The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Topographical organization of the efferent projections of the medial prefrontal cortex in the rat: An anterograde tract‐tracing study with Phaseolus vulgaris leucoagglutinin
Abstract
The purpose of the present investigation was to examine the topographical organization of efferent projections from the cytoarchitectonic divisions of the mPFC (the medial precentral, dorsal anterior cingulate and prelimbic cortices). We also sought to determine whether the efferents from different regions within the prelimbic division were organized topographically. Anterograde transport of Phaseolus vulgaris leucoagglutinin was used to examined the efferent projections from restricted injection sites within the mPFC. Major targets of the prelimbic area were found to include prefrontal, cingulate, and perirhinal cortical structures, the dorsomedial and ventral striatum, basal forebrain nuclei, basolateral amygdala, lateral hypothalamus, mediodorsal, midline and intralaminar thalamic nuclei, periaqueductal gray region, ventral midbrain tegmentum, laterodorsal tegmental nucleus, and raphe nuclei. Previously unreported projections of the prelimbic region were also observed, including efferents to the anterior olfactory nucleus, the piriform cortex, and the pedunculopontine tegmental‐cuneiform region. A topographical organization governed the efferent projections from the prelimbic area, such that the position of terminal fields within target structures was determined by the rostrocaudal, dorsoventral, and mediolateral placement of the injection sites. Efferent projections from the medial precentral and dorsal anterior cingulate divisions (dorsomedial PFC) were organized in a similar topographical fashion and produced a pattern of anterograde labeling different from that seen with prelimbic injection sites. Target structures innervated primarily by the dorsomedial PFC included certain neocortical fields (the motor, somatosensory, and visual cortices), the dorsolateral striatum, superior colliculus, deep mesencephalic nucleus, and the pontine and medullary reticular formation. Previously unreported projections to the paraoculomotor central gray area and the mesencephalic trigeminal nucleus were observed following dorsomedial PFC injections. These results indicate that the efferent projections of the mPFC are topographically organized within and across the cytoarchitectonic divisions of the medial wall cortex. The significance of topographically organized and restricted projections of the rat mPFC is discussed in light of behavioral and physiological studies indicating functional heterogeneity of this region.
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
“It is well documented that the nucleus accumbens receives innervation from multiple brain regions including the prefrontal cortex and hippocampus [85, 86].”
Citations
Cites
Circuitry of Primate Prefrontal Cortex and Regulation of Behavior by Representational Memory
Goldman‐Rakic, P. S. (1987) · Comprehensive Physiology · doi:10.1002/cphy.cp010509 · Cited by 1,960
Flagged first, then by citations
Research works printed but not linked: 115
- 10.1016/0006-8993(77)90291-8 · DOI
- 10.1126/science.3775363 · DOI
- 10.1007/BF00247590 · DOI
- 10.1002/cne.901840104 · DOI
- 10.1093/brain/103.1.23 · DOI
- 10.1177/29.7.6167611 · DOI
- 10.1007/BF00238097 · DOI
- 10.1016/0361-9230(86)90059-6 · DOI
- 10.1016/0006-8993(76)90171-2 · DOI
- 10.1016/0361-9230(86)90237-6 · DOI
