See more Thalamus articles on AOD.

Powered by
Share this page on
Article provided by Wikipedia

( => ( => ( => Thalamus [pageid] => 78227 ) =>
""Brain chrischan thalamus.jpg
thalamus marked ("MRI cross-section)
anterolateral view
Part of "Diencephalon
Parts See "List of thalamic nuclei
"Artery "Posterior cerebral artery and branches
"Latin thalamus dorsalis
"MeSH D013788
"NeuroNames 300
"NeuroLex ID birnlex_954
"TA A14.1.08.101
"TE E5.
"FMA 62007
"Anatomical terms of neuroanatomy

The thalamus (from "Greek θάλαμος, "chamber")[1] is the large mass of "gray matter in the dorsal part of the diencephalon of the brain with several functions such as relaying of "sensory signals, including "motor signals, to the cerebral cortex,[2][3]["page needed] and the regulation of "consciousness, "sleep, and "alertness.[4]

It is a midline symmetrical structure of two halves, within the "vertebrate "brain, situated between the "cerebral cortex and the "midbrain.

It is the main product of the "embryonic "diencephalon, as first assigned by "Wilhelm His, Sr. in 1893.[5]



The thalamus in a 360° rotation

The thalamus is located in the "forebrain which is superior to the midbrain, near the center of the brain, with nerve fibers projecting out to the cerebral cortex in all directions. The medial surface of the thalamus constitutes the upper part of the lateral wall of the "third ventricle, and is connected to the corresponding surface of the opposite thalamus by a flattened gray band, the "interthalamic adhesion.

Blood supply[edit]

The thalamus derives its blood supply from a number of arteries: the polar artery ("posterior communicating artery), paramedian thalamic-subthalamic arteries, inferolateral (thalamogeniculate) arteries, and "posterior (medial and lateral) choroidal arteries.[6] These are all branches of the "posterior cerebral artery.[7]

Some people have the "artery of Percheron, which is a rare anatomic variation in which a single arterial trunk arises from the posterior cerebral artery to supply both parts of the thalamus.

Thalamic nuclei[edit]

Nuclei of the thalamus

The thalamus is part of a nuclear complex structured of four parts, the "hypothalamus, "epithalamus, "prethalamus (formerly called ventral thalamus), and dorsal thalamus.[8]["need quotation to verify]

Derivatives of the "diencephalon also include the dorsally-located "epithalamus (essentially the "habenula and annexes) and the perithalamus (prethalamus) containing the "zona incerta and the "thalamic reticular nucleus. Due to their different "ontogenetic origins, the epithalamus and the perithalamus are formally distinguished from the thalamus proper.

The thalamus comprises a system of "lamellae (made up of "myelinated "fibers) separating different thalamic subparts. Other areas are defined by distinct clusters of "neurons, such as the "periventricular nucleus, the intralaminar elements, the "nucleus limitans", and others.[9] These latter structures, different in structure from the major part of the thalamus, have been grouped together into the "allothalamus as opposed to the "isothalamus.[10] This distinction simplifies the global description of the thalamus.


The thalamus is connected to the spinal cord via the "spinothalamic tract.

The thalamus is manifoldly connected to the hippocampus via the "mammillo-thalamic tract, this tract comprises the "mammillary bodies and "fornix.[11]

The thalamus is connected to the "cerebral cortex via the "thalamocortical radiations.[12]

The "spinothalamic tract is a sensory pathway originating in the spinal cord. It transmits information to the thalamus about pain, temperature, itch and "crude touch. There are two main parts: the "lateral spinothalamic tract, which transmits pain and temperature, and the "anterior (or ventral) spinothalamic tract, which transmits crude touch and pressure.


