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PubMed1984

Development of the axon cap neuropil of the Mauthner cell in the goldfish.

Development of the axon cap neuropil of the Mauthner neuron in post-hatching larval goldfish brains was observed electron-microscopically. The axonal initial segment of newly hatched (day-4) larvae is completely covered with synaptic terminals containing clear spherical synaptic vesicles. Profiles of thin terminal axons, the spiral fibers, containing similar synaptic vesicles, rapidly increase in number around the initial segment and form glomerular neuropil similar to the central core of the adult axon cap by day 7. Three types of synapses are formed in the core neuropil. Bouton-type synapses contacting the initial segment are most abundant in day-4 to -14 larvae; they decrease thereafter and are rare on the distal half of the initial segment of day-40 larvae. Asymmetric axo-axonic synapses are commonly observed between spiral fibers in the core neuropil of day-7 to -19 larvae, but become fewer by day 40. Unique symmetrical axo-axonic synapses showing accumulation of synaptic vesicles on either side of apposed membrane thickenings first appear in day-14 core neuropil, gradually increase in number, and become the predominant type in day-40 core neuropil. Thick myelinated axons, which lose their myelin sheaths in the glial cap cell layer, start to penetrate into the axon cap on day 10. They gradually increase in number and form the peripheral part of the axon cap together with the cap dendrites, which finally grow into the axon cap from the axon hillock region of the Mauthner cell by day 40.

Age Factors↗
PubMed1997

Organization of the stomatogastric neuropil of the crab, Cancer borealis, as revealed by modulator immunocytochemistry.

We used antibodies to a number of neuromodulatory substances, including serotonin, FLRF amide, red pigment-concentrating hormone, substance P, proctolin and cholecystokinin, to investigate the distribution of molecules similar to these substances in the stomatogastric ganglion of the crab, Cancer borealis. No immunoreactivity was seen in the region of the cell bodies that surrounds the neuropil and little was found in the core of the neuropil (where the primary neurites of the intrinsic neurons occupy most of the space). Instead, modulator immunolabel was densely packed in the more peripheral portion of the neuropil that surrounded the core. Within this peripheral neuropil, profiles appeared quite uniformly distributed. Double-labeling showed that there were limited differences in distribution between the labels examined in our study. The only immunolabeled structures that showed a distinct differential distribution within the stomatogastric neuropil were a population of >/=10 microm varicosities that arose from a pair of input fibers that we termed the large varicosity fibers. These varicosities were immunolabelled by antisera for three different peptides. Taken collectively, these data shows that there is a stereotyped distribution of modulator immunoreactivity within the crab stomatogastric neuropil. However, this segregation is more rudimentary than that reported for the intrinsic stomatogastric neurons.

Animals↗
PubMed1988

Intraspinal substance P-containing projections to the sympathetic preganglionic neuropil in pigeon, Columba livia: high-performance liquid chromatography, radioimmunoassay and electron microscopic evidence.

The present study uses quantitative and electron microscopic methods to investigate the hypothesis that intraspinal substance P-sympathetic preganglionic neuron circuitry exists in vertebrates. Radioimmunoassay and high-performance liquid chromatography were used to: (1) characterize the chemical nature of the substance P-like immunoreactivity in the sympathetic preganglionic neuropil; and (2) quantify the relative contributions of brain stem, primary sensory and intraspinal neurons to the substance P content within the sympathetic preganglionic neuropil. Electron microscopic observations on the localization of substance P-like immunoreactivity within the preganglionic neuropil caudal to complete thoracic spinal cord transections are also reported. High-performance liquid chromatographic analyses demonstrate that pigeon substance P-like immunoreactivity co-migrates with synthetic substance P, suggesting that the substance P-like material is authentic substance P content within the sympathetic preganglionic neuropil. Electron microscopic observations on the localization of substance P-like immunoreactivity within the preganglionic neuropil caudal to complete preganglionic cell column (inclusive of intermediate spinal laminae V and VII as well as preganglionic neurons located within nucleus intercalatus spinalis); (2) cutting the dorsal rootlets entering the last cervical (C14) and first two thoracic (T1, T2) spinal segments resulted in massive depletion of substance P content in dorsal horn of T1, but no detectable losses within the preganglionic cell column or ventral horn of T1; and (3) total mid-thoracic (T3-4) spinal cord transection significantly depleted the substance P content in the preganglionic cell column (T3-4) as well as in the dorsal (T1-4) and ventral horns (T2-4). Ultrastructural examination of the sympathetic preganglionic neuropil caudal to spinal transections (survival times of 3-14 days) revealed the presence of numerous, intact, normal appearing substance P-like immunoreactive terminals. Immunolabeled terminals formed asymmetric contacts on medium-sized and small caliber dendrites. Extensive degeneration was evident in this material as well. The ultrastructural features of degenerating processes were distinctive and quite dissimilar in appearance from those exhibiting substance P-like immunoreactive staining. No evidence for damage-induced sequestration of substance P-like material into glial elements was found. The above observations are consistent with earlier findings in rat and pigeon, and provide new quantitative and qualitative evidence to support the hypothesis that intraspinal substance P-containing interneurons contribute t

