The DOI matches its Crossref record; 79 of the 79 references it cites were found in a registry or an index.
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.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“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 101–200 of 1,006
Amaral, D. G., & Insausti, R. (1990) · Elsevier eBooks · doi:10.1016/b978-0-12-547625-6.50026-x · Cited by 300
Role of the nicotinic acetylcholine receptor in Alzheimer's disease pathology and treatment.
Lombardo, S., & Maskos, U. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.11.018 · Cited by 281
Mufson, E. J., Kroin, J. S., Sendera, T. J., & Sobreviela, T. (1999) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00059-8 · Cited by 296
Self-citationSubcortical Dementia Neuropsychology, Neuropsychiatry, and Pathophysiology
Cummings, J. L. (1986) · The British Journal of Psychiatry · doi:10.1192/bjp.149.6.682 · Cited by 298
Datta, S., & MacLean, R. R. (2007) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2007.02.004 · Cited by 307
Human cholinergic basal forebrain: chemoanatomy and neurologic dysfunction
Mufson, E. J., Ginsberg, S. D., Ikonomović, M. D., & DeKosky, S. T. (2003) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(03)00068-1 · Cited by 295
Self-citationTowards a muscarinic hypothesis of schizophrenia
Raedler, T. J., Bymaster, F. P., Tandon, R., Copolov, D., & Dean, B. (2006) · Molecular Psychiatry · doi:10.1038/sj.mp.4001924 · Cited by 298
Luiten, P. G. M., Gaykema, R. P. A., Traber, J., & Spencer, D. G. (1987) · Brain Research · doi:10.1016/0006-8993(87)91014-6 · Cited by 295
A direct GABAergic output from the basal ganglia to frontal cortex
Saunders, A., Oldenburg, I. A., Berezovskii, V. K., Johnson, C. A., Kingery, N. D., Elliott, H. L., Xie, T., Gerfen, C. R., & Sabatini, B. L. (2015) · Nature · doi:10.1038/nature14179 · Cited by 293
The limbic system: an anatomic, phylogenetic, and clinical perspective
Mega, M. S., Cummings, J. L., Salloway, S., & Malloy, P. F. (1997) · Journal of Neuropsychiatry · doi:10.1176/jnp.9.3.315 · Cited by 298
Cholinergic and non-cholinergic septohippocampal pathways
Wainer, B. H., Levey, A. I., Rye, D. B., Mesulam, M. M., & Mufson, E. J. (1985) · Neuroscience Letters · doi:10.1016/s0304-3940(85)80116-6 · Cited by 293
Self-citationSofroniew, M. V., Priestley, J. V., Consolazione, A., Eckenstein, F. P., & Cuello, A. C. (1985) · Brain Research · doi:10.1016/0006-8993(85)90527-x · Cited by 293
Freund, T. F., & Meskenaïte, V. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.2.738 · Cited by 292
Neural inputs into the temporopolar cortex of the rhesus monkey
Morán, M. A., Mufson, E. J., & Mesulam, M. M. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902560108 · Cited by 291
Self-citationHeimer, L., Harlan, R. E., Alheid, G. F., Garcia, M. M., & de Olmos, J. S. (1997) · Neuroscience · doi:10.1016/s0306-4522(96)00405-8 · Cited by 289
Cholinergic systems in mammalian brain identified with antibodies against choline acetyltransferase
Wainer, B. H., Levey, A. I., Mufson, E. J., & Mesulam, M. M. (1984) · Neurochemistry International · doi:10.1016/0197-0186(84)90089-5 · Cited by 287
Self-citationCortés, R., Probst, A., Tobler, H.-J., & Palacios, J. M. (1986) · Brain Research · doi:10.1016/0006-8993(86)90449-x · Cited by 286
Executive function deficits in mild Alzheimer's disease.
