus, and target organs for nuclei and subnuclei are described. The trigeminal nucleus is separated distinctly from the facial and abducens nuclei and consists of two subnuclei. The abducens nucleus consists of two distinct subnuclei, one medial in location, the abducens proper, and the other lateral, the abducens accessorius. The facial nucleus has two subnuclei, and in all but one species it is posterior to the genu facialis. The facial nucleus completely overlaps the glossopharyngeal nucleus and partially overlaps that of the vagus. In bolitoglossine plethodontid salamanders, all of which have highly specialized projectile tongues, the glossopharyngeal and vagus nuclei have moved rostrally to overlap extensively and intermingle with the anterior and posterior subnuclei of the facial nerve. In the bolitoglossines there is less organization of the cells of the brainstem nuclei: dendritic trunks are less parallel and projection fields are wider than in other salamanders. Some aspects of function and development are discussed; comparisons are made to conditions in anurans; and phylogenetic implications are considered.

Organization of the motor nuclei in the cervical spinal cord of salamanders.

The distribution and cytoarchitecture of motor nuclei of the cervical spinal cord were studied by using HRP techniques (whole mounts and sections) in 22 species of salamanders (families Hynobiidae, Dicamptodontidae, Ambystomatidae, Salamandridae, and Plethodontidae) representing a wide variety of life histories and functional modes of feeding. The nucleus of the first spinal nerve extends from the level of, or slightly caudad to, the root of the tenth cranial nerve, almost to the ventral root of the second spinal nerve. Approximately one-half of this nucleus is situated in the brainstem. This anterior extension is longest in bolitoglossine plethodontids. The nucleus of the second spinal nerve extends from the root of the first spinal nerve to the dorsal root of the second spinal nerve. The nuclei of the first and second spinal nerves in all species except bolitoglossines have motor neurons arranged in two columns: a lateral one containing large spindle-shaped cells and a medial one containing pear-shaped or polygonal smaller cells. The primary dendrites of these lateral and medial cells are parallel and their arborization is relatively narrow. In contrast, bolitoglossines lack the lateral motor column. The nucleus of the first spinal nerve consists only of a medial band of pear-shaped and sometimes polygonal cells, and the nucleus of the second spinal nerve is a wider band of pear-shaped and polygonal cells which are always situated inside the periventricular gray matter. The arrangement of the somata in bolitoglossines is less organized and the primary dendrites are less parallel and have a broader arborization than in other salamanders. In all species, cells in the second spinal nucleus are arranged in a less orderly manner than those in the first. All salamanders studied possess a spinal accessory nerve whose motor neurons are located in the cervical spinal cord; the axons leave the brainstem with fibers of the vagus nerve. The rostrocaudal extent of this nucleus differs markedly among species. In bolitoglossines the nucleus is more or less restricted to the region of the nucleus of the second spinal nerve. In all other species studied, the accessory nucleus extends from the obex to the caudal end of the nucleus of the third spinal nerve. In the tribe Plethodontini the cytoarchitecture of the accessory nucleus is similar to that of the second spinal. In desmognathine and hemidactyliine plethodontids as well as in all nonplethodontid species studied the nucleus consists of pear-shaped and cone-shaped cells.(ABSTRACT TRUNCATED AT 400 WORDS)