PubMed Health⌕ Search

Biomedical subjects

B J Dennis

Publications and source records attributed to B J Dennis.

16 recordsLinked to original sources
PubMed1993

Quantitative ultrastructural analysis of the periaqueductal gray in the rabbit.

The fine structure of the periaqueductal gray (PAG) of the rabbit was examined using the transmission electron microscope. On the basis of synaptic polarity, vesicle size, and the nature of the pre- and post-synaptic elements, 10 essentially different synaptic types could be discerned (6 axo-dendritic, 2 axo-somatic, 1 axo-axonic, and 1 dendro-dendritic). Synaptic contacts on the soma of PAG neurons were small and covered, on average, only 1.6% of the soma surface. The most striking feature of the synaptic structure of the PAG was that more than 94.1% of all synapses were axo-dendritic. Of these, 83.5% were of the symmetrical type. Most of these contacts occurred on buttons of small to medium size, and contained either round vesicles of medium size or pleomorphic vesicles of medium size. Boutons containing only flattened vesicles were quite rare. Boutons contacting larger dendrites were generally small-to-medium in size, made asymmetric-type synaptic contacts, and contained pleomorphic vesicles of medium-to-large size. Medium-sized dendrites were contacted principally by small boutons exhibiting either symmetrical or asymmetrical junctions containing medium-sized pleomorphic vesicles, and in addition a few of these boutons contained both large, and small, round vesicles. Dendritic spines were generally provided with only one synaptic contact, stretching the entire width of the spinous process. Boutons and the spines on dendrites were approximately the same size. Synapses between two vesicle-containing structures (axo-axonic or dendro-dendritic synapses) were rare (1.4%). They were generally asymmetric and contained round vesicles of medium size. Complex synapses, where a glial sheet enclosed the synapse, were occasionally observed. Also seen were multiple synapses, with up to 11 contacts on a single dendritic profile. Large dense-core vesicle were seen in approximately 40% of all synapses, whereas small dense-core vesicles were only found in about 3%. Data is provided on how different synaptic features relate to ventral, lateral, dorsal, and medial PAG. Principally this is in relation to neuron size, glia cell content, axonal characterization, and vesicular type.

Animals↗
PubMed1993

A scanning and transmission electron microscopic analysis of the cerebral aqueduct in the rabbit.

An examination of the surface of the cerebral aqueduct with the scanning electron microscope revealed that the walls of the cerebral aqueduct were so heavily ciliated that most of the ependymal surface was obscured, yet certain specialized supraependymal structures could be discerned lying on (or embedded within) this matt of cilia. These structures were determined by transmission electron microscopy and Golgi analysis to be either macrophages, supraependymal neurons, dendrites from medial periaqueductal gray neurons, or axons of unknown origin. Some axons, which were found to contain vesicles, appeared to make synaptic contacts with ependymal cells. Using the transmission electron microscope, the ependymal lining was found to consist of two different cell types: normal ependymal cells and tanycytes which have a long tapering basal process that was observed to contact blood vessels or, more rarely, seemed to terminate in relation to neuronal elements. While there have been previous reports on the structure of the third and lateral ventricles in other species, there are limited reports in the rabbit. The present report is not only the first description for the rabbit, but it is the first complete scanning and transmission electron microscopic analysis of the cerebral aqueduct in any species.

Animals↗
PubMed1991

Efferent projections of the periaqueductal gray in the rabbit.

The efferent projections of the periaqueductal gray in the rabbit have been described by anterograde tract-tracing techniques following deposits of tritiated leucine, or horseradish peroxidase, into circumscribed sites within dorsal, lateral or ventral periaqueductal gray. No attempts were made to place labels in the fourth, extremely narrow (medial), region immediately surrounding the aqueduct whose size and disposition did not lend itself to confined placements of label within it. These anatomically distinct regions, defined in Nissl-stained sections, corresponded to the same regions into which deposits of horseradish peroxidase were made in order for us to describe afferent projections to the periaqueductal gray. In this present study distinct ascending and descending fibre projections were found throughout the brain. Terminal labelling was detected in more than 80 sites, depending somewhat upon which of the three regions of the periaqueductal gray received the deposit. Therefore, differential projections with respect to both afferent and efferent connections of these three regions of the periaqueductal gray have now been established. Ventral deposits disclosed a more impressive system of ramifying, efferent fibres than did dorsal or lateral placements of labels. With ventral deposits, ascending fibres were found to follow two major pathways from periaqueductal gray. The periventricular bundle bifurcates at the level of the posterior commissure to form hypothalamic and thalamic components which distribute to the anterior pretectal region, lateral habenulae, and nuclei of the posterior commissure, the majority of the intralaminar and midline thalamic nuclei, and to almost all of the hypothalamus. The other major ascending pathway from the periaqueductal gray takes a ventrolateral course from the deposit site through the reticular formation or, alternatively, through the deep and middle layers of the superior colliculus, to accumulate just medial to the medial geniculate body. This contingent of fibres travels more rostrally above the cerebral peduncle, distributing terminals to the substantia nigra, ventral tegmental area and parabigeminal nucleus before fanning out and turning rostrally to contribute terminals to ventral thalamus, subthalamus and zona incerta, then continuing on to supply amygdala, substantia innominata, lateral preoptic nucleus, the diagonal band of Broca and the lateral septal nucleus. Caudally directed fibres were also observed to follow two major routes. They either leave the periaqueductal gray dorsally and pass through the gray matter in the floor of the fourth ventricle towards the abducens nucleus and ventral medulla, or are directed ventrally after passing through either the inferior colliculus or parabrachial nucleus. These ventrally directed fibres merge just dorsal to the pons on the ventral surface of the brain.(ABSTRACT TRUNCATED AT 400 WORDS)