The thalamus has multiple functions, generally believed to act as a relay station, or "hub, relaying information between different subcortical areas and the "cerebral cortex.[13] In particular, every sensory system (with the exception of the "olfactory system) includes a thalamic nucleus that receives sensory signals and sends them to the associated primary cortical area.["citation needed] For the visual system, for example, inputs from the "retina are sent to the "lateral geniculate nucleus of the thalamus, which in turn projects to the "visual cortex in the "occipital lobe.["citation needed] The thalamus is believed to both process sensory information as well as relay it—each of the primary sensory relay areas receives strong feedback connections from the cerebral cortex.["citation needed] Similarly the "medial geniculate nucleus acts as a key "auditory relay between the "inferior colliculus of the "midbrain and the "primary auditory cortex.["citation needed] The "ventral posterior nucleus is a key "somatosensory relay, which sends touch and "proprioceptive information to the "primary somatosensory cortex.["citation needed]

The thalamus also plays an important role in regulating states of "sleep and wakefulness.[14] Thalamic nuclei have strong reciprocal connections with the cerebral cortex, forming "thalamo-cortico-thalamic circuits that are believed to be involved with "consciousness.["citation needed] The thalamus plays a major role in regulating arousal, the level of awareness, and activity. Damage to the thalamus can lead to permanent "coma.["citation needed]

The role of the thalamus in the more anterior "pallidal and "nigral territories in the "basal ganglia system disturbances is recognized but still poorly understood. The contribution of the thalamus to vestibular or to "tectal functions is almost ignored. The thalamus has been thought of as a "relay" that simply forwards signals to the cerebral cortex. Newer research suggests that thalamic function is more selective.[15] Many different functions are linked to various regions of the thalamus. This is the case for many of the sensory systems (except for the olfactory system), such as the "auditory, "somatic, "visceral, "gustatory and "visual systems where localized lesions provoke specific sensory deficits. A major role of the thalamus is support of motor and language systems, and much of the circuitry implicated for these systems is shared. The thalamus is functionally connected to the "hippocampus[16] as part of the extended hippocampal system at the thalamic anterior nuclei[17] with respect to spatial memory and spatial sensory datum they are crucial for human episodic memory and rodent event memory.[18][19] There is support for the hypothesis that thalamic regions connection to particular parts of the mesio-temporal lobe provide differentiation of the functioning of recollective and familiarity memory.[11]

The neuronal information processes necessary for motor control were proposed as a network involving the thalamus as a subcortical motor center.[20] Through investigations of the anatomy of the brains of primates[21] the nature of the interconnected tissues of the "cerebellum to the multiple motor cortices suggested that the thalamus fulfills a key function in providing the specific channels from the basal ganglia and "cerebellum to the cortical motor areas.[22][23] In an investigation of the "saccade and "antisaccade[24] motor response in three monkeys, the thalamic regions were found to be involved in the generation of antisaccade eye-movement (that is, the ability to inhibit the reflexive jerking movement of the eyes in the direction of a presented stimulus].[25]

Recent research suggests that the mediodorsal thalamus may play a broader role in cognition. Specifically, the mediodorsal thalamus may "amplify the connectivity (signaling strength) of just the circuits in the cortex appropriate for the current context and thereby contribute to the flexibility (of the mammalian brain) to make complex decisions by wiring the many associations on which decisions depend into weakly connected cortical circuits."[26] Researchers founds that "enhancing MD activity magnified the ability of mice to “think,”[26] driving down by more than 25 percent their error rate in deciding which conflicting sensory stimuli to follow to find the reward." [27]


The thalamic complex is composed of the perithalamus (or prethalamus, previously also known as ventral thalamus), the mid-diencephalic organiser (which forms later the "zona limitans intrathalamica (ZLI) ) and the thalamus (dorsal thalamus).[28][29] The development of the thalamus can be subdivided into three steps.[30] The thalamus is the largest structure deriving from the embryonic "diencephalon, the posterior part of the forebrain situated between the midbrain and the cerebrum.

