Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Neuronal Connectivity”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,477 records · Page 82Linked to original sources

Activation of pyramidal neurons by intrinsic longitudinal connections in the hippocampus.

In the guinea pig, EPSPs and population spikes were found to be generated in the apical dendrites of pyramidal neurons of middle and ventral hippocampus, in response to dorsal hippocampal commissure (PSD) stimulation, without any involvement of dentate gyrus granule cells of corresponding segments. These long-latency synaptic effects were evoked only by repetitive (0.2-2.0 c/sec) PSD stimulation and showed increasing latency in ventral direction. A cross section between dorsal and middle hippocampus was followed by the disappearance of the responses ventrally to the section. The results show that the postsynaptic discharge of dorsal pyramidal neurons is transferred to more ventral hippocampal segments by an intrahippocampal longitudinal association system.

Animals↗

Galanin-immunoreactive axons innervate somatostatin-synthesizing neurons in the anterior periventricular nucleus of the rat.

The anterior periventricular nucleus (PeN) regulates GH secretion by synthesizing and releasing somatotropin release-inhibiting factor (SRIF) into the portal circulation. This territory of the diencephalon is heavily innervated by axons of galanin (GAL)-immunoreactive (IR) neurons. The connections between GAL-IR fibers and hypophysiotropic SRIF neurons were studied by means of immunocytochemical double labeling at the light and electron microscopic levels. Retrograde axonal labeling with Fluoro-Gold revealed the anterior PeN as the main site of hypophysiotropic SRIF-synthesizing neurons. These cells were densely surrounded by GALergic axons that made contacts with their cell bodies and dendrites. At the ultrastructural level, diaminobenzidine-labeled SRIF neurons received synapsing GAL-IR axons marked with silver-gold particles. Both axo-somatic and axo-dendritic forms of connections were observed. These morphochemical data revealed an interaction between GAL- and SRIF-synthesizing neurons in the anterior PeN. Furthermore, the presence of synaptic connections between these neuronal systems suggests a role for GAL in the control of SRIF secretion and, in turn, in the regulation of GH release.

Animals↗

Infrared-guided laser stimulation of neurons in brain slices.

Infrared-guided laser stimulation is a new technique that allows precise and rapid stimulation of visualized neurons in brain slices. Infrared imaging of neurons with a new contrast system is combined with the photolytic release of caged neurotransmitters by an ultraviolet (UV) laser. Addition of caged neurotransmitters to the superfusion medium of neurons in brain slices allows local excitation in the micrometer range with a focused spot of UV light. In this way, the distribution of glutamate or gamma-aminobutyric acid (GABA) receptors on neuronal dendrites can be mapped. Furthermore, this technique can be used to map the connectivity of neuronal networks through the controlled stimulation of neighboring neurons. Because the laser stimulation can be performed much faster than can paired recording, it is also possible to search for synaptic connections between distant neurons that have a low probability of connectivity.

Animals↗

Synaptic connections of cholecystokinin-immunoreactive neurons and terminals in the rat fascia dentata: a combined light and electron microscopic study.

We report here on the fine structure and synaptic connections of neurons and axon terminals in the rat fascia dentata displaying immunoreactivity to antibodies against cholecystokinin octapeptide (CCK). In the fascia dentata and hilar region, CCK-immunoreactivity was confined to nonpyramidal neurons that were similar in appearance to basket cells known to use gamma-aminobutyric acid (GABA) as neurotransmitter. These neurons exhibited dense accumulations of endoplasmic reticulum and infolded nuclei, and established asymmetric and symmetric synaptic contacts with presynaptic terminals. Among those terminals that formed asymmetric synaptic contacts, giant mossy fiber boutons arising from granule cell axons were identified. Cholecystokinin-immunoreactive terminals established symmetric synaptic contacts on the cell bodies and dendrites of granule cells. Similar contacts were formed on nonimmunoreactive hilar neurons. Some of these hilar cells were identified as commissural neurons by retrograde filling with horseradish peroxidase (HRP) following injection of the tracer into the contralateral fascia dentata. Synaptic contacts were rarely observed between immunolabeled pre- and postsynaptic elements. The results are discussed with regard to inhibitory processes in the fascia dentata since other studies have shown that CCK is coexistent with GABA in hippocampal nonpyramidal neurons.

