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The organization of the thalamocortical connections of the mediodorsal thalamic nucleus in the rat, related to the ventral forebrain–prefrontal cortex topography
Abstract
The medial and central segments of the mediodorsal nucleus of the thalamus (MD) receive afferents from the ventral forebrain, including the piriform cortex, the ventral pallidum, and the amygdaloid complex. Because MD is reciprocally interconnected with prefrontal and agranular insular cortical areas, it provides a relay of ventral forebrain activity to these cortical areas. However, there are also direct projections from the piriform cortex and the amygdala to the prefrontal and agranular insular cortices. This study addresses whether this system has a "triangular" organization, such that structures in the ventral forebrain project to interconnected areas in MD and the prefrontal/insular cortex. The thalamocortical projections of MD have been studied in experiments with injections of retrograde tracers into prefrontal or agranular insular cortical areas. In many of the same experiments, projections from the ventral forebrain to MD and to the prefrontal/insular cortex have been demonstrated with anterograde axonal tracers. The connections of the piriform cortex (PC) with MD and the prefrontal/insular cortex form an organized triangular system. The PC projections to the central and medial segments of MD and to the lateral orbital cortex (LO) and the ventral and posterior agranular insular cortices (AIv and AIp) are topographically organized, such that more caudal parts of PC tend to project more medially in MD and more caudally within the orbital/insular cortex. The central and medial portions of MD also send matching, topographically organized projections to LO, AIv and AIp, with more medial parts of MD projecting further caudally. The anterior cortical nucleus of the amygdala (COa) also projects to the dorsal part of the medial segment of MD and to its cortical targets, the medial orbital area (MO) and AIp. The projections of the basal/accessory basal amygdaloid nuclei to MD and to prefrontal cortex, and from MD to amygdaloceptive parts of prefrontal cortex, are not as tightly organized. Amygdalothalamic afferents in MD are concentrated in the dorsal half of the medial segment. Cells in this part of the nucleus project to the amygdaloceptive prelimbic area (PL) and AIp. However, other amygdaloceptive prefrontal areas are connected to parts of MD that do not receive fibers from the amygdala. Ventral pallidal afferents are distributed to all parts of the central and medial segments of MD, overlapping with the fibers from the amygdala and piriform cortex. Fibers from other parts of the pallidum, or related areas such as the substantia nigra, pars reticulata, terminate in the lateral and ventral parts of MD, where they overlap with inputs from the superior colliculus and other brainstem structures.(ABSTRACT TRUNCATED AT 400 WORDS)
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“The medial ventral pallidum, which receives inputs from the medial shell and medial tubercle, sends its efferent to the medial segment of the mediodorsal thalamic nucleus (Zahm et al., 1987; Groenewegen, 1988; Ray and Price, 1992; Zahm et al., 1996; O’Donnell et al., 1997).”
From Dopamine reward circuitry: Two projection systems from the ventral midbrain to the nucleus accumbens–olfactory tubercle complex (2007) · cites this paper as Ray and Price, 1992
In the citing paper
“The medial mediodorsal thalamic nucleus then projects to the infralimbic, prelimbic and agranular insular cortices (Leonard, 1972; Groenewegen, 1988; Ray and Price, 1992), which project to the ventral striatum (Berendse et al., 1992a; Brog et al., 1993).”
From Dopamine reward circuitry: Two projection systems from the ventral midbrain to the nucleus accumbens–olfactory tubercle complex (2007) · cites this paper as Ray and Price, 1992
In the citing paper
“The central segment projects to the ventral agranular insular cortex (Groenewegen, 1988; Ray and Price, 1992), which in turn projects back to the lateral shell and lateral tubercle.”
From Dopamine reward circuitry: Two projection systems from the ventral midbrain to the nucleus accumbens–olfactory tubercle complex (2007) · cites this paper as Ray and Price, 1992
In the citing paper
“However, the ventrolateral ventral pallidum, which receives its afferents from the lateral shell and lateral tubercle, sends its efferent to the central and lateral segments of the dorsomedial thalamic nucleus (Groenewegen, 1988; Ray and Price, 1992; Zahm et al., 1996; O’Donnell et al., 1997).”
