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Thalamus reticular nucleus

A global view of consciousness is that it is generated throughout the entire brain, as a result of synchronisation of relevant neural networks. Specific systems or regions—for example the cerebral cortex, brainstem reticular formation and thalamic nuclei—may be key anatomical integrators. Areas with the most widespread interconnections are pivotal, and on this basis the cortex and thalamus are more relevant than cerebellum and striatum for example. Frontal cortex for example connects with every other brain region, both in terms of input and output, with 80% of such connections accounted for by cortico-cortical connections. Thalamic intralaminar nuclei are, in conjunction with the reticular nucleus, reciprocally connected to all cortical areas. By contrast the cerebellum has very few output pathways and striatal-cortical input is (via the thalamus) confined to frontal lobe. [Pg.5]

The GABAeroic reticular nucleus of the thalamus gates" sensory information transfer from the thalamus to the cortex. [Pg.270]

Receptors containing the ai, a2, a3 or as subunit in combination with any of the P-subimits and the y2 subunit are most prevalent in the brain (Fig. 3). These receptors are sensitive to benzodiazepine modulation. The major receptor subtype is assembled from the subunits aiP2Y2. with only a few brain regions lacking this receptor (granule cell layer of the olfactory bulb, reticular nucleus of the thalamus, spinal cord motoneurons) (Fritschy and Mohler 1995 Pirker et al. 2000 Fritschy and Brunig 2003) (Table 1). [Pg.229]

Similar to all the other thalamic afferent inputs, basal ganglia outputs give off collaterals to the thalamic reticular nucleus traversing this nucleus to enter the thalamus... [Pg.41]

The slow (deep sleep) -waves probably originate in the eortex beeause they survive separation from, or lesions of, the thalamus. However, the rhythm and appearanee of spindles in earlier phases of the sleep eyele do depend on links with the thalamus (see Steriade 1999). Unlike stimulation of the specific sensory relay nuclei in the thalamus, which only affects neurons in the appropriate sensory areas of the cortex, the nonspecific nuclei can produce responses throughout the cortex and may not only control, but also generate, cortical activity. Certainly, in vitro studies show that neurons of the non-specific reticular thalamic nucleus (NspRTN) can fire spontaneously at about 8-12 Hz (equivalent to EEG a-rhythm) or lower, and that low-frequency stimulation of this area can induce sleep. [Pg.484]

Figure 22.5 Pathways involved in cortico-thalamic synchrony and EEG arousal. The ascending reticular activating system (ARAS) extends from the cephalic medulla through the pons and midbrain to the thalamus (see Moruzzi and Mayoun 1949). It is activated by impulses in collaterals of the spinothalamic sensory pathway running to specific thalamic nuclei (SpThNc) and in turn activates much of the cortex, partly through the non-specific thalamic nuclei (NspThNc), which also receive inputs from SpThNc and also via the nucleus basalis (NcB). Its stimulation is followed by EEG arousal. It is probable that reciprocal links between cortical areas and the thalamus, particularly NspThN, lead to slow-wave (8 Hz) cortical EEG synchrony and, in the absence of appropriate sensory input and ARAS activity, a sleep state... Figure 22.5 Pathways involved in cortico-thalamic synchrony and EEG arousal. The ascending reticular activating system (ARAS) extends from the cephalic medulla through the pons and midbrain to the thalamus (see Moruzzi and Mayoun 1949). It is activated by impulses in collaterals of the spinothalamic sensory pathway running to specific thalamic nuclei (SpThNc) and in turn activates much of the cortex, partly through the non-specific thalamic nuclei (NspThNc), which also receive inputs from SpThNc and also via the nucleus basalis (NcB). Its stimulation is followed by EEG arousal. It is probable that reciprocal links between cortical areas and the thalamus, particularly NspThN, lead to slow-wave (8 Hz) cortical EEG synchrony and, in the absence of appropriate sensory input and ARAS activity, a sleep state...
FIGURE 29-1. Anatomy of the extrapyramidal system. The extrapyramidal motor system controls muscle movement through a system of pathways and nerve tracts that connect the cerebral cortex, basal ganglia, thalamus, cerebellum, reticular formation, and spinal neurons. Patients with Parkinson s disease have a loss of dopamine neurons in the substantia nigra in the brain stem that leads to depletion of dopamine in the corpus striatum. The corpus striatum is made up of the caudate nucleus and the lentiform nuclei that are made up of the putamen and the globus pallidus. [Pg.475]

