PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “Reticular Formation”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

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

At least 55 records · Page 3Linked to original sources

Comparative effects of pentylenetetrazol on the sensory responsiveness of lateral geniculate and reticular formation neurons.

The responses of bulbar and mesencephalic reticular formation (MRF) neurons to visual, auditory and/or somatosensory stimuli were considerably enhanced after subconvulsant doses of pentylenetetrazol (PTZ) in a similar fashion suggesting a general action of PTZ on reticular formation (RF) neurons. PTZ enhanced MRF responses evoked by electrical stimuli in the lateral geniculate nucleus (LGN) or cochlear nucleus but only modestly enhanced LGN neuronal responses. These findings indicate that the effects of this convulsant on the first brain sensory 'relay' nuclei and primary sensory receptors do not appear to be sufficient to account for the extensive PTZ-induced enhancement of RF neuronal responses, and direct effects of PTZ on the reticular formation may play a major role in this enhancement.

Animals↗

Excitatory amino acid-mediated responses and synaptic potentials in medial pontine reticular formation neurons of the rat in vitro.

Neurons of the medial pontine reticular formation (mPRF) are involved in the execution of numerous behaviors including initiation of locomotion, eye movements, startle responses, and rapid eye movement sleep phenomena. Approximately half of the afferent projections to mPRF neurons come from within the reticular formation (Shammah-Lagnado et al., 1987). In spite of the importance of reticulo-reticular connections, virtually nothing is known about transmitters mediating these synapses. In order to identify a candidate excitatory neurotransmitter, the actions of excitatory amino acids (EAAs) on the membrane properties of mPRF neurons recorded in rat brainstem slices in vitro were studied. Standard intracellular recording methods, including single-electrode voltage clamp, were used to examine the postsynaptic actions of EAAs. We also tested whether EAA antagonists block EPSPs evoked by stimulation of the contralateral reticular formation in the slices. mPRF neurons responded to both non-NMDA and NMDA agonists. NMDA-induced conductances were voltage dependent and depressed by physiological concentrations of magnesium. Stimulation of the contralateral reticular formation elicited EPSPs that were depressed by the general EAA antagonist kynurenate. Evoked EPSPs were partially depressed by 6,7-dinitroquinoxaline-2,3-dione. The evoked EPSP was further reduced by the NMDA antagonist (+/-)-2-amino-5-phosphonopentanoic acid in some cases. These results suggest that excitatory reticulo-reticular neurotransmission is mediated by an EAA. Both non-NMDA and NMDA receptors contribute to EAA neurotransmission in the mPRF formation and play an integral role in reticular formation function.

Amino Acids↗

[3H]thymidine autoradiographic study in the transit part from the spinal cord to the medulla oblongata of the chick embryo--the ontogenetic relation between the reticular formation and the spinal cord.

In order to examine the ontogenetic structural continuity of the reticular formation to the spinal gray matter, the time of origin of neurons was investigated in the transit part from the spinal cord to the medulla of chick embryos with tritriated thymidine autoradiography. The reticular formation was found to be neurogenetically divided into parvocellular reticular formation (RP), dorsal part of the magnocellular reticular formation (RME) and ventral part of the magnocellular reticular formation (RMI). Neurons in the RP differentiated synchronously with those in the neck and base of the dorsal horn, neurons in the RME with those in the zona intermedia, and neurons in the RMI with those in the ventral horn, suggesting that each synchronously developing region forms an ontogenetic structural unit.

Animals↗

Differences in the distribution of catecholamine varicosities in cat and rat reticular formation.

The distribution of catecholamine varicosities within the brainstem reticular formation of the immature cat was determined by means of the formaldehyde-induced fluorescence technique. A continuous pattern of intense, green, medium-sized varicosities exists at nearly all brainstem levels. At most of these levels the varicosities appear within the boundaries of reticular formation nuclei. However, in rostral mesencephalon, some of the varicosities of the pattern lie in proximity to perikarya of the red nucleus. In addition, numerous varicosities in caudal medulla appear to extend from the pattern into nonreticular formation nuclei. A comparable pattern of reticular formation fluorescence is absent in the rat and this finding is believed to represent a true interspecies difference.