Animals↗
PubMed1981

Aging in the neuropil of cerebral cortex--a quantitative ultrastructural study.

Six age groups, each composed of four animals from each of the following ages, were used to assess age-related ultrastructural changes in the neuropil of the III layer of the frontal cortex in rats: 3, 6, 12, 18, 24 and 30 months old. Random samplings within the neuropil were taken to produce 40 electron micrographs in each rat (totaling 960). The profiles of axon terminals, dendrites and astroglial processes in the neuropil of each micrograph were traced. Then the percentage of their areas for the area of neuropil (relative volume fraction) was examined using the image analyzer system. The relative volume fractions of both the axon terminals and dendrites for the neuropil were found to have decreased in the aged rats. On the contrary, the relative volume fraction of astroglial processes for the neuropil had progressively increased with aging.

Aging↗
PubMed2005

Integration and segregation of inputs to higher-order neuropils of the crayfish brain.

Information about the input and output pathways of higher-order brain neuropils is essential for gaining an understanding of their functions. The present study examines the connectivity of two higher-order neuropils in the central olfactory pathway of the crayfish: the accessory lobe and its target neuropil, the hemiellipsoid body. It is known that the two subregions of the accessory lobe, the cortex and medulla, receive different inputs; the medulla receives visual and tactile inputs, whereas the cortex receives neither (Sandeman et al. [1995] J Comp Neurol 352:263-279). By using dye injections into the olfactory lobe, we demonstrate that the accessory lobe cortex and medulla also have differing connections with the olfactory lobe. These injections show that local interneurons joining the olfactory and accessory lobes branch primarily within the cortex with only limited branching within the medulla. Injections of different dyes into the two subregions of the hemiellipsoid body, HBI and HBII, show that the accessory lobe cortex and medulla also have separate output pathways. HBI is innervated by the output pathway from the cortex while HBII is innervated by the output pathway from the medulla. These injections also show that HBI and HBII are innervated by separate populations of local interneurons with differing connections to higher-order neuropils in the olfactory and visual pathways. These results suggest a segregation of olfactory and multimodal (including olfactory) inputs within both the accessory lobe and the hemiellipsoid body and provide evidence of important functional subdivisions within both neuropils.

Animals↗
PubMed2006

Modular neuropile organization in the Drosophila larval brain facilitates identification and mapping of central neurons.

Elucidating how neuronal networks process information requires identification of critical individual neurons and their connectivity patterns. For this purpose, we used the third-instar Drosophila larval brain and applied reverse-genetic tools, immunolabeling procedures, and 3D digital reconstruction software. Consistent topological definition of neuropile compartments in the larval brain can be obtained through simple fluorescence-immunolabeling methods. The modular neuropiles can be used as a fiducial framework for mapping the projection patterns of individual neurons labeled with green fluorescent protein (GFP). GFP-labeled neurons often exhibit dendrite-like arbors as well as clustered varicose terminals on neurite branches that innervate identifiable neuropile compartments. We identified candidate cholinergic interneurons in genetic mosaic brains that overlap with the larval optic nerve terminus. By using the neuropile framework, we demonstrate that the candidate visual interneurons are not a subset of the previously identified circadian pacemaker neurons that also contact the larval optic nerve terminus; they may represent parallel pathways in the processing of visual inputs. Thus, in the Drosophila larval brain, modular neuropiles can be used as a framework for systematically identifying, mapping, and classifying interneurons; understanding their roles in behavior can then be pursued further.

Animals↗
PubMed1993

Two visual systems in one brain: neuropils serving the principal eyes of the spider Cupiennius salei.

