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The process of secondary neuralation has been studied in the Brazilian opossum, Monodelphis domesticus. Secondary neuralation in this mammal was found to have qualities of secondary neuralation that were present in both the chick and the mouse. In this study, four stages of secondary neuralation were found beginning with the medullary cord stage. Other stages in the differentiation of the secondary neural tube were: differentiation of the neuroepithelium, cavitation of the medullary cord, and proliferation of the neural tube. The process of secondary neuralation proceeded in a rostral-to-caudal direction and was found to be independent of age. Diastematomyelia (doubling of the tube) was found in several animals. The process of cavitation was completed by the joining of several small, focal cavities in a rostral-to-caudal direction. The most distinctive feature of secondary neuralation in this animal was the finding of axons within the secondary neural tube, a feature not characteristic of either the chick or the mouse.

Terminal innervation ratios were determined in normal porcine semiendinosus to test the hypothesis that intramuscular collateral branching of subterminal axons gives rise to fiber type grouping. Innervation ratios were near 1.00 in both the lateral pale portion which exhibits type II predominance and in the medial red portion which exhibits extensive grouping of type I fibers. Type grouping observed in porcine skeletal muscle is not the result of multi-fiber innervation by subterminal axons, but, rather, may be the manifestation of a unique motor unit topography.

Although it has been recognized for some years that each cytoarchitectonic field of Ammon's horn and the subiculum gives rise to a specific pattern of cortical and subcortical projections, it has not been clear whether these various projections arise from different populations of neurons within each field or whether they arise as collaterals from an essentially homogeneous population of cells. We have examined this problem, and the related issue of the origin of the commissural and ipsilateral associational projections of the dentate gyrus, by injecting retrogradely transported fluorescent dyes into two or more of the relevant projection fields in adult rats and subsequently examining the brains for doubly or triply labeled neurons. It is clear from these experiments that at least two of the known efferent projections of field CA1 (to the septum and to the entorhinal cortex) arise from the same pyramidal neurons and also that the commissural, ipsilateral associational, septal, and subicular projections of the other major field of Ammon's horn--field CA3--similarly are due to collaterals. Double-labeling experiments also indicate that at least 80% of the cells in the deep hilar region of the dentate gyrus give rise to both an ipsilateral (associational) and a crossed (or commissural) projection to the dentate granule cells. In contrast, the projection neurons in the dorsal part of the subiculum form a quite heterogeneous population; cells that project to both the septum and the entorhinal area are intermingled with others that project to one or the other area but not to both. The cortical and cortico-subcortical connections of the hippocampal formation thus appear to be quite different from those of the neo-cortex, and the existence of such an extensive system of collateral projections clearly has important consequences for studies of the development of the hippocampus and of its response to selective deafferentation.

In the developing wing of Drosophila a set of early differentiating neurons pioneer the axon courses observed in the adult. The possibility that these first cells are indispensable for establishing the normal neural pathways has been tested. The differentiation of particular neurons was suppressed by inducing cell clones homozygous for two scute deficiencies, mutations that inhibit the differentiation of sensilla and their associated neurons. From the analysis of the nerve patterns in wings lacking specific sensilla, it has been demonstrated that none of the identified neurons are essential for guiding other axons along the correct path. However, the possibility remains that the presence of certain cells may increase the probability of establishing the normal pattern of peripheral nerves.

The effect of hypophysectomy on the hypothalamic neurosecretory system of the catfish, H. fossilis, was studied. Hypophysectomy resulted initially in an accumulation of NSM at the distal ends of the cut axons. The axons had grown and were reorganized into a neurohypophysis-like structure 3 weeks after hypophysectomy, and this persisted even more than 3 years post-hypophysectomy.

In our previous paper, we reported a marked advantage in using collagen gel matrix available for cell culture in combination with a silicone tube as an effective environment for axonal sprouting during peripheral nerve regeneration. In the present experiment, collagen film was substituted for the silicone tube because of its non-toxicity, biocompatibility and better availability. Also, the surgical procedure was simplified, using a fibrin adhesive system instead of suturing. In the second postoperative week, severed proximal and distal stumps became joined together concomitantly with absorption of the collagen matrix and film. On size-frequency histograms, the diameters of both myelinated and unmyelinated axons at 8 weeks after surgery had recovered to their normal ranges. These findings demonstrate that this procedure of enveloping a collagen matrix and severed nerve stumps in bioresorbable collagen film would be an ideal way of forming a perfect perineurium. The regeneration of peripheral nerve axons resulted in normal thickness of the original nerve bundle without exception, unlike the axons on the control side.