Animals↗

Gene expression of Caenorhabditis elegans neurons carries information on their synaptic connectivity.

The claim that genetic properties of neurons significantly influence their synaptic network structure is a common notion in neuroscience. The nematode Caenorhabditis elegans provides an exciting opportunity to approach this question in a large-scale quantitative manner. Its synaptic connectivity network has been identified, and, combined with cellular studies, we currently have characteristic connectivity and gene expression signatures for most of its neurons. By using two complementary analysis assays we show that the expression signature of a neuron carries significant information about its synaptic connectivity signature, and identify a list of putative genes predicting neural connectivity. The current study rigorously quantifies the relation between gene expression and synaptic connectivity signatures in the C. elegans nervous system and identifies subsets of neurons where this relation is highly marked. The results presented and the genes identified provide a promising starting point for further, more detailed computational and experimental investigations.

Animals↗

Multiple connections of medial hypothalamic neurons in the rat.

The responses of 700 single neurons in the hypothalamus to electrical stimulation of the preoptic area, limbic structures, and midbrain were studied to determine the location of neurons with multiple inputs and to identify by antidromic activation the projection areas of those neurons. Converging excitatory inputs, observed in 134 responsive hypothalamic neurons, were principally derived from the preoptic, limbic, and midbrain areas. Inputs from separate nuclei of the amygdala were noted in the response of individual hypothalamic neurons. Two classes of short latency transsynaptic responses to amygdala stimulation were defined, indicating either separate pathways from the amygdala to the medial hypothalamus or two types of fibers conducting at different velocities. Stimulation of single or multiple sites in the preoptic and limbic areas, as well as in the arcuate nucleus and medial forebrain bundle produced inhibition of hypothalamic neuronal activity. Most antidromically identified medial hypothalamic neurons projected to the preoptic area, median eminence (tuberoinfundibular neurons), or midbrain. Evidence is presented for collateral projections of tuberoinfundibular neurons to the preoptic area and reticular formation. Medial hypothalamic neurons received inputs from the preoptic area, lateral septal nucleus, amygdala, ventral hippocampus (subiculum), and fornix. These findings illustrate a pattern of reciprocal connections between the medial hypothalamus and limbic and midbrain structures. It was concluded that the hypothalamus contains a type of neuron that is equipped to perform complex integrations and to coordinate directly the behavior of neurons in a diversity of anatomical regions.

Amygdala↗

Coincidence detection and changes of synaptic efficacy in spiny stellate neurons in rat barrel cortex.

Paired whole-cell voltage recordings were made from synaptically connected spiny stellate neurons in layer 4 of the barrel field in young (P14) rat somatosensory cortex. When postsynaptic action potentials (APs) followed each of 5 presynaptic APs in a 10- or 20-Hz train by less than 25 ms, subsequent unitary EPSP amplitudes were persistently reduced. Induction of long-term depression (LTD) depended on activation of group II metabotropic glutamate receptors, but not on NMDA or AMPA receptors. Reducing postsynaptic increases in intracellular calcium ([Ca2+]i) by intracellular loading with a fast- (BAPTA) or a slow- (EGTA) acting Ca2+ buffer blocked synaptic depression. Analysis of EPSP failures suggested mediation of LTD by a reduction in release probability. We propose a mechanism by which coincident activity results in long-lasting reduction of synaptic efficacy between synaptically connected neurons.

Animals↗

A dynamic neural network with temporal coding and functional connectivity.

A neural network model capable of altering its pattern classifying properties by program input is proposed. Here the "program input" is another source of input besides the pattern input. Unlike most neural network models, this model runs as a deterministic point process of spikes in continuous time; connections among neurons have finite delays, which are set randomly according to a normal distribution. Furthermore, this model utilizes functional connectivity which is dynamic connectivity among neurons peculiar to temporal-coding neural networks with short neuronal decay time constants. Computer simulation of the proposed network has been performed, and the results are considered in light of experimental results shown recently for correlated firings of neurons.

Computer Simulation↗

[Role of interneurons in the lateral corpus geniculatum in mammals].

