Pontine nuclei | |
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![]() Cross section through the lower pons showing the pontine nuclei (#22) and the pontocerebellar fibers emerging from them to become the middle cerebellar peduncle | |
Details | |
Identifiers | |
Latin | nuclei pontis |
NeuroNames | 617 |
NeuroLex ID | birnlex_1516 |
TA98 | A14.1.05.202 |
TA2 | 5926 |
FMA | 72512 |
Anatomical terms of neuroanatomy |
The pontine nuclei (or griseum pontis) are all neurons of the ventral pons collectively. Corticopontine fibres project from the primary motor cortex to the ipsilateral pontine nucleus; pontocerebellar fibers then relay the information to the contralateral cerebellum via the middle cerebellar peduncle.
They involved in motor function: the pontine nulcei are involved in adjusting movements according to their outcome (movement error correction), and are therefore important in learning motor skills.[ citation needed ]
The pontine nuclei encompass all of the about 20 million neurons scattered throughout the basilar part of pons. [1] The pontine nuclei nuclei extend caudally into the medulla oblongata as the arcuate nucleus which is functionally homologous with the pontine nuclei.[ citation needed ]
Corticopontine fibres arise primarily from the neocortex layer V of the premotor, somatosensory, non-striate visual, posterior parietal, and cingulate cerebral cortex; there are also a few fibers originating from the prefrontal, temporal, and striate cortex. [1]
Pontine nuclei also receive afferents from the lateral geniculate nucleus, superior colliculus, pretectal nuclei, hypothalamus, medial mammillary nucleus, cerebellum trigeminal nuclei, dorsal column nuclei, locus coeruleus, periaqueductal gray, raphe nuclei, and reticular formation. [1]
Pontocerebellar fibers are the sole efferent pathway of the pontine nuclei. The fibers mostly decussate within the pons to pass through the (contralateral) middle cerebellar peduncle to terminate in the contralateral cerebellum as mossy fibers; they form terminal synapses in the cerebellar cortex, but also issue collaterals to the cerebellar nuclei. [1]
Likely, all of the neurons of the pontine nuclei are glutaminergic. [1]
The cerebellum is a major feature of the hindbrain of all vertebrates. Although usually smaller than the cerebrum, in some animals such as the mormyrid fishes it may be as large as it or even larger. In humans, the cerebellum plays an important role in motor control and cognitive functions such as attention and language as well as emotional control such as regulating fear and pleasure responses, but its movement-related functions are the most solidly established. The human cerebellum does not initiate movement, but contributes to coordination, precision, and accurate timing: it receives input from sensory systems of the spinal cord and from other parts of the brain, and integrates these inputs to fine-tune motor activity. Cerebellar damage produces disorders in fine movement, equilibrium, posture, and motor learning in humans.
The pons is part of the brainstem that in humans and other mammals, lies inferior to the midbrain, superior to the medulla oblongata and anterior to the cerebellum.
The brainstem is the stalk-like part of the brain that interconnects the cerebrum and diencephalon with the spinal cord. In the human brain, the brainstem is composed of the midbrain, the pons, and the medulla oblongata. The midbrain is continuous with the thalamus of the diencephalon through the tentorial notch.
The cerebral peduncles are the two stalks that attach the cerebrum to the brainstem. They are structures at the front of the midbrain which arise from the ventral pons and contain the large ascending (sensory) and descending (motor) nerve tracts that run to and from the cerebrum from the pons. Mainly, the three common areas that give rise to the cerebral peduncles are the cerebral cortex, the spinal cord and the cerebellum. The region includes the tegmentum, crus cerebri and pretectum. By this definition, the cerebral peduncles are also known as the basis pedunculi, while the large ventral bundle of efferent fibers is referred to as the cerebral crus or the pes pedunculi.