Anatomy, Comparative↗

Behavioral functions of the reticular formation.

Studies of the behavioral correlates of activity in reticular formation cells, usually performed in restrained animals, have found units whose discharge relates to sensory stimuli, pain and escape behavior, conditioning and habituation, arousal, complex motivational states, REM sleep, eye movements, respiration and locomotion. Units with these different behavioral correlates were found in the same anatomical areas. Most studies report that a large proportion of encountered cells related to the behavior being studied. If one adds up the reported percentages, the total far exceeds 100%. Therefore it appears that many investigators are looking at the same cells and reaching very different conclusions about their behavioral roles. On the basis of observations in unrestrained cats, it is hypothesized that discharge in most RF cells is primarily related to the excitation of small groups of muscles. This hypothesis can parsimoniously explain many previous observations on the behavioral correlates of these cells, and is consistent with anatomical, physiological and phylogenetic studies of the reticular formation. The hypothesized simplicity of reticular formation unit function is contrasted with the complexity of the behavioral functions mediated by the RF, and the implications of this contrast discussed.

Animals↗

Changes in intracranial pressure elicited by electrical stimulation of the brainstem reticular formation in spinal cats with vagotomy.

The momentary changes in intracranial pressure (ICP) were explored using electrical stimulation of the brainstem reticular formation and the nucleus fastigii of the cerebellum in cats under artificial ventilation after spinalization (C2) and vagotomy. Regions that yielded an increase in ICP in the arterial pressor area were: the central part of the pontine recticular formation, the dorsal medullary reticular formation, the central part of the medullary reticular formation, and the nucleus fastigii of the cerebellum; and one region in the arterial depressor area was the paramedial and ventral medial region of the medullary reticular formation. Since the arterial blood pressure and respiration was maintained constant during electrical stimulation by spinalization and vagotomy, the increase in ICP in the cranium, a semi-closed box, momentarily reflected an increase in cerebral blood volume due to cerebral vasodilatation. It is suggested that excitation of cell bodies or fibres within these regions may produce cerebral vasodilatation.

Animals↗

Immunohistochemistry and spinal projections of the reticular formation in the northern leopard frog, Rana pipiens.

Over 30 nuclei have been identified in the reticular formation of rats, but only a small number of distinct reticular nuclei have been recognized in frogs. We used immunohistochemistry, retrograde tracing, and cell morphology to identify nuclei within the brainstem of Rana pipiens. FluoroGold was injected into the spinal cord, and, in the same frogs, antibodies to enkephalin, substance P, somatostatin, and serotonin were localized in adjacent sections. We identified many previously unrecognized reticular nuclei. The rhombencephalic reticular formation contained reticularis (r.) dorsalis; r. ventralis, pars alpha and pars beta; r. magnocellularis; r. parvocellularis; r. gigantocellularis; r. paragigantocellularis lateralis and dorsalis; r. pontis caudalis, pars alpha and pars beta; nucleus visceralis secundarius; r. pontis oralis, pars medialis and pars lateralis; raphe obscurus; raphe pallidus; raphe magnus; and raphe pontis. The mesencephalic reticular formation contained locus coeruleus-subcoeruleus, r. cuneiformis, r. subcuneiformis, raphe dorsalis-raphe centralis superior, and raphe linearis. Thus, the reticular formation of frog, which is an anamniote, is organized complexly and is similar to the reticular formation in amniotes. Because many of these nuclei may be homologous to reticular nuclei in mammals, we used mammalian terminology for frog reticular nuclei.

Animals↗

Distribution of cholinergic, GABAergic and serotonergic neurons in the medial medullary reticular formation and their projections studied by cytotoxic lesions in the cat.

