From Wikipedia, the free encyclopedia
  (Redirected from Mesencephalon)
Jump to navigation Jump to search
Human brain inferior view description.JPG
Inferior view midbrain (2), above (3)
Human brainstem-thalamus posterior view description.JPG
Human brainstem midbrain (B)
thalamus (A) pons (C)
medulla oblongata (D)
Latin mesencephalon
MeSH D008636
NeuroNames 462
NeuroLex ID birnlex_1667
TA A14.1.03.005
FMA 61993
Anatomical terms of neuroanatomy

The midbrain or mesencephalon (UK: /ˌmɛsɛnˈsɛfəlɒn, -kɛf-/, US: /ˌmɛzənˈsɛfələn/;[1] from Greek mesos 'middle', and enkephalos 'brain'[2]) is a portion of the central nervous system associated with vision, hearing, motor control, sleep/wake, arousal (alertness), and temperature regulation.[3]



The midbrain comprises the tectum, tegmentum, the cerebral aqueduct, and the cerebral peduncles, as well as several nuclei and fasciculi. Caudally the midbrain adjoins the metencephalon (afterbrain) (pons and cerebellum). Rostrally it adjoins the diencephalon (thalamus, hypothalamus, etc.).[4]

Specifically, the midbrain consists of:


Medial and lateral pathways of tectum[edit]

  • The medial descending pathway comprises the vestibulospinal tracts (lateral and medial tracts with control from the cerebellum), reticulospinal tract, and the tectospinal tract. These tracts run through the medial reticular formation, the lateral and medial vestibular nuclei.[5] These tracts extend rostrally and caudally of the tectum. The vestibulospinal tracts; the medial tract originate in the medial and inferior vestibular nuclei moving caudally to the anterior funiculus controlling muscle tone, while the lateral tract originates from lateral vestibular nuclei also referred to as Deiters' nucleus named after Otto Deiters (1834–1863). The reticulospinal tract consists of dense cortical neurons which direct motor input as the tract terminates sequentially down the spine. The tectospinal tract provides stability and posture control.
  • The lateral descending pathway consists of the rubrospinal tract originating from the red nucleus responsible for voluntary motor movement, and partially of the lateral corticospinal tract as this tract does not originate or terminate in the tectum but does play a critical role with afferent and efferent motor control along sidetone rubrospinal tract of the tectum.

Fourth ventricle[edit]

The ventricular system comprises the choroid plexus, which produces cerebral spinal fluid (CSF), the lateral, third, and fourth ventricles responsible for circulating the CSF. The fourth ventricle is the most caudal aspect of the cerebral ventricular system, and is formed by the pons and medulla. The fourth ventricle is connected to the third ventricle via the cerebral aqueduct, and is the smallest ventricle in the ventricular system. Cerebral spinal fluid originates via the choroid plexus, circulating through the ventricular system and recycled into the subarachnoid space. In the fourth ventricle, CSF is recycled through spinal nerve sheaths through the epidural vein. [6]

Cerebral peduncle[edit]

Substantia nigra[edit]

The substantia nigra is located in the midbrain, with a left and right region, with two primary regions; the substantia nigra pars compact and the substantia nigra pars reticular. This region contains three of the four primary dopaminergic tracts and is responsible for coordination of eye movement and voluntary motor movement. The region undergoes extremely high metabolic synthesis of dopamine and norepinephrine through the metabolic conversion of tyrosine to L-DOPA via enzymatic reaction Tyrosine Hydroxlyase (cat-2), to dopamine through Aromatic L-Amino Acid Decarboxylase, and if not used processed further through Dopamine Beta-Hydroxylase into Norepinephrine or Epinephrine via an additional reaction. This region of the brain has been extensively studied in biomedical research since the loss of dopaminergic neurons in this region contributes to the progression of Parkinson's disease.[7] Currently, there is not a cure for Parkinson's disease but there are short-term effective treatments. Exogenous L-DOPA has been shown to be an effective treatment, however long-term use can result in increased dyskinesia and have deleterious effects on the survival of dopaminergic neurons.[7][8] Extensive biomedical research is underway after the initiation of the BRAIN initiative formed by the Obama administration in 2013 with the audacious goal of creating cures and preventive measures by 2023.

Corpora quadrigemina[edit]

The corpora quadrigemina ("quadruplet bodies") are four solid lobes on the dorsal side of the cerebral aqueduct, where the superior posterior pair are called the superior colliculi and the inferior posterior pair are called the inferior colliculi. The homologous structures are called optic lobes in some lower vertebrates (fishes and amphibians) where they integrate sensory information from the eyes and certain auditory reflexes.[9][10]

The four solid lobes help to decussate several fibres of the optic nerve. However, some fibers also show ipsilateral arrangement (i.e., they run parallel on the same side without decussating.)

The superior colliculus is involved with saccadic eye movements; while the inferior is a synapsing point for sound information. The trochlear nerve comes out of the posterior surface of the midbrain, below the inferior colliculus.