1. This paper presents a summary of the morphological characteristics of I-neurons in the Cgld of mammals. These neurons consist of smaller somata and less dendrites being longer than the P-neurons. In all species investigated until now a short branched axon has been found. The dendritic structures show postsynaptic as well as presynaptic characteristics. 2. The innervation of I-neurons is not cleared up sufficiently. Besides retinal and cortical afferents, recurrent collaterals of P-neurons can be taken into account. Physiologists and morphologists give priority to retinal terminals. 3. The presynaptic dendrites of I-neurons are connected in triads with retinal terminals an P-neuron dendrites. Morphological and physiological findings open up the possibility of triads acting as "quasi interneurons" (HAMORI et al. 1974) and make the tonical activity change into the phasical one. 4. The endings of I-neuron axons being constantly presynaptic, synapse perferably at the somata of P-neurons and act presumably as inhibitors of P-neurons in the margin of a retinal input zone (surroundinhibition). In this connection quantitative considerations are carried out. 5. The morphological specializations of I-neurons are discussed in connection with their supposed physiological properties.

Animals↗

Direct synaptic linkage of ventrolateral nucleus of thalamus terminal with cat fast pyramidal tract neuron.

An electron microscopic study on the synaptic connections between neurons of ventrolateral nucleus of thalamus (VL) and pyramidal tract neurons (PTNs) in cat motor cortex was conducted by means of the anterograde degenerating procedure coupled with horseradish peroxidase (HRP) intracellular staining. Following VL lesions, a large majority of the degenerating terminals were found to terminate on dendritic spines and a few on the dendritic shaft. An asymmetric type synapse formed by a VL degenerating terminal and the dendritic shaft of a branch of apical dendrite of a labeled fast pyramidal tract neuron was demonstrated.

Animals↗

Induction and patterning of neuronal development, and its connection to cell cycle control.

Nervous tissue is derived from early embryonic ectoderm, which also gives rise to epidermal derivatives such as skin. The progression from naive ectoderm to differentiated postmitotic neurons involves multiple steps, two of which are crucial in shaping the final neurogenesis pattern. First, is the identification of the neural plate by the process of neural induction. Second, is the selection of a restricted number of sites within the neural plate where neurogenesis, the process leading to final differentiation of neural precursors, is initiated. Recent findings point to the existence of positive inducers of the neural state, whereas, neurogenesis initiation sites appear to be largely defined by inhibition. However, both neural induction and the initiation of neurogenesis appear to be connected to cell cycle control systems that govern whether stem cell maintenance and cell proliferation, or cell specification and differentiation, take place.

Animals↗

Electron microscopy of aminergic retinal neurons.

The synaptic connections of the dopaminergic retinal neurons of Cynomolgus monkeys and rabbits were studied in the electron microscope. In the Cynomolgus monkeys, a labelling method with 5,6-dihydroxytryptamine was used, whereas an autoradiographic technique with a monoamine oxidase inhibitor and (3H)-dopamine was used in the rabbits. The labelling method with 5,6-dihydroxytryptamine altered the normal ultrastructure of the dopaminergic neurons, but their synaptic structures were still easily recognized. The autoradiographic method left the ultrastructure of the labelled neurons unchanged, and large dense-cored vesicles could therefore be seen to be associated with the dopaminergic neurons in the rabbits. Other morphological characteristics could also be seen. The distribution of dopaminergic perikarya in the inner nuclear layer and dopaminergic processes in the inner plexiform layer was consistent with that of amacrine cells in both Cynomolgus monkeys and rabbits. Furthermore, the dopaminergic processes had output synapses of the conventional kind characteristic of amacrine cells. In both animals, the dopaminergic processes were presynaptic to amacrine cell bodies and both pre- and postsynaptic to other amacrine cell processes. The number of output synapses was larger than the number of input synapses. Serial and convergent synaptic arrangements were common. The synaptic organization of the indoleamine-accumulating neurons in the retinae of rabbits, cats, goldfish and carp were also investigated in the electron microscope. The neurons were labelled with 5,6-dihydroxytryptamine after the otherwise interfering dopaminergic processes had been destroyed. The indoleamine-accumulating neurons of the three species had a distribution of perikarya and processes like that of amacrine cells. They also had synapses of the conventional kind. In the rabbit and the cat, the indoleamine-accumulating processes had mainly reciprocal synapses with rod bipolar terminals in the innermost part of the inner plexiform layer. They were, however, also also pre- and postsynaptic to other amacrine cells, and in the cat, they had synaptic contacts with cone bipolar cells and the dendrites of ganglion cells. The indoleamine-accumulating neurons of the goldfish and carp were mainly pre- and postsynaptic to other amacrine cells, even if contacts with bipolar terminals were also seen. In the retinae of goldfish and carp, a subset of indoleamine-accumulating processes were discovered in the middle part of the inner plexiform layer that had a previously not recognized type of conventional output synapse with two postsynaptic elements. This synapse was called a branched conventional synapse. It was found and investigated in the retinae of normal goldfish and carp. Its presynaptic structures were found to be similar to those seen in certain conventional synapses with presynaptic "globular clusters" and only one postsynaptic element.