In C. punctatus the median eminence includes the subterminal region of the hypothalamus and the anterior neurohypophysis. It is formed of ependymal, fibrous and reticular layers as in the tetrapods. Primary capillary plexus extends from the subterminal region to the extremity of the anterior neurohypophysis. Only few portal vessels from the hypothalamus enter in the pars distalis. All the components of pituitary including the pars intermedia are irrigated by the secondary plexus formed from the portal vessels emerging out of the anterior neurohypophysis. The neurosecretory axons and the ependymal cells are in close morphological contact with the primary plexus. Several axons have perivascular endings at the median eminence. Some axons were found to be only silver or aldehyde fuchsin positive whereas some others take up both. The silver positive axons were abundant in the pars distalis and the AF positive ones were more concentrated in the pars intermedia with greater accumulation of neurosecretory material.

A three-chamber culture system was devised in which neurites growing from small clusters of somas of sympathetic neurons penetrated a virtually fluid-impermeable barrier; thus the local fluid environment of the distal portions of the neurites could be controlled independently of the local fluid environment of the somas and proximal portions of the neurites. Neurites regularly penetrated the barriers if a high concentration of nerve growth factor was present on both sides, but never penetrated into chambers to which no nerve growth factor had been added. After neurites crossed the barrier, local removal of nerve growth factor from the distal portions of the neurites caused the growth of these portions to stop, and they eventually appeared to degenerate even though nerve growth factor was continuously present in the chamber that contained their somas and proximal portions. In contrast, local nerve growth factor was not required at the somas and proximal portions of the neurites; many neurons survived its withdrawal provided their somas were associated with neurite bundles that crossed into a chamber containing nerve growth factor. These results show that the growth, and probably the survival, of neurites depends upon nerve growth factor in their local environment, regardless of the nerve growth factor concentrations to which other portions of the neuron are exposed. This is entirely consistent with the notion that nerve growth factor released by sympathetic target tissues promotes the establishment and maintenance of appropriate neuron-target connections during development.

The innervation of guinea-pig and rat cardiac tissue consists of thin noradrenergic axons running parallel to the myocardial fibres and producing well-developed fluorescent networks which are denser in guinea-pig tissue. Transverse sections of arterial vessels exhibit a marked polar-like disposition of adrenergic nerves, which mainly appear to be concentrated in two opposite areas. Tissue sections from daunomycin-treated animals fluoresced a striking orange-red. This drug-specific fluorescence emanated from all parts of the ventricular tissue, with particular intensity in the nuclei. Neither the density nor the shape of the adrenergic nerves were affected by treatment with the drug. Despite penetration and storage of the antibiotic into the ventricular tissue, cardiotoxicity was not found in the present study.

During prenatal development of the cerebellum in rats, a secondary stem cell layer, the external granular, or germinal, layer (EGL) develops at the pial surface of the cerebellar anlage. The EGL cells arise in a region at the caudolateral margin of the fourth ventricle, and the cells migrate over the surface of the developing cerebellum. A key question is how this migration is guided. We have investigated the possible role of the extracellular matrix protein, fibronectin, and find none present in the EGL during the migration. Instead, we find that the EGL neuroblasts migrate in close contact with axons that are present prior to the onset of migration. It appears that these axons serve as the substrate for EGL neuroblast migration and that axonal guidance of cell migration may be a third general mechanism to be added to the previously studied guidance by glial processes and extracellular matrix.

