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Central connections of the IXth and Xth cranial nerves in the clearnose skate, Raja eglanteria.

The anterograde and retrograde transport of horseradish peroxidase was utilized to identify the motor nuclei and sensory connections of the IXth and Xth cranial nerves in the clearnose skate, Raja eglanteria. The majority of VIIth, IXth, and Xth nerve motoneurons form an ipsilateral dorsal visceromotor column, extending from the level of the posterior lateral line nerve root to the 3rd-4th ventral spinal roots. Within this column, the motor nucleus of IX (IXm) occurs rostral to vagal motoneurons (dorsal motor nucleus of X, Xmd). Vagal motoneurons are also located ventrolaterally in a ventral motor nucleus (Xmv), which extends from the level of the middle vagal rootlets to the 5th-6th ventral spinal roots. IXth and Xth nerve afferents terminate predominantly in the ipsilateral visceral sensory column (vS). Many vagal but few glossopharyngeal afferents form a solitary tract. A distinct nucleus of the solitary tract could not be identified; rather fibers terminate among cells scattered in the tract, adjacent vS, and nucleus of the commissura infima, where some vagal fibers decussate. Vagal and glossopharyngeal somatic sensory fibers were not found.

Afferent Pathways↗

Increase of enkephalin and decrease of substance P immunoreactivity in the dorsal and ventral striatum of the rat after midbrain 6-hydroxydopamine lesions.

Unilateral 6-hydroxydopamine lesions of the mesostriatal dopaminergic system in the rat resulted in a decrease of substance P-immunoreactivity in the ventral striatum, and in a heterogeneously distributed increase of enkephalin-immunoreactivity in the dorsal and ventral striatum and the globus pallidus. The respective decrease and increase are caused by a lower or higher staining intensity of the peptidergic fibers, whereas no changes were found in the cell bodies.

Afferent Pathways↗

Efferent connections from the anterior pretectal nucleus to the diencephalon and mesencephalon in the rat.

The anterior pretectal nucleus has been described as part of the visual pretectal complex. However, several electrophysiological and behavioural studies showed that this area is involved in somatosensory modulation, more specifically, antinociception. The efferents of the anterior pretectal nucleus have not been identified taking into account the different function of this nucleus in relation to the rest of the pretectal complex. In the study herein described, a sensitive anterograde tracer Phaseolus vulgaris leucoagglutinin was used to trace the mesencephalic and diencephalic efferents of the anterior pretectal nucleus in the rat. The majority of the connections were ipsilateral. Fibres with varicosities were observed in discrete areas of the thalamus (central lateral, posterior complex), hypothalamus (lateral, posterior and ventromedial), zona incerta, parvocellular red nucleus, intermediate and deep layers of the superior colliculus, central grey, deep mesencephalon, pontine parabrachial region, and pontine nuclei. Fibres en passant were detected in the medial lemniscus, from the level of the injection site to rostral medullary levels. Some labelled axons were seen coursing to the contralateral side through the posterior commissure and the decussation of the superior cerebellar peduncle. These results show that the anterior pretectal nucleus projects principally to areas involved in somatosensory and motor control in a manner that permits sensory modulation at higher and lower levels of the brain. These connections may explain the antinociceptive and antiaversive effects of stimulating the anterior pretectal nucleus in freely moving animals.

Animals↗

Electrophysiologic evidence of regeneration of lamprey spinal neurons.

Morphologic evidence has shown that the anteriorly projecting axons of giant interneurons (GIs) can regenerate after spinal transection in larval sea lampreys (19). In the present study, we showed that the regenerating neurites of GIs were electrically excitable. We also showed evidence for regeneration of descending afferent connections to GIs. Spinal cords were transected at the level of the cloaca. After at least 70 days recovery, GIs located 1.5 to 17.0 mm below the scar were impaled with microelectrodes. Stimulating electrodes were placed at various distances above the scar. Six of 13 GIs located 4 to 17 mm below the scar could be activated antidromically. For 1 GI, the rostralmost point of stimulation which elicited these responses was 13.5 mm above the scar. For the others, the range was 0.5 to 4.5 mm. Estimated average conduction velocity in regenerated neurites was 0.50 m/s compared with 1.94 m/s for the parent axon. Twelve GIs could be orthodromically activated by fixed-latency EPSPs. The most rostral point of stimulation that could elicit such responses was 0.5 to 8.5 mm above the scar. There was an inverse relationship between the farthest distance of stimulation and the distance of the GI from the scar. These findings are consistent with the hypothesis that regeneration of axons across a spinal transection is limited to neurons whose cell bodies are situated within 1 to 2 cm from the transection, and that regenerating neurites grow only a few millimeters beyond the scar.