From Dopamine reward circuitry: Two projection systems from the ventral midbrain to the nucleus accumbens–olfactory tubercle complex (2007) · cites this paper as Ray and Price, 1992
Citations
Cites
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
Handbook of Chemical Neuroanatomy
Stern, C. D. (1986) · Neurochemistry International · doi:10.1016/0197-0186(86)90021-5 · Cited by 4,160
Effects of Different Brain Lesions on Card Sorting: The Role of the Frontal Lobes
MILNER, B. (1963) · Archives of Neurology · doi:10.1001/archneur.1963.00460070100010 · Cited by 2,217
The autoradiographic demonstration of axonal connections in the central nervous system
Cowan, W. M., Gottlieb, D. I., Hendrickson, A. E., Price, J. L., & Woolsey, T. A. (1972) · Brain Research · doi:10.1016/0006-8993(72)90344-7 · Cited by 1,610
Self-citationNeurotransmitters and neuromodulators in the basal ganglia
Graybiel, A. M. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90104-i · Cited by 1,576
Sesack, S. R., Deutch, A. Y., Roth, R. H., & Bunney, B. S. (1989) · Journal of Comparative Neurology · doi:10.1002/cne.902900205 · Cited by 1,568
Efferent connections of the substantia nigra and ventral tegmental area in the rat
Beckstead, R. M., Domesick, V. B., & Nauta, W. J. H. (1979) · Brain Research · doi:10.1016/0006-8993(79)91001-1 · Cited by 1,293
Krettek, J. E., & Price, J. L. (1978) · Journal of Comparative Neurology · doi:10.1002/cne.901780204 · Cited by 1,293
Self-citationThe cortical projections of the mediodorsal nucleus and adjacent thalamic nuclei in the rat
Krettek, J. E., & Price, J. L. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901710204 · Cited by 1,277
Self-citationA functional anatomical study of unipolar depression
Drevets, W., Videen, T., Price, J., Preskorn, S., Carmichael, S., & Raichle, M. (1992) · The Journal of Neuroscience · doi:10.1523/jneurosci.12-09-03628.1992 · Cited by 1,266
Self-citation
Flagged first, then by citations
Research works printed but not linked: 3
- Cajal S. R., 1955, Histologie du Système Nerveux, 727
- Heimer L., 1975, Golgi Centennial Symposium. Proceedings, 177
- Wiegand S. J., 1980, Olfactory neocortical areas in the rat, Soc. Neurosci. Abstr., 6, 307
Cited by
Sorted by citations
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The orbitofrontal cortex, food intake and obesity
Seabrook, L. T., & Borgland, S. L. (2020) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.190163 · Cited by 95
Mátyás, F., Lee, J.-H., Shin, H., & Acsády, L. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12610 · Cited by 88
Datiche, F., & Cattarelli, M. (1996) · Brain Research Bulletin · doi:10.1016/s0361-9230(96)00082-2 · Cited by 87
Anatomical Relationships Between the Prefrontal Cortex and the Basal Ganglia in the Rat
Groenewegen, H. J., & Berendse, H. W. (1994) · Research and perspectives in neurosciences · doi:10.1007/978-3-642-85007-3_4 · Cited by 86
Organization of afferents to the orbitofrontal cortex in the rat
Murphy, M. J. M., & Deutch, A. Y. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24424 · Cited by 85
Anatomic heterogeneity of the rat amygdaloid complex.
