The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
The Concepts of the Ventral Striatopallidal System and Extended Amygdala
Abstract
ABSTRACT: The concepts of the ventral striatopallidal system and extended amygdala have significantly improved our understanding of basal forebrain organization. As a result of these and other advances during the last twenty years, many of the most prominent basal forebrain structures, including the nucleus accumbens, olfactory tubercle, and amygdaloid body, have all but lost their relevance as independent functional anatomical units. In order to appreciate the distinct differences that exist between the ventral striatopallidal system and the extended amygdala, and as a way of explaining the choice of the terms ventral striatopallidal system and extended amygdala, we will review the discovery and subsequent elaboration of these two systems. On the background of these discussions, we will then proceed to dispel some recently published misgivings regarding the usefulness of the extended amygdaloid concept.
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?
The BST and MeA belong to the extended amygdala, a cohort of nuclei with striking similarities in cytoarchitecture and neurochemistry.
“These two areas belong to the extended amygdala, a cohort of nuclei in the BST and centromedial amygdala with striking similarities in cytoarchitecture and neurochemistry (de Olmos and Heimer, 1999).”
From Sexual differentiation of central vasopressin and vasotocin systems in vertebrates: different mechanisms, similar endpoints (2006) · cites this paper as de Olmos and Heimer, 1999
Citations
Cites
Alheid, G. F., & Heimer, L. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90217-5 · Cited by 1,217
Self-citationEffects of nicotine on the nucleus accumbens and similarity to those of addictive drugs.
Pontieri, F. E., Tanda, G., Orzi, F., & Chiara, G. D. (1996) · Nature · doi:10.1038/382255a0 · Cited by 1,073
Alheid, G. F., Beltramino, C. A., de Olmos, J. S., Forbes, M. S., Swanson, D. J., & Heimer, L. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00560-5 · Cited by 113
Self-citation
Flagged first, then by citations
Research works printed but not linked: 97
- Alexander G.E. M.D. Crutcher & M.R. DeLong. 1990. Basal ganglia‐thalamocortical circuits: parallel substrates for motor oculomotor “prefrontal” and “limbic” functions.InThe Prefrontal Cortex: Its Structure Function and Pathology. H.B.M. Uylings C.G. Van Eden J.P.C. De Bruin M.A. Corner & M.P.G. Feenstra Eds.: 119‐146. Elsevier. Amsterdam. · DOI · Paper page
- 10.1146/annurev.ne.09.030186.002041 · DOI · Paper page
- Alheid G.F. C.A. Beltramino A. Braun R.R. Miselis C. François & J.S. de Olmos. 1994. Transition areas of the striatopallidal system with the extended amygdala in the rat and primate: observations from histochemistry and experiments with mono‐and transsynaptic tracer.InThe Basal Ganglia IV. New Ideas and Data on Structure and Function. G. Percheron J.S. McKenzie & J. Feger Eds.:41:95‐107. Plenum Press. New York. · DOI
- Alheid G.F. J.S. de Olmos & C. A. Beltramino. 1995. Amygdala and extended amygdala.InThe Rat Nervous System 2nd Ed. G. Paxinos Ed.: 495‐578. Academic Press Inc. San Diego.
- 10.1016/S0079-6123(08)61882-8 · DOI
- Alheid G.F. L. Heimer & R. C. Switzer. 1990. Basal ganglia.InThe Human Nervous System. G. Paxinos Ed.: 483‐582. Academic Press Inc. San Diego CA. · DOI
- 10.1002/cne.903550207 · DOI
- 10.1159/000113276 · DOI
- 10.1002/cne.903600203 · DOI
- 10.1016/S0006-8993(97)01074-3 · DOI
- 10.1016/0306-4522(90)90091-H · DOI
- 10.1016/0306-4522(95)00386-X · DOI
- 10.1002/(SICI)1096-9861(19980921)399:2<189::AID-CNE4>3.0.CO;2-X · DOI
- 10.1111/j.1460-9568.1991.tb00064.x · DOI
- 10.1002/cne.903020202 · DOI
- 10.1016/0306-4522(95)00458-0 · DOI
- 10.1159/000125825 · DOI
- de Olmos J.S. 1972. The amygdaloid projection field in the rat as studied with the cupric silver method.InThe Neurobiology of the Amygdala. B.E. Eleftheriou Ed.: 145‐204. Plenum Press. New York. · DOI
- de Olmos J.S. 1990. Amygdala.InThe Human Nervous System. G. Paxinos Ed.: 583‐710. Academic Press. Inc. San Diego CA. · DOI
- de Olmos J.S. G.F. Alheid & C.A. Beltramino. 1985. Amygdala.InThe Rat Nervous System. G. Paxinos Ed.: 223‐334. Academic Press. Sydney.