The laminar and cellular structure of retrosplenial cortex in the rhesus monkey was studied with Nissl stained and rapid Golgi impregnated tissue and the results were used to evaluate morphological features of a cortical transition zone. The granular layer of retrosplenial granular cortex is composed primarily of small, density packed, star pyramidal cells. These cells branch within the granular layer itself, while the apical dendrite enters layer I where it branches infrequently or not at all. This cell type is similar to the star pyramid first described by Lorente de No except in its areal and laminar distribution. Cytoarchitectonic observations of retrosplenial agranular cortex show, that, although this area is relatively "agranular" in comparison to other cortical areas, it does possess an incipient layer II and layer IV. These layers are composed mainly of small and medium sized pyramidal cells, but many non-pyramidal cell types were found in these and other layers in this area in rapid Golgi preparations. Stellate cells with beaded or smooth, lightly spinous dendrites were found throughout layer I-IV, while fusiform cells with smooth or very lightly spinous dendrites appear in layers III-VI. Areas surrounding retrosplenial cortex in the posterior cingulate region were also evaluated in Nissl and Golgi preparations including the indusium griseum, subiculum (dorsal to the corpus callosum) and area 23. The laminar and cellular constitutents of retrosplenial cortex were then evaluated in the context of cortical architectonic transition. The transition from one cellular layer in the indusium griseum to five cellular layers in area 23 is made by the addition of layers II, III, IV and VI in retrosplenial cortex to the one ganglionic layer of the indusium griseum and subiculum. Besides the addition and subdivision of layers in retrosplenial cortex, two aspects of cell morphology were found to change in this region. First, the structure of pyramidal cells progressively changes from those in the indusium griseum which have predominently round or oval somata and a preponderance of apical and few basal dendrites to those in layer V of retrosplenial cortex and area 23 which have pyramidal shaped somata and a great number of basal dendrites which branch frequently and spread horizontally for hundreds of microns. Second, there is a change in the number and distribution of non-pyramidal cell types. Evidence was not found that the indusium griseum, dorsal subiculum or layer V of retrosplenial granular cortex contain a significant number of stellate or fusiform cells. At the retrosplenial granular/agranular border, though, these cells gradually begin to constitute a greater proportion of the cell population and in area 23 form a major component of layer IV...

Interaction between neurons and glia may contribute to the formation of characteristic nerve bundles formed by axon elongation along stereotypic pathways. This study reports the temporal and spatial distribution of identified ensheathing glia during embryonic development in the leech. The development of connective glia was followed 1) using an immunohistochemical probe (monoclonal antibody Lan3-13), which recognized connective glia, and 2) using electron microscopy. Embryonic glia were initially located in the medial region of the lateral connectives and contained intermediate filaments. Glia cells continued to develop throughout embryogenesis; the number and size of glial processes increased, and they ensheathed smaller bundles of axons. The glial cell recognized by Lan3-13 first appeared after axons had already begun to form the connectives. This suggests that these particular glial cells may not function in the initial guidance of axons along stereotypic pathways. However, another cell that contained small bundles of intermediate filaments and glycogen granules was present at early stages of connective formation. These cells may be undifferentiated or transient glia, which could contribute to the formation of characteristic nerve bundles.

We have charted the embryonic development of the epidermal receptive fields of the PV and PD mechanosensory neurons present in each segmental ganglion of the ventral nerve cord of the glossiphoniid leech Haementeria ghilianii. The receptive field of either of these neurons is established by several peripheral axons, each of which grows into its own skin territory, so that the receptive field is subdivided into a quiltwork of contiguous, mutually exclusive subfields of various sizes. The largest subfield develops first from the primary peripheral axon of the PD or PV neuron. The PD and PV primary axons grow directly to their respective territories and begin to innervate them at approximately the same time (see also Kuwada, J.Y., and A.P. Kramer (1983) J. Neurosci. 3: 2098-2111). The smaller secondary and minor subfields develop later from the secondary and intersegmental peripheral axons, respectively. These axons, too, grow directly to their appropriate skin territories. The arborizations of the peripheral axons expand until the adult receptive field pattern is established late in embryogenesis; they do not appear to initially overgrow and later trim down to the normal boundaries of the adult receptive field. The receptive field of the PV neuron develops from a stereotyped skeletal branching pattern of the peripheral axons that is elaborated in a regular way to form a grid-like pattern that matches the arrangement of muscle fibers in the body wall. Thus, this branching pattern may be the result of axon growth along prespecified pathways, perhaps delineated by the muscles. Throughout embryonic development, as in the adult leech, axon branches of neighboring homologous P neurons overlap considerably, but separate axon branches of the same neuron are virtually non-overlapping. These observations suggest that developing branches of a neuron are excluded from territory occupied by other branches of the same cell, in contrast to branches belonging to different neurons which can occupy the same territory.

