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Cholinergic innervation of cortex by the basal forebrain: Cytochemistry and cortical connections of the septal area, diagonal band nuclei, nucleus basalis (Substantia innominata), and hypothalamus in the rhesus monkey
Abstract
The organization of projections from the cholinergic neurons of the basal forebrain to neocortex and associated structures was investigated in the rhesus monkey with the help of horseradish peroxidase transport, acetyl‐cholinesterase histochemistry, and choline acetyltransferase immunohis‐tochemistry. Four groups of neurons contained cholinergic perikarya and were designated as Chl‐Ch4. The Ch1 group corresponds to the medial septal nucleus; about 10% of its neurons are cholinergic, and it provides a substantial projection to the hippocampus. The Ch2 group corresponds to the vertical nucleus of the diagonal band; at least 70% of its neurons are cholinergic, and it is the major source of innervation that the hippocampus and hypothalamus receive from the Chl‐Ch4 complex. The Ch3 group most closely corresponds to the horizontal nucleus of the diagonal band; only 1% of its neurons can definitely be shown to be cholinergic, and it is the major source of Chl‐Ch4 projections to the olfactory bulb. The Ch4 group most closely corresponds to the nucleus basalis of Meynert; at least 90% of its neurons are cholinergic, and it has projections to widespread areas of cortex and to the amygdala. In fact, the Ch4 group provides the single major source of cholinergic innervation for the entire cortical surface. In this respect, it is analogous to the raphe nuclei and to the nucleus locus coeruleus, which constitute the major sources of widespread cortical serotonergic and nor‐adrenergic innervation, respectively. The extensive Ch4 group can be divided into several subdivisions. Each subdivision has a preferential set of targets for its projections even though the connection patterns contain considerable overlap. The anteromedial subdivision of Ch4 is the major source of cholinergic projections to areas on the medial aspect of the cerebral hemispheres; the anterolateral Ch4 sub‐division is the major source of cholinergic projections to frontoparietal op‐ercular areas and to the amygdala; the intermediate Ch4 subdivision pro‐vides the major cholinergic input for a variety of dorsal prefrontal, insular, posterior parietal, inferotemporal, and peristriate areas; and the posterior subdivision of Ch4 provides the major cholinergic innervation of superior temporal and immediately adjacent areas. The basal forebrain in the human contains a cytoarchitechture analogous to that of the monkey. The Ch4 group (nucleus basalis) of the human is very extensive and can be subdivided into the same components that were identfied in the monkey brain. Pathological changes in Ch4 neurons have been described in a variety of human disease. In Alzheimer's disease, the relatively selective depression of neocortical cholinergic innervation may be closely associated with the neuronal loss in Ch4, which has also been described inthis condition. In the rhesus monkey, all types of cortical areas receive substantial projections from the hippocampus. Virtually all of this hypothalamic input into neocortex arises from acetylcholinesterase‐rich neurons which lack choline acetyltransferase. The hypothalamocortical pathway is therefore acetylcholinesterase‐rich but not cholinergic.
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“The NBM provides cholinergic input to the entire cortex63 as well as the amygdala and other regions of the social brain (see Fig. 5 in the recent review by Putnam et al.64 for an anatomical model of NBM connectivity to social neural networks).”
From Effect of age and autism spectrum disorder on oxytocin receptor density in the human basal forebrain and midbrain (2018) · cites this paper as [63]
In the citing paper
“These nuclei are major sources of cholinergic input to the rest of the brain (44-46) and are important regulators of selective attention and motivation (47-52).”
From Comparative Perspectives on Oxytocin and Vasopressin Receptor Research in Rodents and Primates: Translational Implications (2016) · cites this paper as [44]
In the citing paper
“Furthermore, NBM projects to the amygdala and is the primary source of cholinergic input to the basolateral amygdala (44,46,56,57).”
