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PubMed1997

Needle EMG of the tongue: motor unit action potential versus peak ratio analysis in limb and bulbar onset amyotrophic lateral sclerosis.

OBJECTIVES: To find out if conventional and automatic needle EMG of the tongue can be helpful in the diagnosis and differentiation of limb and bulbar onset amyotrophic lateral sclerosis. METHODS: Motor unit action potential (MUAP) analysis and peak ratio interference pattern analysis were performed in the right genioglossus muscle of 30 healthy subjects aged 30-81 years, 10 patients aged 49-73 years with limb onset amyotrophic lateral sclerosis, and eight patients aged 52-75 years with bulbar onset amyotrophic lateral sclerosis. Electrical activity was sampled via standard concentric needle electrodes with a commercially available EMG recorder. RESULTS: Normal mean (2SD) MUAP duration was 6.6 (1.5) ms. Normal mean (2SD) MUAP amplitude was 224 (97.4) microV. Normal mean (2SD) peak ratio (PR), turns/second (T/s), amplitude/turn (A/T), and time intervals (TI1, TI2, TI3) were 1.68 (0.56), 732 (303.9), 446 (180.3) microV, 2.62 (0.34), 2.31 (0.14), and 1.01 (0.50) respectively. Mean MUAP duration and amplitude were significantly increased in limb onset (P=0.0001 and P=0.013) and bulbar onset amyotrophic lateral sclerosis (P=0.0001 and P=0.017). Peak ratio indices stayed unchanged in limb onset amyotrophic lateral sclerosis but were significantly decreased (PR, T/s, A/T, TI1, and TI2) or increased (TI3) in bulbar onset disease. The sensitivity of the MUAP analysis was 70% in limb and 75% in bulbar onset amyotrophic lateral sclerosis. The sensitivity of the peak ratio interference pattern analysis was 20% in limb and 100% in bulbar onset amyotrophic lateral sclerosis. Subclinical involvement of the tongue was found in 20% of the patients with limb onset amyotrophic lateral sclerosis and could be more accurately assessed with MUAP analysis than with automatic EMG. CONCLUSIONS: Both conventional and automatic needle EMG of the tongue are valuable electrophysiological devices to assess the clinical and subclinical involvement of the tongue in patients with limb and bulbar onset amyotrophic lateral sclerosis.

Action Potentials↗
PubMed2006

Cerebral lateralization and its relationship to phylogeny and aggression in anabantoid fishes.

We examined the relationship between aggression and cerebral lateralization, as expressed by eye-use preference in a mirror-response paradigm, in six species of anabantoid fishes in the teleost family Belontiidae. Our objective was to test the hypothesis that frequency-dependent selection should decrease lateralization at the population level in more aggressive species. The mean laterality index did not differ significantly among the six species, nor did any of the species differ from zero, which suggests that populations of these fishes are neither left- nor right-eye biased. In spite of species differences in aggressive behavior, there was no relationship between population-level laterality and aggression as we had originally predicted. The degree of individual lateralization did differ significantly among some species. A phylogenetic generalized least squares (PGLS) analysis showed that these species differences were not due to phylogenetic distance. Individual laterality was also unrelated to aggression. Fishes in the genus Betta were the most individually lateralized, but varied in the intensity of aggressive behavior they displayed toward the mirrors. Taxa such as paradise fish (Macropodus opercularis and Pseudosphromenus dayi) were intermediate in eye-use preferences and gourami (Trichogaster trichopterus) displayed little cerebral lateralization. We also used the PGLS method to reconstruct ancestral values for individual lateralization in this group of fishes, from which we conclude that the ancestral condition was one of low variance in eye-use preference.

Aggression↗
PubMed2005

Identifying the primary epileptogenic hemisphere from electroencephalographic (EEG) and magnetoencephalographic dipole lateralizations in children with intractable epilepsy.