Early brain development[edit]

After "neurulation the anlage of the "prethalamus and the thalamus is induced within the neural tube. Data from different vertebrate model organisms support a model in which the interaction between two "transcription factors, Fez and Otx, are of decisive importance. Fez is expressed in the prethalamus, and functional experiments show that Fez is required for prethalamus formation.[31][32] Posteriorly, Otx1 and Otx2 abut the expression domain of Fez and are required for proper development of the thalamus.[33][34]

Formation of progenitor domains[edit]

Early in thalamic development two progenitor domains form, a caudal domain (TH-C) and a rostral domain (TH-R). The caudal domain gives rise to all of the glutamatergic neurons in the adult thalamus while the rostral domain gives rise to all of the GABAergic neurons in the adult thalamus.[35]

The formation of the mid-diencephalic organiser (MDO)[edit]

At the interface between the expression domains of Fez and Otx, the mid-diencephalic organizer (MDO, also called the ZLI organiser) is induced within the thalamic "anlage. The MDO is the central signalling organizer in the thalamus. A lack of the organizer leads to the absence of the thalamus. The MDO matures from ventral to dorsal during development. Members of the "SHH family and of the "Wnt family are the main principal signals emitted by the MDO.

Besides its importance as signalling center, the organizer matures into the morphological structure of the "zona limitans intrathalamica (ZLI).

Maturation and parcellation of the thalamus[edit]

After its induction, the MDO starts to orchestrate the development of the thalamic anlage by release of signalling molecules such as "SHH.[36] In mice, the function of signaling at the MDO has not been addressed directly due to a complete absence of the "diencephalon in SHH mutants.[37]

Studies in chicks have shown that SHH is both necessary and sufficient for thalamic gene induction.[38] In "zebrafish, it was shown that the expression of two SHH genes, SHH-a and SHH-b (formerly described as twhh) mark the MDO territory, and that SHH signaling is sufficient for the molecular differentiation of both the prethalamus and the thalamus but is not required for their maintenance and SHH signaling from the MDO/alar plate is sufficient for the maturation of prethalamic and thalamic territory while ventral Shh signals are dispensable.[39]

The exposure to SHH leads to differentiation of thalamic neurons. SHH signaling from the MDO induces a posterior-to-anterior wave of expression the proneural gene "Neurogenin1 in the major (caudal) part of the thalamus, and Ascl1 (formerly Mash1) in the remaining narrow stripe of rostral thalamic cells immediately adjacent to the MDO, and in the prethalamus.[40][41]

This zonation of proneural gene expression leads to the differentiation of glutamatergic relay neurons from the Neurogenin1+ precursors and of GABAergic inhibitory neurons from the Ascl1+ precursors. In fish, selection of these alternative neurotransmitter fates is controlled by the dynamic expression of Her6 the homolog of "HES1. Expression of this hairy-like bHLH "transcription factor, which represses Neurogenin but is required for Ascl1, is progressively lost from the caudal thalamus but maintained in the prethalamus and in the stripe of rostral thalamic cells. In addition, studies on chick and mice have shown that blocking the Shh pathway leads to absence of the rostral thalamus and substantial decrease of the caudal thalamus. The rostral thalamus will give rise to the reticular nucleus mainly whereby the caudal thalamus will form the relay thalamus and will be further subdivided in the "thalamic nuclei.[30]

In humans, a common genetic variation in the promotor region of the "serotonin transporter (the SERT-long and -short allele: "5-HTTLPR) has been shown to affect the development of several regions of the thalamus in adults. People who inherit two short "alleles (SERT-ss) have more neurons and a larger volume in the "pulvinar and possibly the limbic regions of the thalamus. Enlargement of the thalamus provides an anatomical basis for why people who inherit two SERT-ss alleles are more vulnerable to "major depression, "posttraumatic stress disorder, and suicide.[42]

Clinical significance[edit]

A cerebrovascular accident ("stroke) can lead to the "thalamic syndrome,[43] which involves a one-sided burning or aching sensation often accompanied by "mood swings. Bilateral "ischemia of the area supplied by the paramedian artery can cause serious problems including "akinetic mutism, and be accompanied by "oculomotor problems. A related concept is "thalamocortical dysrhythmia. The occlusion of the "artery of Percheron can lead to a bilateral thalamus infarction.