Principal (anterior median) eyes of the wandering spider Cupiennius are served by three successive neuropils, the organization of which is distinct from those serving secondary eyes. Photoreceptors terminate in the first optic neuropil amongst second order neurons with overlapping dendritic fields. Second order neurons terminate at various depths in anterior median eye medulla where they are visited by bush-like dendritic trees of third order projection neurons. These supply tracts which extend into the "central body." This crescent-shaped neuropil lies midsagittally in the rear of the brain near its dorsal surface. It is organized into columns and it supplies both columnar and tangential efferents to other brain centers. The supply to and organization of the "central body" neuropil is reminiscent of retinotopic neuropils supplying the lobula of insects. Channels to the "central body" comprise one of two concurrent visual pathways, the other provided by the secondary eyes supplying the "mushroom body." We suggest that principal eye pathways may be involved in form and texture perception whereas secondary eyes detect motion, as is known for jumping spiders. Our data do not support Hanström's classical view that the "central body" is specifically associated with web-building, nor that it is homologous to its namesake in insect brains.

Afferent Pathways↗
PubMed1992

Postnatal development of zinc-containing cells and neuropil in the visual cortex of the mouse.

The postnatal development of zinc-containing synaptic boutons and their cells of origin in the visual cortex of a pigmented mouse is described. Two phases can be distinguished. During the early phase zinc-containing neuropil is first apparent by postnatal day 3. By day 7 a light, but distinct neuropil staining sketches the primary and secondary visual cortices. The primary visual area contains light precipitate in layers V and VI as well as the monocular portion of layer II/III. The secondary visual areas contain slightly denser precipitate in layers II/III through VI. The transition to the second phase is marked by a large increase in precipitate density by day 11. Thereafter, the intensity of the neuropil staining increases to day 28, first in layer II/III and then in layer V, as the adult pattern of neuropil staining gradually develops. In the primary visual cortex precipitate is dense in layers II/III and V, moderate in layer VI, and sparse in layers I and IV. In the secondary visual areas the precipitate is dense in layers II/III and V and moderate in the lower portion of layer I and in layers IV and VI. Cells of origin of zinc-containing boutons are visible by the end of the second postnatal week in layer II/III of the secondary visual cortex. By 21 days of age the pattern of staining in the mature mouse is established, and cells in layers II/III and VI are labeled in both the primary and secondary visual cortices. The developmental sequence of zinc-containing cells and neuropil does not preclude an involvement of zinc in the postnatal regulation of NMDA receptor function.

Animals↗
PubMed1989

Structural inhomogeneity in the neuropil of lamina II/III in rabbit visual cortex.

Due to the bundling of apical dendrites throughout laminae IV-II of the cerebral cortex, two compartments of neuropil are distinguished: (1) the neuropil of the dendrite bundles consisting of closely associated, vertically oriented apical dendrites of pyramidal cells and the fine cell processes between them and (2) the neuropil separating the dendrite bundles. The aim of the present study is to obtain more information concerning differences in composition and arrangement of fine cell processes in the two compartments and to quantify differences in the configuration and size of the extracellular space. To this end, a comparative stereological study of the two compartments has been performed in the upper half of lamina II/III in the visual cortex of 8 adult rabbits. The various constituent elements of the neuropil have been evaluated in electron micrographs with respect (a) to their volume fractions and (b) to their surface fractions, i.e. the surface area of their membranes comprised in a given volume of tissue. It was found that the volume fractions of thin axons, glial processes and spines are significantly higher between than within dendrite bundles, whereas the volume fraction of dendrites is about 50% higher in the compartment of the bundles. However, when excluding the dendrites in both compartments from calculations, the composition of the remaining neuropil within and between dendrite bundles was found to be identical. As far as surface fractions are concerned, significant differences were shown to exist for all kinds of cell processes except dendrites and myelinated axons. Surface fractions of small axons, glial processes and spines are higher between than within dendrite bundles.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1987

Morphological organization of the neuropil in laminae II-V of rabbit visual cortex.