As part of a larger study concerning the role of neurons in the medial medullary reticular formation in sleep-wake states, the distribution and projections of cholinergic, GABAergic and serotonergic neurons were studied within the lower brainstem of the cat. Cells were plotted with the aid of an image analysis system through the medullary reticular formation and raphe in adjacent sections immunostained for choline acetyltransferase, glutamic acid decarboxylase and serotonin. Immunostained fibres and varicosities were examined and quantified by microdensitometry in regions of the medulla, pons and upper spinal cord in normal and quisqualate-injected animals to assess the loss of local and distant projections following cytotoxic destruction of neurons in the medial medullary reticular formation. Choline acetyltransferase-immunoreactive neurons are unevenly and sparsely distributed, though none the less in significant numbers (estimated at approximately 9080 in total), through the medial medullary reticular formation, and are present in all tegmental fields, including the gigantocellular (approximately 3700) and magnocellular (approximately 1760) rostrally and the ventral (approximately 3240) and paramedian (approximately 380) caudally, and are absent in the midline raphe. Glutamic acid decarboxylase-immunoreactive neurons are more evenly and densely distributed in large numbers (estimated at approximately 18,720) through the medial medullary reticular formation, being present in the gigantocellular (approximately 5960), magnocellular (approximately 8260), ventral (approximately 2280) and paramedian (approximately 2220) tegmental fields, and are also numerous within the raphe magnus and pallidus-obscurus nuclei (approximately 3880). Serotonin-immunoreactive cells are sparse in the medial medullary reticular formation (estimated to total approximately 1540), where they are mainly located in the magnocellular tegmental field (approximately 1340), and are concentrated in larger numbers within the raphe nuclei (approximately 8060). Cholinergic varicose fibres were moderately densely distributed through the medial medullary reticular formation, as well as through more distant lateral, rostral and caudal brainstem and upper spinal regions. After cytotoxic lesions focussed in the gigantocellular and magnocellular tegmental fields, a loss of approximately 55% of the cholinergic neurons in the medial medullary reticular formation was associated with a minor decrease (approximately 35% in optical density measures) of local cholinergic fibres. Small and variable reductions in varicose fibres (and their optical density measures) were detected in distant structures (including the pontine lateral, gigantocellular and subcoerular tegmental fields and the caudal spinal trigeminal nucleus), that were none the less correlated with the number of intact medial medullary cholinergic cells, suggesting that these cells may project to distant brainstem targets, in addition to providing a minor proportion of the local cholinergic innervation of the medial medullary reticular formation.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Calretinin mRNA and immunoreactivity in the medullary reticular formation of the rat: colocalization with glutamate receptors.

Calretinin-positive cells were identified in the medullary reticular formation of the rat by both immunohistochemistry and in situ hybridization histochemistry. In addition, double immunocytochemical labeling was used to examine the degree of colocalization of calretinin with GluR2/R3, GluR4 and GluR5-7 glutamate receptor subtypes. Results indicated regional variation in calretinin expression across reticular formation regions with the exception of the largest cells which were mostly calretinin-positive. Calretinin mRNA was particularly abundant in the parvocellular reticular nucleus. Most calretinin-immunoreactive cells also expressed at least one of the glutamate receptor subtypes examined with the exception of the smallest calretinin-positive cells of the parvocellular reticular formation which were generally not immunoreactive for any of the glutamate receptors examined. Calretinin immunoreactivity was colocalized with immunoreactivity for all three glutamate receptor subtypes examined in most of the large cells of the reticular formation. Immunoreactivity for the GluR4 antibody was least abundant in the reticular formation and GluR4 immunoreactive cells were least likely to co-express calretinin. These results suggest that calretinin and glutamate receptor antibodies may be used to identify specific subsets of reticular formation neurons.

Animals↗

Afferent connections of the mesencephalic reticular formation: a horseradish peroxidase study in the rat.

