Efferent projections of infralimbic and prelimbic areas of the medial prefrontal cortex in the Japanese monkey, Macaca fuscata
Abstract
The infralimbic area (IL) and prelimbic area (PL) have been postulated as an autonomic motor region in the medial prefrontal cortex. The present study was conducted to reveal the projection sites of IL and PL of the monkey, Macaca fuscata, using biotinylated dextran amine as an anterograde tracer. IL and PL projected densely to the ventromedial caudate nucleus, the core and shell of the nucleus accumbens (Acb), parvicellular lateral basal and magnocellular accessory basal nuclei of the amygdala, lateral preoptic area, ventromedial hypothalamic nucleus, tubero-mammillary nucleus (TM), medial part of the magnocellular and dorsal part of the parvicellular (MDpc) dorsomedial thalamic nuclei, reunience and medial part of the medial pulvinar nucleus, and dorso-lateral part of the periaqueductal gray (PAGdl) in the mesencephalon. Moderately to weakly projected areas were the intermediate and lateral parts of the agranular insular cortex, orbital part of area 12, agranular and dysgranular part of the temporal pole cortex (TPa-g), auditory temporal cortex, lateral and medial (MS) septal nuclei, bed nucleus of the stria terminalis, diagonal band of Broca, substantia innominata, and medial preoptic area, dorsomedial, lateral, and posterior hypothalamic nuclei, magnocellular lateral basal and lateral amygdaloid nuclei, paratenial, paraventricular (PV), inter-antero-medial (IAM), reticular, central medial (CeM), parafascicular (PF) and limitans nuclei of the thalamus, lateral habenular nucleus, pedunculo-pontine nucleus, dorsal part of the lateral lemniscal nucleus, ventral tegmental area (VTA), dorsal raphe, superior central nucleus, medial and lateral parabrachial nuclei (PBl) and nucleus locus coeruleus (LC). A few scattered terminals were observed in the perifornical nucleus of the hypothalamus and substantia nigra pars compacta. PL and area 24 were characterized by projections to the entorhinal (Ent) and piriform (Pir) cortex as well as to the magnocellular part of the ventral anterior thalamic nucleus (VAmc). The morphology of the terminal arborization in each nuclei was different in appearance, perhaps reflecting the synaptic interaction between the nerve terminals and postsynaptic dendrites. PL projected uniquely to Ent, Pir and VAmc and IL projected uniquely to TPa-g, MS, IAM, CeM, MDpc, PF, PBl and LC. IL projected more strongly than PL to the shell of Acb, amygdaloid nuclei, PV, TM, VTA and PAGdl. The present results support the hypothesis that IL is a major cortical autonomic motor area and PL integrates limbic and autonomic inputs in the primate.
Integrity signals
Registry
Cites
Statistics
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?
ACC and AI project to or are adjacent to VTA and SN, with multisynaptic routes via habenula.
“which project to or are adjacent to VTA and SN3,22,29–33,54,55 (with multisynaptic routes via habenula56,57)”
From Interpretable abstractions of artificial neural networks predict behavior and neural activity during human information gathering (2026) · cites this paper as [30]
Anatomical connectivity data support the homology of rat infralimbic cortex with monkey area 25 and rat prelimbic cortex with monkey area 32.
“Efferent projections from rat IL are similar to those of monkey 25, whereas the efferent projections from rat PrL are similar to those of monkey 32 (33–39).”
From Functional anatomy of ventromedial prefrontal cortex: implications for mood and anxiety disorders (2012) · cites this paper as [35]
There are significant restrictions on inferring mechanisms of rat infralimbic cortex to primate vmPFC because human extinction recall correlates with regions anterior to area 25, and areas 10m and 10r have little connectional similarity to primate 25 or rat IL.
“there remain significant restrictions on the extent to which one can draw inferences from what is known about the neural mechanisms by which rat IL comes to extinguish conditioned fear to claims about the neural mechanisms by which primate vmPFC comes to extinguish conditioned fear; especially since a number of anatomical studies make clear that areas such as 10m and 10r share little connectional”
From Functional anatomy of ventromedial prefrontal cortex: implications for mood and anxiety disorders (2012) · cites this paper as [35]
IL/25 projects directly to autonomic regions that enhance sympathetic activity, including perifornical area, dorsomedial hypothalamus, dorsolateral periaqueductal gray, lateral parabrachial nucleus, cuneiform nucleus, and lateral septum.
“IL/25 projects directly to a number of autonomic regions which have been found to enhance sympathetic activity, including the perifornical area, dorsomedial hypothalamus, dorsolateral periaqueductal gray, lateral parabrachial nucleus, cuneiform nucleus, and lateral septum, among other regions (4, 33, 35–37, 39, 47, 82, 97, 98).”
From Functional anatomy of ventromedial prefrontal cortex: implications for mood and anxiety disorders (2012) · cites this paper as [35]
Rat IL and monkey area 25 send significant projections to inhibitory ITC cells and also project directly to amygdalar regions that enhance amygdalar output, such as basolateral nucleus, medial nucleus, and medial CeA.
