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Trauma or the tourniquet used in orthopedic surgery is often associated with ischemia-reperfusion (I/R) injury with a consequent decrease of muscle power. To explore whether components of the neuromuscular junction (NMJ) are involved in this muscle dysfunction, NMJs were ultrastructurally characterized in the extensor digitorum longus muscle of rats at reperfusion times of 1, 24, 72, and 168 h after a 120-min arterial occlusion. Disorganization of the presynaptic membrane and mitochondrial injury was noted at 1 h, followed by fragmentation and partial engulfment of nerve terminals by Schwann cells at 24 and 72 h. The magnitude of degenerative changes declined at 168 h, suggesting the commencement of regeneration. The postsynaptic membrane remained intact throughout the whole period. In our previous study, deafferentation with pretreatment of the sciatic nerve with capsaicin, which reduces neurogenic inflammation and has a selective effect on nociceptive fibers, improved functional recovery of the muscle after I/R. The present results document a significantly delayed structural regeneration of the motor nerve terminals after combined capsaicin and I/R treatment. Since capsaicin treatment alone had no discernible effect on the structure of NMJs, the findings point to a possibly indirect effect of capsaicin on the motor nerves, which may predispose them to increased susceptibility unmasked only by a subsequent injury. The mismatch between the enhanced functional improvement of the muscle and delayed regeneration of the nerve after capsaicin pretreatment questions the efficient use of such deafferentation to protect the integrity of neuromuscular junctions in I/R injury.

The intrinsic neuronal organisation in the nucleus of the basal optic root of chickens was investigated. The divergent connections with various areas and the functional complexity of the nucleus require a complex intrinsic structural arrangement. Therefore, an analysis of Golgi impregnated material, ultrastructure, GABA-immunocytochemistry and biotinylated dextran-amine anterograde tracer analysis of the nucleus was carried out. In the Golgi analysis, a characteristic dendritic ramification pattern of two types of putative projection neurons was observed. These neurons form dendritic nests with their overlapping dendritic terminal sections, that develop synaptic fields with the optic fibre terminals. These synaptic fields were confirmed by electron microscopy. GABA-immunopositive terminals synapse with distinct loci of the dendritic trees of projection neurons; they may therefore play an important role in the inhibitory-modulatory system of the nucleus of the basal optic root. The GABA-immunopositive terminals derive from small and/or elongated local circuit neurons which receive retinal afferents, and from myelinated fibres afferents to the nucleus of unknown origin.

The principal afferent fibres of the avian optic tectum are the optic fibres of retinal origin. They terminate on the contralateral side, in the external layers (2-7) of the optic tectum (called optic layers) turning into these layers from the external surface. The terminal branchings of the optic fibres develop four densely innervated areas in layers 2, 3, 4-5 and 7. Their terminals are large and of various appearance in the different areas. In the middle third of the optic layer (in layers 4-5), thin dendritic terminal sections of tectal ganglion cells (according to Ramòn y Cajal) of layer 13 terminate into bunches. Phaseolus vulgaris lectin immunotracer corroborates these dendritic endings (further: dendritic terminals) of tectal ganglion cells. The direct connections between these dendritic terminals and the supposed optic fibres were studied under electron microscope and it was found that the large terminals of optic fibres containing round synaptic vesicles establish asymmetrical synapses with several dendritic profiles, among them Phaseolus lectin labelled dendritic terminals of ganglion cells. This result morphologically supports the former physiological observation of a direct synaptic transmission between optic fibres and ganglion cells of layer 13. In addition, on the dendritic terminals of ganglion cells, symmetrical synapses established by GABA-positive terminals were found. The optic terminals, the GABA-immunopositive terminals and the dendritic terminals of ganglion cells form complex synaptic units surrounded with glial sheath, and thus they establish glomerulus-like synaptic units. The size of the dendritic tree and the branching pattern of the dendrites of ganglion cells point to divergence and convergence in visual transmission.