Afferent Pathways↗

The origin of symptoms on the brain-gut axis in functional dyspepsia.

It was hypothesized that symptoms in functional dyspepsia are originated by an altered mechanism at the brain-gut axis (one or several) in the process of gastric accommodation to a meal. To test the key mechanisms potentially involved in symptomatic gastric accommodation, the sensorial responses (on a 0-10 perception score) and the gastric tone responses (by electronic barostat) to either gastric accommodation (n = 10) or to cold stress (n = 10) were measured in 20 patients with functional dyspepsia and 20 healthy controls. The mechanical accommodation of the stomach to gastric distention (compliance) was similar in patients (52 +/- 8 mL/mm Hg) and controls (57 +/- 6 mL/mm Hg). However, isobaric gastric distention elicited more upper abdominal discomfort in dyspeptics than in controls (perception scores, 4.7 +/- 0.9 vs. 1.1 +/- 0.5, respectively; mean +/- SE; P less than 0.005). Cold stress induced a similar gastric relaxatory response in dyspeptics and controls (delta vol, 145 mL +/- 40 mL vs. 141 mL +/- 42 mL, respectively); hand perception (scores, 8.3 +/- 0.4 vs. 7.9 +/- 0.4, respectively) and autonomic responses were also similar. It is concluded that an abnormal afferent sensorial pathway (altered gastric perception) may be a major mechanism of symptom production in functional dyspepsia.

Adult↗

A functional hypothesis concerning the striatal matrix and patches: mediation of S-R memory and reward.

Recent neurochemical and anatomical findings delineating two compartments, the patches and the matrix, in the mammalian striatum, are described. Anatomical and neurochemical aspects of manipulations affecting behaviors related to S-R memory and reward correspond in certain respects to the features of these striatal compartments. These coincidences lead to an hypothesis concerning the function of the striatal compartments and their participation in neural systems controlling both immediate and learned behaviors.

Afferent Pathways↗

The organization of noradrenergic pathways from the brainstem to the paraventricular and supraoptic nuclei in the rat.

Axonal transport and immunohistochemical methods have been used to clarify the organization of pathways from noradrenergic and adrenergic cell groups in the brainstem to the paraventricular (PVH) and supraoptic (SO) nuclei of the hypothalamus. First, the location of such cells was determined with a combined retrograde tracer-immunofluorescence method. The fluorescent tracer, True Blue, was injected into the PVH or the SO, and sections through the brainstem were stained with anti-(rat) DBH, a specific marker for noradrenergic and adrenergic neurons. It was found that, after injections in the PVH, doubly labeled neurons were confined almost exclusively to 3 cell groups, the A1 region of the ventral medulla, which contained a majority of such cells, the A2 region in the dorsal vagal complex, and the locus coeruleus (A6 region). After injections centered in the SO an even greater proportion of doubly labeled cells were found in the A1 region, although some were also found in the A2 and A6 regions. The topography of doubly labeled cells indicates that these projections arise primarily from noradrenergic neurons, although adrenergic cells in both the C1 and the C2 groups probably contribute as well. Because well over 80% of the retrogradely labeled cells in these three regions were also DBH-positive, we next placed injections of [3H]amino acids into each of them in different groups of animals, and traced the course and distribution of the ascending (presumably DBH-positive) projections to the PVH and SO in the resulting autoradiograms. Injections centered in the A1 region labeled a substantial projection to most parts of the parvocellular division of the PVH, and was most dense in the dorsal and medial parts. In addition, terminal fields were labeled on those parts of the magnocellular division of the PVH, and of the SO, in which vasopressinergic cell bodies are concentrated. Injections centered in the A2 region also labeled a projection to the parvocellular division of the PVH that was topographically similar, but less dense, than that from the A1 region. In contrast, [3H]amino acid injections centered in the locus coeruleus labeled a moderately dense projection to the PVH that was limited to the medialmost part of the parvocellular division. Neither the A2 nor the A6 cell groups project to the magnocellular parts of PVH, or to the SO. The autoradiographic material, and additional double-labeling experiments, were used to identify and to characterize projections that interconnect the A1, A2 and A6 regions, as well as possible projections from these cell groups to the spinal cord. These results may be summarized as follows: a substantial projection from the nucleus of the solitary tract to the A1 region was identified, but this pathway does not arise from catecholaminergic neurons in the A2 cell group. DBH-stained cells in the A1 region project back to the dorsal vagal complex, as well as quite massively to the locus coeruleus (A6 region)...

