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Catecholamine innervation of the human cerebral cortex as revealed by comparative immunohistochemistry of tyrosine hydroxylase and dopamine-beta-hydroxylase
Abstract
The organization of the cortical monoamine systems, dopamine (DA), and noradrenaline (NA), which have been studied extensively in the rat and more recently in the monkey, had not yet been investigated directly in the human brain. We report here the first systematic account of the regional and laminar distributions of the catecholamine fibers in the human cerebral cortex, using immunohistochemistry of the catecholamine biosynthetic enzymes, tyrosine hydroxylase (TH), and dopamine‐β‐hydroxylase (DBH) in 13 cytoarchitectonic areas (4, 6, 9, 3b, 5, 40, 17, 18, 23, 24, 29, insula, and hippocampus) sampled postmortem. The noradrenergic (NA) innervation, mapped with DBH‐immunoreactivity (DBH‐IR), displayed a characteristic density gradient in the neocortex (highest in the primary sensorimotor areas, decreasing rostrally and caudally) that contrasted with the more uniform density in the limbic cortices (24, 23, 29, insula, hippocampus). NA axons were present in all cortical layers and were least numerous in layer I. The DBH‐IR fibers were only partly TH‐immunostained (10–50%, on double‐labeled sections), suggesting a heterogeneity of the cortical NA axons. The putative dopaminergic (DA) fibers were identified by comparing alternate or double‐immunolabeled (DBH‐TH) sections, as the TH‐IR fibers which contain no DBH‐IR. A DA‐like innervation was present in all cortical areas, with major regional differences in density and laminar distribution, which closely paralleled cytoarchitectural buildups: (1) the DA‐like innervation was densest in the agranular areas, primary and secondary motor areas, anterior cingulate, and insula; it distributed throughout layers I–VI; (2) density was lower in the granular cortices, areas 9 (prefrontal cortex), 23, 3b, 5, 40, and 18, displaying a bilaminar pattern in layers I and V–VI. In all areas, DA‐like fibers were most abundant in the molecular layer, with a predominant distribution in its deepest part. Convoluted and coily fibers represented a unique morphologic aspect of the CA innervation in the human cortex. These findings are in agreement with findings in nonhuman primates and demonstrate major evolutionary changes in the organization of the cortical aminergic input as compared with rodents. The most striking features are the expansion of the DA innervation to the whole cortex and the peak of highest density in the motor areas. The regional differentiation of NA innervation is also accentuated. Slight differences were found in the laminar distributions of the amines in humans and primates. These data seem quite promising and open new research fields in neurologic and psychiatric diseases.
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In the citing paper
“Notably, many if not all regions of the interoceptive circuit in Figure 7, are characterized by a high density of dopaminergic receptors and terminals across all cortical layers; this is particularly well-established for visceromotor regions like AIC, ACC, or OFC (Gaspar et al., 1989; Hurd et al., 2001; Lewis et al., 2001).”
From Allostatic Self-efficacy: A Metacognitive Theory of Dyshomeostasis-Induced Fatigue and Depression (2016) · cites this paper as Gaspar et al., 1989
In the citing paper
“It is well established that the aIns receives dopaminergic innervations (Gaspar et al., 1989) and processes dopamine-associated RPEs.”
From Cognitive flexibility in adolescence: Neural and behavioral mechanisms of reward prediction error processing in adaptive decision making during development (2015) · cites this paper as Gaspar et al., 1989
In the citing paper
“The entire granular subregion has notably high dopamine utilization (Gaspar et al., 1989) with the aIC having high density D1-subtype receptors surrounding dopaminergic terminals from the VTA and substantia nigra.”