We used electroencephalographic (EEG) and magnetoencephalographic dipole lateralizations to identify the primary epileptogenic hemisphere in 41 children with intractable localization-related epilepsy. We compared EEG and magnetoencephalographic dipole lateralizations, EEG ictal onsets, and magnetic resonance images (MRIs). Concordant lateralization of EEG and magnetoencephalographic dipoles (> 50% of each lateralizing to the same hemisphere) occurred in 34 patients, with EEG ictal onsets in the same hemisphere in 23 (68%) and concordant MRI lesions in 23 (68%). Focal resection in 16 of 20 patients resulted in a good surgical outcome. Of the seven children with nonconcordant magnetoencephalographic and EEG lateralizations, one (14%) had EEG ictal onset and one (14%) had MRI lesions that lateralized; none had surgery. The relationship between lateralized EEG and magnetoencephalographic dipoles forecasts surgical candidacy. Concordant lateralizations predict good seizure control after surgery by identifying the primary epileptogenic hemisphere. Discordant lateralizations signify an undetermined epileptogenic hemisphere and contraindicate surgery without further testing.

Child↗
PubMed2002

Functional and postural lateral preferences in humans: interrelations and life-span age differences.

This study aimed to provide data on lateral preferences among older subjects, to analyze age differences, and to determine interrelations between lateral preferences. Four functional preferences (handedness, footedness, eyedness, earedness) and three postural lateral preferences (hand-clasping, arm-folding, leg-crossing) were assessed in 628 Germans (252 men, 376 women) aged between 19 and 90 years. Sex differences, age differences, and associations between lateralities were analyzed applying chi-square tests. Logistic regression analyses considering age, sex, and interactions between variables were applied to analyze combined effects on laterality measures. Right-sided preference for handedness, footedness, eyedness, earedness, and leg-crossing characterized 86.8%, 77.1%, 70.9%, 67.8%, and 56.6%, respectively, of subjects, while a left-sided preference for hand-clasping and arm-folding characterized 56.4% and 60.2%, respectively, of all participants. Results are within the range of other populations. Only footedness differed between the sexes: there were more left-footed men. Older cohorts showed a rightward shift in handedness, eyedness, earedness, and leg-crossing, the opposite for arm-folding. No age-related differences exist in footedness or hand-clasping. Logistic regression models indicate no interaction between age and sex for each laterality measure. The four functional lateralities are significantly interrelated. All also are positively associated with leg-crossing. Conversely, the postural lateralities generally are not correlated, although leg-crossing and arm-folding are, inversely. The observed relationships among lateralities support the hypothesis that handedness, footedness, leg-crossing, and earedness might be aspects of a larger phenotype that is independent of hand-clasping and arm-folding.

Adult↗
PubMed2000

Psychophysics of taste lateralization on anterior tongue.

There have been very few investigations of the spatial properties of taste stimuli localized to specific areas of the oral cavity. This is surprising, since the spatial localization of taste sensations may contribute to the overall taste percept, much as do quality, intensity, and the temporal characteristics of tastes. The difficulty in eliminating the confounding factor of a tactile sensation may partially account for the paucity of such studies, since a gustatory stimulus cannot be presented as a liquid without a tactile component. As a step toward understanding the localizability of gustatory sensations, we designed a yoked stimulator and an experimental procedure to control for tactile cues. Lateral discrimination was evaluated at the tip of the tongue with four taste stimuli (sodium saccharin, sodium chloride, citric acid, and quinine hydrochloride) by presenting a taste and a blank solution simultaneously at two locations on the tongue. We found that subjects could lateralize all four taste stimuli in the absence of any discriminative tactile cues. Subjects' ability to lateralize varied as a psychometric function of the stimulus concentration. Detection thresholds, measured in a forced-choice two-interval staircase procedure with the same yoked stimulator that was used in the lateralization task, were always lower than lateralization thresholds, and both lateralization and detection thresholds were correlated within subjects. Subjects were unable to lateralize taste cues on a nongustatory surface under the upper lip at the highest tested concentrations, at which performance was 100% on a gustatory surface (dorsal anterior tongue). These results show that (1) taste compounds can be lateralized in the absence of any discriminative mechanical cue (but only on the gustatory epithelium) and (2) although the localization of a compound does not logically require conscious detection of the taste (cf. blind sight), subjects always detected a taste when they were able to lateralize.

Adult↗
PubMedDate not supplied

A molecular genetic approach to amyotrophic lateral sclerosis.