From Comparative Perspectives on Oxytocin and Vasopressin Receptor Research in Rodents and Primates: Translational Implications (2016) · cites this paper as [44]
Citations
Cites
Mesulam, M. M. (1978) · Journal of Histochemistry & Cytochemistry · doi:10.1177/26.2.24068 · Cited by 4,303
Self-citationSELECTIVE LOSS OF CENTRAL CHOLINERGIC NEURONS IN ALZHEIMER'S DISEASE
DAVIES, P. (1976) · The Lancet · doi:10.1016/s0140-6736(76)91936-x · Cited by 3,565
Alzheimer disease: Evidence for selective loss of cholinergic neurons in the nucleus basalis
Whitehouse, P. J., Price, D. L., Clark, A. W., Coyle, J. T., & DeLong, M. R. (1981) · Annals of Neurology · doi:10.1002/ana.410100203 · Cited by 1,736
Human Memory and the Cholinergic System
Drachman, D. A. (1974) · Archives of Neurology · doi:10.1001/archneur.1974.00490320001001 · Cited by 1,398
Asher, R. (1961) · The Lancet · doi:10.1016/s0140-6736(61)91217-x · Cited by 1,293
Jacobowitz, D. M., & Palkovits, M. (1974) · The Journal of Comparative Neurology · doi:10.1002/cne.901570103 · Cited by 1,246
The central cholinergic system studied by choline acetyltransferase immunohistochemistry in the cat
Kimura, H., McGeer, P. L., Peng, J. H., & McGeer, E. G. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.902000202 · Cited by 966
Correlative Anatomy of the Nervous System
Crosby, E. C., Humphrey, T., Lauer, E. W., & Kappers, J. A. (1962) · Biblioteca Digital (Real Academia Nacional de Medicina) · Cited by 844
A cytoarchitectural study of the prefrontal area of the macaque monkey
Walker, A. E. (1940) · The Journal of Comparative Neurology · doi:10.1002/cne.900730106 · Cited by 803
Activity of pallidal neurons during movement.
DeLong, M. R. (1971) · Journal of Neurophysiology · doi:10.1152/jn.1971.34.3.414 · Cited by 734
Flagged first, then by citations
Research works printed but not linked: 19
- Beccari N., 1943, Neurologia Comparata Anatomo‐Funzionale Dei Ver‐tebrati Compresso L'Uomo
- Burton M. J., 1975, Visual and taste neurons in the lateral hypothnlamus and substantia innominata: Modulation of responsiveness by hunger, J. Physiol. (Lond.), 252, 50
- Foix C., 1925, Anatomie Cerebrale Noyaux Gris Cen‐traux et Region Mesencephalo‐Sous‐Optique
- Friedcmann M., 1911, Die Cytoarchitektonikdes Zwischenhirns der Cer‐copithekcn mit besonderer Berucksichtigung des Thalamus opticus, J. Psychol. Neurol. (Leipzig), 18, 309
- Heimer L., 1975, Golgi Centennial Symposium Proceedings, 177
- Hilt D. C., 1982, Pick Disease: Loss of neurons in the nucleus basalis, Neurology, 32, A229
- Kodama S., 1929, Pathologisch‐anatomische Untersuchungen mit Bezug auf die sorgenannten Basalganglien und ihre Adnexe. Neurologische und Psychiatrische Abhandlungen aus dem Schweize, Archiv fur Neu‐rologie und Psychiatrie, 8, 1
- Kolliker A., 1896, Nervensystem
- Levey A. I., 1982, Immunochcmical studies of bovine and Inimnn choline‐o‐acetyltrnnsferase using monoclonal an‐UlniilliiH, .J. Nmmiulliilll., 39, 1652
- McLennan H., 1978, Pharmacological characterization of the excitatory cholinergic receptors of rat central neurons, Neuro‐pharmacology, 17, 329
- Mesulam M.‐M., 1977, Substantia innominata, septal area and nuclei of the diagonal band in the rhesus monkey: Organization of efferents and their acetylcholinesterase his‐tochemistry, Soc. Neurosci. Abstr., 3, 202
- Meynert T., 1872, A Manual of Histology, 650
- Mufson E. J., 1982, Cholinergic projections from the mesencephalic tegmentum to neocortex in rhesus monkey, Soc. Neurosci. Abstr., 8, 135
- Nauta W. J. H., 1969, The Hypothalamus, 136
- Parent A., 1979, Advances in Neurology, 1
- Reichert C. B., 1861, Der Bau Des Menschlichen Gthirns