Afferent Pathways↗
PubMed1990

A multiple Golgi analysis of the periaqueductal gray in the rabbit.

Four variants of the Golgi method have been used, in the rabbit, to reveal the morphological attributes of neurons within the periaqueductal gray. Of these methods, the Golgi-Cox version provided the most satisfactory results in terms of both quality and quantity of cell impregnation. In order to make comparison with other descriptions of Golgi characteristics of the periaqueductal gray, statistical analysis was carried out on the distinguishing features of individual neurons, following two different rationales. One method, primarily based on soma characteristics (shape, area, length, and width) and basic features of the primary dendrites (number, length, and number of end-points) resulted in nine different categories of neurons being recognized: round, ovoid, spindle, pyriform, triangular, pyramidal, rhomboidal, polygonal, and stellate shaped cells. The alternative method principally characterized neurons by an assessment of the degree of dendritic spine development and prominent features of the dendritic tree (number of primary dendrites, length, number of branches, end-points, and degree of spine development). This approach resulted in nine subgroups within three major classes being identified: three spiny, four moderately spiny, and two aspiny classes (subdivision of each of the groups being resultant on neuronal size and/or the degree of dendritic branching). There was no similarity between the nine groups found by the two methods. Some, though little, correlation of neuron type was evidenced with respect to four zonal subdivisions of the periaqueductal gray complex. It remains to be seen how any of these readily recognizable morphological features, or the subgroups (derived on a statistical basis) into which they fall, might be shown to relate to function.

Animals↗
PubMed1990

Quantitative Nissl study of the neuronal types, and recognition of cytoarchitectural subdivisions, within the rabbit periaqueductal gray.

A quantitative analysis of 4,621 Nissl-stained neurons within the periaqueductal gray of the rabbit found that there were four main cell types (stellate/round, ovoid, spindle, and triangular) distributed throughout this complex. Further statistical analysis on these neurons confirmed that there were morphological grounds to subdivide the periaqueductal gray into four cytologically distinct regions: ventral, lateral, dorsal, and medial. Neurons in the narrow medial zone, which completely surrounds the aqueduct, were orientated essentially parallel to the aqueduct. The majority of these neurons were small, ovoid, or spindle in shape, and highly basophilic. The cells in this region had the lowest packing density of those in any periaqueductal gray subdivision. The dorsal subdivision, a small midline region, contains the largest cells of any division and the highest packing density of glial cells. The neurons in this region show no preference for orientation, tend to be round, and are moderately basophilic. Cells in the lateral zone are also quite large and demonstrate a preferred orientation either parallel or perpendicular to the aqueduct. The average cell density within lateral PAG is considerably higher than in other regions. Most of these neurons are round or ovoid, and moderately basophilic. Neurons in the ventral zone are mainly ovoid, of medium size, highly basophilic, and lie fairly sparsely arrayed and are orientated essentially parallel to the aqueductal surface.

Animals↗
PubMed1986

Autoradiographic study of the distribution of [3H]gamma-aminobutyrate-accumulating neural elements in guinea-pig intestine: evidence for a transmitter function of gamma-aminobutyrate.

High affinity uptake, and the distribution of 3H-radiolabelled gamma-aminobutyrate (GABA), cis-3-aminocyclohexanecarboxylic acid, beta-alanine, proline, and leucine have been examined autoradiographically in laminar preparations of the myenteric plexus from the guinea-pig intestine. Following labelling with [3H]proline and [3H]leucine, which are incorporated into neurons, silver grains were concentrated over recognisable perikarya in the ganglia and meshworks of the plexus, whilst [3H]GABA labelled a smaller proportion of neurons and their processes. Specificity of labelling in the sites of [3H]GABA-uptake was established using combinations of labelled and unlabelled GABA, beta-alanine, and cis-3-aminocyclohexanecarboxylic acid, substrates for glial or neuronal high affinity GABA uptake systems. Only myenteric neurons and their processes were labelled significantly by [3H]GABA and its analogue cis-3-[3H]aminocyclohexanecarboxylic acid. Using autoradiographs of laminar preparations and paraffin sections, [3H]GABA labelling was found over nerve fibre bundles that could be traced from their ganglionic origins through the interconnecting meshworks of the myenteric plexus into the innervation of the deep muscular plexus of the circular muscle layer where GABA is evidently concerned with prejunctional modulation of transmitter release. The extensive but selective distribution of [3H]GABA high affinity uptake sites in neural elements of the guinea-pig myenteric plexus is consistent with GABA being an enteric neurotransmitter.