Neurite-inducing factor (NIF) is a novel protein that has been partially purified from mouse submaxillary glands. NIF induces neurite formation in PC12 pheochromocytoma cells, and the NIF-induced neurites are indistinguishable from NGF-induced neurites in both their morphology and the time course of their formation. Neurite-inducing activity can be recovered at a position corresponding to a molecular weight of 20,000 Da after fractionation of partially purified preparations via SDS-PAGE. Partially purified preparations of NIF are about half as potent as pure beta NGF, and since the neurite-inducing activity does not correspond to any of the major proteins in this fraction, specific activity of purified NIF will probably be significantly greater than the 60 ng/ml found for our partially purified material. NIF is distinct from beta NGF by four criteria: (1) antibodies to beta NGF can block the activity of beta NGF, but not the activity of NIF; (2) beta NGF can induce ornithine decarboxylase (ODC) in PC12 cells at concentrations significantly below those required to induce neurites, while NIF induces ODC only at concentrations greatly in excess of those required to induce neurite formation; (3) by the criterion of SDS-PAGE, there is insufficient beta NGF in our partially purified preparations of NIF to explain the biological activity of this fraction; and (4) the biological activity of NIF has a molecular weight (20,000 Da) that is distinct from beta NGF (13,000 Da). We conclude that NIF is probably a novel peptide that is very active in promoting morphological differentiation.(ABSTRACT TRUNCATED AT 250 WORDS)

The use of image plane scanning for the purpose of quantification of data is becoming increasingly important in medicine and biology. Such equipment allows complex geometric-statistical relationships to be investigated by reduction to a counting process in which picture elements are counted (using a photocell), stored, and evaluated. Various absolute values of interest can then be computed using certain mathematical relationships. These methods, using automatically controlled sampling, are fast, and, since they are able to detect small variations in light intensity, very accurate. Furthermore, even in the presence of highly complex patterns, an accurate surface area measurement can be made. Peripheral nerve cells, for example, lend themselves well to such methods, since the strong contrast between individual structural elements provides excellent conditions for automatic measurement.

The radial fibers in the globus pallidus are the striatal efferents. Evidence now indicates that they arise from medium-sized neurons in the striatum. During their transit of the globus pallidus, they give off collaterals in both segments of the globus pallidus and undergo reduction in caliber. It has not been possible to observe the same radial fiber emitting collaterals in both segments of the globus pallidus, and the prospects of ever doing so are not good. The radial fibers in the medial segment of the globus pallidus continue into the substantia nigra by way of the "comb" bundle. The divergence and convergence in the striatal efferent systems is considerable. The afferent plexuses of fine fibers bearing bouton en passant endings, which completely ensheath the long dendrites in the globus pallidus and the substantia nigra and make "longitudinal axodendritic connections," are derived from the convergence of branches off the collaterals of a number of different radial fibers in the globus pallidus and the convergence of "comb" bundle fibers in the substantia nigra. The synaptic endings on these fibers constitute most of the endings in the globus pallidus. They are the endings with large, egg-shaped, synaptic vesicles and form symmetrical synapses.

Hanging drop cultures of rhombencephalon of 6-11 day chick embryos were placed for 15'-24 hours at low temperatures (0 degree, 10 degrees, 15 degrees, 20 degrees, 25 degrees). Phase contrast time-lapse cinemicrography were made of the axons outgrowth from the explants, during recovery of normal temperature (38 degrees). A number of cultures were also filmed during cooling from 38 degrees to 15 degrees or 20 degrees. It was thus possible follow the sequence of the axon changes, especially of its growth cone, and demonstrate the reversible nature of the modifications observed at some subnormal temperatures.

Giant axons from the squid, Loligo pealei, were fixed in glutaraldehyde and postfixed in osmium tetroxide. Calcium chloride (5 mM/liter) was added to all aqueous solutions used for tissue processing. Electron-opaque deposits were found along the axonal plasma membranes, within mitochondria, and along the basal plasma membranes of Schwann cells. X-ray microprobe analysis (EMMA-4) yielded signals for calcium and phosphorus when deposits were probed, whereas these elements were not detected in the axoplasm.