- Rosene D. L., 1978, Centrifugal efferents to the olfactory bulb in the rhesus monkey, Soc. Neurosci. Abstr., 4, 91
- Shute C. C. D., 1970, The Hypothal‐amus, 167
- Stephan H., 1964, Cytoarchitectonics of the septal nuclei in the old world monkeys (Cercopithecus and Colobus), J. Hirnforsch., 7, 1
Cited by
Sorted by citations
Items 601–700 of 1,006
Nickell, W. T., & Shipley, M. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-12-04492.1988 · Cited by 69
Záborszky, L. (1989) · Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions · doi:10.1007/978-3-0348-9138-7_2 · Cited by 69
Chu, Y., Cochran, E. J., Bennett, D. A., Mufson, E. J., & Kordower, J. H. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1284 · Cited by 69
Self-citationCholinergic innervation in the human hippocampal formation including the entorhinal cortex
Lacalle, S. D., Lim, C., Sobreviela, T., Mufson, E. J., Hersh, L. B., & Saper, C. B. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903450302 · Cited by 69
Self-citationCentral cholinergic systems and the P3 evoked potential
Meador, K. J., Loring, D. W., Adams, R. J., Patel, B. R., Davis, H., & Hammond, E. J. (1987) · International Journal of Neuroscience · doi:10.3109/00207458708987404 · Cited by 69
Kristt, D. A., McGowan, R. A., Martin-MacKinnon, N., & Solomon, J. (1985) · Brain Research · doi:10.1016/0006-8993(85)91606-3 · Cited by 69
Wenk, G. L., Harrington, C. A., Tucker, D. A., Rance, N. E., & al, E. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.6.909 · Cited by 69
Peck, C. J., & Salzman, C. D. (2014) · eLife · doi:10.7554/elife.04478 · Cited by 68
Target selectivity of septal cholinergic neurons in the medial and lateral entorhinal cortex
Desikan, S., Koser, D. E., Neitz, A., & Monyer, H. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1716531115 · Cited by 72
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Moeller, I., Paxinos, G., Mendelsohn, F. A. O., Aldred, G. P., CASLEY, D. J., & Chai, S. Y. (1996) · Brain Research · doi:10.1016/0006-8993(95)01482-9 · Cited by 68
Morphologic features of embryonic neocortex grafts in adult rats following frontal cortical ablation
Mufson, E. J., Labbe, R., & Stein, D. G. (1987) · Brain Research · doi:10.1016/0006-8993(87)91177-2 · Cited by 68
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Liu, N., Hadj-Bouziane, F., Jones, K. B., Turchi, J. N., Averbeck, B. B., & Ungerleider, L. G. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1508097112 · Cited by 65
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Casula, E. P., Borghi, I., Maiella, M., Pellicciari, M. C., Bonnı̀, S., Mencarelli, L., Assogna, M., D’Acunto, A., Lorenzo, F. D., Spampinato, D. A., et al. (2022) · Annals of Neurology · doi:10.1002/ana.26514 · Cited by 70
Tinkler, G. P., Tobin, J. R., & Voytko, M. L. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.11028 · Cited by 67
Neurobiology of waking and sleeping
Jones, B. E. (2010) · Handbook of clinical neurology · doi:10.1016/b978-0-444-52006-7.00009-5 · Cited by 67
Emre, M., Heckers, S., Mash, D., Geula, C., & Mesulam, M. (1993) · The Journal of comparative neurology · doi:10.1002/cne.903360110 · Cited by 83
Self-citationVoytko, M. L. (2002) · Behavioral Neuroscience · doi:10.1037//0735-7044.116.2.187 · Cited by 67
Benzing, W. C., Kordower, J. H., & Mufson, E. J. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903360103 · Cited by 67
Self-citationChapter 26 Human brain cholinergic pathways
Mesulam, M. M. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)60908-5 · Cited by 67
Self-citationKoliatsos, V. E., Martin, L. J., Walker, L. C., Richardson, R. T., DeLong, M. R., & Price, D. L. (1988) · Brain Research · doi:10.1016/0006-8993(88)90535-5 · Cited by 67