"Korsakoff's syndrome stems from damage to the "mammillary body, the "mammillothalamic fasciculus or the thalamus.

"Fatal familial insomnia is a hereditary "prion disease in which degeneration of the thalamus occurs, causing the patient to gradually lose his ability to sleep and progressing to a state of total "insomnia, which invariably leads to death. In contrast, damage to the thalamus can result in "coma.

Additional images[edit]

Drawings are by Gray and Carter (1858).[44]

See also[edit]


  1. ^ "Harper - index & "University of Washington Faculty Web Server & Search engine search page + "Perseus Project Retrieved 2012-02-09
  2. ^ Sherman, S. (2006). "Thalamus". Scholarpedia. 1 (9): 1583. "doi:10.4249/scholarpedia.1583. 
  3. ^ Sherman, S. Murray; Guillery, R. W. (2000). Exploring the Thalamus. Academic Press. "ISBN "978-0-12-305460-9. 
  4. ^ "What you can learn from Einsteins quirky habits"
  5. ^ The Thalamus - Springer. "doi:10.1007/978-1-4615-1749-8. 
  6. ^ Percheron, G. (1982). "The arterial supply of the thalamus". In Schaltenbrand; Walker, A. E. Stereotaxy of the human brain. Stuttgart: Thieme. pp. 218–32. 
  7. ^ Knipe, H Jones, J et al. Thalamus
  8. ^ Herrero, María-Trinidad; Barcia, Carlos; Navarro, Juana (2002). "Functional anatomy of thalamus and basal ganglia". Child's Nervous System. 18 (8): 386–404. "doi:10.1007/s00381-002-0604-1. 
  9. ^ Jones Edward G. (2007) "The Thalamus" Cambridge Uni. Press["page needed]
  10. ^ Percheron, G. (2003). "Thalamus". In Paxinos, G.; May, J. The human nervous system (2nd ed.). Amsterdam: Elsevier. pp. 592–675. 
  11. ^ a b Carlesimo, GA; Lombardi, MG; Caltagirone, C (2011). "Vascular thalamic amnesia: A reappraisal". Neuropsychologia. 49 (5): 777–89. "doi:10.1016/j.neuropsychologia.2011.01.026. "PMID 21255590. 
  12. ^ "University of Washington (1991). "Thalamocortical radiations". 
  13. ^ Gazzaniga; Ivry; Mangun, Michael, S.; Richard B.; George R. (2014). Cognitive Neuroscience - The Biology of The Mind. New York: W.W. Norton. p. 45. "ISBN "978-0-393-91348-4. 
  14. ^ Steriade, Mircea; Llinás, Rodolfo R. (1988). "The Functional States of the Thalamus and the Associated Neuronal Interplay". Physiological Reviews. 68 (3): 649–742. "PMID 2839857. 
  15. ^ Leonard, Abigail W. (August 17, 2006). "Your Brain Boots Up Like a Computer". LiveScience. 
  16. ^ Stein, Thor; Moritz, Chad; Quigley, Michelle; Cordes, Dietmar; Haughton, Victor; Meyerand, Elizabeth (2000). "Functional Connectivity in the Thalamus and Hippocampus Studied with Functional MR Imaging". American Journal of Neuroradiology. 21 (8): 1397–401. "PMID 11003270. 
  17. ^ Aggleton, John P.; Brown, Malcolm W. (1999). "Episodic memory, amnesia, and the hippocampal–anterior thalamic axis". Behavioral and Brain Sciences. 22 (3): 425–44; discussion 444–89. "doi:10.1017/S0140525X99002034. "PMID 11301518. 
  18. ^ Aggleton, John P.; O'Mara, Shane M.; Vann, Seralynne D.; Wright, Nick F.; Tsanov, Marian; Erichsen, Jonathan T. (2010). "Hippocampal-anterior thalamic pathways for memory: Uncovering a network of direct and indirect actions". European Journal of Neuroscience. 31 (12): 2292–307. "doi:10.1111/j.1460-9568.2010.07251.x. "PMC 2936113Freely accessible. "PMID 20550571. 