“Rat IL and monkey area 25—the only regions in rat/monkey mPFC that appear to send significant projections to the inhibitory ITC cells in the amygdala—also send direct projections to amygdalar regions that are thought to enhance amygdalar output: e.g., the basolateral nucleus and medial nucleus (in rats and monkeys) and medial CeA (in rats) (35, 36, 39).”
From Functional anatomy of ventromedial prefrontal cortex: implications for mood and anxiety disorders (2012) · cites this paper as [35]
In monkey brain, amygdala projections are stronger from the subgenual than the pregenual cingulate region.
“The strength of connections from different cingulate subregions is rarely systematically compared in macaque, but it has been claimed that, as we have found for the human brain, amygdala projections are stronger from the subgenual than the pregenual cingulate region in the monkey brain (Chiba et al. 2001).”
From Anatomical connectivity of the subgenual cingulate region targeted with deep brain stimulation for treatment-resistant depression (2008) · cites this paper as Chiba et al. 2001
Cites
The rat brain in stereotaxic coordinates
Palkovits, M. (1983) · Neuropeptides · doi:10.1016/0143-4179(83)90049-5 · Cited by 28,959 · see citing works
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works
Insensitivity to future consequences following damage to human prefrontal cortex
Bechara, A., Damasio, A. R., Damasio, H., & Anderson, S. W. (1994) · Cognition · doi:10.1016/0010-0277(94)90018-3 · Cited by 6,128 · see citing works
Deciding advantageously before knowing the advantageous strategy
Bechara, A., Damasio, H., Tranel, D., & Damasio, A. R. (1997) · Science · doi:10.1126/science.275.5304.1293 · Cited by 3,547 · see citing works
From motivation to action: Functional interface between the limbic system and the motor system
MOGENSON, G., JONES, D., & YIM, C. (1980) · Progress in Neurobiology · doi:10.1016/0301-0082(80)90018-0 · Cited by 2,331 · see citing works
DAMASIO, A. (1990) · Behavioural Brain Research · doi:10.1016/0166-4328(90)90144-4 · Cited by 1,275 · see citing works
Perirhinal and parahippocampal cortices of the macaque monkey: Cortical afferents
Suzuki, W., & Amaral, D. G. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903500402 · Cited by 1,134 · see citing works
Central regulation of autonomic functions
(1991) · General Pharmacology The Vascular System · doi:10.1016/0306-3623(91)90107-h · Cited by 1,115 · see citing works
Functional characteristics of the midbrain periaqueductal gray.
Behbehani, M. M. (1995) · Progress in Neurobiology · doi:10.1016/0301-0082(95)00009-k · Cited by 879 · see citing works
(1964) · McGraw-Hill eBooks · Cited by 838 · see citing works
Efferent projections of the infralimbic cortex of the rat
Hurley, K. M., Herbert, H., Moga, M. M., & Saper, C. B. (1991) · Journal of Comparative Neurology · doi:10.1002/cne.903080210 · Cited by 777 · see citing works
Neurobiology of Cingulate Cortex and Limbic Thalamus
Vogt, B. A., & Gabriel, M. (1993) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4899-6704-6 · Cited by 772 · see citing works
The frontal granular cortex and behavior
Pribram, K. H. (1965) · Neuropsychologia · doi:10.1016/0028-3932(65)90022-9 · Cited by 705 · see citing works
McDonald, A. J., Mascagni, F., & Guo, L. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00417-3 · Cited by 689 · see citing works
Sensory and premotor connections of the orbital and medial prefrontal cortex of macaque monkeys
Carmichael, S. T., & Price, J. L. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903630409 · Cited by 678 · see citing works
Architectonic subdivision of the orbital and medial prefrontal cortex in the macaque monkey
Carmichael, S. T., & Price, J. L. (1994) · Journal of Comparative Neurology · doi:10.1002/cne.903460305 · Cited by 656 · see citing works
Cortical and subcortical afferents to the amygdala of the rhesus monkey (Macaca mulatta)
Aggleton, J. P., Burton, M. J., & Passingham, R. E. (1980) · Brain Research · doi:10.1016/0006-8993(80)90279-6 · Cited by 610 · see citing works
The orbital and medial prefrontal circuit through the primate basal ganglia
Haber, S., Kunishio, K., Mizobuchi, M., & Lynd-Balta, E. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-07-04851.1995 · Cited by 605 · see citing works
Cytoarchitecture and neural afferents of orbitofrontal cortex in the brain of the monkey
Morecraft, R. J., Geula, C., & Mesulam, M. ‐. (1992) · Journal of Comparative Neurology · doi:10.1002/cne.903230304 · Cited by 539 · see citing works
Krettek, J. E., & Price, J. L. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901720409 · Cited by 535 · see citing works
Direct and indirect pathways from the amygdala to the frontal-lobe in rhesus-monkeys
Porrino, L. J., Crane, A. M., & Goldman‐Rakic, P. S. (1981) · Journal of Comparative Neurology · doi:10.1002/cne.901980111 · Cited by 491 · see citing works
Autonomic responses and efferent pathways from the insular cortex in the rat
Yasui, Y., Breder, C. D., Safer, C. B., & Cechetto, D. F. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903030303 · Cited by 480 · see citing works
Russchen, F. T., Amaral, D. G., & Price, J. L. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902560202 · Cited by 416 · see citing works
Ray, J. P., & Price, J. L. (1993) · Journal of Comparative Neurology · doi:10.1002/cne.903370102 · Cited by 402 · see citing works
Is the histaminergic neuron system a regulatory center for whole-brain activity?