Lafleche, G., & Albert, M. (1995) · Neuropsychology · doi:10.1037/0894-4105.9.3.313 · Cited by 308
Záborszky, L., Csordás, A., Mosca, K., Kim, J., Gielow, M. R., Vadász, C., & Nádasdy, Z. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht210 · Cited by 284
Abitbol, M. M., Ménini, C., Delezoide, A., Rhyner, T. A., Vekemans, M. J. J., & Mallet, J. J. (1993) · Nature Genetics · doi:10.1038/ng0693-147 · Cited by 284
Correspondence between the Dopamine islands and striosomes of the mammalian striatum
Graybiel, A. M. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90293-8 · Cited by 282
Neural associations of the substantia innominata in the rat: Afferent connections
Grove, E. A. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902770302 · Cited by 281
Cell loss and shrinkage in the nucleus basalis Meynert complex in Alzheimer's disease
Vogels, O. J. M., Broere, C. A. J., Laak, H. J. T., ten Donkelaar, H. J., Nieuwenhuys, R., & Schulte, B. P. M. (1990) · Neurobiology of Aging · doi:10.1016/0197-4580(90)90056-6 · Cited by 279
Mufson, E. J., Bothwell, M. A., & Kordower, J. H. (1989) · Experimental Neurology · doi:10.1016/0014-4886(89)90124-6 · Cited by 279
Self-citationSemba, K., Reiner, P. B., McGeer, E. G., & Fibiger, H. C. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902670311 · Cited by 277
Levey, A. I., Wainer, B. H., Rye, D. B., Mufson, E. J., & Mesulam, M. M. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90234-3 · Cited by 276
Self-citationThe Cholinergic Hypothesis of Neuropsychiatric Symptoms in Alzheimer's Disease
Cummings, J. L., & Back, C. (1998) · American Journal of Geriatric Psychiatry · doi:10.1097/00019442-199821001-00009 · Cited by 276
Cognitive dysfunction and dementia in Parkinson?s disease
Bosboom, J. L. W., Stoffers, D., & Wolters, E. C. (2004) · Journal of Neural Transmission · doi:10.1007/s00702-004-0168-1 · Cited by 274
Directions in neurogenetic gradients and patterns of anatomical connections in the telencephalon
Bayer, S. A., & Altman, J. (1987) · Progress in Neurobiology · doi:10.1016/0301-0082(87)90015-3 · Cited by 276
Chan‐Palay, V. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902730409 · Cited by 273
Carlsen, J., Záborszky, L., & Heimer, L. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902340203 · Cited by 271
The afferent connections of the substantia innominata in the monkey,Macaca fascicularis
Russchen, F. T., Amaral, D., & Price, J. L. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902420102 · Cited by 270
Haxby, J. V., Grady, C. L., Duara, R., Schlageter, N. L., Berg, G., & Рапопорт, С. И. (1986) · Archives of Neurology · doi:10.1001/archneur.1986.00520090022010 · Cited by 270
Value-dependent selection in the brain: Simulation in a synthetic neural model
Friston, K. J., Tononi, G., Reeke, G. N., Sporns, O., & Edelman, G. M. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90592-4 · Cited by 268
Distribution of gabaergic and cholinergic neurons in the rat diagonal band
Brashear, H. R., Záborszky, L., & Heimer, L. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90258-7 · Cited by 268
The serotonergic system in ageing and Alzheimer's disease
Rodriguez, J. J., Noristani, H. N., & Verkhratsky, A. (2012) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.06.010 · Cited by 274
Scott, S. A., Mufson, E. J., Weingartner, J. A., Skau, K., & Crutcher, K. A. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-09-06213.1995 · Cited by 264
Self-citationMemory: Anatomical Organization of Candidate Brain Regions
Amaral, D. G. (1987) · Comprehensive physiology · doi:10.1002/cphy.cp010507 · Cited by 265
Deep brain stimulation of the nucleus basalis of Meynert in Alzheimer’s dementia
Kuhn, J., Hardenacke, K., Lenartz, D., Gruendler, T. O. J., Ullsperger, M., Bartsch, C., Mai, J. K., Zilles, K., Bauer, A., Matusch, A., et al. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.32 · Cited by 262