Pitkänen, A., Jolkkonen, E., & Kemppainen, S. (2000) · PubMed · Cited by 85
Ray, J. P., Russchen, F. T., Fuller, T. A., & Price, J. L. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903200403 · Cited by 85
Self-citationChang, J.-Y., Zhang, L., Janak, P. H., & Woodward, D. J. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00012-7 · Cited by 83
Nonsensory target-dependent organization of piriform cortex
Chen, C. F., Zou, D., Altomare, C. G., Xu, L., Greer, C. A., & Firestein, S. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1411266111 · Cited by 78
Oyoshi, T., Nishijo, H., Asakura, T., Takamura, Y., & Ono, T. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-18-05812.1996 · Cited by 85
Architectonic Subdivisions of Neocortex in the Tree Shrew (Tupaia belangeri)
Wong, P., & Kaas, J. H. (2009) · The Anatomical Record · doi:10.1002/ar.20916 · Cited by 77
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Wong, P., & Kaas, J. H. (2008) · The Anatomical Record · doi:10.1002/ar.20758 · Cited by 75
Chang, J., Janak, P. H., & Woodward, D. J. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00218-9 · Cited by 74
Werd, H. J. J. M. V. D., & Uylings, H. B. M. (2008) · Brain Structure and Function · doi:10.1007/s00429-007-0164-y · Cited by 73
Transient Extracellular Glutamate Events in the Basolateral Amygdala Track Reward-Seeking Actions
Wassum, K. M., Tolosa, V., Tseng, T. T. ‐., Balleine, B. W., Monbouquette, H. G., & Maidment, N. T. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5780-11.2012 · Cited by 74
Lasseter, H. C., Wells, A. M., Xie, X., & Fuchs, R. A. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2010.209 · Cited by 72
Corticocortical and thalamocortical projections to layer I of the frontal neocortex in rats
Mitchell, B. D., & Cauller, L. J. (2001) · Brain Research · doi:10.1016/s0006-8993(01)03084-0 · Cited by 71
Senapati, A. K., LaGraize, S. C., Huntington, P. J., Wilson, H., Fuchs, P. N., & Peng, Y. B. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00040.2005 · Cited by 71
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Samuelsen, C. L., & Fontanini, A. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1926-16.2016 · Cited by 73
Prisco, G. V. D., & Vertes, R. P. (2006) · Synapse · doi:10.1002/syn.20271 · Cited by 70
Debeir, T., Ginestet, L., François, C., Laurens, S., Martel, J., Chopin, P., Marien, M. R., Colpaert, F. C., & Raisman‐Vozari, R. (2005) · Experimental Neurology · doi:10.1016/j.expneurol.2005.01.007 · Cited by 73
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Georgescu, I. A., Popa, D., & Zăgrean, L. (2020) · Brain Sciences · doi:10.3390/brainsci10090624 · Cited by 72
Hamani, C., Amorim, B. O., Wheeler, A. L., Diwan, M., Driesslein, K., Covolan, L., Butson, C. R., & Nóbrega, J. N. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.08.007 · Cited by 71
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
Gulcebi, M. I., Ketenci, S., Linke, R., Hacıoğlu, H., Yananlı, H. R., Velı́šková, J., Moshé, S. L., Onat, F., & Çavdar, S. (2011) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2011.11.005 · Cited by 68
Thalamic olfaction: characterizing odor processing in the mediodorsal thalamus of the rat
Courtiol, E., & Wilson, D. A. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00741.2013 · Cited by 68
Antal, M., Beneduce, B. M., & Regehr, W. G. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0236-14.2014 · Cited by 63
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Gonçalves, L., Nogueira, M. I., Shammah‐Lagnado, S. J., & Metzger, M. (2008) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2008.11.012 · Cited by 69
Jones, E. G. (1998) · Handbook of chemical neuroanatomy · doi:10.1016/s0924-8196(98)80003-1 · Cited by 66
Topographic organization of orbitofrontal projections to the parahippocampal region in rats
Kondo, H., & Witter, M. P. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23442 · Cited by 72
Nguyen, A. D., Shenton, M. E., & Levitt, J. J. (2010) · Harvard Review of Psychiatry · doi:10.3109/10673229.2010.511060 · Cited by 65
Numan, M. J., FLEMING, A., & Lévy, F. (2006) · Elsevier eBooks · doi:10.1016/b978-012515400-0/50040-3 · Cited by 63