- 10.1007/BF01245232 · DOI
- 10.1002/neu.480210503 · DOI · Paper page
- Fallon J.H., 1983, The islands of Calleja complex of rat basal forebrain, II. Connections of medium and large sized cells. Brain Res. Bull., 10, 775
- 10.1126/science.6144184 · DOI
- 10.1016/0006-8993(67)90166-7 · DOI
- 10.1016/0006-8993(94)01395-X · DOI
- Freund‐Mercier M.J., 1988, Quantitative autoradiographic mapping of neurohypophysial hormone binding sites in the rat forebrain and pituitary gland, II. Comparative study on the Long-Evans and Brattleboro strains. Neuroscience, 26, 273
- 10.1002/cne.902940403 · DOI
- 10.1016/0306-4522(88)90339-9 · DOI · Paper page
- Groenewegen H.J. 1996. Cortical‐subcortical relationships and the limbic forebrain.InContemporary Behavioral Neurology. M.R. Trimble & J.L. Cummings Eds.: 29‐48. Blue Books of Practical Neurology Vol. 16. C.D. Marsden & A.K. Ashbury Series Eds. Butterworth‐Heineman. Boston.
- Groenewegen H.J. & H.W. Berendse. 1994. Anatomical relationships between the prefrontal cortex and the basal ganglia in the rat.InMotor and Cognitive Functions of the Prefrontal Cortex. A.M. Thierry J. Glowinski P.S. Goldman‐Rakic & Y. Christen Eds.: 31‐77. Springer‐Verlag. Berlin Heidelberg. · DOI
- 10.1002/cne.902770303 · DOI
- 10.1002/cne.902770302 · DOI
- 10.1016/0306-4522(83)90291-9 · DOI
- 10.1038/scientificamerican0771-48 · DOI
- Heimer L., 1972, The olfactory connections of the diencephalon in the rat, An experimental light-and electron-microscopic study with special emphasis on the problem of terminal degeneration. Brain Behav. Evol., 6, 484
- Heimer L. 1978. The olfactory cortex and the ventral striatum.InLimbic Mechanisms. K.E. Livingston & O. Hornykiewicz Eds.: 95‐187. Plenum Press. New York. · DOI
- 10.1176/jnp.9.3.354 · DOI
- Heimer L. G.F. Alheid & D.S. Zahm. 1993. Basal forebrain organization: an anatomical framework for motor aspects of drive and motivation.InLimbic Motor Circuits and Neuropsychiatry. P.W. Kalivas & C.D. Barnes Eds.: 1‐43. CRC Press. Boca Raton Florida. · DOI
- Heimer L. J. de Olmos G.F. Alheid J. Pearson M. Sakamoto J. Marksteiner & R.C. Switzer III. 1999. The human basal forebrain part 2.InHandbook of Chemical Neuroanatomy Vol. 15. The Primate Nervous System Part III. F.E. Bloom A. Björklund & T. Hökfelt Eds. Elsevier. Amsterdam. In press. · DOI · Paper page
- 10.1016/S0079-6123(08)63050-2 · DOI
- 10.1016/S0306-4522(96)00405-8 · DOI
- Heimer L. & G.W. Van Hoesen. 1979. Ventral striatum.InThe Neostriatum. I. Divac & G.E. Oberg Eds.: 147‐158. Pergamon Press. New York. · DOI
- Heimer L. & R.D. Wilson. 1975. The subcortical projections of allocortex: similarities in the neuronal associations of the hippocampus the piriform cortex and the neocortex.InGolgi Centennial Symposium Proceedings. M. Santini Ed.: 173‐193. Raven Press. New York.
- Heimer L., 1987, The ventral striatopallidothalamic projection, I. The striatopallidal link originating in the striatal parts of the olfactory tubercle. J. Comp. Neurol., 255, 571
- Heimer L. D.S. Zahm & G.F. Alheid. 1995. Basal ganglia.InThe Rat Nervous System 2nd edition. G. Paxinos Ed.: 579–628. Academic Press. San Diego CA.