The internal capsule is a white matter structure situated in the inferomedial part of each cerebral hemisphere of the brain. It carries information past the basal ganglia, separating the caudate nucleus and the thalamus from the putamen and the globus pallidus. The internal capsule contains both ascending and descending axons, going to and coming from the cerebral cortex. It also separates the caudate nucleus and the putamen in the dorsal striatum, a brain region involved in motor and reward pathways.
The spinocerebellar tract is a nerve tract originating in the spinal cord and terminating in the same side (ipsilateral) of the cerebellum.
The upper part of the posterior district of the medulla oblongata is occupied by the inferior cerebellar peduncle, a thick rope-like strand situated between the lower part of the fourth ventricle and the roots of the glossopharyngeal and vagus nerves.
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 dentate nucleus is responsible for the planning, initiation and control of voluntary movements. The dorsal region of the dentate nucleus contains output channels involved in motor function, which is the movement of skeletal muscle, while the ventral region contains output channels involved in nonmotor function, such as conscious thought and visuospatial function.
The fastigial nucleus is located in each hemisphere of the cerebellum. It is one of the four deep cerebellar nuclei.
The flocculus is a small lobe of the cerebellum at the posterior border of the middle cerebellar peduncle anterior to the biventer lobule. Like other parts of the cerebellum, the flocculus is involved in motor control. It is an essential part of the vestibulo-ocular reflex, and aids in the learning of basic motor skills in the brain.
Cerebellar peduncles connect the cerebellum to the brain stem. There are six cerebellar peduncles in total, three on each side:
The middle cerebellar peduncle is a paired structure of the brain. It connects the pons to the cerebellum, with fibres originating from the pontine nucleus and travelling to the opposite hemisphere of the cerebellar cortex. It is supplied by the anterior inferior cerebellar artery (AICA) and branches from the basilar artery. It conveys information from the cerebrum and the pons to the cerebellum.
The projection fibers consist of efferent and afferent fibers uniting the cortex with the lower parts of the brain and with the spinal cord. In human neuroanatomy, bundles of axons called tracts, within the brain, can be categorized by their function into association fibers, projection fibers, and commissural fibers.
The frontopontine fibers or frontopontine tract are corticopontine fibers projecting from the cortex of the frontal lobe to the pons. In the internal capsule, the fibers descend predominately in the anterior limb, passing inferior to the thalamus to reach the mesencephalon (midbrain) where they descend in the medial portion of base of the cerebral peduncles. In the pons, the fibers flare out between the pontine nuclei.
The reticulotegmental nucleus, tegmental pontine reticular nucleus is an area within the floor of the pons, in the brain stem. This area is known to affect the cerebellum with its axonal projections.
The basilar part of pons, also known as basis pontis, is the ventral part of the pons; the dorsal part is known as the pontine tegmentum.
The juxtarestiform body is the smaller, medial subdivision of each inferior cerebellar peduncle.
The pontocerebellar fibers are the second-order fibers of the corticopontocerebellar tract. They arise from the nuclei pontis as the second leg of the path of the corticopontocerebellar tract, and deecussate (cross-over) in the pons before passing through the middle cerebellar peduncle to reach and terminate in the contralateral posterior lobe of cerebellum (neocerebellum). It is part of a pathway involved in coordination of voluntary movements.
Corticopontine fibers are projections from the cerebral cortex to the pons. Depending upon the lobe of origin, they can be classified as frontopontine fibers, parietopontine fibers, temporopontine fibers or occipitopontine fibers.
The anatomy of the cerebellum can be viewed at three levels. At the level of gross anatomy, the cerebellum consists of a tightly folded and crumpled layer of cortex, with white matter underneath, several deep nuclei embedded in the white matter, and a fluid-filled ventricle in the middle. At the intermediate level, the cerebellum and its auxiliary structures can be broken down into several hundred or thousand independently functioning modules or compartments known as microzones. At the microscopic level, each module consists of the same small set of neuronal elements, laid out with a highly stereotyped geometry.