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Kumar, V., Mang, S. C., & Grodd, W. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0748-2 · Cited by 59
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Jelsing, J., Hay‐Schmidt, A., Dyrby, T. B., Hemmingsen, R., Uylings, H. B. M., & Pakkenberg, B. (2006) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2006.06.009 · Cited by 62
Lavı́n, A., Moore, H. M., & Grace, A. A. (2005) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300696 · Cited by 62
Pathological Activity in Mediodorsal Thalamus of Rats with Spinal Cord Injury Pain
Whitt, J. L., Masri, R. M., Pulimood, N. S., & Keller, A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2639-12.2013 · Cited by 62
Rosas-Vidal, L. E., Lozada-Miranda, V., Cantres-Rosario, Y. M., Vega-Medina, A., Meléndez, L. M., & Quirk, G. J. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0176-8 · Cited by 63
Groenewegen, H. J., & Witter, M. P. (2004) · Elsevier eBooks · doi:10.1016/b978-012547638-6/50018-3 · Cited by 66
Malvaez, M., Greenfield, V. Y., Wang, A. S., Yorita, A. M., Feng, L., Linker, K. E., Monbouquette, H. G., & Wassum, K. M. (2015) · Scientific Reports · doi:10.1038/srep12511 · Cited by 61
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Lane, G., Zhou, G., Noto, T., & Zelano, C. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113304 · Cited by 76
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Kamigaki, T. (2018) · Neuroscience Research · doi:10.1016/j.neures.2018.08.017 · Cited by 69
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Santiago, A. C., & Shammah‐Lagnado, S. J. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20028 · Cited by 58
Efferent connections of the rostral linear nucleus of the ventral tegmental area in the rat
Del-Fava, F., Hasue, R. H., Ferreira, J. G. P., & Shammah-Lagnado, S. J. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.12.039 · Cited by 56
Schilman, E. A., Klavir, O., Winter, C., Sohr, R., & Joel, D. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.208 · Cited by 55
McGuier, N. S., Padula, A. E., Lopez, M. F., Woodward, J. J., & Mulholland, P. J. (2014) · Alcohol · doi:10.1016/j.alcohol.2014.07.017 · Cited by 52
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Constantinople, C. M., Piet, A. T., Bibawi, P., Akrami, A., Kopec, C. D., & Brody, C. D. (2019) · eLife · doi:10.7554/elife.49744 · Cited by 49
Banerjee, P., & Snead, O. C. (1994) · Epilepsy Research · doi:10.1016/0920-1211(94)90050-7 · Cited by 52
The human mediodorsal thalamus: Organization, connectivity, and function
Li, K., Fan, L., Cui, Y. J., Wei, X., He, Y., Yang, J., Lu, Y., Li, W., Shi, W., Cao, L., et al. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.118876 · Cited by 52
Thalamic‐insular dysconnectivity in schizophrenia: Evidence from structural equation modeling
Corradi‐Dell’Acqua, C., Tomelleri, L., Bellani, M., Rambaldelli, G., Cerini, R., Mucelli, R. P., Balestrieri, M., Tansella, M., & Brambilla, P. (2011) · Human Brain Mapping · doi:10.1002/hbm.21246 · Cited by 52
Barreiros, I. V., Panayi, M. C., & Walton, M. E. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.02.017 · 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
Cartography of 5-HT1Aand 5-HT2AReceptor Subtypes in Prefrontal Cortex and Its Projections
Mengod, G., Palacios, J. M., & Cortés, R. (2015) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.5b00023 · Cited by 52
Dynamic cortical lateralization during olfactory discrimination learning
Cohen, Y., Putrino, D. F., & Wilson, D. A. (2015) · The Journal of Physiology · doi:10.1113/jphysiol.2014.288381 · Cited by 49
Contribution of infralimbic cortex in the cardiovascular response to acute stress
Müller-Ribeiro, F. C. D. F., Zaretsky, D. V., Zaretskaia, M. V., Santos, R. A. S., DiMicco, J. A., & Fontes, M. A. P. (2012) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00573.2011 · Cited by 49
Cortico-amygdala circuits: Role in the conditioned stress response
Berretta, S. (2005) · Stress · doi:10.1080/10253890500489395 · Cited by 49
Mathiasen, M. L., Aggleton, J. P., & Witter, M. P. (2023) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2023.1131167 · Cited by 46