In the present study the telencephalic connections between the centres of the tectofugal and thalamofugal pathways were investigated with Phaseolus vulgaris leucoagglutinin and biotinylated dextran-amine anterograde tracers in chicken using light and electron microscopy. No direct connection was found between the visual Wulst and the ectostriatum or the telencephalic centres of the tectofugal and thalamofugal pathways. Besides other projections, the visual Wulst emitted fibres also to the middle and lateral parts of the hyperstriatum ventrale. Further experiments revealed that the middle part of the hyperstriatum ventrale projected to the ectostriatum centrale and periphericum and established an indirect connection between the visual Wulst and the ectostriatum. The lateral part of the hyperstriatum ventrale sent a few efferent fibres toward the diencephalon and brainstem, but projected massively to the ectostriatum periphericum, neostriatum intermedium pars laterale, the ventral part of the neostriatum caudale and the archistriatum dorsale. Considering that these areas are structures of the tectofugal circuitry as well, the presence of these connections may result in a more elaborate visual processing. The neostriatum may be an associative visual center and possibly a modulatory area toward the archistriatum intermedium dorsale, by which visual information may mediate, modulate and control the movements.

In Golgi preparations of the chicken diencephalon, various types of cells and fibres were studied in the nucleus dorsolateralis anterior thalami (DLA). Two groups of neurons were found: projection neurons with long axons and interneurons with locally branching axons. The projection neurons varied in the different areas of the DLA. In the medial part the neurons are large cells with long, moderately spiny dendrites, and in the dorsal part there are small cells with short, wavy and moderately spiny dendrites. These neurons differ completely from those found in the rostral and lateral parts, where the neurons have medium-sized cell bodies and curving, spiny dendrites, which branch tuft-like or with bifurcations. In the rostral and lateral parts of the DLA, thick afferent fibres were impregnated which developed their terminal branchings among the neurons. Owing to their terminal branching pattern and the shape of the terminals they are thought to be optic fibres. The terminal pattern of these fibres is similar to the optic terminals in the LGB of the mammalian brain. The interneurons are GABA positive, as attested by immunostaining in light microscopic and EM specimens. There are rather few of them. The HRP-filled projection neurons and the surrounding neuropil were investigated under EM: synaptic connections around the large terminals and/or around dendrites were identified, but this synaptic arrangement does not display the characteristics of a synaptic glomerulus.

After PhA-L injection into the tectum opticum of chickens, column-like labelled terminal arborizations were found in tectum and also labelled neurons of Ipc and Imc in the corresponding sections. The PhA-L labele proved the projection from both Imc and Ipc neurons to tectum; their terminal axonarborizations were clearly discernible. Column-like terminal arborizations of different sizes were found both in PHA-L and Golgi impregnated preparations. GABA immunostaining displayed GABA positive neurons in Imc. The EM-Golgi study corroborated that the axon-terminals of Imc neurons established symmetrical synapses in the tectum. The results of the present study support the existence of an inhibitory feedback loop from Imc neurons to the tectum.

The projection from the chick optic tectum to the nucleus rotundus was investigated by iontophoresis of the anterograde tracer Phaseolus vulgaris lectin (PHA-L) into the optic tectum and by Golgi impregnation. PHA-L labelled fibres were observed within the ipsilateral nucleus rotundus and to course through the supraoptic decussation to the contralateral nucleus rotundus. They appeared similar to fibres evident in Golgi impregnated material. Before reaching the nucleus rotundus, PHA-L labelled fibres gave off short terminal branches in the caudoventral thalamic nucleus. Within the ipsilateral nucleus rotundus, the labelled fibres formed an extensive fibre net with a dense core and a less dense periphery. PHA-L labelled fibres in the contralateral nucleus rotundus exhibited a qualitatively similar but sparser distribution. There appeared to be a topographic representation of the optic tectum within the nucleus rotundus. Electron microscopy revealed that PHA-L labelled tectal fibres established asymmetric synapses with principal neurons in the nucleus rotundus.

Having injected Phaseolus Vulgaris Lectin (PhA-L) iontophoretically to subpretectal (SP) and postero-ventralis (PV) thalamic nuclei, labelled fibers and terminals appeared in nucleus rotundus (Rt). The PhA-L immunostained fibers are divided dichotomically and they develop long terminal sections with large varicosities. In EM preparates PhA-L labelled terminals were observed establishing axo-somatic, axo-dendritic symmetrical synapses. These terminals were stained by GABA immunogold procedure and proved to be GABA-ergic, i.e. the neurons of SP and PV nuclei supply the principal neurons of Rt with GABA positive terminals, which are located on specific, exponent loci of the principal neuron.