Afferent Pathways↗

Is spinal cord dorsolateral funiculus involved in hypoalgesia induced by counter-irritation?

Several previous studies have demonstrated that, depending upon the behavioral test used, counter-irritation (i.e. the pain-relieving effects of pain elicited from heterotopic body areas) can produce hypoalgesia. In the present study, behavioral responses were elicited in the rat by increasing calibrated pressure applied to a hindpaw (Randall-Selitto test; 'passive' stimulus) and were studied before and after a subcutaneous formalin injection ('active' stimulus). The vocalization threshold to the pressure was clearly increased after injection of the algogenic solution either in the forepaw or in the cheek. Using this vocalization threshold, the counter-irritation-produced hypoalgesia was generally unchanged by unilateral dorsolateral funiculus (DLF) lesions. Following bilateral DLF lesions, hypoalgesia was decreased when formalin was injected in the forepaw, but was unaffected when the algogen was injected in the cheek. The present results partly contrast with previous papers from our group, where it has been assumed that the DLF is mainly involved in the neural circuitry subserving diffuse noxious inhibitory controls (DNIC), which have been considered as one possible neurophysiological basis for counter-irritation phenomena. They are discussed with reference to various hypotheses, including DNIC, as explanations for counter-irritation.

Afferent Pathways↗

Anatomical relationship between neuropeptide-containing fibers and efferent vagal neurons projecting to the rat corpus.

Injections of the retrograde tracers into the posterior surface of the stomach at the greater curvature resulted in labelling of the right half of the dorsal motor nucleus of the vagus. Whereas injections into the anterior and posterior surfaces of the corpus resulted in bilateral labelling in the medulla. Immunocytochemical staining of the labelled sections using antisera to substance P was confined to a dense network of fibers within the dorsal motor nucleus of the vagus and the nucleus tractus solitarius with no cell bodies being detected. Calcitonin gene-related peptide-immunoreactivity was detected in nerve fibers in the nucleus tractus solitarius and cell bodies of the hypoglossal nucleus. Finally, neuropeptide Y-immunoreactivity was confined to nerve fibers within the vagal complex. Of the neurons labelled by the retrograde tracers injected into the corpus all were in close spatial contact with fibers containing substance P-immunoreactivity. A smaller number were associated with neuropeptide Y-containing fibers with a few adjacent to calcitonin gene-related peptide-immunoreactive fibers. These results indicate that substance P and neuropeptide Y may directly regulate efferent neurons controlling gastric motility and acid secretion. Calcitonin gene-related peptide, however, is unlikely to directly modulate the cell bodies of the neurons in the dorsal motor nucleus but may modulate the dendrites from these neurons in the nucleus tractus solitarius.

Animals↗

Sympathetic and afferent neurons projecting in the splenic nerve of the cat.

Afferent and sympathetic postganglionic nerve cell bodies projecting in the splenic nerve of the cat have been labeled retrogradely with horseradish peroxidase (HRP) in order to study numbers and locations of these neurons. Labeled somata were found bilaterally in dorsal root and sympathetic paravertebral ganglia T3-L2 with a maximum in T10-T13 and in the coeliac superior mesenteric ganglion complex. About 13,200 neurons project into the splenic nerve of the cat, 12,550 being postganglionic and 650 afferent. About 98% of the postganglionic neurons were located in prevertebral and 2% in paravertebral sympathetic ganglia. About 73% of the afferent and 66% of the postganglionic paravertebral neurons were located on the left side. The density of the splenic innervation is about 3-4 times higher than that of the kidneys when normalized to the weight of both organs. It is discussed whether the afferent and sympathetic innervation of the spleen is not only involved in cardiovascular functions but also in regulation of the immune response of this organ.

Afferent Pathways↗

Substantia nigra influences on the reticulospinal neurons: an electrophysiological and ionophoretic study in cats and rats.