From The Insula: A Brain Stimulation Target for the Treatment of Addiction (2019) · cites this paper as Gaspar et al., 1989
In the citing paper
“Furthermore, the insula has a high level of endogenous opioids (Gaspar et al., 1989), high density of µ-subtype opioid receptors (Baumgartner et al., 2006), high density of hypocretin subtype-1 receptors (Hollander et al., 2008), and a high level of nicotinic acetylcholine receptors (nAChRs) containing the β2 subunit”
From The Insula: A Brain Stimulation Target for the Treatment of Addiction (2019) · cites this paper as Gaspar et al., 1989
Citations
Cites
Parallel organization of functionally segregated circuits linking basal ganglia and cortex
Alexander, G. E., DeLong, M. R., & Strick, P. L. (1986) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.09.030186.002041 · Cited by 8,527
Handbook of chemical neuroanatomy
(2005) · Handbook of chemical neuroanatomy · doi:10.1016/s0924-8196(05)80001-6 · Cited by 906
Everitt, B. J., Hökfelt, T. G. M., Terenius, L. Y., Tatemoto, K., Mutt, V., & Goldstein, M. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90036-8 · Cited by 871
Scatton, B., Javoy-Agid, F., Rouquier, L., Dubois, B., & Agid, Y. (1983) · Brain Research · doi:10.1016/0006-8993(83)90993-9 · Cited by 727
Muakkassa, K. F., & Strick, P. L. (1979) · Brain Research · doi:10.1016/0006-8993(79)90928-4 · Cited by 630
Afferent and efferent projections of the inferior area 6 in the macaque monkey
Matelli, M., Camarda, R., Glickstein, M., & Rizzolatti, G. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902510302 · Cited by 525
REACTION TIME IN PARKINSON'S DISEASE
Evarts, E. V., Teräväinen, H., & Calne, D. B. (1981) · Brain · doi:10.1093/brain/104.1.167 · Cited by 515
Tramu, G., Pillez, A., & Léonardelli, J. (1978) · Journal of Histochemistry & Cytochemistry · doi:10.1177/26.4.207771 · Cited by 506
Hendry, S., Jones, E. G., & Emson, P. C. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-10-02497.1984 · Cited by 415
Organization of catecholamine neurons projecting to the frontal cortex in the rat
Lindvall, O., Björklund, A., & Divac, I. (1978) · Brain Research · doi:10.1016/0006-8993(78)90173-7 · Cited by 412
Research works printed but not linked: 12
- Berger B., 1976, Axones catecholaminergiques du cortex cérébral humain. Observation, en histofluorscence, de biopsiescérébrales dont 2 cas de maladie d'Alzheimer, Rev. Neurol., 132, 183
- Berger B., 1980, Enzymes and Neurotransmitters in Mental Disease, 317
- Berger B., 1986, Differential distribution of dopamine and serotonin axons in monkey cerebral cortex. A radioautographic study, Neurosci. Lett. Suppl., 26, S105
- Burke W. J., 1987, Geriatrics Clinical Pharmacology, 47
- Hökfelt T., 1977, Immunohistochemical studies on the localization and distribution of monoamine neuron systems in the rat. IITyrosine‐hydroxylase in the telencephalon, Med. Bio., 55, 21
- Hökfelt T., 1984, Handbook of Chemical Neuroanatomy, 277
- Javoy‐Agid F., 1987, Distribution of monoaminergic, cholinergic and peptidergic markers in the human cerebral cortex, Soc. Neurosci. Abstr., 13, 527
- Kitt C. A., 1984, Contribution of catecholaminergic systems to neurites in plaques of aged primates, Ann. Neurol., 16, 118
- Mann D. M. A., 1983, The pathology of the human locus coeruleus, Clinical Neuropathol., 2, 1
- Marin‐Padilla M., 1986, Cerebral Cortex, 447
- Sanidés F., 1964, The cyto‐myeloarchitecture of the human frontal lobe, its relation to phylogenetic differentiation of the cerebral cortex, J. für Hirnforsch., 6, 269
- Von Economo C. V., 1972, L'architecture cellulaire normale de l'écorce cérébrale
Cited by