- 10.1016/0306-4522(91)90202-Y · DOI · Paper page
- 10.1007/BF00235319 · DOI
- 10.1016/S0006-8993(97)01143-8 · DOI
- 10.1016/S0006-8993(98)00765-3 · DOI
- 10.1016/0306-4522(81)90223-2 · DOI
- 10.1016/0960-0760(93)90253-S · DOI
- 10.1002/cne.900350502 · DOI · Paper page
- 10.1007/BF02245004 · DOI
- 10.1016/0006-8993(90)90002-S · DOI
- 10.1126/science.278.5335.52 · DOI · Paper page
- 10.1016/0006-8993(94)90961-X · DOI
- 10.1002/(SICI)1096-9861(19970707)383:3<349::AID-CNE6>3.0.CO;2-3 · DOI · Paper page
- 10.1002/cne.903190306 · DOI
- 10.1176/jnp.6.4.358 · DOI
- Meredith G.E. & S. Totterdell. 1999. Microcircuits in nucleus accumbens' shell and core involved in cognition and reward. Psychobiology. In press. · DOI
- 10.1002/cne.902280409 · DOI
- 10.1176/jnp.1.1.27 · DOI
- 10.1002/cne.902950408 · DOI
- 10.1016/0306-4522(93)90241-7 · DOI
- Mugnaini E. & W.H. Oertel. 1985. An atlas of the distribution of GABAergic neurons and terminals in the rat CNS as revealed by GAD immunohistochemistry.InHandbook of Chemical Neuroanatomy Vol. 4. GABA and Neuropeptides in the CNS Part 1. A. Björklund & T. Hökfelt Eds.: 436–608. Elsevier. Amsterdam.
- 10.1002/cne.901910204 · DOI
- Paxinos G. & C. Watson. 1986. The Rat Brain in Stereotaxic Coordinates 2nd Edition. Academic Press. Sydney.
- Paxinos G. & C. Watson. 1997. The rat brain.InStereotaxic Coordinates 3rd Edition. Academic Press. San Diego.
- Pierce R.C., 1995, Amphetamine produces sensitized increases in locomotion and extracellular dopamine preferentially in the nucleus accumbens shell of rats administered repeated cocaine, J. Pharmacol. Exp. Ther., 275, 1019
- 10.1002/(SICI)1096-9861(19961209)376:2<278::AID-CNE9>3.0.CO;2-0 · DOI
- 10.1073/pnas.92.26.12304 · DOI
- 10.1002/(SICI)1096-9861(19981116)401:2<163::AID-CNE2>3.0.CO;2-D · DOI
- 10.1016/0361-9230(94)00217-O · DOI
- 10.1176/jnp.6.2.93 · DOI
- Sanides F., 1957, Die Insulae terminales des Erwachsenen Gehirns des Menschen, J. Hirnforsch., 3, 243
- Schwaber J.S., 1982, Amygdaloid and basal forebrain direct connections with the nucleus of the solitary tract and the dorsal motor nucleus, J. Neurosci., 2, 424, 10.1523/JNEUROSCI.02-10-01424.1982 · DOI
- 10.1002/cne.902260102 · DOI
- Shammah‐Lagnado S.J. G.F. Alheid & L. Heimer. 1999. Afferent connections of the interstitial nucleus of the posterior limb of the anterior commissure and adjacent amygdalostriatal transition area in the rat. Neuroscience. Submitted. · DOI
- 10.1073/pnas.84.7.2087 · DOI
- Skofitsch G., 1985, Calcitonin gene-related peptide: detailed immunohistochemical distribution in the central nervous system Peptides, 6, 721
- Skofitsch G. & D.M Jacobowitz. 1992. Calcitonin‐and calcitonin gene‐related peptide: receptor binding sites in the central nervous system.InHandbook of Chemical Neuroanatomy Vol. 11. Neuropeptide Receptors in the CNS. A. Björklund T. Hökfelt & M.J. Kuhar Eds.: 97–144. Elsevier. Amsterdam.