Previous studies of the olfactory nerve, mainly in higher vertebrates, have indicated that axonal injury causes total degeneration of the mature neurons, followed by replacement of new neuronal cells arising from undifferentiated mucosal cells. A similar regeneration process was confirmed in the garfish olfactory system. Regeneration of the nerve, crushed 1.5 cm from the cell bodies, is found to produce three distinct populations of regenerating fibers. The first traverses the crush site 1 wk postoperative and progresses along the nerve at a rate of 5.8 +/- 0.3 mm/d for the leading fibers of the group. The second group of fibers traverses the crush site after 2 wk postcrush and advances at a rate of 2.1 +/- 0.1 mm/d for the leading fibers. The rate of growth of this group of fibers remains constant for 60 d but subsequently falls to 1.6 +/- 0.2 for the leading population of fibers. The leading fibers in the third group of regenerating axons traverse the crush site after 4 wk and advance at a constant rate of 0.8 +/- 0.2 mm/d. The multiple populations of regenerating fibers with differing rates of growth are discussed in the context of precursor cell maturity at the time of nerve injury and possible conditioning effects of the lesion upon these cells. Electron microscopy indicates that the number of axons decreases extensively after crush. The first two phases of regenerating axons represent a total of between 6 and 10% of the original axonal population and are typically characterized by small fascicles of axons surrounded by Schwann cells and large amounts of collagenous material. The third phase of fibers represents between 50 and 70% of the original axonal population.

Neurons from the abdominal ganglion of the mollusc Aplysia californica regenerate neurite processes in dissociated cell culture. Both the nature of neurite outgrowth and the morphology of the cells are influenced by the presence of adult Aplysia hemolymph in the growth medium and the presence of a portion of a cell's original axonal process. Aplysia hemolymph enhances cell survival, the initiation of neurite outgrowth from multiple sites on the cell body surface, the linear growth of the processes, and the amount of branching by those processes. Hemolymph also decreases the diameter of the outgrowing neurite fascicles and the diameter of the individual neurites within the fascicles. The presence of a cell's original axon reduces the time required for the initiation of neurite outgrowth and restricts the formation of multipolar processes. In addition, the presence of an initial axonal segment is essential for neurite regeneration from large adult neurons.

Medial giant (MGA) and lateral giant (LGA) axons of crayfish were doubly cut in order to selectively isolate axonal segments from perikaryal and transsynaptic sources of trophic input. Isolated MGA segments remained morphologically intact for over 43 days, whereas isolated LGA segments usually degenerated within one week. The glial sheaths around isolated MGA segments had significantly increased in thickness within one week, but severed LGA segments showed no increase in sheath thickness at any time after lesioning. These data suggest that cells of the surrounding glial sheath can provide trophic support to isolated MGA segments but not to isolated LGA segments. Extent of glial hypertrophy seems dependent upon specific spatiotemporal parameters. The diameters of isolated MGA segments decreased more rapidly than the diameters of singly cut MGA segments. These data suggest that the MGA also receives some trophic support from pre- or postsynaptic sources. Conversely, some singly cut LGA segments completely degenerated within one week, whereas other singly cut LGA segments remained intact for at least 43 days after lesioning. Such results suggest that the LGA receives a significant trophic input from pre- or postsynaptic structures.

Three neurons located in the dorsal horn (Lamina III) have been reconstructed using Golgi-stained serial sections. These cells including dendritic and axonal branchings appear to remain within the dorsal horn and to belong to small-sized local interneurons of the dorsal horn proper. The measurements have been made with various criteria: the medio-lateral, dorso-ventral and rostro-caudal extents of the dendritic tree as well as the axonal branchings, total dendritic and axonal length, number of axonal endings and distance from the starting point of the axon at the dendrite to the point where the dendrite joins the soma (S-A distance).

A quantitative study was carried out on the adult cat optic nerve near the eyeball by systematically measuring the perimeters of all the axons seen through the optic microscope. The main purpose of this study was to define the topographical distribution of these axons in function of their size. Statistical studies show the existence of an area of maximal concentration of large axons in crescent form situated in the temporal zone of the nerve. The neurophysiological implications are discussed.

