Medial dorsal nucleus | |
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Details | |
Identifiers | |
Latin | nucleus mediodorsalis thalami |
MeSH | D020645 |
NeuroNames | 312 |
NeuroLex ID | birnlex_1543 |
TA98 | A14.1.08.622 |
TA2 | 5681 |
FMA | 62156 |
Anatomical terms of neuroanatomy |
The medial dorsal nucleus (or mediodorsal nucleus of thalamus, dorsomedial nucleus, dorsal medial nucleus, or medial nucleus group) is a large nucleus in the thalamus. [1] [2] It is separated from the other thalamic nuclei by the internal medullary lamina.
The medial dorsal nucleus is interconnected with the prefrontal cortex, therefore involved in prefrontal functions. Damage to the interconnected tract or the nucleus itself will result in similar damage to the prefrontal cortex. [3] It is also believed to play a role in memory. [4]
The medial dorsal nucleus relays inputs from the amygdala and olfactory cortex and projects to the prefrontal cortex and the limbic system, [5] [6] and in turn relays them to the prefrontal association cortex. As a result, it plays a crucial role in attention, planning, organization, abstract thinking, multi-tasking, and active memory.[ citation needed ]
The connections of the medial dorsal nucleus have even been used to delineate the prefrontal cortex of the Göttingen minipig brain. [7]
By stereology the number of brain cells in the region has been estimated at around 6.43 million neurons in the adult human brain and 36.3 million glial cells, with the newborn having quite different numbers: around 11.2 million neurons and 10.6 million glial cells. [8]
The medial dorsal nucleus has four parts. [9]
While both the ventral and medial dorsal nuclei process pain, the medial dorsal nucleus bypasses primary cortices, sending their axons directly to secondary and association cortices. The cells also send axons directly to many parts of the brain, including nuclei of the limbic system such as the lateral nucleus of the amygdala, the anterior cingulate, and the hippocampus. This part of the sensory system, known as the non-classical or extralemniscal system is less accurate, and less detailed in regards to sensory signal analysis. This processing is known colloquially as "fast and dirty" rather than the "slow and accurate" processing of the classical or lemniscal system. This pathway activates parts of the brain that evoke emotional responses.[ citation needed ]
The medial dorsal nucleus is also presumed to play a role in monitoring internal movements of the eye. Specifically, its function is to relay the information about how the eyes will be moved (efference copy, also known as corollary discharge) from the superior colliculus to the frontal eye fields (FEF) in order to aid the neurons in FEF to change their receptive fields to where the visual stimuli will appear after the saccade. [10]
Damage to the medial dorsal nucleus has been associated with Korsakoff's syndrome. [11]
The thalamus is a large mass of gray matter on the lateral walls of the third ventricle forming the dorsal part of the diencephalon. Nerve fibers project out of the thalamus to the cerebral cortex in all directions, known as the thalamocortical radiations, allowing hub-like exchanges of information. It has several functions, such as the relaying of sensory and motor signals to the cerebral cortex and the regulation of consciousness, sleep, and alertness.
The spinothalamic tract is a nerve tract in the anterolateral system in the spinal cord. This tract is an ascending sensory pathway to the thalamus. From the ventral posterolateral nucleus in the thalamus, sensory information is relayed upward to the somatosensory cortex of the postcentral gyrus.
The pulvinar nuclei or nuclei of the pulvinar are the nuclei located in the thalamus. As a group they make up the collection called the pulvinar of the thalamus, usually just called the pulvinar.
The solitary nucleus(SN) (nucleus of the solitary tract, nucleus solitarius, or nucleus tractus solitarii) is a series of neurons whose cell bodies form a roughly vertical column of grey matter in the medulla oblongata of the brainstem. Their axons form the bulk of the enclosed solitary tract. The solitary nucleus can be divided into different parts including dorsomedial, dorsolateral, and ventrolateral subnuclei.
In the anatomy of the brain, the centromedian nucleus, also known as the centrum medianum, is a nucleus in the posterior group of the intralaminar thalamic nuclei (ITN) in the thalamus. There are two centromedian nuclei arranged bilaterally.
The reticular formation is a set of interconnected nuclei in the brainstem that spans from the lower end of the medulla oblongata to the upper end of the midbrain. The neurons of the reticular formation make up a complex set of neural networks in the core of the brainstem. The reticular formation is made up of a diffuse net-like formation of reticular nuclei which is not well-defined. It may be seen as being made up of all the interspersed cells in the brainstem between the more compact and named structures.
The Papez circuit, or medial limbic circuit, is a neural circuit for the control of emotional expression. In 1937, James Papez proposed that the circuit connecting the hypothalamus to the limbic lobe was the basis for emotional experiences. Paul D. MacLean reconceptualized Papez's proposal and coined the term limbic system. MacLean redefined the circuit as the "visceral brain" which consisted of the limbic lobe and its major connections in the forebrain – hypothalamus, amygdala, and septum. Over time, the concept of a forebrain circuit for the control of emotional expression has been modified to include the prefrontal cortex.