Disorders of the motor neurons may affect both the upper and lower neurons, primarily the lower motor neurons as in the spinal muscular atrophies are primarily the upper motor neurons as in the familial spastic paraplegias. Amyotrophic lateral sclerosis is a degenerative disorder of the motor neuron that results in paralysis and wasting of voluntary muscles. Large motor neurons in the cerebral cortex, brain stem and spinal cord degenerate or are lost. Hyaline inclusions may be seen in the cytoplasm of surviving motor neurons. Acute axonal degeneration of peripheral motor fibers occurs at all levels, including the distal axon. Subclinical involvement of the spinecerebellar tracts, posterior column and Clarke's column as well as loss of large neurons in the dorsal root ganglia and neurons of oculomotor nuclei has been reported. The average duration of life onset of symptoms of amyotrophic lateral sclerosis is three years and ninety per cent of patients died within 5 years. The basic mechanism of disease in amyotrophic lateral sclerosis remains unknown. There is no known treatment that will prevent, reverse or otherwise alter the course of the disease. Autosomal dominant and autosomal recessive forms of amyotrophic lateral sclerosis are genetic models of amyotrophic lateral sclerosis which may provide insight into the disease mechanism of sporadic amyotrophic lateral sclerosis, five to ten percent of adult cases of amyotrophic lateral sclerosis with early onset of symptoms and a more benign course. It is conceivable that both genetic and sporadic forms of amyotrophic lateral sclerosis result from failure of the same or similar neuronal mechanism triggered by defective genes and by an environment agent in sporadic amyotrophic lateral sclerosis.

Amyotrophic Lateral Sclerosis↗
PubMed1989

[Motor and sensory laterality in the population of Prague].

Laterality is a developmental (not pathological) deviation in shape functional symmetry of paired motor and sensory organs. As it is one of the most specific features of the human being, great attention is paid to it during recent decades. These problems are important also form the point of view of findings of laterality changes in schizophrenics. The authors present results of examination of a normal Prague population sample. The estimated data on stratification of laterality findings in this group may serve as standard control figures for comparison and evaluation of findings in various defects and illnesses. 754 Prague blood donors (367 males and 387 females) aged 18-60 years (mean age 31.1 years) were examined. Probands in whom it could be the case of either pathological or out of necessity laterality or who had a history of mental disease were not included in this population. The motor (hand, foot) and sensory (eye, ear) phenotype of the probands were ascertained using Matĕjcek and Zlab test (8) which was expanded by several important operations. Moreover, the examination was supplemented by aimed questions on some operations. The total numbers found in this population were following: 74% of right-handed, 13.9% of ambidextrous and 12% of left-handed individuals. As for the motor laterality of the lower limbs, an ambiguous laterality of the foot is present more frequently (34.9%), right laterality in 56.9% and left only in 8.2%. The sensory left-sided laterality is generally higher than the motor left-sided laterality--left-sided vision in 26.7% and left-sided hearing in 23.3%.(ABSTRACT TRUNCATED AT 250 WORDS)

Adolescent↗
PubMed1999

Synaptic targets of cholinergic terminals in the cat lateral posterior nucleus.

We examined profiles in the neuropil of the lateral division of the lateral posterior (LP) nucleus of the cat stained with antibodies against choline acetyl transferase (ChAT) or gamma-aminobutyric acid (GABA), and several differences in the synaptic circuitry of the lateral LP nucleus compared with the pulvinar nucleus and lateral geniculate nucleus (LGN) were identified. In the lateral LP nucleus, there are fewer glomerular arrangements, fewer GABAergic terminals, and fewer cholinergic terminals. Correspondingly, the neuropil of the lateral LP nucleus appears to be composed of a higher percentage of small type I cortical terminals (RS profiles). Similar to the pulvinar nucleus and the LGN, the cholinergic terminals present in the lateral LP nucleus contact both GABA-negative profiles (thalamocortical cells; 74%) and GABA-positive profiles (interneurons; 26%). However, in contrast to the pulvinar nucleus and the LGN, the majority of cholinergic terminals in the lateral LP nucleus contact small-caliber dendritic shafts outside of glomeruli (60 of 82; 73%). Consequently, most cholinergic terminals are in close proximity to RS profiles. Therefore, whereas the cholinergic input to the LGN and pulvinar nucleus appears to be positioned to selectively influence the response of thalamocortical cells to terminals that innervate glomeruli (retinal terminals or large type II cortical terminals), the cholinergic input to the lateral LP nucleus may function primarily in the modulation of responses to terminals that innervate distal dendrites (small type I cortical terminals).