  19. ^ Burgess, Neil; Maguire, Eleanor A; O'Keefe, John (2002). "The Human Hippocampus and Spatial and Episodic Memory". Neuron. 35 (4): 625–41. "doi:10.1016/S0896-6273(02)00830-9. "PMID 12194864. 
  20. ^ Evarts, E V; Thach, W T (1969). "Motor Mechanisms of the CNS: Cerebrocerebellar Interrelations". Annual Review of Physiology. 31: 451–98. "doi:10.1146/ "PMID 4885774. 
  21. ^ Orioli, PJ; Strick, PL (1989). "Cerebellar connections with the motor cortex and the arcuate premotor area: An analysis employing retrograde transneuronal transport of WGA-HRP". The Journal of Comparative Neurology. 288 (4): 612–26. "doi:10.1002/cne.902880408. "PMID 2478593. 
  22. ^ Asanuma C, Thach WT, Jones EG (May 1983). "Cytoarchitectonic delineation of the ventral lateral thalamic region in the monkey". Brain Research. 286 (3): 219–35. "doi:10.1016/0165-0173(83)90014-0. "PMID 6850357. 
  23. ^ Kurata, K (2005). "Activity properties and location of neurons in the motor thalamus that project to the cortical motor areas in monkeys". Journal of Neurophysiology. 94 (1): 550–66. "doi:10.1152/jn.01034.2004. "PMID 15703228. 
  24. ^["full citation needed]
  25. ^ Kunimatsu, J; Tanaka, M (2010). "Roles of the primate motor thalamus in the generation of antisaccades". Journal of Neuroscience. 30 (14): 5108–17. "doi:10.1523/JNEUROSCI.0406-10.2010. "PMID 20371831. 
  26. ^ a b "New Role Discovered For Brain Region". Neuroscience News. 2017-05-03. Retrieved 2017-12-03. 
  27. ^ Schmitt, L. Ian; Wimmer, Ralf D.; Nakajima, Miho; Happ, Michael; Mofakham, Sima; Halassa, Michael M. (11 May 2017). "Thalamic amplification of cortical connectivity sustains attentional control". Nature. 545 (7653): 219–223. "doi:10.1038/nature22073. "ISSN 1476-4687. "PMC 5570520Freely accessible. "PMID 28467827. 
  28. ^ Kuhlenbeck, Hartwig (1937). "The ontogenetic development of the diencephalic centers in a bird's brain (chick) and comparison with the reptilian and mammalian diencephalon". The Journal of Comparative Neurology. 66: 23–75. "doi:10.1002/cne.900660103. 
  29. ^ Shimamura, K; Hartigan, DJ; Martinez, S; Puelles, L; Rubenstein, JL (1995). "Longitudinal organization of the anterior neural plate and neural tube". Development. 121 (12): 3923–33. "PMID 8575293. 
  30. ^ a b Scholpp, Steffen; Lumsden, Andrew (2010). "Building a bridal chamber: Development of the thalamus". Trends in Neurosciences. 33 (8): 373–80. "doi:10.1016/j.tins.2010.05.003. "PMC 2954313Freely accessible. "PMID 20541814. 
  31. ^ Hirata, T.; Nakazawa, M; Muraoka, O; Nakayama, R; Suda, Y; Hibi, M (2006). "Zinc-finger genes Fez and Fez-like function in the establishment of diencephalon subdivisions". Development. 133 (20): 3993–4004. "doi:10.1242/dev.02585. "PMID 16971467. 
  32. ^ Jeong, J.-Y.; Einhorn, Z.; Mathur, P.; Chen, L.; Lee, S.; Kawakami, K.; Guo, S. (2007). "Patterning the zebrafish diencephalon by the conserved zinc-finger protein Fezl". Development. 134 (1): 127–36. "doi:10.1242/dev.02705. "PMID 17164418. 
