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A conductor hidden in the orchestra? Role of the habenular complex in monoamine transmission and cognition

Lecourtier, Lucas, Kelly, Peter H.·2007·Neuroscience & Biobehavioral Reviews

DOI 10.1016/j.neubiorev.2007.01.004

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Abstract

Influences of the habenular complex on electrophysiological and neurochemical aspects of brain functioning are well known. However, its role in cognition has been sparsely investigated until recently. The habenular complex, composed of medial and lateral subdivisions, is a node linking the forebrain with midbrain and hindbrain structures. The lateral habenula is the principal actor in this direct dialogue, while the medial habenula mostly conveys information to the interpeduncular nucleus before this modulates further regions. Here we describe neuroanatomical and physiological aspects of the habenular complex, and its role in cognitive processes, including new behavioral, electrophysiological and imaging findings. Habenular complex lesions result in deficits in learning, memory and attention, some of which decline during repeated testing, while others become worse, consistent with multiple roles in cognition. The habenular complex is particularly responsive to feedback about errors. Electrophysiological studies indicate a role in metaplasticity, the modulation of neuroplasticity. These studies thus reveal important roles of the habenular complex in learning, memory and attention.

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Untitled work
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010
Place navigation impaired in rats with hippocampal lesions
Morris, R. G. M., Garrud, P., Rawlins, J. N. P., & O'Keefe, J. (1982) · Nature · doi:10.1038/297681a0 · Cited by 6,340
The hippocampus as a cognitive map
Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128
The medial temporal lobe
Squire, L. R., Stark, C. E. L., & Clark, R. E. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144130 · Cited by 2,680
Expression of c- fos Protein in Brain: Metabolic Mapping at the Cellular Level
Sagar, S. M., Sharp, F. R., & Curran, T. (1988) · Science · doi:10.1126/science.3131879 · Cited by 1,925
Molecular cloning, functional properties, and distribution of rat brain alpha 7: a nicotinic cation channel highly permeable to calcium
Séguéla, P., Wadiche, J. I., Dineley‐Miller, K., Dani, J., & Jw, P. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-02-00596.1993 · Cited by 1,471
Neuronal Coding of Prediction Errors
Schultz, W., & Dickinson, A. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.473 · Cited by 1,427
Efferent connections of the substantia nigra and ventral tegmental area in the rat
Beckstead, R. M., Domesick, V. B., & Nauta, W. J. H. (1979) · Brain Research · doi:10.1016/0006-8993(79)91001-1 · Cited by 1,293
The 5-choice serial reaction time task: behavioural pharmacology and functional neurochemistry
Robbins, T. (2002) · Psychopharmacology · doi:10.1007/s00213-002-1154-7 · Cited by 1,282

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Leiva-Santana, 2006, Levodopa and cognitive disorders in Parkinson's disease, Revista de Neurologia, 43, 95

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Authors: Lecourtier, L., & Kelly, P. H.
Affiliations: University of Pittsburgh (US)
Novartis (Switzerland) (CH)
Corresponding author: Lecourtier, Lucas
ORCID: Lecourtier, Lucas
Venue: Neuroscience & Biobehavioral Reviews
Publisher: Elsevier BV
Published: 2007-01
Volume: 31
Issue: 5
Pages: 658-672
ISSN: 0149-7634 (ISSN-L)
DOI: 10.1016/j.neubiorev.2007.01.004
OpenAlex: W1969480244
Cited by: 283
References: 170
Citations by year: 2026: 5 · 2025: 4 · 2024: 10 · 2023: 4 · 2022: 10 · 2021: 15 · 2020: 9 · 2019: 12 · 2018: 15 · 2017: 25 · 2016: 19 · 2015: 13 · 2014: 30 · 2013: 28 · 2012: 11
FWCI: 1.30
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Neuroscience & Biobehavioral Reviews (publishedVersion)
PubMed (publishedVersion)
HAL (submittedVersion)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords: lateral habenula, medial habenula, interpeduncular nucleus, cognition, learning and memory, attention, metaplasticity, neuroplasticity, error feedback, neuroanatomy
MeSH terms: Animals, Cognition, Humans, Synaptic Transmission, Biogenic Monoamines, Habenula

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A conductor hidden in the orchestra? Role of the habenular complex in monoamine transmission and cognition

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