Wada, H., Inagaki, N., Yamatodani, A., & Watanabe, T. (1991) · Trends in Neurosciences · doi:10.1016/0166-2236(91)90034-r · Cited by 380 · see citing works
Neurobiology of cingulate cortex and limbic thalamus : a comprehensive handbook
Vogt, B. A., & Gabriel, M. (1993) · Medical Entomology and Zoology · Cited by 378 · see citing works
Romanski, L. M., Giguere, M., Bates, J. F., & Goldman-Rakic, P. S. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970317)379:3 · Cited by 325 · see citing works
Neafsey, E. J. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)62679-5 · Cited by 305 · see citing works
Diverse thalamic projections to the prefrontal cortex in the rhesus monkey
Barbas, H., Henion, T. H. H., & Dermon, C. R. (1991) · Journal of Comparative Neurology · doi:10.1002/cne.903130106 · Cited by 292 · see citing works
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 · see citing works
Takagishi, M., & Chiba, T. (1991) · Brain Research · doi:10.1016/0006-8993(91)91677-s · Cited by 284 · see citing works
Self-citationIlinsky, I. A., & Kultas‐Ilinsky, K. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902620303 · Cited by 281 · see citing works
Connections of the Monkey Cingulate Cortex
Hoesen, G. W. V., Morecraft, R. J., & Vogt, B. A. (1993) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4899-6704-6_9 · Cited by 276 · see citing works
Pandya, D. Ν., & Yeterian, E. H. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)62676-x · Cited by 255 · see citing works
Lovick, T. A. (1993) · Progress in Neurobiology · doi:10.1016/0301-0082(93)90036-r · Cited by 215 · see citing works
Deutch, A. Y. (1993) · Journal of Neural Transmission · doi:10.1007/bf01245232 · Cited by 212 · see citing works
Sesack, S. R., & Bunney, B. S. (1989) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)24159-3 · Cited by 200 · see citing works
Central Neural Integration for the Control of Autonomic Responses Associated with Emotion
Smith, O. A., & Devito, J. L. (1984) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.07.030184.000355 · Cited by 191 · see citing works
Gabbott, P. L. A., & Bacon, S. J. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960122)364:4 · Cited by 165 · see citing works
Neafsey, E. J., Terreberry, R. R., Hurley, K. M., Ruit, K. G., & Frysztak, R. J. (1993) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4899-6704-6_7 · Cited by 159 · see citing works
Role of the Cerebral Cortex in Autonomic Function
Cechetto, D. F., & Saper, C. B. (1990) · doi:10.1093/oso/9780195051063.003.0012 · Cited by 154 · see citing works
Three cerebral cortical systems affecting autonomic function
Wall, P. D., & Davis, G. D. (1951) · Journal of Neurophysiology · doi:10.1152/jn.1951.14.6.507 · Cited by 153 · see citing works
Origin of neuronal inputs to the region of the tuberomammillary nucleus of the rat brain
Ericson, H., Blomqvist, A. G., & Köohler, C. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903110105 · Cited by 149 · see citing works
Valentino, R. J., Page, M. E., Luppi, P., Zhu, Y., Bockstaele, E. V., & Aston‐Jones, G. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90320-4 · Cited by 148 · see citing works
Bailey, P., & Sweet, W. H. (1940) · Journal of Neurophysiology · doi:10.1152/jn.1940.3.3.276 · Cited by 144 · see citing works
Circulatory effects of cortical stimulation.
Jm, D. (1960) · PubMed · Cited by 116 · see citing works
Brinley-Reed, M., Mascagni, F., & MCDONALD, A. (1995) · Neuroscience Letters · doi:10.1016/0304-3940(95)12212-5 · Cited by 114 · see citing works
Bacon, S. J., & Smith, A. D. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90242-8 · Cited by 100 · see citing works
Thalamic and temporal cortex input to medial prefrontal cortex in rhesus monkeys
Bachevalier, J., Meunier, M., Lu, M., & Ungerleider, L. G. (1997) · Experimental Brain Research · doi:10.1007/pl00005713 · Cited by 93 · see citing works
Datiche, F., & Cattarelli, M. (1996) · Brain Research Bulletin · doi:10.1016/s0361-9230(96)00082-2 · Cited by 87 · see citing works
Vickery, R. M., Morris, S. H., & Bindman, L. J. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.6.3039 · Cited by 80 · see citing works
Zagon, A., Totterdell, S., & Jones, R. S. G. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903400402 · Cited by 70 · see citing works
Rétaux, S., Besson, M., & Penit-Soria, J. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90296-z · Cited by 56 · see citing works
Cingulothalamic and Prefrontal Control of Autonomic Function
Buchanan, S. L., & Powell, D. A. (1993) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4899-6704-6_14 · Cited by 51 · see citing works
Afferent projections of the infralimbic cortex (area 25) in rats: a WGA-HRP study.