In neuroanatomy, thalamocortical radiations, also known as thalamocortical fibers, are the efferent fibers that project from the thalamus to distinct areas of the cerebral cortex. They form fiber bundles that emerge from the lateral surface of the thalamus.
The dentate nucleus is a cluster of neurons, or nerve cells, in the central nervous system that has a dentate – tooth-like or serrated – edge. It is located within the deep white matter of each cerebellar hemisphere, and it is the largest single structure linking the cerebellum to the rest of the brain. It is the largest and most lateral, or farthest from the midline, of the four pairs of deep cerebellar nuclei, the others being the globose and emboliform nuclei, which together are referred to as the interposed nucleus, and the fastigial nucleus.
The medial geniculate nucleus (MGN) or medial geniculate body (MGB) is part of the auditory thalamus and represents the thalamic relay between the inferior colliculus (IC) and the auditory cortex (AC). It is made up of a number of sub-nuclei that are distinguished by their neuronal morphology and density, by their afferent and efferent connections, and by the coding properties of their neurons. It is thought that the MGN influences the direction and maintenance of attention.
The septal area, consisting of the lateral septum and medial septum, is an area in the lower, posterior part of the medial surface of the frontal lobe, and refers to the nearby septum pellucidum.
The basal ganglia form a major brain system in all vertebrates, but in primates there are special differentiating features. The basal ganglia include the striatum, pallidus, substantia nigra and subthalamic nucleus. In primates the pallidus is divided into an external and internal globus pallidus, the external globus pallidus is present in other mammals but not the internal globus pallidus. Also in primates, the dorsal striatum is divided by a large nerve tract called the internal capsule into two masses named the caudate nucleus and the putamen. These differences contribute to a complex circuitry of connections between the striatum and cortex that is specific to primates, reflecting different functions in primate cortical areas.
The amygdalofugal pathway is one of the three major efferent pathways of the amygdala, meaning that it is one of the three principal pathways by which fibers leave the amygdala. It leads from the basolateral nucleus and central nucleus of the amygdala. The amygdala is a limbic structure in the medial temporal lobe of the brain. The other main efferent pathways from the amygdala are the stria terminalis and anterior commissure.
The mammillothalamic tract (MMT) is an efferent pathway of the mammillary bodies which project to the anterior nuclei of the thalamus. The mammillothalamic tract is part of the Papez circuit, starting and finishing in the hippocampus. The fibers of the MMT are heavily myelinated.
The isothalamus is a division used by some researchers in describing the thalamus.
Synaptic gating is the ability of neural circuits to gate inputs by either suppressing or facilitating specific synaptic activity. Selective inhibition of certain synapses has been studied thoroughly, and recent studies have supported the existence of permissively gated synaptic transmission. In general, synaptic gating involves a mechanism of central control over neuronal output. It includes a sort of gatekeeper neuron, which has the ability to influence transmission of information to selected targets independently of the parts of the synapse upon which it exerts its action.
The ventral lateral nucleus (VL) is a nucleus in the ventral nuclear group of the thalamus.
The ventral posterolateral nucleus (VPL) is one of the subdivisions of the ventral posterior nucleus in the ventral nuclear group of the thalamus. It relays sensory information from the second-order neurons of the neospinothalamic tract and medial lemniscus which synapse with the third-order neurons in the nucleus. These then project to the primary somatosensory cortex in the postcentral gyrus.
The trisynaptic circuit or trisynaptic loop is a relay of synaptic transmission in the hippocampus. The trisynaptic circuit is a neural circuit in the hippocampus, which is made up of three major cell groups: granule cells in the dentate gyrus, pyramidal neurons in CA3, and pyramidal neurons in CA1. The hippocampal relay involves 3 main regions within the hippocampus which are classified according to their cell type and projection fibers. The first projection of the hippocampus occurs between the entorhinal cortex (EC) and the dentate gyrus (DG). The entorhinal cortex transmits its signals from the parahippocampal gyrus to the dentate gyrus via granule cell fibers known collectively as the perforant path. The dentate gyrus then synapses on pyramidal cells in CA3 via mossy cell fibers. CA3 then fires to CA1 via Schaffer collaterals which synapse in the subiculum and are carried out through the fornix. Collectively the dentate gyrus, CA1 and CA3 of the hippocampus compose the trisynaptic loop.
The parabrachial nuclei, also known as the parabrachial complex, are a group of nuclei in the dorsolateral pons that surrounds the superior cerebellar peduncle as it enters the brainstem from the cerebellum. They are named from the Latin term for the superior cerebellar peduncle, the brachium conjunctivum. In the human brain, the expansion of the superior cerebellar peduncle expands the parabrachial nuclei, which form a thin strip of grey matter over most of the peduncle. The parabrachial nuclei are typically divided along the lines suggested by Baxter and Olszewski in humans, into a medial parabrachial nucleus and lateral parabrachial nucleus. These have in turn been subdivided into a dozen subnuclei: the superior, dorsal, ventral, internal, external and extreme lateral subnuclei; the lateral crescent and subparabrachial nucleus along the ventrolateral margin of the lateral parabrachial complex; and the medial and external medial subnuclei