We obtained human cruciate ligaments at the time of total knee replacement and from autopsy and amputation specimens, and examined histological sections of the ligaments for the presence of mechanoreceptors using the Bodian, Bielschowsky, and Ranvier gold-chloride stains for axons and nerve-endings. The cruciate ligaments obtained at the time of total knee replacement were too distorted by disease processes to be of use. The autopsy and amputation specimens, however, contained fusiform mechanoreceptor structures measuring 200 by seventy-five micrometers, with a single axon exiting from the capsule of the receptor. One to three receptors were found at the surface of each ligament beneath the synovial membrane, and were absent from the joint capsules and menisci. Morphologically the receptors resembled Golgi tendon organs, and it seems likely that they provide proprioceptive information and contribute to reflexes inhibiting injurious movements of the knee. This is the first histological demonstration of mechanoreceptors in human cruciate ligaments.

An impulse propagating in a cell with nonuniform geometry sees an increased electrical load at regions of increasing diameter or at branch points with certain morphologies. We present here theoretical and experimental studies on the changes in membrane current and axial current associated with diameter changes. The theoretical studies were done with numerical solutions for cable equations that were generalized to include a varying diameter; the Hodgkin-Huxley equations were used to represent the membrane properties. The experimental studied were done using squid axons with the axial insertion of platinized platinum wires to create a localized region of increased electrical load. As an action potential approaches a region of increased electrical load, the action potential amplitude and rate of rise decrease, but there is a marked increase in the magnitude of the inward sodium current. The time integrals of the inward and outward currents are not constant along the fiber and indicate net inward charge movement at regions subjected to an increased electrical load. Changes in the waveform of the axial current at such a region help to explain the temperature dependence of propagation failure at regions of increasing electrical load.

Neurons having large cell bodies in the anterior dorsal median cluster in the metathoracic ganglion of the locust Schistocerca gregaria and the grasshopper Romalea microptera were studied by direct dye injection and reverse filling combined with elyctrical stimulation and recording. Eight, possibly nine, are of the unpaired type, with a T branch leading into left and right axons that leave the ganglion to terminate in muscles. Another six are probably paired, and may be interneurons. Five of the 8 or 9 unpaired neurons have one axonal branch in both N4 and N5, on both sides: the others have but a single branch. One of the nine, DUMETi, has left and right axons exclusively innervating the jumping muscles, and another, DUMDL, has left and right axons exclusively innervating the dorsal longitudinal flight muscles. Neither the locations, sizes or numbers of somata, nor their locations were as constant as is the case for ordinary ventral motoneurons.

Anatomy, histology and innervation of the heart of spiny lizard, U. hardwickii have been described. The heart is typically reptilian and comprises four chambers: sinus venosus, two atria and a ventricle. The sinus venosus is a small, thin-walled chamber present on the dorsal side of right atrium. The sinuatrial opening is protected by a pair of valves. The auriculoventricular opening is also protected by a pair of muscular valves. The presence of a cardiac conducting system is reaffirmed. The conducting system comprises sinuatrial and atrioventricular nodes. The sinuatrial node is present at the sinuatrial junction very close to the interauricular septum. The atrioventricular node is quite conspicuous and located at the caudal end of the interauricular septum. The atrioventricular bundle is absent. There is present an atrioventricular cushion which serves the purpose of atrioventricular bundle. The heart is richly innervated, as is evident by the presence of a large number of nerve fibres and ganglion cells at the different levels of the heart. Both the nodes and the atrioventricular cushion are supplied by the fine nerve fibres, but ganglion cells could not be found in any one of these components. The myogenic theory of conduction systems is supported.

A three-dimensional reconstruction of the rat's hypothalamo-neurohypophysial system, depicting the neurons that project to the neuro-intermediate lobe of the pituitary, has been made by using retrograde transport of horseradish peroxidase injected into the neuro-intermediate lobe and by using immunocytochemistry with antisera to vasopressin and somatostatin. The overall picture illustrates the neurons situated in the walls of a pair of ill-defined cone-shaped tunnels, the apices pointing anteriorly. Among the neuronal aggregates in the tunnel wall two, the paraventricular and forniceal nuclei, appear similar in shape but clearly separated by a gap of at least 150 micrometers. Many of the vasopressin-positive neurons lie in the same nuclear aggregates with two notable exceptions: the suprachiasmatic nucleus contains many vasopressin-positive cells but does not project to the pituitary, and the forniceal aggregate, which does project to the pituitary, contains no vasopressin-positive cells. Somatostatin-positive cells are situated close to the third ventricle and their size is intermediate between parvocellular and magnocellular. Cell counts show only half the cells in the system lying in the supraoptic and paraventricular nuclei, the rest being in "accessory nuclei".