Voogd, J., Nieuwenhuys, R., van Dongen, P. A. M., & ten Donkelaar, H. J. (1998) · Springer eBooks · doi:10.1007/978-3-642-18262-4_22 · Cited by 46
Zhang, C. H., Sha, Z., Mundahl, J., Liu, S., Lu, Y., Henry, T. R., & He, B. (2015) · NeuroImage Clinical · doi:10.1016/j.nicl.2015.07.014 · Cited by 45
Vertes, R. P., Linley, S. B., Groenewegen, H. J., & Witter, M. P. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-374245-2.00016-4 · Cited by 45
Kobayashi, M. (2011) · International review of neurobiology · doi:10.1016/b978-0-12-385198-7.00011-4 · Cited by 45
Martínez‐Garciá, F., Novejarque, A., Gutiérrez‐Castellanos, N., & Lanuza, E. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-369497-3.10006-8 · Cited by 48
Kuroda, M., Murakami, K., Igarashi, H., & Okada, A. (1996) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1996.tb01596.x · Cited by 45
Kuroda, M., Murakami, K., Kishi, K., & Price, J. (1995) · The Journal of comparative neurology · doi:10.1002/cne.903560110 · Cited by 51
Self-citationKuroda, M., Murakami, K., Oda, S., Shinkai, M., & Kishi, K. (1993) · Brain Research · doi:10.1016/0006-8993(93)91683-j · Cited by 48
Pattern of distribution of serotonergic fibers to the orbitomedial and insular cortex in the rat
Linley, S. B., Hoover, W. B., & Vertes, R. P. (2013) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2012.12.006 · Cited by 43
Hassiotis, M., Paxinos, G., & Ashwell, K. W. S. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20193 · Cited by 43
Miller, P. J., & Záborszky, L. (1997) · Experimental Neurology · doi:10.1006/exnr.1997.6522 · Cited by 43
McBride, S., & Slotnick, B. M. (1997) · Behavioral Neuroscience · doi:10.1037//0735-7044.111.6.1273 · Cited by 42
Miyamoto, Y., & Jinnai, K. (1994) · Brain Research · doi:10.1016/0006-8993(94)91079-0 · Cited by 42
Optical recording of the rat piriform cortex activity
Litaudon, P., Datiche, F., & Cattarelli, M. (1997) · Progress in Neurobiology · doi:10.1016/s0301-0082(97)00027-0 · Cited by 40
The cerebellum regulates fear extinction through thalamo-prefrontal cortex interactions in male mice
Frontera, J. L., Sala, R. W., Georgescu, I. A., Baba Aissa, H., d’Almeida, M. N., Popa, D., & Léna, C. (2023) · Nature Communications · doi:10.1038/s41467-023-36943-w · Cited by 38
Determining the Neural Substrate for Encoding a Memory of Human Pain and the Influence of Anxiety
Tseng, M., Kong, Y., Eippert, F., & Tracey, I. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0750-17.2017 · Cited by 40
Connections of the laterodorsal tegmental nucleus with the habenular‐interpeduncular‐raphe system
Bueno, D., Lima, L. B., Souza, R., Gonçalves, L., Leite, F., Souza, S., Furigo, I. C., Donato, J., & Metzger, M. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24729 · Cited by 46
MEDIAL PREFRONTAL CORTEX LESIONS ABOLISH CONTEXTUAL CONTROL OF COMPETING RESPONSES
Haddon, J. E., & Killcross, S. (2005) · Journal of the Experimental Analysis of Behavior · doi:10.1901/jeab.2005.81-04 · Cited by 37
Kuroda, M., Yokofujita, J., Oda, S., & Price, J. L. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20249 · Cited by 36
Self-citationMediodorsal Thalamic Lesions Impair Trace Eyeblink Conditioning in the RabbitPreprint
Powell, D. A., & Churchwell, J. C. (2002) · Learning & Memory · doi:10.1101/lm.45302 · Cited by 36
Congenital olfactory impairment is linked to cortical changes in prefrontal and limbic brain regions
Karstensen, H. G., Vestergaard, M. D., Baaré, W. F. C., Skimminge, A., Djurhuus, B. D., Ellefsen, B., Brüggemann, N., Klausen, C., Leffers, A.-M., Tommerup, N., et al. (2018) · Brain Imaging and Behavior · doi:10.1007/s11682-017-9817-5 · Cited by 36
Jackson, R. L., Bajada, C. J., Ralph, M. A. L., & Cloutman, L. L. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz079 · Cited by 34
Négyessy, L., Hámori, J., & Bentivoglio, M. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00559-9 · Cited by 35
The Insular Cortex and the Amygdala: Shared Functions and Interactions
Moraga‐Amaro, R., & Stehberg, J. (2012) · InTech eBooks · doi:10.5772/48495 · Cited by 37
What Can Different Brains Do with Reward?