Maurer, S. V., & Williams, C. L. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01489 · Cited by 276
Rosene, D. L., & Van Hoesen, G. W. (1987) · Cerebral Cortex · doi:10.1007/978-1-4615-6616-8_9 · Cited by 422
Parkinson's disease: Neuron loss in the nucleus basalis without concomitant Alzheimer's disease
Nakano, I., & Hirano, A. (1984) · Annals of Neurology · doi:10.1002/ana.410150503 · Cited by 260
Mild cognitive impairment: pathology and mechanisms
Mufson, E. J., Binder, L. I., Counts, S., DeKosky, S. T., deToledo‐Morrell, L., Ginsberg, S. D., Ikonomović, M. D., Perez, S. E., & Scheff, S. W. (2011) · Acta Neuropathologica · doi:10.1007/s00401-011-0884-1 · Cited by 268
Self-citationChanges in Nicotinic and Muscarinic Cholinergic Receptors in Alzheimer‐Type Dementia
Shimohama, S., Taniguchi, T., Fujiwara, M., & Kameyama, M. (1986) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1986.tb12960.x · Cited by 258
Ginsberg, S. D., Che, S., Wuu, J., Counts, S., & Mufson, E. J. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03764.x · Cited by 253
Self-citationWenk, G. L., Stoehr, J. D., Quintana, G., Mobley, S., & Wiley, R. G. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-10-05986.1994 · Cited by 252
Subcortical evidence for a contribution of arousal to fMRI studies of brain activity
Liu, X., de Zwart, J. A., Schölvinck, M. L., Chang, C., Ye, F. Q., Leopold, D. A., & Duyn, J. H. (2018) · Nature Communications · doi:10.1038/s41467-017-02815-3 · Cited by 243
Z�borszky, L., Heimer, L., Eckenstein, F. P., & Leranth, C. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902500303 · Cited by 249
Measurement of basal forebrain atrophy in Alzheimer's disease using MRI
Teipel, S. J., Flatz, W. H., Heinsen, H., Bokde, A. L. W., Schoenberg, S. O., Stöckel, S., Dietrich, O., Reiser, M. F., Möller, H., & Hampel, H. J. (2005) · Brain · doi:10.1093/brain/awh589 · Cited by 248
The neurobiologie consequences of down syndrome
Coyle, J. T., Oster-Granite, M. L., & Gearhart, J. D. (1986) · Brain Research Bulletin · doi:10.1016/0361-9230(86)90074-2 · Cited by 248
Regional Cerebral Blood Flow in Mood Disorders
Sackeïm, H. A. (1990) · Archives of General Psychiatry · doi:10.1001/archpsyc.1990.01810130062009 · Cited by 247
Neuron loss in key cholinergic and aminergic nuclei in Alzheimer disease: a meta-analysis
Lyness, S. (2003) · Neurobiology of Aging · doi:10.1016/s0197-4580(02)00057-x · Cited by 240
Cognitive and neurobiologic markers of early Alzheimer disease
Albert, M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.24.13547 · Cited by 254
Insausti, R., & Amaral, D. G. (2004) · Elsevier eBooks · doi:10.1016/b978-012547626-3/50024-7 · Cited by 256
Mufson, E. J., Bothwell, M. A., Hersh, L. B., & Kordower, J. H. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902850204 · Cited by 245
Self-citationSmith, D. E., Roberts, J. A., Gage, F. H., & Tuszynski, M. H. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.19.10893 · Cited by 244
The Basal Forebrain Corticopetal System Revisited
Záborszky, L., Pang, K. C. H., Somogyi, J., Nádasdy, Z., & Kalló, I. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09276.x · Cited by 244
Akaike, A., Tamura, Y., Yokota, T., Shimohama, S., & Kimura, J. (1994) · Brain Research · doi:10.1016/0006-8993(94)91678-0 · Cited by 240
Gilmor, M. L., Erickson, J. D., Varoqui, H., Hersh, L. B., Bennett, D. A., Cochran, E. J., Mufson, E. J., & Levey, A. I. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990906)411:4 · Cited by 243
Self-citationLysakowski, A., Wainer, B. H., Bruce, G., & Hersh, L. B. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90180-2 · Cited by 239