The neural structures involved in the promotion of the waking (W) state are located in the (1) brainstem [dorsal raphe nucleus (DRN), median raphe nucleus (MRN), locus coeruleus (LC), laterodorsal and pedunculopontine tegmental nuclei (LDT/PPT), and medial-pontine reticular formation (mPRF)] (2) hypothalamus [tuberomammillary nucleus (TMN) and lateral hypothalamus (LH)[ (3) basal forebrain (BFB) (medial septal area, nucleus basalis of Meynert) and (4) midbrain ventral tegmental area (VTA) and substantia nigra pars compacta (SNc) (Pace-Schott Hobson, 2002 Jones, 2003). The following neurotransmitters function to promote W (1) acetylcholine (ACh LDT/PPT, BFB) (2) noradrenaline (NA LC) (3) serotonin (5-HT DRN, MRN) (4) histamine (HA TMN) (5) glutamate (GLU mPRF, BFB, thalamus) (6) orexin (OX LH) and (7) dopamine (DA VTA, SNc) (Zoltoski et al, 1999 Monti, 2004). [Pg.244]

Structures implicated in the production or maintenance of sleep include the nucleus of the solitary tract, dorsal medullary reticular formation, raphe nuclei, thalamus, anterior hypothalamus, preoptic area, basal forebrain, orbitofrontal cortex, caudate nucleus, basal ganglia, and cerebral cortex. None of these structures are individually necessary for sleep. No lesion has produced a long lasting total insomnia. After some sleep-reducing lesions, sleep returns toward normal if sufficient time is allowed for recovery. [Pg.567]

The nucleus basalis of Meynert, located in the basal forebrain, is the main location of the cholinergic neurons. The cholinergic neurons project to the amygdala, hippocampus and other parts of the neocortex. Additional cholinergic neurons in the reticular system also project to the cerebral cortex, the limbic system, the hypothalamus, and the thalamus. Acetylcholine is... [Pg.27]

Schematic diagram of the gustatory pathway in rodents. Taste receptor cells are innervated by one of three cranial nerves (VII, IX, or X), which project topographically into the rostral portion of nucleus of the solitary tract (NST). Cells within the NST send projections into the reticular formation (RF), through which connections are made to oral motor nuclei V, VII, and XII and the nucleus ambiguous (NA). Ascending fibers connect to the parabrachial nuclei (PbN) of the pons, from which two parallel pathways emerge. One pathway carries taste information to the insular cortex (IC) via the ventral posterior medial nucleus, parvicellularis (VPMpc), of the thalamus. The other pathway projects into areas of the limbic forebrain involved in food and water regulation, reinforcement, reward, and stress, including the lateral hypothalamus (LH), the central nucleus ofthe amygdala (CeA), and the bed nucleus of the stria terminalis (BST). These areas and the IC are interconnected and send descending projections back to both the PbN and NST... Schematic diagram of the gustatory pathway in rodents. Taste receptor cells are innervated by one of three cranial nerves (VII, IX, or X), which project topographically into the rostral portion of nucleus of the solitary tract (NST). Cells within the NST send projections into the reticular formation (RF), through which connections are made to oral motor nuclei V, VII, and XII and the nucleus ambiguous (NA). Ascending fibers connect to the parabrachial nuclei (PbN) of the pons, from which two parallel pathways emerge. One pathway carries taste information to the insular cortex (IC) via the ventral posterior medial nucleus, parvicellularis (VPMpc), of the thalamus. The other pathway projects into areas of the limbic forebrain involved in food and water regulation, reinforcement, reward, and stress, including the lateral hypothalamus (LH), the central nucleus ofthe amygdala (CeA), and the bed nucleus of the stria terminalis (BST). These areas and the IC are interconnected and send descending projections back to both the PbN and NST...

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See also in sourсe #XX -- [ Pg.268 ]

See also in sourсe #XX -- [ Pg.12 , Pg.41 , Pg.42 , Pg.86 , Pg.542 , Pg.545 ]




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