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Falzone, T. L., Gelman, D. M., Young, J. I., Grandy, D. K., Low, M. J., & Rubinstein, M. (2002) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01842.x · Cited by 109
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Traub, R. D., & Whittington, M. A. (2010) · doi:10.1093/acprof:oso/9780195342796.001.0001 · Cited by 108
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Wacker, J., Chavanon, M., & Stemmler, G. (2009) · Journal of Research in Personality · doi:10.1016/j.jrp.2009.12.004 · Cited by 106
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Szabadi, E. (2012) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2012.00094 · Cited by 111
Huntley, G. W., Morrison, J. H., Prikhozhan, A., & Sealfon, S. C. (1992) · Molecular Brain Research · doi:10.1016/0169-328x(92)90107-m · Cited by 100
Kébir, O., Tabbane, K., Sengupta, S. M., & Joober, R. (2009) · Journal of Psychiatry and Neuroscience · doi:10.1139/jpn.0913 · Cited by 98
Monoaminergic–cholinergic interactions in the primate basal forebrain
Smiley, J. F., Subramanian, M., & Mesulam, M.-M. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00116-5 · Cited by 79
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Glass, M., & Dragunow, M. (1995) · Brain Research Reviews · doi:10.1016/0165-0173(95)00005-n · Cited by 98
Goldsmith, S. K., & Joyce, J. N. (1994) · Hippocampus · doi:10.1002/hipo.450040318 · Cited by 96
Stavropoulos, K. K. M., & Carver, L. J. (2014) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.12270 · Cited by 105
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Aalto, S., Ihalainen, J. A., Hirvonen, J., Kajander, J., Scheinin, H., Tanila, H., Någren, K., Vilkman, H., Gustafsson, L. L., Syvälahti, E. K. G., et al. (2005) · Psychopharmacology · doi:10.1007/s00213-005-0092-6 · Cited by 95
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Poletti, M., Enrici, I., Bonuccelli, U., & Adenzato, M. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.01.010 · Cited by 94
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Keyser, J. D., Backer, J. D., Vauquelin, G., & Ebinger, G. (1990) · Brain Research · doi:10.1016/0006-8993(90)91672-4 · Cited by 93
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Mottaghy, F. M., Willmes, K., Horwitz, B., Müller, H.-W., Krause, B. J., & Sturm, W. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.07.034 · Cited by 85
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Murphy, M. J. M., & Deutch, A. Y. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24424 · Cited by 85
Périn, B., Godefroy, O., Fall, S., & de Marco, G. (2009) · Brain and Cognition · doi:10.1016/j.bandc.2009.09.010 · Cited by 86
Kritzer, M. F., & Kohama, S. G. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990705)409:3 · Cited by 126
Krimer, L. S., Jakab, R. L., & Goldman‐Rakic, P. S. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-19-07450.1997 · Cited by 85
Verney, C., Zečević, N., Nikolic, B., Alvarez, C., & Berger, B. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90351-s · Cited by 84
Self-citationLecci, S., Cataldi, J., Betta, M., Bernardi, G., Heinzer, R. C., & Siclari, F. (2020) · SLEEP · doi:10.1093/sleep/zsaa094 · Cited by 83
Raghanti, M. A., Stimpson, C. D., Marcinkiewicz, J. L., Erwin, J. M., Hof, P. R., & Sherwood, C. C. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm089 · Cited by 81
Masilamoni, G. J., & Smith, Y. (2017) · Journal of Neural Transmission · doi:10.1007/s00702-017-1774-z · Cited by 86
Levodopa/Carbidopa Treatment for Amblyopia in Older Children
Leguire, L. E., Walson, P. D., Rogers, G. L., Bremer, D. L., & McGregor, M. L. (1995) · Journal of Pediatric Ophthalmology & Strabismus · doi:10.3928/0191-3913-19950501-05 · Cited by 78