Azuma, M., & Chiba, T. (1996) · PubMed · Cited by 21 · see citing works
Self-citationTopographic organization of efferent projections of medial frontal cortex
Zeng, D., & Stuesse, S. L. (1993) · Brain Research Bulletin · doi:10.1016/0361-9230(93)90075-m · Cited by 17 · see citing works
NAKANO, K., Kayahara, T., & Chiba, T. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09297.x · Cited by 16 · see citing works
Self-citationLovick, T. A., & Stezhka, V. V. (1999) · Experimental Brain Research · doi:10.1007/s002210050599 · Cited by 12 · see citing works
2418 Projection sites of infralimbic cortex (area 25) of the monkey
Chiba, T., & Nakano, K. (1997) · Neuroscience Research · doi:10.1016/s0168-0102(97)90776-8 · Cited by 1 · see citing works
Self-citationAn, X., Bandler, R., �ng�r, D., & Price, J. L. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19981130)401:4
Flagged first, then by citations
4 of the 64 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Bardo, M. T., & Hammer, R. P. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90226-e · Cited by 3,229 · see citing works
Emotional processing in anterior cingulate and medial prefrontal cortex
Etkin, A., Egner, T., & Kalisch, R. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.11.004 · Cited by 3,059 · see citing works
Interoceptive predictions in the brain
Barrett, L. F., & Simmons, W. K. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3950 · Cited by 1,766 · see citing works
Neural Mechanisms of Extinction Learning and Retrieval
Quirk, G. J., & Mueller, D. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301555 · Cited by 1,645 · see citing works
Differential projections of the infralimbic and prelimbic cortex in the rat
Vertes, R. P. (2004) · Synapse · doi:10.1002/syn.10279 · Cited by 1,550 · see citing works
Anatomical analysis of afferent projections to the medial prefrontal cortex in the rat
Hoover, W. B., & Vertes, R. P. (2007) · Brain Structure and Function · doi:10.1007/s00429-007-0150-4 · Cited by 1,365 · see citing works
Amygdala, medial prefrontal cortex, and hippocampal function in PTSD
SHIN, L. M., RAUCH, S. L., & PITMAN, R. K. (2006) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1364.007 · Cited by 1,203 · see citing works
Mental fatigue: Costs and benefits
Boksem, M. A. S., & Tops, M. (2008) · Brain Research Reviews · doi:10.1016/j.brainresrev.2008.07.001 · Cited by 1,142 · see citing works
Shin, L. M., Wright, C. I., Cannistraro, P. A., Wedig, M. M., McMullin, K., Martis, B., Macklin, M. L., Lasko, N. B., Cavanagh, S. R., Krangel, T. S., et al. (2005) · Archives of General Psychiatry · doi:10.1001/archpsyc.62.3.273 · Cited by 960 · see citing works
Frontocingulate Dysfunction in Depression: Toward Biomarkers of Treatment Response
Pizzagalli, D. A. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2010.166 · Cited by 945 · see citing works
Tohen, M., Vieta, E., Calabrese, J., Ketter, T. A., Sachs, G., Bowden, C., Mitchell, P. B., Centorrino, F., Risser, R., Baker, R. W., et al. (2003) · Archives of General Psychiatry · doi:10.1001/archpsyc.60.11.1079 · Cited by 908 · see citing works
Orbitofrontal Cortex and Its Contribution to Decision-Making
Wallis, J. D. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094334 · Cited by 895 · see citing works
The cingulate cortex and limbic systems for emotion, action, and memory
Rolls, E. T. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01945-2 · Cited by 859 · see citing works
Vertes, R. P. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.06.027 · Cited by 811 · see citing works
Ghashghaei, H. T., & Barbas, H. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00446-3 · Cited by 785 · see citing works
Shin, L. M., Orr, S. P., Carson, M. A., Rauch, S. L., Macklin, M. L., Lasko, N. B., Peters, P. M., Metzger, L. J., Dougherty, D. D., Cannistraro, P. A., et al. (2004) · Archives of General Psychiatry · doi:10.1001/archpsyc.61.2.168 · Cited by 790 · see citing works
Anterior cingulate cortex: unique role in cognition and emotion
Stevens, F. L., Hurley, R. A., & Taber, K. H. (2011) · The Journal of Neuropsychiatry and Clinical Neurosciences · doi:10.1176/jnp.23.2.jnp121 · Cited by 779 · see citing works
Extinction circuits for fear and addiction overlap in prefrontal cortex
Peters, J., Kalivas, P. W., & Quirk, G. J. (2009) · Learning & Memory · doi:10.1101/lm.1041309 · Cited by 736 · see citing works
Emotion and the prefrontal cortex: an integrative review
Dixon, M. L., Thiruchselvam, R., Todd, R., & Christoff, K. (2017) · Psychological Bulletin · doi:10.1037/bul0000096 · Cited by 745 · see citing works