The influences exerted by the substantia nigra on reticulospinal neurons and the nature of the synaptic transmitter subserving these projections have been studied in adult cats and rats. Nigral stimulation evokes discharge changes in a significant number of reticulospinal cells (32.4% in cats and 39.1% in rats) on both ipsi- and contralateral sides. The responses were short-latency inhibitions (69.5% in cats and 76.5% in rats), short-latency excitations (22.2% in cats and 23.6% in rats) and in the remaining few cases long-latency excitations. Short-latency excitations, quite similar to the nigra-induced ones, were the predominant response pattern (95.2% in cats and 96.9% in rats) elicited on reticulospinal cells following stimulation of cerebral peduncle. The stimulation of substantia nigra in rats submitted to chronic ablation of sensorimotor cortex elicited only inhibitory responses while stimulation of nigral area in rats with intranigral injection of kainic acid was still capable of evoking short-latency excitations but not short-latency inhibitions. Therefore, the former can be ascribed to activation of corticoreticular fibers running in the cerebral peduncle whereas the latter can be considered as depending on activation of nigral efferents. The nigra-influenced cells were both 'fast' and 'slow' reticulospinal neurons and resulted mainly located in most rostral regions of reticular formation. Ionophoretic application of GABA suppressed the spontaneous firing of reticulospinal cells while no effect was observed following application of dopamine. The nigra-induced inhibitions were abolished by GABA-antagonist bicuculline and not by dopamine-antagonist fluphenazine.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

The indusium griseum in the mouse: architecture, Timm's histochemistry and some afferent connections.

The Indusium griseum (IG) is an enigmatic cortical field classically felt to be a part of the hippocampus (HC). In the mouse, IG lies just dorsal to the corpus callosum at the base of the anterior half of cingulate cortex. In coronal sections the field is small but constitutes a fairly long rostro-caudal strip. The connections of the IG are poorly understood. The Timm's staining pattern of the IG is reminiscent of a mini-dentate gyrus (DG) comprising a layer of granule cells with two bands of staining in the molecular layer. In the DG there are three bands which correspond to inputs from the lateral and medial entorhinal area (LEA and MEA) and the ipsi- and contralateral association systems. Using anterograde transport of HRP we have found that the LEA and MEA also terminate in the molecular layer of the IG. This suggests that the IG is a displaced portion of the DG. The olfactory system is known to have a strong indirect influence on the HC via primary and secondary bulbar projections to the LEA. Wheat germ agglutinin-HRP injections confined to the main olfactory bulb (MOB) show a direct projection from the MOB to IG. Both the olfactory bulb itself and retrobulbar structures such as the piriform cortex (PC) convey olfactory information to the LEA; the LEA supplies a major input to the DG. Our results suggest that there is a more direct pathway whereby olfactory information may influence a cortical region, IG, whose histochemistry and direct afferents from the entorhinal cortex suggest that it is part of or closely related to the DG. Thus, IG may represent a phylogenetically old olfacto-recipient outpost of the hippocampus.

Afferent Pathways↗

Local cerebral metabolic effects induced by nigral stimulation following ventromedial thalamic lesions. II: Sensory motor, reticular and limbic systems.

The involvement of the ventromedial thalamic nucleus (VM) in mediating the local cerebral metabolic effects induced by unilateral substantia nigra (SN) electrical stimulation was investigated in the awake rat. Local cerebral glucose utilization (LCGU) was measured during ipsilateral SN-stimulation in VM-intact rats as well as in animals bearing 8 or 30 days old electrolytic VM-lesions, using the 14C-deoxyglucose quantitative autoradiographic method. In VM-intact rats, SN-stimulation enhanced LCGU in several bilateral components of the sensory motor, reticular, and limbic systems despite the lack of direct anatomical connections. Almost all these metabolic activations were no longer apparent one week following VM-lesion. In contrast, one month after the VM-injury, the above activations reappeared even more dramatically than in VM-intact animals especially on the contralateral side. It is concluded that SN-stimulation activates several brain regions of both hemispheres beyond the traditional motor areas, the role of the VM in mediating these activations is crucial, and the plasticity of the adult CNS allows for recovery of metabolic responsiveness in a disturbed system.

Afferent Pathways↗

Descending projections to the dorsal and ventral divisions of the cochlear nucleus in guinea pig.