Verney, C., Milosevic, A., Alvarez, C., & Berger, B. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903360303 · Cited by 77
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Kessi, M., Duan, H., Xiong, J., Chen, B., He, F., Yang, L., Ma, Y., Bamgbade, O. A., Peng, J., & Yin, F. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.925049 · Cited by 93
Grossman, M., Crino, P. B., Reivich, M., Stem, M. B., & Hurtig, H. I. (1992) · Cerebral Cortex · doi:10.1093/cercor/2.6.513 · Cited by 75
Brefel‐Courbon, C., Thalamas, C., Paul, H. P. S., Sénard, J., Montastruc, J., & Rascol, O. (1998) · CNS Drugs · doi:10.2165/00023210-199810030-00004 · Cited by 71
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Clemens, B., Wagels, L., Bauchmüller, M., Bergs, R., Habel, U., & Kohn, N. (2017) · Scientific Reports · doi:10.1038/srep40180 · Cited by 70
Berger, B., Febvret, A., Greengard, P., & Goldman‐Rakic, P. S. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902990306 · Cited by 70
Self-citationKébir, O., & Joober, R. (2011) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-011-0207-5 · Cited by 71
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Ramakrishnan, A., Byun, Y. W., Rand, K., Pedersen, C. E., Lebedev, M., & Nicolelis, M. A. L. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1703668114 · Cited by 71
Melega, W. P., Grafton, S. T., Huang, S., Satyamurthy, N., Phelps, M. E., & Barrio, J. R. (1991) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1991.154 · Cited by 69
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Leguire, L. E., Rogers, G. L., Walson, P. D., Bremer, D. L., & McGregor, M. L. (1998) · Journal of American Association for Pediatric Ophthalmology and Strabismus · doi:10.1016/s1091-8531(98)90080-5 · Cited by 67
Montorsi, F. (2003) · European Urology · doi:10.1016/s0302-2838(03)00053-8 · Cited by 66
Gaspar, P., Duyckaerts, C. J., Febvret, A., Benoit, R., Beck, B., & Berger, B. (1989) · Brain Research · doi:10.1016/0006-8993(89)90424-1 · Cited by 65
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Kieling, C., Genro, J. P., Hutz, M. H., & Rohde, L. A. (2008) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30636 · Cited by 65
Greenwood, P. M., Fossella, J., & Parasuraman, R. (2005) · Journal of Cognitive Neuroscience · doi:10.1162/089892905774597281 · Cited by 64
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Samson, Y., Wu, J. J., Friedman, A. H., & Davis, J. N. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902980209 · Cited by 64
Jaworska, N., Yücel, K., Courtright, A., MacMaster, F. P., Sembo, M., & MacQUEEN, G. M. (2015) · Journal of Affective Disorders · doi:10.1016/j.jad.2015.10.064 · Cited by 63
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Cunnington, R., Egan, G. F., O’Sullivan, J. D., Hughes, A. J., Bradshaw, J. L., & Colebatch, J. G. (2001) · Movement Disorders · doi:10.1002/mds.1181 · Cited by 64
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Lewis, D. A. (1992) · Springer eBooks · doi:10.1007/978-3-7091-9211-5_9 · Cited by 65
Chavanon, M., Wacker, J., & Stemmler, G. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00117 · Cited by 64
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Bl�mcke, I., L�bach, M., Wolf, H. K., & Wiestler, O. D. (1999) · Microscopy Research and Technique · doi:10.1002/(sici)1097-0029(19990701)46:1 · Cited by 82
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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
Febvret, A., Berger, B., Gaspar, P., & Verney, C. (1991) · Brain Research · doi:10.1016/0006-8993(91)90572-d · Cited by 61
Self-citationAlm, P. A. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.661880 · Cited by 65