- 10.1002/cne.901780102 · DOI
- 10.1016/0006-8993(88)90515-X · DOI
- Clugnet M. C., 1986, Olfactory input to the prefrontal cortex in the rat, Chem. Senses, 11, 590
- 10.1016/0006-8993(74)90649-0 · DOI
- Dahlström A., 1964, Evidence for the existence of monoaminecontaining neurons in the central nervous system. I. Demonstration of monoamines in the cell bodies of brain stem neurons, Acta Physiol. Scand, 62, 1
- 10.1016/0306-4522(81)90149-4 · DOI
- 10.1002/cne.901800105 · DOI
- 10.1016/0006-8993(69)90002-X · DOI
- 10.1016/0006-8993(86)91658-6 · DOI
- 10.1159/000121803 · DOI
- 10.1016/0306-4522(86)90128-4 · DOI
- 10.1016/0006-8993(87)90450-1 · DOI
- Freeman W., 1925, The relationship of the radix mesencephalica trigemini to the extraocular muscles, Arch. Neurol. Psychiatry, 14, 111
- 10.1002/cne.902580302 · DOI
- Fuster J. M., 1985, The prefrontal cortex, mediator of cross‐temporal contingencies, Hum. Neurobiol, 4, 169
- 10.1038/311461a0 · DOI
- Gerfen C. R., 1988, Laminar origin of patch‐ and matrix‐directed corticostriatal projections in the rat, Proc. Soc. Neurosci, 14, 76
- 10.1016/0006-8993(84)90940-5 · DOI
- 10.1002/cne.901710305 · DOI
- Goldman‐Rakic P. S., 1987, Handbook of Physiology, 373
- 10.1016/0306-4522(84)90166-0 · DOI
- 10.1002/cne.901750105 · DOI
- Greatex R. M., 1982, Demonstration of synaptic input from prefrontal cortex to the habenula in the rat, Brain Res, 238, 192, 10.1016/0006-8993(82)90782-X · DOI
- 10.1016/0306-4522(88)90339-9 · DOI · Paper page
- 10.1002/cne.902770302 · DOI
- 10.1002/cne.902770303 · DOI
- 10.1002/cne.902150203 · DOI
- 10.1016/0006-8993(74)90076-6 · DOI
- 10.1016/0304-3940(86)90054-6 · DOI
- 10.1007/BF00248217 · DOI
- 10.1016/0304-3940(81)90183-X · DOI
- Heimer L., 1975, Golgi Centennial Symposium, Proceedings, 177
- 10.1002/cne.901730107 · DOI
- 10.1016/0304-3940(80)90290-6 · DOI
- 10.1016/0006-8993(86)91635-5 · DOI
- 10.1016/0306-4522(81)90223-2 · DOI
- 10.1016/0006-8993(75)90815-X · DOI
- 10.1016/0306-4522(85)90216-7 · DOI
- 10.1016/0006-8993(85)91254-5 · DOI
- 10.1016/0006-8993(81)91244-0 · DOI
- 10.1002/cne.902710204 · DOI
- 10.1016/S0091-6773(74)91924-5 · DOI
- 10.1016/0165-0173(84)90018-3 · DOI
- 10.1002/cne.901710204 · DOI
- 10.1016/0306-4522(84)90061-7 · DOI
- 10.3758/BF03326684 · DOI
- 10.1007/BF00248801 · DOI
- 10.1002/cne.902280307 · DOI
- 10.1002/cne.902280306 · DOI
- 10.1016/0006-8993(69)90003-1 · DOI
- 10.1523/JNEUROSCI.01-09-00956.1981 · DOI
- 10.1016/0361-9230(83)90212-5 · DOI
- 10.3758/BF03326611 · DOI
- 10.1002/cne.902260204 · DOI
- Mogenson G. J., 1983, Neuronal projections from nucleus accumbens to globus pallidus, substantia innominata, and lateral preoptic‐lateral hypothalamic area: An anatomical and electrophysiological investigation in the rat, J. Neurosci., 3, 189, 10.1523/JNEUROSCI.03-01-00189.1983 · DOI
- 10.1016/0306-4522(78)90041-6 · DOI
- 10.1016/0165-0173(86)90011-1 · DOI
- 10.1016/0006-8993(86)90867-X · DOI
- 10.1002/cne.902050104 · DOI
- Passingham R. E., 1988, Premotor cortex in the rat, Behav. Neurosci, 102, 101, 10.1037/0735-7044.102.1.101 · DOI
- 10.1016/B978-0-12-547620-1.50007-2 · DOI
- 10.1002/cne.900900102 · DOI
- 10.1002/cne.900910202 · DOI
- 10.1159/000118849 · DOI
- 10.1016/0304-3940(84)90030-2 · DOI
- 10.1016/0361-9230(87)90086-4 · DOI
- 10.1002/cne.902080304 · DOI
- Room P., 1985, Efferent connections of the prelimbic (area 32) and the infralimbic (area 25) cortices: An anterograde tracing study in the cat, J. Comp. Neurol., 212, 40, 10.1002/cne.902420104 · DOI