Animals↗

Radial correlation contrast--a functional connectivity MRI contrast to map changes in local neuronal communication.

A functional connectivity MRI method that groups neighboring voxels in relation to their degree of temporal cross-correlation between their time courses is presented. This grouping generates a vector field, which is assumed to provide insights into the local organization of neuronal activity. Application with high spatial resolution fMRI rat data subjected to electric forepaw sensory stimulation (156 . 156 . 1000 micron1) shows a significant localized increase of the vector field amplitude in cortical layers 4 and 2/3 of the primary sensory cortex and in layer 2/3 of the primary motor cortex, suggesting a strong correlation with local neuronal communication. Vector field phases exhibit a transition with neuronal activation from random-like orientations during rest to clusters of common orientations. Cluster size is shown to be weakly dependent on the radii of the vector field calculation, and shuffling voxel position within clusters generates a random-like vector orientation instead. This suggests that changes in vector orientations upon activation represent changes in the internal correlation between voxels that is interpreted as a change in the internal neuronal communication.

Animals↗

[Organization of neocortical neuronal networks].

Multiple unit activity in deep layers of the frontal and motor cortices was recorded by chronically implanted semimicroelectrodes in waking cats with different levels of food motivation. From four to seven neuronal spike trains were selected from the recorded multiunit activity. Interactions between neighbouring neurons in the motor and frontal areas of the neocortex (within the local neuronal networks) and between the neurons of these areas (distributed neuronal networks) were estimated by means of statistical crosscorrelation analysis of spike trains within the range of delays from 0 to 100 ms. Neurons in the local networks were divided in two subgroups: the neurons with higher spike amplitudes with the dominance of divergent connections and neurons with lower spike amplitudes with the dominance of convergent connections. Strong monosynaptic connections (discharges with a delay of less than 2 ms) between the neurons with high- and low-amplitude spikes formed the background of the local networks. Connections between low-amplitude neurons in the frontal cortex and high-amplitude neurons in the motor cortex dominated in the distributed networks. A 24-hour food deprivation predominantly altered the late interneuronal crosscorrelations with time delays within the range of 2-100 ms in both local and distributed networks.

Animals↗

Intra- and interganglionic synaptic connections in the CNS of Aplysia.

Synaptic connections were found between two groups of neurons in the CNS of Aplysia, the cerebral ganglion A and B cluster neurons which are involved in the control of pedal and parapodial movements and neurons in the pleural ganglion which has been shown to modulate locomotion. The A and B neurons made synaptic connections in both the cerebral and pleural ganglia. Pleural neurons had synaptic connections among themselves and with A and B neurons. The A neurons made excitatory monosynaptic connections with the B neurons and a minimum of 6 pleural neurons including the left giant cell (LGC). All of the A neuron synapses found were excitatory. The B neurons received excitatory synaptic input from two other groups of neurons in the cerebral ganglion and both excitatory and inhibitory input from pleural neurons. The latter were identified on the basis of their synaptic connections with the LGC and A neurons. The B neurons and LGC had several common synaptic inputs. The A neurons received monosynaptic input from only 2 pleural neurons. Complex synaptic circuits between A and B neurons and pleural neurons were found. These included recurrent inhibition of B neurons by A neurons via a pleural interneuron, feedforward summation of A neuron synaptic input to the LGC, and reciprocal excitatory synaptic connections between B and the pleural neurons. The activity of the B neurons was modulated by direct inhibitory and excitatory synaptic connections from pleural neurons. The A neurons were modulated primarily by a polysynaptic pathway through the B neurons. The modulation of cerebral A and B neurons by pleural neurons is consistent with behavioral results obtained studying locomotion.

Animals↗