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Grossman, M., Carvell, S., Gollomp, S. M., Stern, M. B., Reivich, M., Morrison, D. F., Alavi, A. A., & Hurtig, H. I. (1993) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1993.5.4.480 · Cited by 60
Smiley, J. F., & Mesulam, M. M. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00202-4 · Cited by 60
The Interface Between Dopamine Neurons and the Amygdala: Implications for Schizophrenia
Haber, S. N., & Fudge, J. L. (1997) · Schizophrenia Bulletin · doi:10.1093/schbul/23.3.471 · Cited by 60
Anterior cingulate pyramidal neurons display altered dendritic branching in depressed suicides
Hercher, C., Canetti, L., Turecki, G., & Mechawar, N. (2009) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2009.08.011 · Cited by 59
Olfactory impairment in Parkinson’s disease is a consequence of central nervous system decline
Iannilli, E., Stephan, L., Hummel, T. R., Reichmann, H., & Haehner, A. (2017) · Journal of Neurology · doi:10.1007/s00415-017-8521-0 · Cited by 56
The neuroanatomy of schizophrenia: circuitry and neurotransmitter systems
Fallon, J. H., Opole, I. O., & Potkin, S. G. (2003) · Clinical Neuroscience Research · doi:10.1016/s1566-2772(03)00022-7 · Cited by 53
Ventral tegmental area connections to motor and sensory cortical fields in humans
Hosp, J. A., Coenen, V. A., Rijntjes, M., Egger, K. E., Urbach, H., Weiller, C., & Reisert, M. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01939-0 · Cited by 59
Zilles, K., Gross, G., Schleicher, A., Schildgen, S., Bauer, A., Bahro, M., Schwendemann, G., Zech, K., & Kolassa, N. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90122-5 · Cited by 55
Pogarell, O. M., Tatsch, K., Juckel, G., Hamann, C., Mulert, C., Pöpperl, G., Folkerts, M., Choukèr, M., Riedel, M. J., Zaudig, M., et al. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300537 · Cited by 55
Montorsi, F., Perani, D., Anchisi, D., Salonia, A., Scifo, P., Rigiroli, P., Zanoni, M. L., Heaton, J., Rigatti, P., & Fazio, F. (2003) · International Journal of Impotence Research · doi:10.1038/sj.ijir.3900999 · Cited by 54
Local Application of Dopamine Inhibits Pyramidal Tract Neuron Activity in the Rodent Motor Cortex
Awenowicz, P. W., & Porter, L. L. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00078.2002 · Cited by 51
Tsubomoto, M., Kawabata, R., Zhu, X., Minabe, Y., Chen, K., Lewis, D. A., & Hashimoto, T. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy227 · Cited by 54
Effects of atypical and typical neuroleptics on anterior cingulate volume in schizophrenia
McCormick, L. M., Decker, L. C., Nopoulos, P., Ho, B., & Andreasen, N. C. (2005) · Schizophrenia Research · doi:10.1016/j.schres.2005.06.022 · Cited by 52
Autonomic physiological coupling of the global fMRI signal
Bolt, T., Wang, S., Nomi, J. S., Setton, R., Gold, B. P., Frederick, B. B., Yeo, B. T. T., Chen, J. J., Picchioni, D., Duyn, J. H., et al. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-01945-y · Cited by 71
ADHD pharmacogenetics across the life cycle: New findings and perspectives
Bruxel, E. M., Akutagava-Martins, G. C., Salatino-Oliveira, A., Contini, V., Kieling, C., Hutz, M., & Rohde, L. (2014) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32240 · Cited by 44
Mash, D. C. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00435 · Cited by 53
Monoamine systems in the cerebral cortex: evidence for anatomical specificity
PAPADOPOULOS, G., & Parnavelas, J. G. (1991) · Progress in Neurobiology · doi:10.1016/0301-0082(91)90030-5 · Cited by 51
Ádori, C., Glück, L., Barde, S. S., Yoshitake, T., Kovács, G. G., Mulder, J., Maglóczky, Z., Havas, L., Bölcskei, K., Mitsios, N., et al. (2015) · Acta Neuropathologica · doi:10.1007/s00401-015-1394-3 · Cited by 53