Evidence for a large-scale brain system supporting allostasis and interoception in humans
Kleckner, I. R., Zhang, J., Touroutoglou, A., Chanes, L., Xia, C., Simmons, W. K., Quigley, K. S., Dickerson, B. C., & Feldman Barrett, L. (2017) · Nature Human Behaviour · doi:10.1038/s41562-017-0069 · Cited by 641 · see citing works
Johansen-Berg, H., Gutman, D. A., Behrens, T. E. J., Matthews, P. M., Rushworth, M. F. S., Katz, E., Lozano, A. M., & Mayberg, H. S. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm167 · Cited by 561 · see citing works
Regulation of affect by the lateral septum: implications for neuropsychiatry
Sheehan, T. P., Chambers, R. A., & Russell, D. S. (2004) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.04.009 · Cited by 514 · see citing works
The subcallosal cingulate gyrus in the context of major depression
Hamani, C., Mayberg, H., Stone, S., Laxton, A., Haber, S., & Lozano, A. M. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.09.034 · Cited by 508 · see citing works
The Neural Representation of Abstract Words: The Role of Emotion
Vigliocco, G., Kousta, S. T., Rosa, P. A. D., Vinson, D., Tettamanti, M., Devlin, J. T., & Cappa, S. F. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht025 · Cited by 493 · see citing works
The nucleus accumbens: a comprehensive review
Salgado, S., & Kaplitt, M. G. (2015) · Stereotactic and Functional Neurosurgery · doi:10.1159/000368279 · Cited by 489 · see citing works
A Role for the Human Dorsal Anterior Cingulate Cortex in Fear Expression
Milad, M. R., Quirk, G. J., Pitman, R. K., Orr, S. P., Fischl, B., & Rauch, S. L. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.04.032 · Cited by 485 · see citing works
Brain reward circuitry beyond the mesolimbic dopamine system: a neurobiological theory
Ikemoto, S. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.02.001 · Cited by 454 · see citing works
Anatomical insights into the interaction of emotion and cognition in the prefrontal cortex
Ray, R. D., & Zald, D. H. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.08.005 · Cited by 446 · see citing works
Allostatic Self-efficacy: A Metacognitive Theory of Dyshomeostasis-Induced Fatigue and Depression
Stephan, K. E., Manjaly, Z. M., Mathys, C. D., Weber, L. A. E., Paliwal, S., Gard, T., Tittgemeyer, M., Fleming, S. M., Haker, H., Seth, A. K., et al. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00550 · Cited by 437 · see citing works
“…to both the body and the physical and social world outside the body; this is for notational brevity only and not meant to disregard differences in how bodily, social and physical states can influence brain activity in general and the emergence of fatigue in particular; a topic we return to below.”
BackgroundEmotional Perseveration: An Update on Prefrontal-Amygdala Interactions in Fear ExtinctionPreprint
Sotres-Bayón, F., Bush, D. E. A., & LeDoux, J. E. (2004) · Learning & Memory · doi:10.1101/lm.79504 · Cited by 407 · see citing works
Lisman, J. E., & Otmakhova, N. A. (2001) · Hippocampus · doi:10.1002/hipo.1071 · Cited by 402 · see citing works
Serial pathways from primate prefrontal cortex to autonomic areas may influence emotional expression
Barbas, H., Saha, S., Rempel-Clower, N., & Ghashghaei, T. (2003) · BMC Neuroscience · doi:10.1186/1471-2202-4-25 · Cited by 380 · see citing works
Receptor architecture of human cingulate cortex: Evaluation of the four‐region neurobiological model
Palomero‐Gallagher, N., Vogt, B. A., Schleicher, A., Mayberg, H. S., & Zilles, K. (2008) · Human Brain Mapping · doi:10.1002/hbm.20667 · Cited by 346 · see citing works
McNally, R. J. (2007) · Clinical Psychology Review · doi:10.1016/j.cpr.2007.01.003 · Cited by 348 · see citing works
Functional anatomy of ventromedial prefrontal cortex: implications for mood and anxiety disorders
Myers-Schulz, B., & Koenigs, M. (2012) · Molecular Psychiatry · doi:10.1038/mp.2011.88 · Cited by 333 · see citing works
Saalmann, Y. B. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00083 · Cited by 323 · see citing works
Circuit-Based Corticostriatal Homologies Between Rat and Primate
Heilbronner, S. R., Rodríguez-Romaguera, J., Quirk, G. J., Groenewegen, H. J., & Haber, S. N. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.05.012 · Cited by 321 · see citing works
Catechol- <i>O</i> -Methyltransferase Genotype and Dopamine Regulation in the Human Brain
Akil, M., Kolachana, B. S., Rothmond, D. A., Hyde, T. M., Weinberger, D. R., & Kleinman, J. E. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-06-02008.2003 · Cited by 325 · see citing works