- Rose J. E., 1948, The orbitofrontal cortex and its connections with the mediodorsal nucleus in rabbit, sheep and cat, Res. Publ. Assoc. Res. Nerv. Ment. Dis, 27, 210
- Rosenkilde C. E., 1983, Functions of the prefrontal cortex: Behavioral investigations using ablation and electrophysiological techniques in rats, cats, dogs, and monkeys, Acta Physiol. Scand, 514, 4
- 10.1002/cne.902570206 · DOI
- 10.1002/cne.902590403 · DOI
- 10.1002/cne.902100207 · DOI
- 10.1016/0006-8993(82)90493-0 · DOI
- 10.1002/cne.902220302 · DOI
- 10.1159/000121804 · DOI
- 10.1016/0361-9230(83)90029-1 · DOI
- 10.1002/cne.902360302 · DOI
- 10.1002/cne.902530302 · DOI
- 10.1007/BF00237879 · DOI
- 10.1002/cne.902290209 · DOI
- Sesack S. R., 1986, Projection neurons of the rat medial prefrontal cortex: anatomical studies and electrophysiological analysis of dopamine sensitivity, Proc. Soc. Neurosci, 12, 137
- 10.1016/0006-8993(77)91048-4 · DOI
- 10.1016/0006-8993(86)90684-0 · DOI
- 10.1016/0031-9384(84)90098-2 · DOI
- 10.1016/0006-8993(84)90319-6 · DOI
- 10.1016/0166-2236(79)90005-5 · DOI
- Swanson L. W., 1983, Neurobiology of the Hippocampus, 3
- 10.1523/JNEUROSCI.06-10-03010.1986 · DOI
- 10.1016/0006-8993(84)90827-8 · DOI
- 10.1016/0006-8993(84)90500-6 · DOI
- 10.1016/0006-8993(83)90246-9 · DOI
- 10.1016/0361-9230(87)90050-5 · DOI · Paper page
- 10.1002/cne.902430107 · DOI
- Tohyama M., 1978, Organization and projections of the neurons in the dorsal tegmental area of the rat, J. Hirnforsch., 19, 163
- Vander Kooy D., 1982, Visceral cortex: A direct connection from prefrontal cortex to the solitary nucleus in rat Neurosci, Lett, 33, 123
- 10.1002/cne.902240102 · DOI
- 10.1002/cne.902440307 · DOI
- 10.1016/0014-4886(88)90094-5 · DOI
- 10.1016/0006-8993(87)90878-X · DOI
- 10.1002/cne.902080303 · DOI
- 10.1016/0306-4522(85)90271-4 · DOI
- 10.1016/0006-8993(85)91402-7 · DOI
- 10.1016/0006-8993(87)90802-X · DOI
- 10.1016/0006-8993(84)91448-3 · DOI
Cited by
Sorted by citations
Items 101–145 of 145
Inhibitory Gating of Basolateral Amygdala Inputs to the Prefrontal Cortex
McGarry, L. M., & Carter, A. G. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.0874-16.2016 · Cited by 169
Floresco, S. B., Braaksma, D. N., & Phillips, A. G. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-24-11061.1999 · Cited by 181
Individual Differences and Social Influences on the Neurobehavioral Pharmacology of Abused Drugs
Bardo, M. T., Neisewander, J. L., & Kelly, T. H. (2013) · Pharmacological Reviews · doi:10.1124/pr.111.005124 · Cited by 167
Hart, G., Leung, B. K., & Balleine, B. W. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.11.003 · Cited by 166
Mannella, F., Gurney, K., & Baldassarre, G. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00135 · Cited by 166
Gabbott, P. L. A., Warner, T. A., Jays, P. R. L., & Bacon, S. J. (2003) · Brain Research · doi:10.1016/j.brainres.2003.08.056 · Cited by 157
Prefrontal cortical inputs to the basal amygdala undergo pruning during late adolescence in the rat
Cressman, V. L., Balaban, J., Steinfeld, S., Shemyakin, A., Graham, P., Parisot, N., & Moore, H. (2010) · Journal of Comparative Neurology · doi:10.1002/cne.22359 · Cited by 161
Baratta, M. V., Christianson, J. P., Gomez, D. M., Zarza, C. M., Amat, J., Masini, C. V., Watkins, L. R., & Maier, S. F. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.03.042 · Cited by 156
Kim, J. H., Hamlin, A. S., & Richardson, R. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.0596-09.2009 · Cited by 154