The origins of extrinsic projections to the guinea pig dorsal and ventral cochlear nuclei were identified by examining the retrograde transport of horseradish peroxidase conjugated to wheatgerm agglutinin following its injection into each of these divisions. Major projections originated in periolivary regions of the superior olivary complex, the contralateral cochlear nucleus and the inferior colliculus. There was no contribution from the nuclei of the lateral lemniscus to these pathways. The heaviest projection from the periolivary regions to both divisions of the cochlear nucleus arose bilaterally in the ventral nucleus of the trapezoid body. The ipsilateral lateral nucleus of the trapezoid body also projected heavily to dorsal and ventral cochlear nucleus. In addition, the ventral cochlear nucleus received a substantial projection from the dorsal aspect of the ipsilateral dorsomedial periolivary nucleus. Projections originating bilaterally in the central nucleus of the inferior colliculus terminated in the deep layers of dorsal cochlear nucleus. These projections appear to be more strongly ipsilateral and specific than those reported in the cat.

Animals↗

Electrophysiological and pharmacological characterisation of ascending anterolateral axons in the in vitro mouse spinal cord.

Here we describe a procedure to obtain electrophysiological recordings from cut ends of ascending axons of the spinal cord white matter. This procedure involves the use of an in vitro preparation of the neonate mouse spinal cord and suction microelectrodes of about 10 microm tip diameter. Using this procedure, we have recorded from axons of the anterolateral quadrant at the thoracic level which responded to electrical stimulation of a lumbar dorsal root. Using adequate stimulation parameters, we have identified axons responding exclusively to activation of C-fibres and axons responding to activation of A- and C-fibres. These axons are likely to originate at dorsal horn second order sensory neurons of different functional types. Simultaneous recordings from a lumbar ventral root and from ascending axons were used to assess the effects of noradrenaline and sevoflurane on motor and sensory pathways. The results obtained show that noradrenaline can potentiate responses of motor neurons to dorsal root stimulation while depressing responses of ascending axons to the same stimulus. In contrast both motor and sensory pathways were inhibited by sevoflurane. We believe that the procedures developed here may be of great interest to assess spinal nociceptive and antinociceptive mechanisms in vitro.

Action Potentials↗

The effect of a simulated knee joint effusion on postural control in healthy subjects.

OBJECTIVE: To determine the effects of a simulated knee joint effusion on center of pressure (COP) path and mean power frequency (MPF) during standing. DESIGN: Quasi-experimental design. SETTING: Sports injury research laboratory in a university setting. PARTICIPANTS: Twenty healthy volunteers, 10 of whom (age, 20.1+/-2.4y; height, 168.0+/-8.1cm; weight, 70.4+/-13.3kg) were assigned to an effusion group and 10 of whom (age, 25+/-3.8y; height, 169.4+/-8.9cm; weight, 74.7+/-7.7kg) were assigned to a control group. INTERVENTIONS: COP data were collected before and after a 60-mL injection of sterile saline into the knee joint space. MAIN OUTCOME MEASURES: COP path and mediolateral and anteroposterior MPF. RESULTS: COP path decreased after the effusion (pre-effusion mean, 92.2+/-21.9cm; posteffusion mean, 77.27+/-23.0cm). No change was found within the control group for COP path (P>.05). No differences were detected before or after joint effusion when the MPF was examined (P>.05). CONCLUSIONS: Possible explanations for the improved postural control after the effusion include additional somatosensory feedback, an augmented neural drive to the soleus, and/or increased capsular tension.

Adult↗

Neural circuitry of the kidney: NO-containing neurons.

The neurons synthesizing nitric oxide (NO) that are part of the renal sympathetic pathways were located by double-staining for the neuronal isoform of nitric oxide synthase (nNOS) using immunocytochemistry to identify NO-synthesizing neurons and transneuronal tracing following infection of the left kidney with pseudorabies virus (PRV). Following kidney injection with PRV, the animals survived 4-day post-inoculation prior to sacrifice and tissue processing. PRV-infected neurons that double-stained for nNOS were found in the paraventricular hypothalamic nucleus (PVN), the raphe obscurus nucleus (ROb), the ventromedial medulla (VMM), the rostral ventrolateral medulla (rVLM) and the A5 cell group. In the thoracolumbar spinal cord, nNOS neurons co-localized with PRV-infected cells in the dorsal horn in laminae I, III-V ipsilateral to the injected kidney and in lamina X, the intermediolateral cell column, the lateral funiculus, the intercalated nucleus and the central autonomic area. We conclude that NO synthesizing cells may significantly affect renal autonomic pathways in the rat by interacting with the renal sensory and sympathomotor circuitry at multiple sites.

Afferent Pathways↗