Weighing up the benefits of work: Behavioral and neural analyses of effort-related decision making
Walton, M. E., Kennerley, S. W., Bannerman, D. M., Phillips, P. E. M., & Rushworth, M. F. S. (2006) · Neural Networks · doi:10.1016/j.neunet.2006.03.005 · Cited by 305 · see citing works
Mother–infant bonding and the evolution of mammalian social relationships
Broad, K. D., Curley, J. P., & Keverne, E. B. (2006) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2006.1940 · Cited by 283 · see citing works
Dysfunction of the Default Mode Network in Parkinson Disease
van Eimeren, T., Monchi, O., Ballanger, B., & Strafella, A. P. (2009) · Archives of Neurology · doi:10.1001/archneurol.2009.97 · Cited by 262 · see citing works
Central representation of visceral and cutaneous hypersensitivity in the irritable bowel syndrome
Verne, N. G., Himes, N. C., Robinson, M. E., Gopinath, K., Briggs, R. W., Crosson, B., & Price, D. D. (2003) · Pain · doi:10.1016/s0304-3959(02)00416-5 · Cited by 255 · see citing works
Friedman, D. P., Aggleton, J. P., & Saunders, R. C. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10336 · Cited by 245 · see citing works
Medial and orbital frontal cortex in decision-making and flexible behavior
Klein-Flügge, M. C., Bongioanni, A., & Rushworth, M. F. S. (2022) · Neuron · doi:10.1016/j.neuron.2022.05.022 · Cited by 244 · see citing works
Taren, A. A., Gianaros, P. J., Greco, C. M., Lindsay, E. K., Fairgrieve, A., Brown, K. W., Rosen, R. K., Ferris, J. L., Julson, E., Marsland, A. L., et al. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv066 · Cited by 236 · see citing works
Neural structures mediating expression and extinction of platform-mediated avoidance
Bravo-Rivera, C., Roman-Ortiz, C., Brignoni-Perez, E., Sotres-Bayon, F., & Quirk, G. J. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.0191-14.2014 · Cited by 206 · see citing works
Cools, R., & Arnsten, A. F. T. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01100-8 · Cited by 206 · see citing works
French, S. J., & Totterdell, S. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10191 · Cited by 202 · see citing works
Raphe GABAergic Neurons Mediate the Acquisition of Avoidance after Social Defeat
Challis, C., Boulden, J., Veerakumar, A., Espallergues, J., Vassoler, F. M., Pierce, R. C., Beck, S. G., & Berton, O. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2383-13.2013 · Cited by 197 · see citing works
Bissonette, G. B., Powell, E. M., & Roesch, M. R. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.04.037 · Cited by 189 · see citing works
Ascending visceral regulation of cortical affective information processing
Berntson, G. G., Sarter, M. F., & Cacioppo, J. T. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02967.x · Cited by 185 · see citing works
Gianaros, P. J., & Sheu, L. K. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.04.073 · Cited by 180 · see citing works
Austin, M. C., Janosky, J. E., & Murphy, H. A. (2003) · Molecular Psychiatry · doi:10.1038/sj.mp.4001250 · Cited by 162 · see citing works
Flow of information for emotions through temporal and orbitofrontal pathways
Barbas, H. (2007) · Journal of Anatomy · doi:10.1111/j.1469-7580.2007.00777.x · Cited by 167 · see citing works
Mannella, F., Gurney, K., & Baldassarre, G. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00135 · Cited by 166 · see citing works
Brain systems for baroreflex suppression during stress in humans
Gianaros, P. J., Onyewuenyi, I. C., Sheu, L. K., Christie, I. C., & Critchley, H. D. (2012) · Human Brain Mapping · doi:10.1002/hbm.21315 · Cited by 166 · see citing works
Sensitivity of Locus Ceruleus Neurons to Reward Value for Goal-Directed Actions
Bouret, S., & Richmond, B. J. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4553-14.2015 · Cited by 163 · see citing works
Dougherty, D. D., Rauch, S. L., Deckersbach, T., Marci, C., Loh, R., Shin, L. M., Alpert, N. M., Fischman, A. J., & Fava, M. (2004) · Archives of General Psychiatry · doi:10.1001/archpsyc.61.8.795 · Cited by 161 · see citing works
The cingulate cortex and limbic systems for action, emotion, and memory
Rolls, E. T. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64196-0.00002-9 · Cited by 155 · see citing works
The Lateral Habenula:No Longer Neglected
Geisler, S., & Trimble, M. (2008) · CNS Spectrums · doi:10.1017/s1092852900016710 · Cited by 149 · see citing works
The multifaceted abstract brain