Amat, J., Paul, E., Watkins, L. R., & Maier, S. F. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.04.005 · Cited by 153
Wright, C. I., & Groenewegen, H. J. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00592-7 · Cited by 148
Jay, T. M., Rocher, C., Hotte, M., Naudon, L., Gurden, H., & Spedding, M. (2004) · Neurotoxicity Research · doi:10.1007/bf03033225 · Cited by 141
Rogers, R. D., Baunez, C., Everitt, B. J., & Robbins, T. W. (2001) · Behavioral Neuroscience · doi:10.1037/0735-7044.115.4.799 · Cited by 140
Kim, U., & Lee, T. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08030.x · Cited by 133
The medial prefrontal cortex shapes dopamine reward prediction errors under state uncertainty
Starkweather, C. K., Gershman, S. J., & Uchida, N. (2018) · Neuron · doi:10.1016/j.neuron.2018.03.036 · Cited by 136
Brain areas that influence general anesthesia
Leung, L. S., Luo, T., Ma, J., & Herrick, I. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2014.08.001 · Cited by 126
Pathway-Selective Adjustment of Prefrontal-Amygdala Transmission during Fear Encoding
Arruda-Carvalho, M., & Clem, R. L. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.2664-14.2014 · Cited by 127
Functional implications of glutamatergic projections to the ventral tegmental area
Geisler, S., & Wise, R. A. (2008) · Reviews in the Neurosciences · doi:10.1515/revneuro.2008.19.4-5.227 · Cited by 125
Jaferi, A., & Bhatnagar, S. (2006) · Endocrinology · doi:10.1210/en.2005-1393 · Cited by 122
The effects of amygdala lesions on conditioned stimulus- potentiated eating in rats.
Holland, P. C., Petrovich, G. D., & Gallagher, M. (2002) · Physiology & Behavior · doi:10.1016/s0031-9384(02)00688-1 · Cited by 117
Cho, S. S., Koshimori, Y., Aminian, K., Obeso, I., Rusjan, P., Lang, A. E., Daskalakis, Z. J., Houle, S., & Strafella, A. P. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2014.211 · Cited by 112
The study of active avoidance: a platform for discussion
Diehl, M. M., Bravo-Rivera, C., & Quirk, G. J. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.09.010 · Cited by 95
Baratta, M. V., Zarza, C. M., Gomez, D. M., Campeau, S., Watkins, L. R., & Maier, S. F. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06867.x · Cited by 106
Gabbott, P., Headlam, A., & Busby, S. (2002) · Brain Research · doi:10.1016/s0006-8993(02)02487-3 · Cited by 101
Shibata, H., & Naito, J. (2005) · Brain Research · doi:10.1016/j.brainres.2005.08.025 · Cited by 97
Topographic organization of the striatal and thalamic connections of rat medial agranular cortex
Reep, R. L., & Corwin, J. V. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01779-5 · Cited by 91
A Connectomic Analysis of the Human Basal Ganglia Network
Cacciola, A., Calamuneri, A., Milardi, D., Mormina, E., Chillemi, G., Marino, S., Naro, A., Rizzo, G., Anastasi, G., & Quartarone, A. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00085 · Cited by 81
Marinho, A. L. Z., Vila-Verde, C., Fogaça, M. V., & Guimarães, F. S. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.02.023 · Cited by 68
Lesions of the medial prefrontal cortex and sexual behavior in the male rat
Ågmo, A., Villalpando, A., Picker, Z., & Fernández, H. (1995) · Brain Research · doi:10.1016/0006-8993(95)00852-h · Cited by 64
Milstein, J. A., Elnabawi, A., Vinish, M., Swanson, T., Enos, J. K., Bailey, A. M., Kolb, B., & Frost, D. O. (2013) · PLoS ONE · doi:10.1371/journal.pone.0057308 · Cited by 57
Learning and the motivation to eat: forebrain circuitry.