Animals↗
PubMed1980

An electromyographic study of the human lateral pterygoid muscles.

An electromyographic investigation of the lateral pterygoid muscles was undertaken to determine their activity relative to isolated and functional movements of the mandible. Daerally in the lateral and medial pterygoid muscles. Surface electrodes were placed bilaterally on the skin over the temporalis and masseter muscles. Our data strongly suggest that separate roles for the superior and inferior heads of the lateral pterygoid cannot be supported electromyographically. In addition, the lateral pterygoid is active in protrusive movements, including an incisor clench, and not active in retrusion or a molar clench. Both lateral pterygoid muscles initiate depression of the mandible and the contralateral muscle initiates a lateral transversion. The ipsilateral activity present is not sufficient to be an active stabilizer of the temporomandibular joint. In the chewing cycle, the lateral pterygoids are bilaterally active, both in alternation with and overlapping the elevating musculature. The sequence of the lateral pterygoid activity in the chewing cycle is led by the ipsilateral lateral pterygoid muscle.

Adult↗
PubMed2004

Fiber connections of the lateral valvular nucleus in a percomorph teleost, tilapia (Oreochromis niloticus).

Fiber connections of the lateral valvular nucleus were investigated in a percomorph teleost, the tilapia (Oreochromis niloticus), by tract-tracing methods. Following tracer injections into the lateral valvular nucleus, neurons were labeled in the ipsilateral dorsal part of dorsal telencephalic area, corpus glomerulosum pars anterior, dorsomedial thalamic nucleus, central nucleus of the inferior lobe, mammillary body, semicircular torus, valvular and cerebellar corpus, in the bilateral rostral regions of the central part of dorsal telencephalic area, dorsal region of the medial part of dorsal telencephalic area, habenula, anterior tuberal nucleus, posterior tuberal nucleus, and spinal cord, and in the contralateral lateral funicular nucleus. Labeled fibers and terminals were found in the ipsilateral cerebellar corpus and bilateral valvula of the cerebellum. Tracers were injected into portions of the telencephalon, pretectum, inferior lobe, and cerebellum to confirm reciprocally connections with the lateral valvular nucleus and to determine afferent terminal morphology in the lateral valvular nucleus. Telencephalic fibers terminated mainly in a dorsolateral portion of the lateral valvular nucleus. Terminals from the corpus glomerulosum pars anterior, central nucleus of the inferior lobe, and mammillary body showed more diffuse distributions and were not confined to particular portions of the lateral valvular nucleus. Labeled terminals in the lateral valvular nucleus were cup-shaped or of beaded morphology. These results indicate that the lateral valvular nucleus receives projections from various sources including the telencephalon, pretectum, and inferior lobe to relay information to the valvular and cerebellar corpus. In addition, the corpus glomerulosum pars anterior in tilapia is considered to be homologous to the magnocellular part of superficial pretectal nucleus in cyprinids.

Animals↗
PubMed1977

Distinct auditory and lateral line nuclei in the midbrain catfishes.