A combined light- and electronmicroscopic study of tangential serial sections through the visual cortex of the rabbit has been performed in order to find out whether or not the vertical bundles of apical dendrites in laminae IV/V and II/III on one hand and the areas between these bundles on the other differ with respect to composition and/or spatial organization of the neuropil. Lightmicroscopically only thick profiles such as apical dendrites of pyramidal cells and myelinated axons contribute to the structural characteristics of the neuropil. The appearance of the areas between the dendrite bundles is determined by the presence or absence of radiate bundles of myelinated axons. Lamina-dependent variations were seen in the neuropil of the dendrite bundles as well as in that of the areas between them. Ultrastructurally, the dendrite bundles and the areas between them were observed to be different also with respect to the distribution of the various types of small dendritic profiles and thin axons. The neuropil within the dendrite bundles except for the shafts and thick branches of apical dendrites contains thin unmyelinated axons and numerous spines of apical dendrites contracted by axon terminals. Small irregularly shaped dendrites are few in number. The neuropil between the dendrite bundles contains a larger number of thin unmyelinated axons than that within the bundles, and, instead of spines of apical dendrites, small irregularly shaped smooth and spiny dendrites represent the prevailing postsynaptic structures. Hence, areas within dendrite bundles differ from areas between them by thickness and orientation of their profiles and by the quantitative relation of the various kinds of processes accumulating in each compartment.

Animals↗
PubMed1991

The effect of neonatal hypoxia-ischemia on striatal cholinergic neuropil: a quantitative morphologic analysis.

Little is known about the alterations in the neurochemical anatomy of the brain in the static encephalopathies of childhood, of which one cause is hypoxia-ischemia. We and others have previously shown in neonatal rodent that experimental hypoxia-ischemia results in an increase in the density of striatal cholinergic neurons (number/mm3). There is a rostrocaudal gradient for this effect within the striatum, with as much as a 50% increase in density caudally. It has not been known what effect this injury has on the distribution of striatal cholinergic neuropil. We have therefore investigated effects on striatal cholinergic neuropil, demonstrated with a monoclonal antibody to choline acetyltransferase (CAT) and the immunoperoxidase technique. Because individual CAT-positive fibers in the striatum are too numerous to be directly counted, we have quantified relative effects on neuropil at the population level using segmented field analysis within the same section. We find that hypoxic-ischemic injury results in a significant increase in the proportion of the injured striatum occupied by high density CAT-positive neuropil staining. This change is persistent, as it is also observed in adult rats. The increase is uniform in the rostrocaudal dimension. Our measure of CAT-positive neuropil staining, being relative, cannot determine whether the observed increase in staining is strictly due to striatal shrinkage with compaction of fibers or whether, in addition, there has been sprouting. The latter possibility is suggested by the lack of a correlation between the degree of shrinkage and changes in area occupied by positive staining. While the functional significance of these changes is not known, they support the concept that striatal cholinergic systems are resistant to hypoxic-ischemic injury and that an abnormal predominance of these systems may play a role in the persistent alterations of motor control observed clinically in this form of injury.

Aging↗
PubMed1987

Increases in ribosomal RNA within the denervated neuropil of the dentate gyrus during reinnervation: evaluation by in situ hybridization using DNA probes complementary to ribosomal RNA.

Previous studies have revealed that there are increases in the incorporation of [3H]amino acids into protein in the denervated neuropil of the dentate gyrus during periods of reactive synaptogenesis. The present study evaluates whether the increase in incorporation reflects an increase in protein synthetic machinery (ribosomes) in the denervated zone. We evaluated the distribution of ribosomal RNA (rRNA) in the denervated dentate gyrus 2-14 days after unilateral destruction of the entorhinal cortex using DNA probes complementary to rRNA for in situ hybridization. Animals with comparable lesions were injected with [3H]leucine 30 min prior to sacrifice and prepared for autoradiography in order to define the extent of protein synthesis within the denervated neuropil. Quantitative analyses revealed that the increases in [3H]leucine incorporation were accompanied by increases in labeling with the rRNA probe. In both cases, the increases were first apparent at 2 days postlesion, reached a peak on day 6, and then declined between 8 and 14 days postlesion. Plots of grain density across the neuropil revealed that the increases in rRNA, like the increases in amino acid incorporation, occurred selectively within the denervated portion of the neuropil. We propose that increased incorporation of protein precursor is the result of an increase in protein synthetic machinery within the denervated neuropil. These increases may reflect in part the increases that we have previously noted in polyribosomes under dendritic spines.

Animals↗
PubMed1994

Increase of c-fos and ras oncoproteins in the denervated neuropil of the rat dentate gyrus.