The afferent connections of the mesencephalic reticular formation were studied experimentally in the rat by the aid of the retrograde horseradish peroxidase tracer technique. The results suggest that the rostral portion of the mesencephalic reticular formation receives its main input from the cerebral cortex, the zona incerta and the fields of Forel, the central gray substance, the nuclei reticularis pontis oralis and caudalis, and the deep cerebellar nuclei. Substantial input to the same territory of the mesencephalic reticular formation appears to come from the superior colliculus, the substantia nigra, the parabrachial area, the spinal trigeminal nucleus, and the nucleus reticularis gigantocellularis, whereas several other brain structures, among which the locus coeruleus and the raphe complex, seem to represent modest but consistent additional input sources. The afferentation of more caudal portions of the mesencephalic reticular formation appears to conform to the general pattern outlined above with only three exceptions; the cerebral cortex, the deep cerebellar nuclei and the spinal trigeminal nucleus seem to be relatively modest sources of projections to these levels. Considering that the mesencephalic reticular formation is a critical structure in the "ascending activating systems" the present results, confirming and extending those of many other investigators, characterize a set of pathways that seem to be an important part of the anatomical substrate of the sleep-walking cycle.

Afferent Pathways↗

[Sensory organization of the reticular formation: Specific integrative activity].

On the basis of personal investigations including 1) electrophysiological methods (EEG, averaged evoked potentials), 2) behavior methods, 3) destruction of various parts of the brain (mesencephalic reticular formation, auditory pathways) and 4) pharmacological methods, conducted in the years 1953-1974 the author put forward a concept of sensory organization of reticular formation postulating existence of special systems in the reticular formation differing in their relative physiological and chemical specificity. This relative specificity is, in this concept, the ability of the so-called non-specific neurons in the reticular formation to be included under certain experimental conditions into specific functional systems. The author suggests the term "paraspecific systems" for designating these relatively specific systems. It seems that these systems determine the integrative role of reticular formation in the process of learning. In contrast to this important role the reticular formation is without any greater importance for the process of memory storage. The dynamic and relatively specific functional organization of reticular formation provides potential possibilities of its utilization in the processes of reeducation or rehabilitation in central nervous system damage and in pharmacological treatment of psychic disturbances.

Acoustic Stimulation↗

Ascending projections of the brain stem reticular formation in a nonmammalian vertebrate (the lizard Varanus exanthematicus), with notes on the afferent connections of the forebrain.

In the present study an attempt has been made to analyze the ascending reticular projections in the lizard Varanus exanthematicus by means of the horseradish peroxidase (HRP) technique. Reticular projections ascending to the telencephalon were found to arise in the mesencephalon, but not caudal to the mesorhombencephalic border. HRP injections into the dorsal thalamus have demonstrated retrogradely labeled cells in the mesencephalic reticular formation, particularly at the level of the oculomotor nerve and in the medial magnocellular zone of the rhombencephalic reticular formation, predominantly rostrally. HRP infiltrations at the mesodiencephalic border damaged most of the fibers passing beyond this junction, resulting in the uptake of HRP by the damaged axons and subsequent labeling of the cell bodies or origin of ascending reticular projections to the diencephalon and telencephalon. From a comparison of cell-labeling patterns in cases of HRP injections of, respectively, the dorsal thalamus and the mesodiencephalic border, it seems likely that the nucleus reticularis medius and more sparsely the nucleus reticularis inferior project to ventral diencephalic structures (ventral thalamus and hypothalamus), whereas the midbrain reticular formation and the rostral parts of the rhombencephalic reticular formation (nuclei reticulares isthmi and superior) project to both the dorsal thalamus and more ventral diencephalic structures. Projections arising throughout the rhombencephalic reticular formation, but predominantly in the nucleus reticularis inferior, were found to ascend to the midbrain reticular formation. The present experimental data in the lizard Varanus exanthematicus are comparable to the findings in mammals, with the exception of the reticulo-oculomotor pathways which have not been analyzed so far in reptiles. In addition to the aforementioned ascending reticular projections, the present study has demonstrated projections ascending from monoamine cell groups, various diencephalic structures, as well as from neuronal groups involved in somatosensory, auditory, and gustatory systems. Projections were found from the locus coeruleus and the nucleus raphes superior to the telencephalon, as well as from the substantia nigra and the presumable reptilian homologue of the mammalian ventral tegmental area to the basal forebrain and the dorsal thalamus. Bilateral projections were demonstrated from the principal trigeminal nucleus to the telencephalon, reminiscent of the quintofrontal tract of birds. Ascending projections to the diencephalon were found to originate bilaterally in the descending trigeminal nucleus and the dorsal funicular nucleus. Auditory projections to the midbrain arise bilaterally in the superior olivary complex and in the cochlear nuclear complex. Finally, the ascending gustatory pathway arising in the nucleus of the solitary tract was found to project to the "parabrachial region," which in its turn has extensive projections to the forebrain.