The Human Basal Forebrain Integrates the Old and the New
Rosa, E. D., Desmond, J. E., Anderson, A. K., Pfefferbaum, A., & Sullivan, E. V. (2004) · Neuron · doi:10.1016/s0896-6273(04)00080-7 · Cited by 64
Fujishiro, H., Umegaki, H., Isojima, D., Akatsu, H., Iguchi, A., & Kosaka, K. (2006) · Acta Neuropathologica · doi:10.1007/s00401-005-0004-1 · Cited by 66
Knox, D., & Keller, S. M. (2015) · Hippocampus · doi:10.1002/hipo.22553 · Cited by 70
The NGF Metabolic Pathway in the CNS and its Dysregulation in Down Syndrome and Alzheimer's Disease
Iulita, M. F., & Cuello, A. C. (2015) · Current Alzheimer Research · doi:10.2174/1567205012666150921100030 · Cited by 69
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Kish, S. J., Kleinert, R., Minauf, M., Gilbert, J., Walter, G. F., Slimovitch, C., Maurer, E., Rezvani, Y., Myers, R., & Hornykiewicz, O. (1990) · American Journal of Psychiatry · doi:10.1176/ajp.147.10.1358 · Cited by 66
Cantero, J. L., Atienza, M., Lage, C., Záborszky, L., Vilaplana, E., López‐García, S., Pozueta, A., Rodríguez‐Rodríguez, E., Blesa, R., Alcolea, D. A., et al. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz224 · Cited by 65
The cholinergic system in subtypes of Alzheimer’s disease: an in vivo longitudinal MRI study
Machado, A., Ferreira, D., Grothe, M. J., Eyjolfsdottir, H., Almqvist, P. M., Cavallin, L., Lind, G., Lind, G., Seiger, Å., Teipel, S., et al. (2020) · Alzheimer s Research & Therapy · doi:10.1186/s13195-020-00620-7 · Cited by 65
Siˇmić, G., Mrzljak, L., Fucic, A., Winblad, B. G., Lovrić, H., & Kostović, I. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00304-2 · Cited by 65
Alzheimer plaques and cortical cholinergic innervation
Mesulam, M. M. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90242-3 · Cited by 65
Self-citationVisuospatial learning impairment following lesion of the cholinergic projection to the hippocampus
Ridley, R. M., Samson, N. A., Baker, H. F., & Johnson, J. A. (1988) · Brain Research · doi:10.1016/0006-8993(88)90348-4 · Cited by 63
Wainer, B. H., Steininger, T. L., Roback, J. D., Burke, M. A., Mufson, E. J., & Kordower, J. H. (1993) · Progress in brain research · doi:10.1016/s0079-6123(08)62378-x · Cited by 65
Self-citationCentral Cholinergic Pathways Neuroanatomy and Some Behavioral Implications
Mesulam, M. M. (1988) · Springer eBooks · doi:10.1007/978-1-4613-0925-3_15 · Cited by 65
Self-citationCell loss in the nucleus basalis is related to regional cortical atrophy in Alzheimer's disease
Cullen, K. M., Halliday, G. M., Double, K. L., Brooks, W. S., Creasey, H. M., & Broe, G. A. (1997) · Neuroscience · doi:10.1016/s0306-4522(96)00569-6 · Cited by 65
Liu, A. K. L., Chau, T. W., Lim, E., Ahmed, I., Chang, R. C., Kalaitzakis, M. E., Graeber, M. B., Gentleman, S., & Pearce, R. K. B. (2019) · Acta Neuropathologica Communications · doi:10.1186/s40478-019-0717-3 · Cited by 64
Counts, S. (2003) · Molecular Interventions · doi:10.1124/mi.3.3.137 · Cited by 64
Alzheimers Disease and Neural Transplantation as Prospective Cell Therapy
de Oliveira, A. A., & Hodges, H. R. (2005) · Current Alzheimer Research · doi:10.2174/1567205052772759 · Cited by 63
Neural Systems of the Non‐human Primate Forebrain Implicated in Memorya
Hoesen, G. W. V. (1985) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1985.tb37582.x · Cited by 64
Cholinergic neurons within the rat hippocampus: Response to fimbria‐fornix transection
Blaker, S. N., Armstrong, D. M., & Gage, F. H. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902720109 · Cited by 64
Visual agnosia contrasted with visual-verbal disconnection
Larrabee, G. J., Levin, H. S., Huff, F. J., Kay, M. C., Guinto, F. C., Huff, F. J., & Kay, M. C. (1985) · Neuropsychologia · doi:10.1016/0028-3932(85)90039-9 · Cited by 64