Petrovich, G. D. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.04.059 · Cited by 57
Pinto, A., Fuentes, C., & Paré, D. (2006) · Journal of Comparative Neurology · doi:10.1002/cne.20905 · Cited by 55
Ultrastructural organization of medial prefrontal inputs to the rhinal cortices
Apergis‐Schoute, J., Pinto, A., & Paré, D. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04894.x · Cited by 51
Churchill, L., Zahm, D. S., Duffy, P., & Kalivas, P. W. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00352-j · Cited by 50
Rodriguez-Romaguera, J., Do-Monte, F. H., Tanimura, Y., Quirk, G. J., & Haber, S. N. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.20 · Cited by 48
Kim, J. H., Li, S., Hamlin, A. S., McNally, G. P., & Richardson, R. (2012) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.09.005 · Cited by 46
Modulation of sensitivity to alcohol by cortical and thalamic brain regions
Jaramillo, A. A., Randall, P. A., Frisbee, S., & Besheer, J. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13374 · Cited by 42
Learned stressor resistance requires extracellular signal-regulated kinase in the prefrontal cortex
Christianson, J. P., Flyer-Adams, J. G., Drugan, R. C., Amat, J., Daut, R. A., Foilb, A. R., Watkins, L. R., & Maier, S. F. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00348 · Cited by 39
Forebrain circuits and control of feeding by learned cues
Petrovich, G. D. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2010.10.003 · Cited by 37
Pezze, M. A., Marshall, H. J., Fone, K. C., & Cassaday, H. J. (2017) · Learning & Memory · doi:10.1101/lm.044784.116 · Cited by 35
McNair, L. F., & Kohlmeier, K. A. (2015) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s2040174414000439 · Cited by 22
Chakroborty, S., Geisbush, T. R., Dale, E., Pehrson, A. L., Sánchez, C., & West, A. R. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00764 · Cited by 13
Fritz, B. M., & Boehm II, S. L. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.07.020 · Cited by 10
Haddon, J. E., Titherage, D., Heckenast, J. R., Carter, J., Owen, M. J., Hall, J., Wilkinson, L. S., & Jones, M. W. (2024) · Translational Psychiatry · doi:10.1038/s41398-024-02969-x · Cited by 6
“It is well documented that the nucleus accumbens receives innervation from multiple brain regions including the prefrontal cortex and hippocampus [85, 86].”
BackgroundLayer-specific input to medial prefrontal cortex is linked to stress susceptibility
Solakoğlu, S. T., Erdener, Ş. E., Gliko, O., Can, A., Sümbül, U., & Eren-Koçak, E. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03258-x · Cited by 5
Metadata
- Authors
- Sesack, S. R., Deutch, A. Y., Roth, R. H., & Bunney, B. S.
- Affiliations
- Yale University (US)
- ORCID
- Sesack, Susan R.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1989-12-08
- Volume
- 290
- Issue
- 2
- Pages
- 213-242
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2128312680
- Cited by
- 1,568
- References
- 1
- Citations by year
- 2026: 15 · 2025: 18 · 2024: 23 · 2023: 25 · 2022: 39 · 2021: 34 · 2020: 39 · 2019: 41 · 2018: 59 · 2017: 50 · 2016: 51 · 2015: 43 · 2014: 63 · 2013: 65 · 2012: 50
- FWCI
- 12.54
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Public Health Service
- National Institute of Mental Health (MH-45124, MH 25642, MH 28849)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Keywords
- medial prefrontal cortex, efferent projections, topographic organization, prelimbic cortex, dorsal anterior cingulate cortex, Phaseolus vulgaris leucoagglutinin, thalamic projections, striatum, amygdala, raphe nuclei, pedunculopontine nucleus
- MeSH terms
- Animals, Brain Mapping, Frontal Lobe, Male, Neural Pathways, Phytohemagglutinins, Rats, Inbred Strains, Rats
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