Gottfried, J. A. (2011) · CRC Press eBooks · doi:10.1201/b10776-10 · Cited by 33
Kuroda, M., López‐Mascaraque, L., & Price, J. L. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903260106 · Cited by 33
Self-citationHarte, M., & O'Connor, W. T. (2004) · Brain Research · doi:10.1016/j.brainres.2004.05.027 · Cited by 33
Wang, Z., Feng, X., & Zheng, P. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00113-6 · Cited by 32
The role of mediodorsal thalamic nucleus in fear extinction
Lee, S., & Shin, H. (2016) · Journal of Analytical Science & Technology · doi:10.1186/s40543-016-0093-6 · Cited by 32
Neural Encoding in the Orbitofrontal Cortex Related to Goal‐Directed Behavior
Furuyashiki, T., & Gallagher, M. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.037 · Cited by 31
Yamamuro, K., Yoshino, H., Ogawa, Y., Okamura, K., Nishihata, Y., Makinodan, M., Saito, Y., & Kishimoto, T. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00105 · Cited by 29
Roesch, M. R., & Schoenbaum, G. M. (2006) · doi:10.1093/acprof:oso/9780198565741.003.0008 · Cited by 29
Magalhães, R. J. D. S., Novais, A., Barrière, D. A., Marques, P., Marques, F., Sousa, J. C., Cerqueira, J., Cachia, A., Jay, T. M., Bottlaender, M., et al. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2192-18.2019 · Cited by 29
Architectonic structure of the orbital and medial prefrontal cortex
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Self-citationPrefrontal connections of the perirhinal and postrhinal cortices in the rat
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Souza, R., Bueno, D., Lima, L. B., Muchon, M. J., Gonçalves, L., Donato, J., Shammah‐Lagnado, S. J., & Metzger, M. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02538-2 · Cited by 30
A limited role for mediodorsal thalamus in devaluation tasks.
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Functional dissociation between dorsal and ventral regions of the medial prefrontal cortex in rats
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The role of mediodorsal thalamus in temporal differentiation of reward-guided actions
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Effects of stressor controllability on diurnal physiological rhythms
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Metadata
- Authors
- Ray, J. P., & Price, J. L.
- Affiliations
- Washington University in St. Louis (US)
- Corresponding author
- Price, Joseph L.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1992-09-08
- Volume
- 323
- Issue
- 2
- Pages
- 167-197
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2044537936
- Cited by
- 326
- References
- 90
- Citations by year
- 2026: 7 · 2024: 5 · 2023: 8 · 2022: 9 · 2021: 7 · 2020: 13 · 2019: 7 · 2018: 11 · 2017: 10 · 2016: 10 · 2015: 13 · 2014: 17 · 2013: 19 · 2012: 12
- FWCI
- 4.03
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute on Deafness and Other Communication Disorders (R01DC000093, R01 DC00093)
- National Institute of General Medical Sciences (T32GM008151, T32 GM08151)
- 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 dynamics and brain function
- Keywords
- mediodorsal thalamus, thalamocortical connections, ventral forebrain, piriform cortex, amygdala, prefrontal cortex, agranular insular cortex, topographic organization, ventral pallidum
- MeSH terms
- Amygdala, Animals, Cerebral Cortex, Female, Globus Pallidus, Injections, Male, Neural Pathways, Neurons, Afferent, Phytohemagglutinins, Thalamic Nuclei, Thalamus, Prosencephalon, Rats, Sprague-Dawley, Rats
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