Haring, J. H., & Wang, R. Y. (1986) · Brain Research · doi:10.1016/0006-8993(86)91290-4 · Cited by 64
[3H]Vesamicol binding in human brain cholinergic deficiency disorders
Kish, S. J., DiStefano, L. M., Dozić, S., Robitaille, Y., Rajput, A. H., Deck, J. H. N., & Hornykiewicz, O. (1990) · Neuroscience Letters · doi:10.1016/0304-3940(90)90689-7 · Cited by 64
Pedata, F., Giovannelli, L., & Pepeu, G. (1984) · Journal of Neuroscience Research · doi:10.1002/jnr.490120226 · Cited by 64
Afferent cortical connections of the motor cortical larynx area in the rhesus monkey
Simonyan, K., & Jürgens, U. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.08.031 · Cited by 62
Babiloni, C., Squitti, R., Percio, C. D., Cassetta, E., Ventriglia, M. C., Ferreri, F., Tombini, M., Frisoni, G. B., Binetti, G. G., Gurzì, M., et al. (2007) · Clinical Neurophysiology · doi:10.1016/j.clinph.2007.03.016 · Cited by 64
Monoaminergic afferents to cortex modulate structural plasticity in the barrelfield of the mouse
Osterheld-Haas, M. C., der Loos, H. V., & Hornung, J. (1994) · Developmental Brain Research · doi:10.1016/0165-3806(94)90196-1 · Cited by 63
Mufson, E. J., Desan, P. H., Mesulam, M. M., Wainer, B. H., & Levey, A. I. (1984) · Brain Research · doi:10.1016/0006-8993(84)90269-5 · Cited by 63
Self-citationHeterogeneous distribution of D1, D2 and D5 receptor mRNAs in monkey striatum
Rappaport, M. S., Sealfon, S. C., Prikhozhan, A. V., Huntley, G. W., & Morrison, J. H. (1993) · Brain Research · doi:10.1016/0006-8993(93)90215-9 · Cited by 63
Lapchak, P. A., Jenden, D. J., & Hefti, F. F. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-09-02821.1991 · Cited by 63
Stichel, C. C., & Singer, W. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902580107 · Cited by 63
Kelley, C. M., Powers, B. E., Velázquez, R., Ash, J. A., Ginsberg, S. D., Strupp, B. J., & Mufson, E. J. (2013) · Brain Pathology · doi:10.1111/bpa.12073 · Cited by 63
Self-citationRaghanti, M. A., Stimpson, C. D., Marcinkiewicz, J. L., ERWIN, J. M., Hof, P. R., & Sherwood, C. C. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21546 · Cited by 62
Ferman, T. J., & Boeve, B. F. (2007) · Neurologic Clinics · doi:10.1016/j.ncl.2007.03.001 · Cited by 68
Cholinergic neurons in the telencephalon of the reptile Caiman crocodilus
Brauth, S. E., Kitt, C. A., Price, D. L., & Wainer, B. H. (1985) · Neuroscience Letters · doi:10.1016/0304-3940(85)90170-3 · Cited by 62
Self-citationThe Nucleus Basalis of Meynert
Ezrin‐Waters, C., & Resch, L. (1986) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100035721 · Cited by 62
Armstrong, D. M., Benzing, W. C., Evans, J. A., Terry, R. D., Shields, D., & Hansen, L. A. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90431-4 · Cited by 63
Cholinergic innervation displays strikingly different laminar preferences in several cortical areas
Lysakowski, A., Wainer, B. H., Rye, D. B., Bruce, G., & Hersh, L. B. (1986) · Neuroscience Letters · doi:10.1016/0304-3940(86)90671-3 · Cited by 62
Self-citationAllen, T. G. J., Sim, J. A., & Brown, D. A. (1993) · The Journal of Physiology · doi:10.1113/jphysiol.1993.sp019461 · Cited by 62
Fisone, G., Bartfai, T., Nilsson, S., & Hökfelt, T. G. M. (1991) · Brain Research · doi:10.1016/0006-8993(91)91409-t · Cited by 62
Cortically projecting nucleus basalis neurons in rat are physiologically heterogeneous
Aston‐Jones, G., Shaver, R., & Dinan, T. G. (1984) · Neuroscience Letters · doi:10.1016/0304-3940(84)90192-7 · Cited by 62
The Amygdala and Basal Forebrain as a Pathway for Motivationally Guided Attention
Peck, C. J., & Salzman, C. D. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2106-14.2014 · Cited by 62