The catfish torus semicircularis (TS) comprises two major nuclei, which are specialized to process separately inputs of three acousticolateral modalities: VIII nerve acoustic input in one, and lateral line mechanoreceptive and electroreceptive input in the other. Electrophysiological recording and mapping experiments demonstrate a medial auditory region, a lateral electroreceptive region, and an intercalated mechanoreceptive region in the TS Nissl and Golgi-Cox preparations distinguished two rostrocaudally elongate, nuclear divisions, which correlate, one with the auditory and the other with the mechano- and electroreceptive regions. The medially positioned auditory nucleus is here called the nucleus centralis. The nucleus centralis appears as a rostrally flattened cylinder of uniformly packed cells, covered dorsally and laterally by a fiber rind. Cells within this nucleus conform to one of three general cell types based upon somatic and dendritic morphology: type 1 cells, which are the most abundant" have a single major primary dendrite and an axon typically arising from the same somatic pole; type 2 cells have two major primary dendrites and an axon, which issues from a third distinct somatic pole; and type 3 cells have several major primary dendrites and their axons are associated with one of the major somatic poles. No systematic orientation of dendrites could be found in the nucleus centralis. The laterally positioned lateral line nucleus, to be called the nucleus lateralis, includes two subdivisions: a large pars lateralis containing predominantly electroreceptive units, and a smaller, ventromedial pars medialis encompassing predominantly mechanoreceptive units. Each subdivision is found to be somatotopically organized, inputs from the head projecting to rostral areas and inputs from the tail to caudal areas. Although the cell types resemble those described for the nucleus centralis, a greater degree of cytoarchitectural orderliness is discernible: (a) cells in the nucleus lateralis group into four, alternating cell-poor cell-rich, layers; and (b) the dendritic fields of many type 1 and type 2 cells located in layer II tend to orient in a rostrodorsal-caudoventral attitude, perpendicular to the laminar planes. Fink-Heimer preparations of brains with unilateral, lateral line lobe lesions demonstrate heavy fiber and terminal degeneration confined to the nucleus lateralis on both sides. Lateral line fibers ascend bilaterally in the lateral halves of the lateral lemnisci. At the level of the dorsal oculomotor nucleus the lemniscal fibers in this portion split into two fascicles, one proceeding rostrally to innervate the rostral portion of the nucleus lateralis, and the other arching back dorsolaterally to innervate the caudal portions of the nucleus.

Animals↗
PubMed1981

Projections from visual areas of the middle suprasylvian sulcus onto the lateral posterior complex and adjacent thalamic nuclei in cat.

The distribution of corticothalamic projections from lateral suprasylvian areas AMLS, PMLS, ALLS, and PLLS was investigated with the autoradiographic method. Areas AMLS and PMLS were both found to project retinotopically upon the medial interlaminar nucleus and the lateral and pulvinar zones of the lateral posterior complex, as well as to the ventral lateral geniculate nucleus, intralaminar nuclei, and thalamic reticular complex. Retinotopic projections to the dorsal lateral geniculate nucleus were demonstrated from PMLS but not AMLS, and projections to zona incerta were demonstrated from AMLS but not PMLS. Areas PLLS and ALLS were both found to project retinotopically upon the interjacent zone of the lateral posterior complex, as well as to the intermediate and suprageniculate divisions of the posterior nuclear group, the magnocellular division of the medial geniculate complex, the thalamic reticular complex, and central lateral nucleus. Area ALLS was also found to project onto the dorsal division of the medial geniculate complex and lateral division of the posterior nuclear group. Differences between the four cortical areas in the pattern and density of their thalamic projections supports the parcellation of these areas as proposed by Palmer et al. ('78). The projection patterns of areas PMLS, AMLS, PLLS, and ALLS were found to respect the boundaries of the zones of the lateral posterior complex, which had been identified and defined previously (Updyke, '77), and the results thus support the hypothesis that these zones are the functional units of organization of visual traffic between the cat's extrastriate visual areas.

Animals↗
PubMed1983

A cobalt study of medullary sensory projections from lateral line nerves, associated cutaneous nerves, and the VIIIth nerve in adult Xenopus.