This paper details the in vitro techniques used to establish cells in culture from the brains of 40 patients, most of whom had chronic neurologic disease. The clinical and pathologic features of these patients are given. The success in establihsing cell lines was dependent upon the origin of tissue (biopsy vs. autopsy), the site of removal from the brain, and various environmental and technical manipulations in vitro.

The properties of the giant cerebral serotonin-containing neurons of the opisthobranch mollusc Aplysia californica were studied and were compared to the existing data on the giant serotonin-containing neurons (metacerebral cells) of pulmonate mulluscs. Among the properties examined were: axonal distribution, synaptic input and output, pharmacological responses, biophysical characteristics, and plasticity. With only minor exceptions, the properties of the serotonin-containing neurons of Aplysia and of pulmonate molluscs were remarkably similar, and it was concluded that these identified neurons are true homologues. The establishment of the homology of the metacerebral cells of Aplysia to the metacerebral cells of pulmonate molluscs extends the known distribution of these neurons to a second major subclass (Opisthobranchiata) of molluscs. Since pulmonate and opisthobranch molluscs differ substantially in behavioral and anatomical features, the study of the metacerebral cells of these two groups may promote the understanding of the evolutionary adaptation of the nervous system to different environmental pressures.

This paper describes the vasopressin (VP) and oxytocin (OXT) immunoreactive structures in the brain and upper spinal cord of the adult male and female Macaca fascicularis. Immunocytochemistry following intraventricular application of colchicine displayed VP neurons in the diagonal band of Broca (DBB), bed nucleus of the stria terminalis (BST), medial amygdaloid nucleus, dorsomedial hypothalamic nucleus, area of the locus coeruleus (LC), solitary tract nuclei (NTS), and the dorsal horn of the cervical spinal cord in addition to those known to exist in the paraventricular, supraoptic, and suprachiasmatic hypothalamic nuclei. Furthermore, a dense accumulation of VP fibers was observed in areas such as the DBB, medial septum, BST, amygdala, hippocampus, ventral tegmental area, periaquaductal gray, dorsal and ventral raphe, area of Forel, LC region, parabrachial nuclei, and NTS. The lateral septum and lateral habenula displayed no and very few VP fibers, respectively. No extrahypothalamic OXT neurons were found in the brain of this macaque monkey. Dense concentrations of OXT fibers were demonstrated in the amygdala, NTS, and marginal layer of the cervical spinal cord. No sexual dimorphism was found in this primate VP or OXT system. The results show a distribution of the central VP and OXT systems in this primate which is quite different from that in the rat. However, in various aspects it agrees with current data on the VP and OXT systems of the human brain. The present results suggest, therefore, that this monkey might serve as a better model for the human VP system than the rat.

Catecholamine axons have been visualized in human cerebral cortex obtained during routine neurosurgical operations. The fluorescence histochemical method of Lindvall et al. was used, slightly modified (calcium-deprived buffer, glyoxylic acid fixation followed by formaldehyde vapours exposition). The frontal cortex was more richely provided with catecholamine terminals than the parietal cortex. Two general types of axon morphology are evident. The most frequent is thin and sinous, sometimes forming clews, or loose basket-like arrangement around presumed nerve cells. The other one is moniliform and demonstrates spherical evenly-spaced varicosities. They look like, respectively, the well characterized dopaminergic and noradrenergic axons of the rat cerebral cortex. In two cases of Alzheimer's disease, noradrenergic-like fibers were missing and voluminous green-fluorescent varicosities, sometimes in obvious connection with typical axons, were observed in the proximity of senile plaques.

Cross-sectional areas at different levels, number of axons, maximal diameters, and number and maximal diameters of vessels were measured comparing autologous transplants with synthetic implants and nonlesion controls in a rat nerve regeneration model. The corresponding electrophysiologic data have been reported earlier in this journal. Although similar in many aspects, transplants led to the overall more reliable and slightly superior results, still lacking a substantial percentage of numerical qualities found in normal nerve, at least within the 3-month regeneration in this study.