Pharmacological Dissociation of Novelty Responses in the Human Brain
Bunzeck, N., Guitart‐Masip, M., Dolan, R. J., & Düzel, E. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs420 · Cited by 57
The Neuroanatomy of the Reticular Nucleus Locus Coeruleus in Alzheimer’s Disease
Giorgi, F. S., Ryskalin, L., Ruffoli, R., Biagioni, F., Limanaqi, F., Ferrucci, M., Busceti, C. L., Bonuccelli, U., & Fornai, F. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00080 · Cited by 63
Musiol, I. M., & Feldman, D. (1997) · Endocrinology · doi:10.1210/endo.138.1.4858 · Cited by 61
Xuereb, J. H., Perry, E. K., Candy, J., Bonham, J. R., Perry, R. H., & Marshall, E. (1990) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(90)90155-g · Cited by 61
Irle, E. (1990) · Brain Research Reviews · doi:10.1016/0165-0173(90)90001-5 · Cited by 61
Three-dimensional synaptic organization of the human hippocampal CA1 field
Montero-Crespo, M., Dominguez-Alvaro, M., Rondon-Carrillo, P., Alonso-Nanclares, L., DeFelipe, J., & Blazquez-Llorca, L. (2020) · eLife · doi:10.7554/elife.57013 · Cited by 60
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Lockhofen, D. E. L., & Mulert, C. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.643597 · Cited by 66
Proulx, É., Piva, M., Tian, M. K., Bailey, C. D. C., & Lambe, E. K. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1481-3 · Cited by 66
Down's Syndrome Individuals Begin Life with Normal Levels of Brain Cholinergic Markers
Kish, S. J., Karlinsky, H., Becker, L. E., Gilbert, J. J., Rebbetoy, M., Chang, L., DiStefano, L. M., & Hornykiewicz, O. (1989) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1989.tb01864.x · Cited by 60
Topographic projections to the visual cortex from the basal forebrain in the rat
Carey, R. G., & Rieck, R. W. (1987) · Brain Research · doi:10.1016/0006-8993(87)91463-6 · Cited by 60
Smiley, J. F., & Mesulam, M. M. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00202-4 · Cited by 60
Self-citationHedreen, J. C., Bacon, S. J., Cork, L. C., Kitt, C. A., Crawford, G. D., Salvterra, P. M., & Price, D. L. (1983) · Neuroscience Letters · doi:10.1016/0304-3940(83)90183-0 · Cited by 60
Kordower, J. H., Bartus, R. T., Marciano, F. F., & Gash, D. M. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902790403 · Cited by 60
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Hollander, E., Mohs, R. C., & Davis, K. L. (1986) · Neurobiology of Aging · doi:10.1016/0197-4580(86)90164-8 · Cited by 60
Alberch, J., Pérez‐Navarro, E., Arenas, E., & Marsa, J. (1991) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1991.tb06342.x · Cited by 60
Distribution of choline acetyltransferase-immunoreactive axons in monkey frontal cortex
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Pale Neurites, Premature α‐Synuclein Aggregates with Centripetal Extension from Axon Collaterals
Kanazawa, T., Adachi, E., Orimo, S., Nakamura, A., Mizusawa, H., & Uchihara, T. (2011) · Brain Pathology · doi:10.1111/j.1750-3639.2011.00509.x · Cited by 57
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Akaike, A., Shimohama, S., & Misu, Y. (2018) · Springer eBooks · doi:10.1007/978-981-10-8488-1 · Cited by 61
Semba, K. (2004) · Progress in brain research · doi:10.1016/s0079-6123(03)45001-2 · Cited by 58
Baskerville, K. A., Chang, H. T., & Herron, P. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903350407 · Cited by 59
Griffin, S. L., van Reekum, R., & Masanic, C. A. (2003) · Journal of Neuropsychiatry · doi:10.1176/appi.neuropsych.15.1.17 · Cited by 59
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Armstrong, D. M., Bruce, G., Hersh, L. B., & Terry, R. D. (1986) · Neuroscience Letters · doi:10.1016/0304-3940(86)90564-1 · Cited by 59