The medullary projections of the anterior lateral line nerve, dorsal branch (Alln.d), the posterior lateral line nerve, dorsal branch (PLLn.d), associated cutaneous nerves, and the VIIIth nerve in Xenopus laevis have been delineated by axonal infusion of cobalt chloride and silver intensification. The peripheral innervation of the posterior lateral line sense organs has also been traced. From wholemount and sectioned preparations, we describe three central projections, extending the length of the ipsilateral medulla but occupying distinct zones: lateral line afferents dorsomedially, stato-acoustic dorsolaterally, and cutaneous ventrolaterally. Arborizations of ALLn.d and PLLn.d afferents are morphologically similar, intermingling throughout the lateral line lobe. Each divides into ascending and descending limbs bearing collaterals, which terminate in the lateral line neuropile and nucleus. Evidence is presented for directional and positional mapping in the branching of individual PLLn.d afferents and for topography in the ALLn.d projection. Second-order neurones have been identified by transneuronal staining and their axons traced into the contralateral torus semicircularis. The morphology of efferent neurones is also described. Rostral branches of PLLn.d also contain cutaneous afferents which run through the medulla into the spinal cord, similar to the nerve V (cutaneous) projection. In nerve VIII preparations, the projection to the compact cochlear nucleus and the massive vestibular projection are identified. Cutaneous and vestibular but not lateral line afferents extend into the cerebellum. The separation of VIIIth nerve and lateral line afferents in Xenopus medulla is considered as evidence against the validity of the acousticolateralis concept. Information processing in the lateral line lobe is discussed in relation to connectivity patterns between first- and second-order neurones.

Afferent Pathways↗
PubMed1987

Organization of subcortical pathways for sensory projections to the limbic cortex. II. Afferent projections to the thalamic lateral dorsal nucleus in the rat.

Afferent projections to the thalamic lateral dorsal nucleus were examined in the rat by the use of retrograde axonal transport techniques. Small iontophoretic injections of horseradish peroxidase were placed at various locations within the lateral dorsal nucleus, and the location and morphology of cells of origin of afferent projections were identified by retrograde labeling. For all cases examined, subcortical retrogradely labeled neurons were most prominent in the pretectal complex, the intermediate layers of the superior colliculus, and the ventral lateral geniculate nucleus. Labeled cells were also seen in the thalamic reticular nucleus and the zona incerta. Within the cerebral cortex, labeled cells were prominent in the retrosplenial areas (areas 29b, 29c, and 29d) and the presubiculum. Labeled cells were also seen in areas 17 and 18 of occipital cortex. Peroxidase injections in the dorsal lateral part of the lateral dorsal nucleus result in labeled neurons in all of the ipsilateral pretectal nuclei, but especially those that receive direct retinal afferents. Labeled cells were also seen in the ventral lateral geniculate nucleus and the rostral tip of laminae IV-VI of the superior colliculus. In contrast, peroxidase injections in ventral medial portions of the lateral dorsal nucleus result in fewer labeled pretectal cells, and these labeled cells are found exclusively in the pretectal nuclei that do not receive retinal afferents. Other labeled cells following injections in the rostral and medial portions of the lateral dorsal nucleus are seen contralaterally in the medial pretectal region and nucleus of the posterior commissure, and bilaterally in the rostral tips of laminae IV and V of the superior colliculus. Camera lucida drawings of HRP labeled cells reveal that projecting cells in each pretectal nucleus have a characteristic soma size and dendritic branching pattern. These results are discussed with regard to the type of sensory information that may reach the lateral dorsal nucleus and then be relayed on to the medial limbic cortex.

Afferent Pathways↗
PubMed1988

Intrinsic connections of the retrohippocampal region in the rat brain: III. The lateral entorhinal area.