Afferent Pathways↗

Collision-like interactions between acoustic and electrical signals that produce startle reflexes in reticular formation sites.

A startle-like response can be evoked at low currents by one-pulse electrical stimulation of reticular formation sites from the rostrolateral pons to the caudomedial medulla. To test whether this response is mediated by the same reticular formation neurons as those that mediate the acoustic startle, we delivered a brief, subthreshold acoustic stimulus followed by an 0.1-ms electrical pulse to one side of the reticular formation of rats. The current thresholds for electrical startle were usually powerfully reduced (50-80%) whenever the acoustic stimulation was presented within 5 ms of the electrical pulse. This summation was, however, interrupted by brief (0.2-1.0 ms) spike-like increases in threshold when the electrical pulse was delivered 4.0-4.6 ms after the offset of the acoustic stimulus. The timing of the spike-like increase in threshold shifted to longer intervals in more caudal sites, consistent with the conduction of action potentials in the startle pathway. For example, the increase occurred at an interval of 4.1 ms near the ventral lateral lemniscus (VLL) and at intervals of 4.4-4.6 ms for sites in the pontine or medullary reticular formation. The increases in startle threshold are attributed to collisions between antidromic action potentials evoked by the electrical pulses and orthodromic action potentials evoked by the acoustic stimuli. These results suggest that the neurons in reticular formation that produce the acoustic startle reflex overlap greatly with the neurons that mediate electrically evoked startle-like responses. Also, the acoustic signals mediating the startle reflex must be, in large part, a synchronous volley of action potentials conducted by longitudinal bundles of reticular formation axons.

Acoustic Stimulation↗

Single cholinergic mesopontine tegmental neurons project to both the pontine reticular formation and the thalamus in the rat.

Microinjections of the cholinergic agonist carbachol into a caudal part of the pontine reticular formation of the rat induce a rapid eye movement sleep-like state. This carbachol-sensitive region of the pontine reticular formation is innervated by cholinergic neurons in the pedunculopontine and laterodorsol tegmental nuclei. The same population of cholinergic neurons also project heavily to the thalamus, where there is good evidence that acetylcholine facilitates sensory transmission and blocks rhythmic thalamocortical activity. The present study was undertaken to examine the degree to which single cholinergic neurons in the mesopontine tegmentum project to both the carbachol-sensitive region of the pontine reticular formation and the thalamus, by combining double fluorescent retrograde tracing and immunofluorescence with a monoclonal antibody to choline acetyltransferase in the rat. The results indicated that a subpopulation (5-21% ipsilaterally) of cholinergic neurons in the mesopontine tegmentum projects to both the thalamus and the carbachol-sensitive site of the pontine reticular formation, and these neurons represented the majority (45-88%) of cholinergic neurons projecting to the pontine reticular formation site. The percentage of cholinergic neurons with dual projections was higher in the pedunculopontine tegmental nucleus (6-27%) than in the laterodorsal tegmental nucleus (4-11%). In addition, mixed with cholinergic neurons in the mesopontine tegmentum, there was a small population of dually projecting neurons that did not appear to be cholinergic. Mesopontine cholinergic neurons with dual projections may simultaneously modulate neuronal activity in the pontine reticular formation and the thalamus, and thereby have the potential of concurrently regulating different aspects of rapid eye movement sleep.