Self-citationSaper, C., Wainer, B. H., & German, D. C. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90063-7 · Cited by 239
Self-citationA histamine-containing neuronal system in human brain
Panula, P., Airaksinen, M. S., Pirvola, U., & Kotilainen, E. (1990) · Neuroscience · doi:10.1016/0306-4522(90)90307-p · Cited by 239
Umbriaco, D., Watkins, K. C., Descarries, L., Cozzari, C., & Hartman, B. K. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903480304 · Cited by 237
Therapeutic Opportunities for Muscarinic Receptors in the Central Nervous System
Felder, C. C., Bymaster, F. P., Ward, J. S., & DeLapp, N. W. (2000) · Journal of Medicinal Chemistry · doi:10.1021/jm990607u · Cited by 235
Subregional Basal Forebrain Atrophy in Alzheimer's Disease: A Multicenter Study
Kilimann, I., Grothe, M. J., Heinsen, H., Alho, E. J. L., Grinberg, L. T., Amaro, E., dos Santos, G. A. B., da Silva, R. E., Mitchell, A. J., Frisoni, G. B., et al. (2014) · Journal of Alzheimer s Disease · doi:10.3233/jad-132345 · Cited by 244
The cholinergic system and spatial learning
Deiana, S., Platt, B., & Riedel, G. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.11.036 · Cited by 245
Quantitation of cerebral atrophy in preclinical and end-stage Alzheimer’s disease
de la Monte, S. M. (1989) · Annals of Neurology · doi:10.1002/ana.410250506 · Cited by 229
Targeting Plasticity with Vagus Nerve Stimulation to Treat Neurological Disease
Hays, S. A., Rennaker, R. L., & Kilgard, M. P. (2013) · Progress in brain research · doi:10.1016/b978-0-444-63327-9.00010-2 · Cited by 235
Associative representational plasticity in the auditory cortex: a synthesis of two disciplines
Weinberger, N. M. (2007) · Learning & Memory · doi:10.1101/lm.421807 · Cited by 223
Counts, S., & Mufson, E. J. (2005) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/64.4.263 · Cited by 223
Self-citationEfferent connections of the substantia innominata in the rat
Grove, E. A. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902770303 · Cited by 222
Vascular determinants of cholinergic deficits in Alzheimer disease and vascular dementia.
Román, G. C., & Kalaria, R. N. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.10.004 · Cited by 213
Changes in cortical acetylcholine output induced by modulation of the nucleus basalis
Casamenti, F., Deffenu, G., Abbamondi, A. L., & Pepeu, G. (1986) · Brain Research Bulletin · doi:10.1016/0361-9230(86)90140-1 · Cited by 217
Mufson, E. J., Ma, S. Y., Cochran, E. J., Bennett, D. A., Beckett, L., Jaffar, S., Saragovi, H. U., & Kordower, J. H. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20001106)427:1 · Cited by 219
Self-citationCortés, R., Probst, A., & Palacios, J. M. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90006-6 · Cited by 215
The entorhinal cortex of the monkey: III. Subcortical afferents
Insausti, R., Amaral, D. G., & Cowan, W. M. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902640307 · Cited by 214
The Basal Forebrain Regulates Global Resting-State fMRI Fluctuations
Turchi, J. N., Chang, C., Ye, F. Q., Russ, B. E., Yu, D. K., Cortes, C. R., Monosov, I. E., Duyn, J. H., & Leopold, D. A. (2018) · Neuron · doi:10.1016/j.neuron.2018.01.032 · Cited by 221
Etienne, P. E., Robitaille, Y., Wood, P. L., Gauthier, S. G., Nair, N. P. V., & Quirion, R. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90142-9 · Cited by 213
Wainer, B. H., Bolam, J. P., Freund, T. F., Henderson, Z., Totterdell, S., & Smith, A. D. (1984) · Brain Research · doi:10.1016/0006-8993(84)90918-1 · Cited by 213
Self-citationJones, B. E. (1993) · Progress in brain research · doi:10.1016/s0079-6123(08)62381-x · Cited by 212
The anatomy of the CNS cholinergic neurons
Cuello, A. C., & Sofroniew, M. V. (1984) · Trends in Neurosciences · doi:10.1016/s0166-2236(84)80161-7 · Cited by 212
The cholinergic innervation of the human cerebral cortex.