The terminals of rotundal fibers labelled with Phaseolus Lectin anterograde tracer were studied in ectostriatum periphericum and neostriatum intermedium laterale with EM. These terminals belong to the fibers which cross the ectostriatum centrale before they enter the ectostriatum periphericum and neostriatum intermedium laterale. These terminals establish synapses with dendrites, spines and also with GABA immunogold stained somata. The EM results prove the connections of ectostriatum periphericum and neostriatum intermedium laterale with the visual system.

Investigation of the chick archistriatum revealed that it was not possible to distinguish distinct sub-regions on the basis of their Golgi architecture, despite the fact that the pigeon archistriatum has been suggested to comprise "amygdaloid" and "sensorimotor" divisions. Nine sub-types of projection neuron and four of local circuit neuron were identified in the chick archistriatum. Projection neurons were generally larger with thicker dendrites than those in other regions of the chick telencephalon. A greater proportion of these projection neurons also had highly densely spiny dendrites. These findings suggest that archistriatal neurons receive a large, possibly complex afferentation and project considerable distances. Large and medium-sized local circuit neurons with varicose axon branches and relatively large neurogliaform cells were characteristic of the archistriatum. All types of archistriatal neuron were identified in both 28 and one day old chicks. However, presumptive highly densely spiny projection neurons appeared relatively immature in the one day old chick archistriatum.

Phaseolus vulgaris leucoagglutinin extracellular injection was performed in nucleus rotundus thalami and the course of labelled fibers and their termination were examined in chicken. The labelled fibers terminate in ectostriatum centrale, ectostriatum perifericum and neostriatum intermedium. The course and termination of the fibers are analysed in detailed.

After having iontophoretically injected Phaseolus vulgaris Lectin into nucleus rotundus, labelled terminals were examined in ectostriatum centrale by EM. These terminals contained round synaptic vesicles. They were observed earlier by Golgi method and proved to be of rotundal origin by Phaseolus Lectin tracing method. The labelled terminals establish synapses, on large and small dendritic truncs of projection and local circuit neurons, and also contact spines and dendritic processes of projection neurons. They were observed on soma of GABA immunopositive local circuit neurons, and also on dendrites. Some observations completed the already known data on fine structure of the chicken ectostriatum centrale.

The EM preparates displayed in the nucleus rotundus also symmetrical type of synapses with flattened vesicles, known this type as inhibitory synapsis. To prove this supposition and to find the sources of inhibitory terminals GABA-immunostaining was applied in the diencephalon of chicks. The preparates were examined by light- and electronmicroscope. In nucl. rotundus the large terminal profiles on the cell membrane of principal neurons, on the dendrites and branching areas of terminal branchings of dendrites proved to be GABA positive. The sources of GABA-ergic fibers seemed to be the subpretectal and ventral posterior thalamic nuclei.

The analysis of EM structure of nucleus rotundus completes the results got by Golgi study. The fine structure of neurons and neuropil of the nucleus and the synaptic relations were studied by EM. The fine structural details of principal neuron were described. Several synapses of symmetrical type with flattened vesicles in large terminals contacted the cell body and also the origin and proximal part of the main dendrites. In the neuropil synaptic junctions were formed by terminals that contained (1) spherical vesicles with occasionally very few dense core vesicles, (2) flattened synaptic vesicles. Terminals that contained spherical vesicles were associated with asymmetric synaptic densities, and terminals that contained flattened vesicles formed symmetric junctions. Synapses of asymmetric type associated mostly with terminal sections of dendrites forming glomerular-like structure. Synapses of symmetric type with flattened synaptic vesicles contacted the branching areas of dendritic terminals and side-branches, the origin of main dendrites and the cell surface of principal neuron.

The structural arrangement of nucleus rotundus was studied by Golgi method. Large, multiangular principal neurons, their dendrites and dendritic terminals were observed. The long dendrites and their side-branches course parallel and/or perpendicular to each-other and they are arranged about in dorso-ventral latero-medial and rostro-caudal directions. The dendrites and their side-branches develop characteristic terminal branchings. These dendritic terminals overlap each-other and the area is called dendritic terminal field. The tecto-rotundal fibers traverse the nucleus in large bundles and the final sections of fibers join to the dendrites of principal neuron and terminate in dendritic terminal fields.