Animals↗

Strychnine effects on the sensory response patterns of reticular formation neurons.

Strychnine (ST) administration results in enhanced responses of reticular formation neurons of the cat to visual, auditory, or somatosensory stimuli. Neurons in the bulbar reticular formation (BRF) also exhibited ST-induced spike-bursting which coincides with the onset of 10--20 Hz high amplitude rhythmic discharge in the lower brain stem often obscuring sensory response enhancement. Mesencephalic reticular formation (MRF) neurons showed enhanced sensory responsiveness at higher doses of ST but rarely showed spike-bursting. The rhythmic discharge in the EEG of BRF and spike-bursting in BRF neurons was not observed in animals with spinal cord transection suggesting that this bursting activity is due to the action of ST on the spinal cord. The enhancement of sensory responses may be due in part to reversal of repetition-induced response attenuation (habituation) mechanisms in RF neurons. The ST-induced enhancement of RF neuronal responses to sensory stimuli is similar to that reported previously with pentylenetetrazol. These findings extend the concept that enhancement of RF responses to sensory stimuli may be indicative of a general neuronal action of convulsant agents which may be important in sensory-induced seizures.

Animals↗

The differential effects of halothane and isoflurane on electroencephalographic responses to electrical microstimulation of the reticular formation.

Isoflurane and halothane cause electroencephalographic (EEG) depression and neuronal depression in the reticular formation, a site critical to consciousness. We hypothesized that isoflurane, more than halothane, would depress EEG activation elicited by electrical microstimulation of the reticular formation. Rats were anesthetized with either halothane or isoflurane and stimulating electrodes were positioned in the reticular formation. In a crossover design, anesthetic concentration was adjusted to 0.8 and 1.2 minimum alveolar concentration (MAC) of halothane or isoflurane and electrical microstimulation was performed and the EEG responses were recorded. Microstimulation increased the spectral edge and median edge frequencies 2-2.5 Hz at 0.8 MAC for halothane and isoflurane and 1.2 MAC halothane. At 1.2 MAC isoflurane, burst suppression occurred and microstimulation decreased the period of isoelectricity (24% +/- 19% to 8% +/- 7%; P < 0.05), whereas the spectral edge and median edge frequencies were unchanged. At anesthetic concentrations required to produce immobility, the cortex remains responsive to electrical microstimulation of the reticular formation, although the EEG response is depressed in the transition from 0.8 to 1.2 MAC. These data indicate that cortical neurons remain responsive to synaptic input during isoflurane and halothane anesthesia.

Anesthetics, Inhalation↗

Divergence of lamina VII and VIII neurones of S1 and S2 segments of the cat's spinal cord to the cerebellum and the reticular formation.

Cerebellar and reticular projections of neurones located in sacral segments of the spinal cord were electrophysiologically investigated in alpha-chloralose anaesthetized cats. Antidromic action potentials were recorded following stimulation of the contralateral restiform body (coRB), contralateral gigantocellular nucleus (coGRN) as well as ipsi- and contralateral lateral funiculus of the 13th thoracic segment (iTh13 and coTh13). Eighty-seven neurones were found in the medial lamina VII and lamina VIII of the gray matter of S1 and S2 segments. Their axons ascended in lateral funiculi on the contralateral side and in 46 cases also on the ipsilateral side of the spinal cord. A projection to coRB was found in 20 neurones, to coGRN in 10 and dual projections to both coRB and coGRN in 20 neurones. Axons of the remaining 37 cells were found to ascend to the level of Th13 only. Conduction velocities of neurones investigated were comprised in the range 35-83 m/s and no significant differences were found between particular groups. However, an evident decrease in conduction was observed in most neurones when comparing proximal to distal parts of their axons, suggesting the possibility of more extensive divergence than indicated in this study. The pattern of projections revealed that the information from the periphery is conveyed in parallel to various supraspinal and possibly also spinal centres.

Animals↗