When the entorhinal cortical input to the rat dentate gyrus is destroyed, the process of sprouting and synaptogenesis begins within the denervated dendritic laminae. The present study used immunohistochemical methods to determine whether there was an increase in the oncoproteins c-fos and ras within the denervated neuropil of the dentate gyrus during this period of terminal growth and synapse formation. Animals were prepared for immunolabeling one, three, six and 30 days after unilateral lesion of the entorhinal cortex. Rats were perfused with paraformaldehyde fixative and brain sections were incubated with antibodies to either c-fos or ras oncoprotein. Qualitative light microscopic analysis showed a marked increase in both c-fos and ras proteins over the denervated zone at three days postlesion when compared to both the intact contralateral control and the naive control. At one- and six-day postlesion intervals there was also an increase in labeling over the denervated neuropil with each oncoprotein; however, the intensity of label was reduced relative to that of the three-day time interval. No increase in labeling over the denervated zone was visible for either antibody at 30 days postlesion. The high level of both c-fos and ras labeling in the denervated molecular layer was confirmed with Western blot analysis of dissected molecular layers from lesioned and contralateral control hippocampi. Controls for antibody and method specificity showed that the labeling was specific for c-fos and ras proteins. The high level of c-fos labeling over the denervated molecular layer was uniform with scattered punctate sites of reaction product interspersed in the neuropil. Glial cell bodies in the neuropil contained the highest levels of c-fos oncoprotein. The granule cell nuclei showed an apparent reduction in the level of c-fos labeling at one, three and six days postlesion when compared with the nuclear staining of naive control cases. At 30 days postlesion, high levels of labeling over the denervated zone were not visible and c-fos localization had returned to the typical predominant nuclear sites seen in controls. Ras oncoprotein localization was diffuse in the cell processes of the molecular layer, with intermittent glial labeling within the denervated zone. No cell nuclei labeling was observed with antibodies to ras protein. These results show that both c-fos and ras oncoproteins are increased within the denervated neuropil of the dentate gyrus during sprouting and synapse formation.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1987

[Avesicular intercellular contacts in the neuropil of the ganglia of the subpharyngeal complex and in the nerves of the edible snail].

Intercellular interconnections in neuropil of dorsal ganglia in the subpharyngeal complex and nerves have been studied in a mature snail (Helix pomatia), dimensions of the shell--3.0 X 3.5 sm, after double fixation (glutaraldehyde and osmium tetraoxide) and treatment with phosphoric tungsten acid. Zones of the neuropil in the left pleural and parietal ganglia have been investigated--where the nerves leave ganglia and in the area of giant cells; neuropil of the central part of both parietal ganglia; central part of the visceral ganglion and nerves--left palial, intestinal and left pleural commissure. The most spread forms of avesicular intercellular contacts in the neuropil are symmetrical. Besides the latter, processes of the neuropil form fissural and desmosomal junctions. Localization of the avesicular contacts supposes presence of dendro-dendritic junctions of desmosomal and fissural types and axo-axonal ones--of desmosomal type. Various types of the contacts differ from each other by their ultrastructural organization.

Animals↗
PubMed1981

[Role of neuronal and neuropile serotonin in the visual analyzer].

The serotonin content was estimated in bulk-separated neuronal and neuropil fractions of visual and motor brain cortex in normal, dark-reared and light-exposured rats. In normal rats, the serotonin content in neuropil in visual and motor cortex was equal to 182.66 +/- 21.19 and 164.10 +/- 27.70 ng/mg protein, respectively, and exceeded its content in neuronal fractions 2.7-fold (for visual cortex) and 2.2-fold (for motor cortex). Under dark-rearing the serotonin content in neuropil of visual and motor cortex decreased by 46.7 and 51.6%, respectively, as compared with normal. Light exposure of dark-reared rats for 3 hours produced a sharp increase in the serotonin content only in neuropil of visual cortex (2.7-fold higher in comparison with dark-reared rats). There were no significant changes in the serotonin content in neurons of both cortical regions under the experimental conditions used as compared with normal. The results are discussed from the point of view of functional heterogeneity of serotonin metabolism in neurons and neuropil.

Animals↗
PubMed2000

Effects of ATP and derivatives on neuropile glial cells of the leech central nervous system.