This paper describes the retrohippocampal projections of individual layers of the lateral entorhinal area as studied by the method of anterograde transport of the lectin Phaseolus vulgaris leucoagglutinin (PHA-L) in the rat. As in the medial entorhinal area (EA), (Köhler, '86a) PHA-L injections restricted to individual layers of the lateral EA resulted in labeling of sparse projections to the subicular complex (e.g., subiculum, pre- and parasubiculum), whereas projections to the perirhinal area and piriform cortex were prominent. All PHA-L injections resulted in the labeling of axons projecting longitudinally within the entorhinal area, in both dorsal and ventral directions, albeit the ventral projections were the most prominent ones. PHA-L injections into layers 2a and 2b resulted in labeling of axons that could be followed into layers 2a, 2b, and layer 1 on both sides of the injection site. Whereas numerous axons appeared to terminate in layer 2, most fibers ascended into layer 1, where they ran in a medial direction, passing the medial EA, around the parasubiculum to the presubiculum. Numerous axons were found to take a lateral route running past the lateral aspect of the lateral EA to the piriform cortex. The axons running medial in layer 2 did not enter the medial EA. After PHA-L injections into layer 3, a large number of axons left the labeled cells on both sides of the injection site, in addition to massive projections that ascended into layers 2b, 2a and 1, just above the injection. Few axons entered layers 2-6 of the medial EA, but numerous axons innervated layer 1, where they were found to run in the outer half of this layer. The axons running in a medial direction reached layer 1 of the presubiculum, whereas the laterally oriented ones innervated the molecular layer of the piriform cortex. PHA-L injections into layer 4 resulted in massive labeling of projections to all superficially located layers. Layers 1, and 2b through 5 were innervated lateral to, and layer 4 medial to, the injection site. After a PHA-L injection into layer 5, ascending projections were found innervating layers 1 through 4. The terminal fields were found to be particularly dense in the deep parts of layer 3 and in layer 1. This projection expanded laterally, but few projections reached into the medial sector of the lateral EA or into the medial EA.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1989

Somatotopic organization of the lateral sulcus of owl monkeys: area 3b, S-II, and a ventral somatosensory area.

Multiunit microelectrode recordings and injections of horseradish peroxidase (HRP) were used to reveal neuron response properties, somatotopic organization, and interconnections of somatosensory cortex in the lateral sulcus (sylvian fissure) of New World owl monkeys. There were a number of main findings. 1) Representations of the face and head in areas 3b, 1, and S-II are found on the upper bank of the lateral sulcus. Most of the mouth and lip representations of area 3b were found in a rostral extension along the lip of the lateral sulcus. Adjacent cortex deeper in the lateral sulcus represented the nose, eye, ear, and scalp. 2) S-II was located on the upper bank of the lateral sulcus and extended past the fundus onto the deepest part of the lower bank. The face was represented most superficially in the sulcus, with the hand, foot, and trunk located in a rostrocaudal sequence deeper in the sulcus. The orientation of S-II is "erect," with the limbs pointing away from area 3b. 3) Neurons in S-II were activated by light tactile stimulation of the contralateral body surface. Receptive fields were several times larger than for area 3b neurons. 4) A 1-2-mm strip of cortex separating the face and hand representations in S-II was consistently responsive to the stimulation of deep receptors but was unresponsive to light cutaneous stimulation. 5) Injections of horseradish peroxidase in the electrophysiologically identified hand or foot representations of area 3b revealed somatotopically matched interconnections with mapped hand and foot representations in S-II. 6) A systematic representation of the body, termed the "ventral somatic" area, VS, was found extending laterally from S-II on the lower bank of the lateral sulcus. Within VS, the hand and foot were represented deep in the sulcus along the hand and foot regions of S-II, and the face was lateral near the ventral lip of the sulcus. 7) Neurons at most recording sites in the VS region were activated by contralateral cutaneous stimuli. However, a few sites had neurons with bilateral receptive fields. Receptive field sizes were comparable to those in S-II. In addition, neurons in islands of cortex in the VS region had properties that suggested that they were activated by pacinian receptors, while other regions were difficult to activate by light tactile stimuli but responded to stimuli that would activate deep receptors. 8) A few recording sites caudal to S-II on the upper bank of the lateral sulcus were responsive to somatic stimuli.(ABSTRACT TRUNCATED AT 400 WORDS)

Afferent Pathways↗
PubMed1989

Immunoreactivity in Limulus: III. Morphological and biochemical studies of FMRFamide-like immunoreactivity and colocalized substance P-like immunoreactivity in the brain and lateral eye.