Desai, R. H., Reilly, M., & van Dam, W. O. (2018) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2017.0122 · Cited by 142 · see citing works
Different Pedunculopontine Tegmental Neurons Signal Predicted and Actual Task Rewards
Okada, K., Toyama, K., Inoue, Y., Isa, T., & Kobayashi, Y. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4415-08.2009 · Cited by 138 · see citing works
Challis, C., Beck, S. G., & Berton, O. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00043 · Cited by 137 · see citing works
Deep brain stimulation for treatment-resistant depression: Efficacy, safety and mechanisms of action
Anderson, R. J., Frye, M. A., Abulseoud, O. A., Lee, K. H., McGillivray, J., Berk, M., & Tye, S. J. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.06.001 · Cited by 137 · see citing works
Prefrontal Cortical Projections to the Midbrain in Primates: Evidence for a Sparse Connection
Frankle, W., Laruelle, M., & Haber, S. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300990 · Cited by 141 · see citing works
Kim, U., & Lee, T. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08030.x · Cited by 133 · see citing works
Palomero‐Gallagher, N., Eickhoff, S. B., Hoffstaedter, F., Schleicher, A., Mohlberg, H., Vogt, B. A., Amunts, K., & Zilles, K. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.04.053 · Cited by 133 · see citing works
Karachi, C., Yelnik, J., Tandé, D., Tremblay, L., Hirsch, É. C., & François, C. (2004) · Movement Disorders · doi:10.1002/mds.20302 · Cited by 130 · see citing works
Food‐Related Odor Probes of Brain Reward Circuits During Hunger: A Pilot fMRI Study
Bragulat, V., Dzemidzic, M., Bruno, C., Cox, C. A., Talavage, T., Considine, R. V., & Kareken, D. A. (2010) · Obesity · doi:10.1038/oby.2010.57 · Cited by 128 · see citing works
Specialized Elements of Orbitofrontal Cortex in Primates
Barbas, H. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.015 · Cited by 127 · see citing works
Anatomical Pathways for Auditory Memory in Primates
Muñoz, M., Mohedano‐Moriano, A., & Insausti, R. (2010) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2010.00129 · Cited by 128 · see citing works
Omelchenko, N., & Sesack, S. R. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.02.016 · Cited by 121 · see citing works
Hahn, J. D., & Swanson, L. W. (2010) · Brain Research Reviews · doi:10.1016/j.brainresrev.2010.02.002 · Cited by 121 · see citing works
Gianaros, P. J., Marsland, A. L., Kuan, D. C.-H., Schirda, B. L., Jennings, J. R., Sheu, L. K., Hariri, A. R., Gross, J. J., & Manuck, S. B. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.10.012 · Cited by 119 · see citing works
Déjean, C., Courtin, J., Rozeske, R. R., Bonnet, M. C., Dousset, V., Michelet, T., & Herry, C. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.03.017 · Cited by 120 · see citing works
Kalisch, R., & Gerlicher, A. M. V. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.02.002 · Cited by 118 · see citing works
Alexander, L., Wood, C. M., Gaskin, P. L. R., Sawiak, S. J., Fryer, T. D., Hong, Y. T., McIver, L., Clarke, H. F., & Roberts, A. C. (2020) · Nature Communications · doi:10.1038/s41467-020-19167-0 · Cited by 100 · see citing works
Frontal-thalamic circuits associated with language
Barbas, H., García‐Cabezas, M. Á., & Zikopoulos, B. (2012) · Brain and Language · doi:10.1016/j.bandl.2012.10.001 · Cited by 115 · see citing works
Cortical Connections Position Primate Area 25 as a Keystone for Interoception, Emotion, and Memory
Joyce, M. K. P., & Barbas, H. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2363-17.2017 · Cited by 112 · see citing works
Neuropeptide Regulation of Signaling and Behavior in the BNST
Kash, T. L., Pleil, K. E., Marcinkiewcz, C. A., Lowery‐Gionta, E. G., Crowley, N. A., Mazzone, C. M., Sugam, J. A., Hardaway, J. A., & McElligott, Z. A. (2014) · Molecules and Cells · doi:10.14348/molcells.2015.2261 · Cited by 105 · see citing works
Distribution of mGluR1α and mGluR5 immunolabeling in primate prefrontal cortex
Muly, E. C., Maddox, M., & Smith, Y. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10937 · Cited by 108 · see citing works
Sensory-motor gating and cognitive control by the brainstem cholinergic system
Kobayashi, Y., & Isa, T. (2002) · Neural Networks · doi:10.1016/s0893-6080(02)00059-x · Cited by 108 · see citing works
Cingulate cortex in the three limbic subsystems
Vogt, B. A. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64196-0.00003-0 · Cited by 106 · see citing works
Kobayashi, Y., Inoue, Y., Yamamoto, M., Isa, T., & Aizawa, H. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.88.2.715 · Cited by 104 · see citing works