We investigated the effects of ATP (adenosine 5'-triphosphate) and derivatives on leech neuropile glial cells, focusing on exposed glial cells. ATP dose-dependently depolarized or hyperpolarized neuropile glial cells in situ as well as exposed neuropile glial cells. These potential shifts varied among cells and repetitive ATP application did not change their amplitude, duration or direction. In exposed neuropile glial cells, ATP most frequently induced a Na(+)-dependent depolarization and decreased the input resistance. The agonist potency ATP > ADP (adenosine 5'-diphosphate) > AMP (adenosine 5'-monophosphate) > adenosine indicates that P2 purinoceptors mediate this depolarization. The P2Y agonist 2-methylthio-ATP mimicked the ATP-induced depolarization, whereas the P2Y antagonist PPADS (pyridoxal-phosphate-6-azophenyl-2', 4'-disulphonic acid) reduced it. P2X agonists were without effect. Because the P1 antagonist 8-SPT (8-(p-sulphophenyl)-theophylline) also depressed ATP-induced depolarizations and some ATP-insensitive glial cells responded to adenosine, we suggest coexpression of metabotropic P2Y and P1 purinoceptors. The ATP-induced depolarization requires activation of Na(+) channels or nonselective cation channels, whereas the ATP-induced hyperpolarization indicates activation of K(+) channels. ATP also increased the intracellular Ca(2+) concentration ([Ca(2+)](i)), that is independent of Ca(2+) influx but reflects intracellular Ca(2+) release possibly triggered by IP(3) formation. ADP and AMP also increased [Ca(2+)](i), but were less efficient than ATP; adenosine and 2-methylthio-ATP did not affect [Ca(2+)](i). In view of the mobilization of intracellular Ca(2+), ATP is clearly different from other leech neurotransmitters, because it enables intracellular Ca(2+) signaling without causing prominent changes in glial membrane potential. Thus disturbance of the extracellular microenvironment and the demand for metabolic energy are minimized.

Adenosine Triphosphate↗
PubMed2002

The phylogenetic significance of crustacean optic neuropils and chiasmata: a re-examination.

Recent molecular data challenge the traditional hypotheses of arthropod phylogeny founded on morphologic characters. In this discussion, the structure of the visual systems in Pterygota (Hexapoda) and Decapoda (Malacostraca, Crustacea) is an important argument. Although many components of their visual systems depict structural homology, differences exist between Pterygota/Decapoda on the one side and Branchiopoda (Entomostraca) on the other in that the latter do not have a third optic neuropil or optic chiasmata. Therefore, the goals of the current study were to explore whether the third optic neuropils in Pterygota and Decapoda are homologous, to examine the formation of the first two optic neuropils and the chiasmata in Crustacea, and to compare these processes with Pterygota. For this purpose, five species of entomostracan and malacostracan crustaceans were analyzed by examination of serial sections, fluorescence labeling with phallotoxins, and anti-histamine immunohistochemistry. We found that the chiasmata of Decapoda and Pterygota are characterized by striking similarities regarding both the level of individually identifiable classes of neurons and ontogenetic mechanisms, which are clearly different from those in Branchiopoda. Furthermore, the third optic neuropil of Decapoda and Pterygota, the lobula, shares an ontogenetic protocerebral origin and an innervation by corresponding sets of histamine-immunoreactive neurons, suggesting homology of the lobula in these two groups. In conclusion, the characteristics of the visual system are in conflict with the traditional classification of Arthropoda. Instead, they support a sister-group relationship of Hexapoda and Malacostraca, as suggested by some of the molecular studies.

Animals↗
PubMed2003

Stereotyped neuropil branching of an identified stomatogastric motor neuron.

Anatomical studies of the crab stomatogastric ganglion (STG) have suggested only minimal organization within the neuropil of this structure. Here, we present evidence that, for at least one intrinsic neuron type, the ventricular dilator (VD) neuron, a highly organized and stereotyped branching structure exists within the stomatogastric neuropil. Specifically, we show the morphology of the VD neuron consists of a single primary neurite that projects from the soma into the neuropil and bifurcates into a pair of subprimary neurites, which in turn exit the neuropilar region, one entering the left and the other the right medial ventricular nerve. Nearly all secondary neurite branching of the VD neuron is from the subprimary neurites. There are approximately 22 secondary branches/neuron (range 14-28), with no significant difference between the number of secondary branches off the right vs. the left subprimary neurite, although the ratio of secondary branches between subprimaries varies (range 0.4-1.6). The fine neurites that branch from the secondary processes segregate hemispherically within the neuropil, based on the subprimary neurite of origin. Within this hemispherical organization, another level of fine neurite segregation is present, namely, the fine neurites derived from each secondary branch are restricted to discrete regions of the hemisphere with only minimal overlap with those derived from other secondary branches. Monte Carlo simulations show that this segregation differs significantly from a random distribution. The organization of branching seen in the VD neuron may play a critical role in the electrotonic and local computational organization of this neuron and sets the stage for physiological experimentation addressing these issues.

Animals↗