Mufson, E. J., Conner, J. M., Varon, S. S., & Kordower, J. H. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903410407 · Cited by 59
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Doucette, R., Fisman, M., Hachinski, V. C., & Mersky, H. (1986) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100037070 · Cited by 58
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Vinters, H. V., Miller, B. L., & Pardridge, W. M. (1988) · Annals of Internal Medicine · doi:10.7326/0003-4819-109-1-41 · Cited by 58
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Lowes, P., Gertz, H., Ferszt, R., & Cervós‐Navarro, J. (1989) · Archives of Gerontology and Geriatrics · doi:10.1016/0167-4943(89)90066-6 · Cited by 58
Monosov, I. E., Leopold, D. A., & Hikosaka, O. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0051-15.2015 · Cited by 56
Powers, B. E., Kelley, C. M., Velázquez, R., Ash, J. A., Strawderman, M. S., Alldred, M. J., Ginsberg, S. D., Mufson, E. J., & Strupp, B. J. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.11.001 · Cited by 55
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Markello, R. D., Spreng, R. N., Luh, W., Anderson, A. K., & Rosa, E. D. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.02.042 · Cited by 57
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Nyíri, G., Szabadits, E., Cserép, C., Mackie, K., Shigemoto, R., & Freund, T. F. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04146.x · Cited by 55
Smiley, J. F., Levey, A. I., & Mesulam, M. M. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00524-1 · Cited by 57
Self-citationAlonso, J. R., & Amaral, D. G. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903550202 · Cited by 57
Candy, J., Perry, E. K., Perry, R. H., COURT, J. A., Oakley, A. E., & Edwardson, J. A. (1986) · Progress in brain research · doi:10.1016/s0079-6123(08)64300-9 · Cited by 57
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Cummings, J. L. (2000) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145700001917 · Cited by 57
Quirion, R. (1987) · Synapse · doi:10.1002/syn.890010403 · Cited by 57
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Ishida, H., Inoue, K., Takada, M., & Hoshi, E. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13127 · Cited by 56
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Hreib, K. K., Rosene, D. L., & Moss, M. B. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902770304 · Cited by 56
Metadata
- Authors
- Mesulam, M. ‐., Mufson, E. J., Levey, A. I., & Wainer, B. H.
- Affiliations
- Beth Israel Deaconess Medical Center (US)
- University of Chicago (US)
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1983-02-20
- Volume
- 214
- Issue
- 2
- Pages
- 170-197
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2013854477
- Cited by
- 1,962
- References
- 79
- Citations by year
- 2026: 30 · 2025: 42 · 2024: 43 · 2023: 51 · 2022: 45 · 2021: 61 · 2020: 53 · 2019: 39 · 2018: 71 · 2017: 36 · 2016: 45 · 2015: 46 · 2014: 47 · 2013: 35 · 2012: 29
- FWCI
- 33.65
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
- Keywords
- cholinergic innervation, basal forebrain, nucleus basalis of Meynert, diagonal band of Brodmann, medial septum, substantia innominata, hypothalamus, neocortex, choline acetyltransferase, acetylcholinesterase, cholinergic projections, rhesus monkeys, hippocampus, amygdala, olfactory bulb
- MeSH terms
- Adult, Afferent Pathways, Animals, Brain Mapping, Cerebral Cortex, Cholinergic Fibers, Diencephalon, Humans, Hypothalamus, Macaca mulatta, Male, Septal Nuclei, Telencephalon
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