Alanine↗
PubMed1986

Afferent projections to the periaqueductal gray in the rabbit.

The afferents to the periaqueductal gray in the rabbit have been described following hydraulic pressure injection of horseradish peroxidase at various sites throughout this structure. Every third section was reacted with tetramethylbenzidine, for the localization of afferent neurons. At the site of the deposit alternate sections were reacted with tetramethylbenzidine, Hanker-Yates reagent, or diaminobenzidine, for comparative assessment of the injection site. A large number of retrogradely labelled cells, assessed by bright- and dark-field microscopy, were observed in a wide range of areas throughout the brain. Major labelled areas within the telencephalon were cortical areas 5, 20, 21, 32 and 40. Within the diencephalon, the hypothalamus contained quantitatively by far the largest number of labelled cells. Of these nuclei, the dorsal pre-mammillary nucleus contained the largest number of labelled cells. Considerable labelling was also found within medial and lateral preoptic nuclei, anterior hypothalamic area, and ventromedial hypothalamic nucleus. Another diencephalic region containing a significant number of retrogradely labelled neurons was the zona incerta. At midbrain, pontine and medullary levels, additional labelled regions were: the substantia nigra, cuneiform nucleus, parabigeminal nucleus, raphe magnus, and reticular areas. Heavy labelling was seen within the periaqueductal gray itself, rostral and caudal to deposits placed within each subdivision. In addition, a large number of other areas labelled throughout the brain (Tables 2A-D). Not only were some differences noted in the pattern of labelled cells with deposits placed rostrally or caudally within periaqueductal gray, but certain topographical differences with respect to the degree of labelling within nuclei were also seen with injection sites ventral, lateral or dorsal to the aqueduct. In addition, a further difference was noted, in that over one third of the areas labelled with deposits in just one or other of the "divisions" within periaqueductal gray. The results therefore suggest that the periaqueductal gray might be divisible to some extent on the basis of connectivity with intrinsic subdivisions of the complex. It is hoped that, with time, it might prove possible to resolve any such differential input in functional terms. The wide variety of afferent input to the periaqueductal gray, and its strategic location, would seem to place it in a unique position for integrating and modifying a diversity of motor, autonomic, hormonal, sensory and limbic influences.(ABSTRACT TRUNCATED AT 400 WORDS)

Afferent Pathways↗
PubMed1983

A rabbit head holder for attachment to a conventional stereotaxic machine.

A device is described for holding the head of a rabbit in a stereotaxic apparatus, employing the principle of anchorage by counter thrust applied between orbital clamps and a plate inserted against the upper molars, which bears the weight of the head. Rotation in the sagittal plane is accomplished by pivoting the head-holder assembly on a U-frame which bolts to a conventional stereotaxic machine. Rigid support of the head by this device has been proven in many experiments, and accurate reproducibility of stereotaxic placement of probes with reference to bregma has been confirmed in animals within limited ranges of size.

Animals↗
PubMed1975

Olfactory bulb connections with basal rhinencephalon in the ferret: an evoked potential and neuroanatomical study.

The lateral olfactory tract (LOT) of the ferret has been shown to project to most of the pyriform lobe, as in the cat. Only a small medio-posterior region of the pyriform cortex (the angular cortex), which has a distinctly different appearance in Nissl stained sections, proves to be devoid of olfactory connections. Despite the fact that sub-areas can be recognized within olfactory cortex, there is an underlying constancy in design throughout. Latency measurements indicate that fine collateral branches of theLOT reach the posterior olfactory cortex, whereas mainly larger diameter (faster conducting) fibres comprise the contribution to anterior olfactory cortex. Thus in the present context it is sufficient to recognise just an anterior and posterior subdivisionof olfactory cortex, contingent on the above criterion and correlated with cytoarchitectural features, chiefly variations in cortical layers II and III of the regions concerned. Pyriform cortex directly in receipt of LOT fibres, and associated deeper cortical zones, generated potentials in the olfactory bulbs which can only be attributed to centrifugal input, thus further substantiating an olfactory role for this cortex. In addition, non-cortical regions in receipt of LOT fibres, namely the anterior olfactory nucleus, olfactory tubercle, cortical amygdaloid nucleus and nucleus of the lateral olfactory tract, also contribute centrifugal input to the bulbs. All these regions are thereby capable of providing a rather direct feedback on olfactory bulb activity. The exact pathways concerned have yet to be determined.

Animals↗