The integrative role of the pedunculopontine nucleus in human gait
Lau, B., Welter, M., Belaïd, H., Fernández-Vidal, S., Bardinet, É., Grabli, D., & Karachi, C. (2015) · Brain · doi:10.1093/brain/awv047 · Cited by 101 · see citing works
Kawai, T., Yamada, H., Sato, N., Takada, M., & Matsumoto, M. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.030 · Cited by 98 · see citing works
Vogt, B. A., Hof, P. R., Zilles, K., Vogt, L. J., Herold, C., & Palomero‐Gallagher, N. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23409 · Cited by 98 · see citing works
The Developmental Decrease in REM Sleep: The Role of Transmitters and Electrical Coupling
García‐Rill, E., Charlesworth, A. G., Heister, D. S., Ye, M., & Hayar, A. M. (2008) · SLEEP · doi:10.1093/sleep/31.5.673 · Cited by 96 · see citing works
Altered neural response of the appetitive emotional system in cocaine addiction: an fMRI Study
Asensio, S., Romero, M. J., Palau, C., Sanchez, A., Senabre, I., Morales, J. L., Carcelen, R., & Romero, F. J. (2010) · Addiction Biology · doi:10.1111/j.1369-1600.2010.00230.x · Cited by 95 · see citing works
Duncan, N. W., Wiebking, C., Tiret, B., Marjańska, M., Hayes, D. J., Lyttleton, O., Doyon, J., & Northoff, G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060312 · Cited by 95 · see citing works
miR-323a regulates ERBB4 and is involved in depression
Fiori, L. M., Kos, A., Lin, R., Théroux, J.-F., Lopez, J. P., Kühne, C., Eggert, C., Holzapfel, M., Huettl, R.-E., Mechawar, N., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-020-00953-7 · Cited by 88 · see citing works
Social reward monitoring and valuation in the macaque brain
Noritake, A., Ninomiya, T., & Isoda, M. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0229-7 · Cited by 86 · see citing works
Prefrontal Pathways Provide Top-Down Control of Memory for Sequences of Events
Jayachandran, M., Linley, S. B., Schlecht, M., Mahler, S. V., Vertes, R. P., & Allen, T. A. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.06.053 · Cited by 84 · see citing works
Challis, C., & Berton, O. (2015) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.5b00007 · Cited by 81 · see citing works
Afferents of vocalization-controlling periaqueductal regions in the squirrel monkey
Gruber-Dujardin, E., & Jürgens, U. (2005) · Brain Research · doi:10.1016/j.brainres.2004.11.048 · Cited by 84 · see citing works
Cyders, M. A., Džemidžić, M., Eiler, W. J. A., Coskunpinar, A., Karyadi, K. A., & Kareken, D. A. (2013) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.12266 · Cited by 83 · see citing works
Sex differences in connectivity of the subgenual anterior cingulate cortex
Wang, G., Erpelding, N., & Davis, K. D. (2014) · Pain · doi:10.1016/j.pain.2014.01.005 · Cited by 82 · see citing works
The anterior cingulate cortex as a key locus of ketamine’s antidepressant action
Alexander, L., Jelen, L. A., Mehta, M. A., & Young, A. H. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.05.003 · Cited by 83 · see citing works
Bienkowski, M. S., & Rinaman, L. (2013) · Brain Structure and Function · doi:10.1007/s00429-012-0393-6 · Cited by 80 · see citing works
Manza, P., Zhang, S., Li, C.-S. R., & Leung, H. (2015) · Human Brain Mapping · doi:10.1002/hbm.23056 · Cited by 79 · see citing works
- Authors
- Chiba, T., Kayahara, T., & Nakano, K.
- Affiliations
- Chiba University (JP)
- Mie University (JP)
- Corresponding author
- Chiba, Tanemichi
- Venue
- Brain Research
- Publisher
- Elsevier BV
- Published
- 2001-01
- Volume
- 888
- Issue
- 1
- Pages
- 83-101
- ISSN
- 0006-8993 (ISSN-L)
- OpenAlex
- W1994008515
- Cited by
- 290
- References
- 64
- Citations by year
- 2026: 6 · 2025: 9 · 2024: 13 · 2023: 7 · 2022: 14 · 2021: 15 · 2020: 14 · 2019: 14 · 2018: 10 · 2017: 13 · 2016: 10 · 2015: 14 · 2014: 13 · 2013: 14 · 2012: 14
- FWCI
- 5.75
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Brain Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ministry of Education, Culture, Sports, Science and Technology
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- medial prefrontal cortex, efferent projections, Japanese macaque, nucleus accumbens, amygdala, periaqueductal gray, thalamus, hypothalamus, ventral tegmental area, entorhinal cortex, piriform cortex
- MeSH terms
- Animals, Biotin, Dextrans, Efferent Pathways, Female, Fluorescent Dyes, Limbic System, Macaca, Male, Medulla Oblongata, Mesencephalon, Spinal Cord, Prefrontal Cortex
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