FMRFamide-like immunoreactivity (FLI) and the colocalization of FMRFamide and substance P-like (SPLI) immunoreactivities were examined in the brain and lateral eye of the horseshoe crab with FITC- and TRITC-labeled secondary antibody techniques. In the brain, fibers with FLI were localized in the neuropils of the lamina, medulla, central body, corpus pedunculatum, optic tract, circumesophageal connective, and central neuropil. An extensive network of reactive fibers innervatives the brain's vascular sheath. Somata with FLI were found in the dorsal medial group, dorsal lateral posterior groups #1 and #2, and ventral posterior lateral groups #1 and #2. Several distinct subgroups of reactive somata were noted in both the medullar and ventral medial groups. The distribution of fibers in the brain with colocalized FLI and SPLI includes those which innervate the vascular sheath and widespread populations of small-diameter beaded fibers in the central neuropil and circumesophageal connective. Somata with colocalized FLI and SPLI constitute minority populations in the medullar and dorsal medial groups but form the majority population of a subgroup in the ventral medial group. Overall localization of SPLI was reevaluated and is reported here according to the nomenclature of the new Chamberlain and Wyse brain atlas. In addition to those previously reported, somata with SPLI were found in the dorsal lateral posterior groups #1 and #2, the ventral lateral posterior groups #1 and #2, and several distinct subgroups of the medial and ventral medial groups. In the retina of the lateral eye, fibers with both FLI and SPLI ramify in the lateral plexus and ultimately innervate the corneal epidermis. Brain homogenates were examined for immunoreactive (ir) FMRFamide and ir-substance P with radioimmunoassay techniques. Ir-FMRFamide and ir-substance P eluted in different fractions from both gel filtration chromatography and HPLC. Furthermore, the binding curves for both substances were similar to those of the corresponding synthetic compounds. Brain homogenates were also bioassayed on the lateral eye. Three gel filtration fractions mimic natural circadian activity by increasing the sensitivity of the lateral eye, but they were not coincident with ir-FMRFamide or ir-substance P. Although it is not completely resolved what the active molecules in these fractions are, it is clear that neither ir-FMRFamide nor ir-substance P is a possible candidate.

Animals↗
PubMed1990

Projections from the lateral geniculate nucleus to the hypothalamus of the Mongolian gerbil (Meriones unguiculatus): an anterograde and retrograde tracing study.

The lateral geniculate nucleus of the thalamus sends efferents to the hypothalamic suprachiasmatic nucleus, which is involved in generation and entrainment of several circadian rhythms. It seems reasonable to believe that the lateral geniculate conveys visual information about the length of the photoperiod to the circadian oscillator. In order to study in more detail the topographical relationship between the lateral geniculate and the suprachiasmatic nucleus, anterograde tracing with Phaseolus vulgaris leucoagglutinin (PHA-L) and retrograde tracing with wheatgerm agglutinin coupled to horseradish peroxidase (WGA-HRP) were performed in the gerbil. After iontophoretic injections of PHA-L in the lateral geniculate, a large number of PHA-L-immunoreactive fibers and nerve terminals were observed in the ventrolateral part of the suprachiasmatic nucleus. Nerve fibers were also present in the ventromedial and dorsolateral portions, particularly in the caudal half of the nucleus. PHA-L-immunoreactive nerve fibers continued outside the borders of the suprachiasmatic nucleus to the adjacent anterior hypothalamic, the periventricular, and the subparaventricular areas. A moderate number of fibers entered the lateral hypothalamic area and the tuber cinerum via the optic tract and chiasm. Moreover, the paraventricular nucleus, the supraoptic nucleus, the medial preoptic area, the lateral preoptic area, and the supramammillary nucleus contained a few labeled fibers. In all parts of the hypothalamus receiving an input from the lateral geniculate, fine beaded immunoreactive fibers with varicosities and nerve terminals were observed, some of which were found in close apposition to hypothalamic neurons. Only after labeling of neurons in the intergeniculate leaflet of the lateral geniculate nucleus, fibers were found in the hypothalamus. This topographical organization of the geniculohypothalamic pathway was supported by retrograde tracing after injections of WGA-HRP in the suprachiasmatic area. In these experiments, retrograde labeled neurons were observed in the intergeniculate leaflet and, in agreement with the anterograde studies, most of labeling was observed in the ipsilateral side. These results confirm that the suprachiasmatic nucleus receives a substantial input from the intergeniculate leaflet of the lateral geniculate. Moreover, the present data demonstrate that the suprachiasmatic nucleus is not the only nucleus that receives a direct visual input. Thus other hypothalamic areas might be influenced by a direct rhythmic neuronal input as well.

Animals↗