- 10.1016/0306-4522(93)90536-O · DOI
- 10.1016/0165-3806(94)00145-6 · DOI
- Strenge H., 1977, Über den Nucleus striae terminalis im Gehirn des erwachsenen Menschen, Z. Mikrosk. Anat. Forsch. Leipzig, 91, 105
- 10.1016/0006-8993(75)90278-4 · DOI
- 10.1016/S0166-2236(98)01265-X · DOI · Paper page
- 10.1017/S0140525X00047488 · DOI · Paper page
- 10.1016/0306-4522(82)90005-7 · DOI
- Tribollet E. 1992. Vasopressin and oxytocin receptors in the rat brain.InHandbook of Chemical Neuroanatomy Vol. 11. Neuropeptide Receptors in the CNS. A. Björklund T. Hökfelt & M.J. Kuhar Eds.: 289–320. Elsevier. Amsterdam.
- 10.1002/(SICI)1096-9861(19970707)383:3<305::AID-CNE3>3.0.CO;2-7 · DOI · Paper page
- Young W.S., 1984, The ventral pallidal projection to the mediodorsal thalamus: a study with fluorescent retrograde tracers and immunohistofluorescence, J. Neurosci., 4, 1626, 10.1523/JNEUROSCI.04-06-01626.1984 · DOI
- 10.1016/0306-4522(85)90302-1 · DOI
- 10.1615/CritRevNeurobiol.v12.i3.50 · DOI
- 10.1016/0306-4522(92)90202-D · DOI · Paper page
- Zahm D.S., 1987, The ventral striatopallidothalamic projection, III. Striatal cells of the olfactory tubercle establish direct synaptic contact with ventral pallidal cells projecting to mediodorsal thalamus. Brain Res., 404, 327
- 10.1002/cne.902550410 · DOI
Cited by
Sorted by citations
Nestler, E. J., Barrot, M., DiLeone, R. J., Eisch, A. J., Gold, S. J., & Monteggia, L. M. (2002) · Neuron · doi:10.1016/s0896-6273(02)00653-0 · Cited by 3,217
Fears, phobias, and preparedness: toward an evolved module of fear and fear learning
Öhman, A., & Mineka, S. (2001) · Psychological Review · doi:10.1037/0033-295x.108.3.483 · Cited by 3,147
Reward Processing by the Opioid System in the Brain
Le Merrer, J., Becker, J. A. J., Befort, K., & Kieffer, B. L. (2009) · Physiological Reviews · doi:10.1152/physrev.00005.2009 · Cited by 1,013
depue, R. A., & morrone-strupinsky, J. V. (2005) · Behavioral and Brain Sciences · doi:10.1017/s0140525x05000063 · Cited by 958
The neuropsychological basis of addictive behaviour
Everitt, B. J., Dickinson, A., & Robbins, T. W. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00088-1 · Cited by 808
Topography of projections from amygdala to bed nuclei of the stria terminalis
Dong, H.-W., Petrovich, G. D., & Swanson, L. W. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00079-0 · Cited by 714
Sturm, V., Lenartz, D., Koulousakis, A., Treuer, H., Herholz, K., Klein, J. C., & Klosterkötter, J. (2003) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2003.09.003 · Cited by 567
Ventral pallidum roles in reward and motivation
Smith, K. S., Tindell, A. J., Aldridge, J. W., & Berridge, K. C. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.09.038 · Cited by 548
Kim, Y., Yang, G. R., Pradhan, K., Venkataraju, K. U., Bota, M., García del Molino, L. C., Fitzgerald, G., Ram, K., He, M., Levine, J. M., et al. (2017) · Cell · doi:10.1016/j.cell.2017.09.020 · Cited by 389
Neural correlates of individual ratings of emotional salience: A trial-related fMRI study
Phan, K. L., Taylor, S. F., Welsh, R. C., Ho, S.-H., Britton, J. C., & Liberzon, I. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.09.072 · Cited by 416
Decreased Volume of the Brain Reward System in Alcoholism
Makris, N., Oscar-Berman, M., Jaffin, S. K., Hodge, S. M., Kennedy, D. N., Caviness, V. S., Marinkovic, K., Breiter, H. C., Gasic, G. P., & Harris, G. J. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.01.018 · Cited by 372
Human Bed Nucleus of the Stria Terminalis Indexes Hypervigilant Threat Monitoring
Somerville, L. H., Whalen, P. J., & Kelley, W. M. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.04.002 · Cited by 351
“Liking” and “wanting” in eating and food reward: Brain mechanisms and clinical implications