Chapter VI Dopamine systems in the primate brain
Lewis, D. A., & Sesack, S. R. (1997) · Handbook of chemical neuroanatomy · doi:10.1016/s0924-8196(97)80008-5 · Cited by 50
PET imaging of neocortical monoaminergic terminals in Parkinson's disease
Marie, R., Barré, L., Rioux, P. P., Allain, P., Lechevalier, B., & Baron, J. (1995) · Journal of Neural Transmission - Parkinsons Disease and Dementia Section · doi:10.1007/bf02252963 · Cited by 53
Differential cingulate and caudate activation following unexpected nonrewarding stimuli
Davidson, M. C., Horvitz, J. C., Tottenham, N., Fossella, J., Watts, R., Uluğ, A. M., & Casey, B. J. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.07.049 · Cited by 52
Dopamine D2 receptors are organized in bands in normal human temporal cortex
Goldsmith, S. K., & Joyce, J. N. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00132-7 · Cited by 50
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Islam, K. U. S., Meli, N., & Blaess, S. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.746582 · Cited by 55
Vaucher, E., Tong, X., Cholet, N., Lantin, S., & Hamel, É. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000529)421:2 · Cited by 126
P2 receptor expression in the dopaminergic system of the rat brain during development
Heine, C., Wegner, A., Grosche, J., Allgaier, C., Illés, P., & Franke, H. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.07.015 · Cited by 48
Dopaminergic Neuromodulation of Semantic Processing: A 4-T fMRI Study with Levodopa
Copland, D. A., McMahon, K. L., Silburn, P. A., & de Zubicaray, G. I. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp017 · Cited by 47
Counts, S., & Mufson, E. J. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374236-0.10012-4 · Cited by 44
Task-Related Interaction between Basal Ganglia and Cortical Dopamine Release
Garraux, G., Peigneux, P., Carson, R. E., & Hallett, M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1595-07.2007 · Cited by 47
Neurotensin innervation of the human cerebral cortex: lack of colocalization with catecholamines
Gaspar, P., Berger, B., & Febvret, A. (1990) · Brain Research · doi:10.1016/0006-8993(90)91282-l · Cited by 47
Self-citationClemens, B., Zvyagintsev, M., Sack, A. T., Heinecke, A., Willmes, K., & Sturm, W. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025453 · Cited by 47
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Metadata
- Authors
- Gaspar, P., Berger, B., Febvret, A., Vigny, A., & Henry, J. P.
- Affiliations
- Inserm (FR)
- Institut de Biologie Physico-Chimique (FR)
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1989-01-08
- Volume
- 279
- Issue
- 2
- Pages
- 249-271
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2069412440
- Cited by
- 395
- References
- 79
- Citations by year
- 2026: 4 · 2025: 11 · 2024: 7 · 2023: 8 · 2022: 5 · 2021: 14 · 2020: 13 · 2019: 9 · 2018: 9 · 2017: 11 · 2016: 8 · 2015: 11 · 2014: 11 · 2013: 12 · 2012: 9
- FWCI
- 5.64
- 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 › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Medicine › Clinical Neurology › Parkinson's Disease Mechanisms and Treatments
- Keywords
- catecholamine innervation, human cerebral cortex, noradrenergic innervation, dopaminergic innervation, tyrosine hydroxylase, dopamine beta-hydroxylase, cortical laminar distribution, cytoarchitectonic areas, molecular layer, neocortex, limbic cortex, norepinephrine, postmortem brain
- MeSH terms
- Adult, Aged, Aged, 80 and over, Catecholamines, Cerebral Cortex, Dopamine beta-Hydroxylase, Female, Humans, Immunohistochemistry, Male, Middle Aged, Nerve Fibers, Tyrosine 3-Monooxygenase
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