  33. ^ Acampora, D; Avantaggiato, V; Tuorto, F; Simeone, A (1997). "Genetic control of brain morphogenesis through Otx gene dosage requirement". Development. 124 (18): 3639–50. "PMID 9342056. 
  34. ^ Scholpp, S.; Foucher, I.; Staudt, N.; Peukert, D.; Lumsden, A.; Houart, C. (2007). "Otx1l, Otx2 and Irx1b establish and position the ZLI in the diencephalon". Development. 134 (17): 3167–76. "doi:10.1242/dev.001461. "PMID 17670791. 
  35. ^ Song, Hobeom; Lee, Bumwhee; Pyun, Dohoon; Guimera, Jordi; Son, Youngsook; Yoon, Jaeseung; Baek, Kwanghee; Wurst, Wolfgang; Jeong, Yongsu (2015-02-15). "Ascl1 and Helt act combinatorially to specify thalamic neuronal identity by repressing Dlxs activation". Developmental Biology. 398 (2): 280–291. "doi:10.1016/j.ydbio.2014.12.003. "ISSN 1095-564X. "PMID 25512300. 
  36. ^ Puelles, L; Rubenstein, JL (2003). "Forebrain gene expression domains and the evolving prosomeric model". Trends in Neurosciences. 26 (9): 469–76. "doi:10.1016/S0166-2236(03)00234-0. "PMID 12948657. 
  37. ^ Ishibashi, M; McMahon, AP (2002). "A sonic hedgehog-dependent signaling relay regulates growth of diencephalic and mesencephalic primordia in the early mouse embryo". Development. 129 (20): 4807–19. "PMID 12361972. 
  38. ^ Kiecker, C; Lumsden, A (2004). "Hedgehog signaling from the ZLI regulates diencephalic regional identity". Nature Neuroscience. 7 (11): 1242–9. "doi:10.1038/nn1338. "PMID 15494730. 
  39. ^ Scholpp, S.; Wolf, O; Brand, M; Lumsden, A (2006). "Hedgehog signalling from the zona limitans intrathalamica orchestrates patterning of the zebrafish diencephalon". Development. 133 (5): 855–64. "doi:10.1242/dev.02248. "PMID 16452095. 
  40. ^ Scholpp, S.; Delogu, A.; Gilthorpe, J.; Peukert, D.; Schindler, S.; Lumsden, A. (2009). "Her6 regulates the neurogenetic gradient and neuronal identity in the thalamus". Proceedings of the National Academy of Sciences. 106 (47): 19895–900. "doi:10.1073/pnas.0910894106. "PMC 2775703Freely accessible. "PMID 19903880. 
  41. ^ Vue, Tou Yia; Bluske, Krista; Alishahi, Amin; Yang, Lin Lin; Koyano-Nakagawa, Naoko; Novitch, Bennett; Nakagawa, Yasushi (2009). "Sonic Hedgehog Signaling Controls Thalamic Progenitor Identity and Nuclei Specification in Mice". Journal of Neuroscience. 29 (14): 4484–97. "doi:10.1523/JNEUROSCI.0656-09.2009. "PMC 2718849Freely accessible. "PMID 19357274. 
  42. ^ Young, Keith A.; Holcomb, Leigh A.; Bonkale, Willy L.; Hicks, Paul B.; Yazdani, Umar; German, Dwight C. (2007). "5HTTLPR Polymorphism and Enlargement of the Pulvinar: Unlocking the Backdoor to the Limbic System". Biological Psychiatry. 61 (6): 813–8. "doi:10.1016/j.biopsych.2006.08.047. "PMID 17083920. 
  43. ^ Dejerine, J.; Roussy, G. (1906). "Le syndrome thalamique". Revue Neurologique. 14: 521–32. 
  44. ^ Gray, H. & Carter, H. V. (1858), Anatomy Descriptive and Surgical, London: John W. Parker and Son, Retrieved (16 October 2011) [2012-02-10] → [1]

External links[edit]

) )