Morales, I., & Berridge, K. C. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.113152 · Cited by 346
De Vries, G. J., & Panzica, G. C. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.07.050 · Cited by 346
Salmaso, N., Rodaros, D., Stewart, J., & Erb, S. (2001) · Psychopharmacology · doi:10.1007/s002130000642 · Cited by 291
Li, S., & Kirouac, G. J. (2008) · Journal of Comparative Neurology · doi:10.1002/cne.21502 · Cited by 261
The olfactory bulb as the entry site for prion-like propagation in neurodegenerative diseases
Rey, N. L., Wesson, D. W., & Brundin, P. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.12.013 · Cited by 257
Olive, M. F., Koenig, H. N., Nannini, M. A., & Hodge, C. W. (2002) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(01)00748-1 · Cited by 237
Northoff, G., Wiebking, C., Feinberg, T., & Panksepp, J. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.12.007 · Cited by 222
The emotional modulation of cognitive processing: an fMRI study
Simpson, J. R., Öngür, D., Akbudak, E., Conturo, T. E., Ollinger, J. M., Snyder, A. Z., Gusnard, D. A., & Raichle, M. E. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/089892900564019 · Cited by 190
McNally, G. P., & Akil, H. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00105-7 · Cited by 141
Brain imaging of the self-conceptual, anatomical and methodological issues
Northoff, G., Qin, P., & Feinberg, T. E. (2011) · Consciousness and Cognition · doi:10.1016/j.concog.2010.09.011 · Cited by 135
Genetically identified amygdala–striatal circuits for valence-specific behaviors
Zhang, X., Guan, W., Yang, T., Furlan, A., Xiao, X., Yu, K., An, X., Galbavy, W., Ramakrishnan, C., Deisseroth, K., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00927-0 · Cited by 126
Roozendaal, B., de Quervain, D. J.-F., Ferry, B., Setlow, B., & McGaugh, J. L. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-07-02518.2001 · Cited by 128
Rood, B. D., Stott, R. T., You, S., Smith, C. J. W., Woodbury, M. E., & De Vries, G. J. (2013) · Journal of Comparative Neurology · doi:10.1002/cne.23288 · Cited by 120
Inputs to the ventrolateral bed nucleus of the stria terminalis
Shin, J., Geerling, J. C., & Loewy, A. D. (2008) · Journal of Comparative Neurology · doi:10.1002/cne.21870 · Cited by 115
Striatal structure and function in mood disorders: a comprehensive review
Marchand, W. R., & Yurgelun‐Todd, D. (2010) · Bipolar Disorders · doi:10.1111/j.1399-5618.2010.00874.x · Cited by 91
Erb, S., Shaham, Y., & Stewart, J. (2001) · Stress · doi:10.3109/10253890109014753 · Cited by 73
Numa, C., Nagai, H., Taniguchi, M., Nagai, M., Shinohara, R., & Furuyashiki, T. (2019) · Scientific Reports · doi:10.1038/s41598-019-52997-7 · Cited by 71
Oler, J. A., Birn, R. M., Patriat, R., Fox, A. S., Shelton, S. E., Burghy, C. A., Stodola, D. E., Essex, M. J., Davidson, R. J., & Kalin, N. H. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.045 · Cited by 67
Role of the Bed Nucleus of the Stria Terminalis (BST) in the Expression of Conditioned Fear
MELONI, E. G., JACKSON, A., GERETY, L. P., COHEN, B. M., & CARLEZON, W. A. (2006) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1364.059 · Cited by 41
Davis, M., & Walker, D. L. (2014) · Brain Structure and Function · doi:10.1007/s00429-013-0616-5 · Cited by 35
Narayanaswamy, J. C., Jose, D., Kalmady, S., Venkatasubramanian, G., & Reddy, Y. J. (2013) · Australian & New Zealand Journal of Psychiatry · doi:10.1177/0004867413491153 · Cited by 8
Metadata
- Authors
- DE OLMOS, J. S., & HEIMER, L.
- Venue
- Annals of the New York Academy of Sciences
- Publisher
- Wiley
- Published
- 1999-06
- Volume
- 877
- Issue
- 1
- Pages
- 1-32
- ISSN
- 0077-8923
- 1749-6632
- Cited by
- 281
- References
- 3
- Language
- en
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