Basilar part of pons | |
---|---|
Details | |
Identifiers | |
Latin | Pars basilaris pontis, basis pontis |
NeuroNames | 616 |
NeuroLex ID | birnlex_1043 |
TA98 | A14.1.05.101 |
TA2 | 5925 |
FMA | 72244 |
Anatomical terms of neuroanatomy |
The basilar part of pons, also known as basis pontis, or basilar pons, is the ventral part of the pons (ventral pons) in the brainstem; the dorsal part (dorsal pons) is known as the pontine tegmentum.
The basilar part of the pons makes up two thirds of the pons. [1] It has a ridged appearance with a shallow groove at the midline. This groove is the basilar sulcus and is covered by the basilar artery. [2] The basilar artery feeds into the circle of Willis providing blood supply to the brainstem and cerebellum. [3] The ridged appearance is due to the fibers that come out of the pons to enter the cerebellum. [2] The basilar pons contains fibers from the corticospinal tract (a descending pathway for neurons to reach other structures in the body), pontine nuclei, and transverse pontine fibers. [1] The corticospinal tract carries fibres from the primary motor cortex to the spinal cord, aiding in voluntary motor movement of the body. In addition to passing through the ventral pons, corticospinal tract fibers go through other structures of the brainstem, including the internal capsule and the crus cerebri. [4]
Integral to the basilar pons are the pontine nuclei. The pontine nuclei are responsible for projecting fibers that go to the opposite cerebellar hemisphere through the middle cerebellar peduncle, changing the fibers into transverse pontine fibers. [1] The fibers of the pontine nuclei are all important to motor function, including fiber bundles such as the corticospinal fibers and corticopontine-pontocerebellar system. [5] Specifically, the basilar part of the pons contains all the corticofugal fibers, which include the corticospinal, corticobulbar (or corticonuclear), and corticopontine fibers. [6] The basal pontine nuclei provides most of the cortical information to the cerebellum received from the corticopontine fibers. [7]
Tissue death (infarction), in this region can impair motor functioning. [8] A lacunar stroke of the base of the pons is known to cause contralateral dysarthria-clumsy hand syndrome.
The basilar pons undergoes demyelination in the condition known as central pontine myelinolysis. This disorder is due to the rapid intravenous correction of hyponatremia.
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 posterior stalk-like part of the brain that connects the cerebrum 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, and sometimes the diencephalon is included in the brainstem.
The midbrain or mesencephalon is the rostral-most portion of the brainstem connecting the diencephalon and cerebrum with the pons. It consists of the cerebral peduncles, tegmentum, and tectum.
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) 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 paired white matter structure, as a two-way tract, carrying ascending and descending fibers, to and from the cerebral cortex. The internal capsule is situated in the inferomedial part of each cerebral hemisphere of the brain. It carries information past the subcortical basal ganglia. As it courses it separates the caudate nucleus and the thalamus from the putamen and the globus pallidus. It also separates the caudate nucleus and the putamen in the dorsal striatum, a brain region involved in motor and reward pathways.
The medial longitudinal fasciculus (MLF) is a prominent bundle of nerve fibres which pass within the ventral/anterior portion of periaqueductal gray of the mesencephalon (midbrain). It contains the interstitial nucleus of Cajal, responsible for oculomotor control, head posture, and vertical eye movement.
The corticobulbartract is a two-neuron white matter motor pathway connecting the motor cortex in the cerebral cortex to the medullary pyramids, which are part of the brainstem's medulla oblongata region, and are primarily involved in carrying the motor function of the non-oculomotor cranial nerves, like muscles of the face, head and neck. The corticobulbar tract is one of the pyramidal tracts, the other being the corticospinal tract.
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 pontine nuclei 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.
The spinocerebellar tracts are nerve tracts originating in the spinal cord and terminating in the same side (ipsilateral) of the cerebellum. The two main tracts are the dorsal spinocerebellar tract, and the ventral spinocerebellar tract. Both of these tracts are located in the peripheral region of the lateral funiculi. Other tracts are the rostral spinocerebellar tract, and the cuneocerebellar tract.
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 globose nucleus is one of the deep cerebellar nuclei. It is located medial to the emboliform nucleus, and lateral to the fastigial nucleus. The globose nucleus and emboliform nucleus are known collectively as the interposed nuclei.
The interposed nucleus is the combined paired globose and emboliform nuclei, on either side of the cerebellum. It is located in the roof of the fourth ventricle, lateral to the fastigial nucleus. The emboliform nucleus is the anterior interposed nucleus, and the globose nucleus is the posterior interposed nucleus.
In the human brain, the superior cerebellar peduncle is one of the three paired cerebellar peduncles of bundled fibers that connect the cerebellum to the brainstem. The superior cerebellar peduncle connects to the midbrain. It consists mainly of efferent fibers, the cerebellothalamic tract that runs from a cerebellar hemisphere to the contralateral thalamus, and the cerebellorubral tract that runs from a cerebellar hemisphere to the red nucleus. It also contains afferent tracts, most prominent of which is the ventral spinocerebellar tract. Other afferent tracts are the ventral trigeminal tract, tectocerebellar fibers, and noradrenergic fibers from the locus coeruleus. The superior peduncle emerges from the upper and medial parts of the white matter of each cerebellar hemisphere and is placed under cover of the upper part of the cerebellum.
The middle cerebellar peduncle is one of three paired cerebellar peduncles connecting the brainstem to the cerebellum. The connection is from the pons. It connects the pons to the cerebellum, with fibres originating from the pontine nuclei, and travelling to the opposite cerebellar hemisphere. 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 pontocerebellar fibers are the second-order neuron fibers of the corticopontocerebellar tracts that cross to the other side of the pons and run within the middle cerebellar peduncles, from the pons to the contralateral cerebellum. They arise from the pontine nuclei as the second part of the corticopontocerebellar tract, and decussate (cross-over) in the pons before passing through the middle cerebellar peduncles to reach and terminate in the contralateral posterior lobe of the cerebellum (neocerebellum). It is part of a pathway involved in the coordination of voluntary movements.
The central tegmental tract is a structure in the midbrain and pons. It is situated in the central portion of the reticular formation. It contains:
Corticopontine fibers are projections from layer V of the cerebral cortex to the pontine nuclei of the ventral pons. They represent the first link in a cortico-cerebello-cortical pathway mediating neocerebellar control of the motor cortex. The pathway is especially important for voluntary movements.
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.
This article incorporates text in the public domain from page 785 of the 20th edition of Gray's Anatomy (1918)