Cerebral peduncle[edit]

The cerebral peduncles are paired structures, present on the ventral side of the cerebral aqueduct, and they further carry tegmentum on the dorsal side and cresta or pes on the ventral side, and both of them accommodate the corticospinal tract fibres, from the internal capsule (i.e., ascending + descending tracts = longitudinal tract.) the middle part of cerebral peduncles carry substantia nigra[citation needed] (literally "Black Matter"), which is a type of basal nucleus. It is the only part of the brain that carries melanin pigment.

Between the peduncles is the interpeduncular fossa, which is a cistern filled with cerebrospinal fluid.[citation needed] The oculomotor nerve comes out between the peduncles, and the trochlear nerve is visible wrapping around the outside of the peduncles. The oculomotor is responsible for pupil constriction (parasympathetic) and certain eye movements.[11]

Anatomical features of cross-sections through the midbrain[edit]

Cross-section of the midbrain at the level of the superior colliculus.
Cross-section of the midbrain at the level of the inferior colliculus.

The midbrain is usually sectioned at the level of the superior and inferior colliculi.

Mesencephalon of human embryo

One mnemonic for remembering the structures of the midbrain involves visualizing the mesencephalic cross-section as an upside down bear face. The two red nuclei are the eyes of the bear and the cerebral crura are the ears. The tectum is the chin and the cerebral peduncles are the face and ears.


During embryonic development, the midbrain arises from the second vesicle, also known as the mesencephalon, of the neural tube. Unlike the other two vesicles, the forebrain and hindbrain, the midbrain remains undivided for the remainder of neural development. It does not split into other brain areas. while the forebrain, for example, divides into the telencephalon and the diencephalon.[13]

Throughout embryonic development, the cells within the midbrain continually multiply and compress the still-forming cerebral aqueduct. Partial or total obstruction of the cerebral aqueduct during development can lead to congenital hydrocephalus.[14]


The mesencephalon is considered part of the brainstem. Its substantia nigra is closely associated with motor system pathways of the basal ganglia. The human mesencephalon is archipallian in origin, meaning that its general architecture is shared with the most ancient of vertebrates. Dopamine produced in the substantia nigra and ventral tegmental area plays a role in excitation, motivation and habituation of species from humans to the most elementary animals such as insects. Laboratory house mice from lines that have been selectively bred for high voluntary wheel running have enlarged midbrains.[15] The midbrain helps to relay information for vision and hearing.

See also[edit]


  1. ^ "mesencephalon". Oxford English Dictionary (3rd ed.). Oxford University Press. September 2005.  (Subscription or UK public library membership required.)
  2. ^ Mosby's Medical, Nursing & Allied Health Dictionary,≈ Fourth Edition, Mosby-Year Book 1994, p. 981
  3. ^ Breedlove, Watson, & Rosenzweig. Biological Psychology, 6th Edition, 2010, pp. 45-46
  4. ^ "Archived copy". Archived from the original on 2011-04-27. Retrieved 2011-03-05. 
  5. ^ Kandel, Eric (2000). Principles of Neural Science. McGraw-Hill. p. 669. ISBN 0-8385-7701-6. 
  6. ^ Laterra, John. "Blood—Cerebrospinal Fluid Barrier". NCBI. 
  7. ^ a b Damier, P.; Hirsch, E. C.; Agid, Y.; Graybiel, A. M. (1999-08-01). "The substantia nigra of the human brainII. Patterns of loss of dopamine-containing neurons in Parkinson's disease". Brain. 122 (8): 1437–1448. doi:10.1093/brain/122.8.1437. ISSN 0006-8950. 
  8. ^ Smith, L.M.; Parr-Brownlie, L.C.; Duncan, E.J.; Black, M.A.; Gemmell, N.J.; Dearden, P.K.; Reynolds, J.N.J. "Striatal mRNA expression patterns underlying peak dose l-DOPA-induced dyskinesia in the 6-OHDA hemiparkinsonian rat". Neuroscience. 324: 238–251. doi:10.1016/j.neuroscience.2016.03.012. 
  9. ^ Collins Dictionary of Biology, 3rd ed. © W. G. Hale, V. A. Saunders, J. P. Margham 2005
  10. ^ Ferrier, David (1886). "Functions of the optic lobes or corpora quadrigemina". doi:10.1037/12789-005. 
  11. ^ Haines, Duane E. Neuroanatomy : an atlas of structures, sections, and systems (8th ed.). Philadelphia: Wolters Kluwer/ Lippincott Williams & Wilkins Health. p. 42. ISBN 978-1-60547-653-7. 
  12. ^ a b c Martin. Neuroanatomy Text and Atlas, Second edition. 1996, pp. 522-525.
  13. ^ Martin. Neuroanatomy Text and Atlas, Second Edition, 1996, pp. 35-36.
  14. ^ "Hydrocephalus Fact Sheet". National Institute of Neurological Disorders and Stroke. February 2008. Retrieved 2011-03-23. 
  15. ^ Kolb, E. M., E. L. Rezende, L. Holness, A. Radtke, S. K. Lee, A. Obenaus, and Garland T, Jr. 2013. Mice selectively bred for high voluntary wheel running have larger midbrains: support for the mosaic model of brain evolution. Journal of Experimental Biology 216:515-523.