Mesulam, M.-M. (2004) · Progress in Brain Research · doi:10.1016/s0079-6123(03)45004-8 · Cited by 211
Self-citationBrain iron deposition is linked with cognitive severity in Parkinson’s disease
Thomas, G. E. C., Leyland, L., Schrag, A. E., Lees, A. J., Acosta‐Cabronero, J., & Weil, R. S. (2020) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2019-322042 · Cited by 211
Montero‐Menei, C. N., & Hefti, F. F. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-08-02986.1988 · Cited by 211
Neurotrophins and neurodegeneration
Dawbarn, D., & Allen, S. J. (2003) · Neuropathology and Applied Neurobiology · doi:10.1046/j.1365-2990.2003.00487.x · Cited by 217
Freeman, S. M., & Young, L. J. (2016) · Journal of Neuroendocrinology · doi:10.1111/jne.12382 · Cited by 196
“These nuclei are major sources of cholinergic input to the rest of the brain (44-46) and are important Freeman and Young Page 5”
BackgroundSchulz, J., Pagano, G., Bonfante, J. A. F., Wilson, H., & Politis, M. (2018) · Brain · doi:10.1093/brain/awy072 · Cited by 230
Afferent connections of the zona incerta: A horseradish peroxidase study in the rat
Shammah‐Lagnado, S. J., Negrão, N., & Ricardo, J. A. (1985) · Neuroscience · doi:10.1016/0306-4522(85)90127-7 · Cited by 209
Comparison of subcortical connections of inferior temporal and posterior parietal cortex in monkeys
Baizer, J. S., Desimone, R., & Ungerleider, L. G. (1993) · Visual Neuroscience · doi:10.1017/s0952523800003229 · Cited by 209
Lehéricy, S., Hirsch, É. C., Cervera, P., Hersh, L. B., Bakchine, S., Piette, F., Duyckaerts, C. J., Hauw, J., Javoy-Agid, F., & Agid, Y. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903300103 · Cited by 208
The cholinergic systems in brain and spinal cord
Kása, P. (1986) · Progress in Neurobiology · doi:10.1016/0301-0082(86)90016-x · Cited by 208
Nimgampalle, M., Chakravarthy, H., Sharma, S., Shree, S., Bhat, A. R., Pradeepkiran, J. A., & Devanathan, V. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101994 · Cited by 207
Estrogen therapy and cognition: a review of the cholinergic hypothesis
Gibbs, R. B. (2010) · Endocrine Reviews · doi:10.1210/er.2009-0036 · Cited by 206
Bucci, D. J., Holland, P. C., & Gallagher, M. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-19-08038.1998 · Cited by 204
Role of attention in the generation and modulation of tinnitus
Roberts, L. E., Husain, F. T., & Eggermont, J. J. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.07.007 · Cited by 202
Cools, R., & Arnsten, A. F. T. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01100-8 · Cited by 216
“Perestroika” in the basal forebrain: Opening the border between neurology and psychiatry
Heimer, L., de Olmos, J. S., Alheid, G. F., & Záborszky, L. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)63050-2 · Cited by 203
Metherate, R., & Ashe, J. H. (1993) · Synapse · doi:10.1002/syn.890140206 · Cited by 203
Alzheimer's disease: Neurofibrillary tangles in nuclei that project to the cerebral cortex
German, D. C., White, C. L., & Sparkman, D. R. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90123-0 · Cited by 204
Chapter 32 Hippocampal formation: anatomy and the patterns of pathology in Alzheimer's disease
Hoesen, G. W. V., & Hyman, B. T. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)61268-6 · Cited by 201
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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review