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Inputs to the ventrolateral bed nucleus of the stria terminalis
Open accessAbstract
The ventrolateral bed nucleus of the stria terminalis (BSTvl) receives direct input from two specific subpopulations of neurons in the nucleus tractus solitarius (NTS). It is heavily innervated by aldosterone‐sensitive NTS neurons, which are selectively activated by sodium depletion, and by the A2 noradrenergic neurons, which are activated by visceral and immune‐ and stress‐related stimuli. Here, we used a retrograde neuronal tracer to identify other brain sites that innervate the BSTvl. Five general brain regions contained retrogradely labeled neurons: cerebral cortex (infralimbic and insular regions), rostral forebrain structures (subfornical organ, organum vasculosum of the lamina terminalis, taenia tecta, nucleus accumbens, lateral septum, endopiriform nucleus, dorsal BST, substantia innominata, and, most prominently the amygdala—primarily its basomedial and central subnuclei), thalamus (central medial, intermediodorsal, reuniens, and, most prominently the paraventricular thalamic nucleus), hypothalamus (medial preoptic area, perifornical, arcuate, dorsomedial, parasubthalamic, and posterior hypothalamic nuclei), and brainstem (periaqueductal gray matter, dorsal and central superior raphe nuclei, parabrachial nucleus, pre‐locus coeruleus region, NTS, and A1 noradrenergic neurons in the caudal ventrolateral medulla). In the arcuate hypothalamic nucleus, some retrogradely labeled neurons contained either agouti‐related peptide or cocaine/amphetamine‐regulated transcript. Of the numerous retrogradely labeled neurons in the perifornical hypothalamic area, few contained melanin‐concentrating hormone or orexin. In the brainstem, many retrogradely labeled neurons were either serotoninergic or catecholaminergic. In summary, the BSTvl receives inputs from a variety of brain sites implicated in hunger, salt and water intake, stress, arousal, and reward. J. Comp. Neurol. 511:628–657, 2008. © 2008 Wiley‐Liss, Inc.
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“In the LN, these changes may directly affect fear conditioning, whereas changes in the BN may impact on hippocampal context learning, and involvement of the CE, ME and ABN suggests direct effects on the bed nucleus of the stria terminalis, speculatively impacting on sustained fear mechanisms.95, 96, 97, 98”
From Aggrecan and chondroitin-6-sulfate abnormalities in schizophrenia and bipolar disorder: a postmortem study on the amygdala (2015) · cites this paper as [95]
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The rat brain in stereotaxic coordinates
Palkovits, M. (1983) · Neuropeptides · doi:10.1016/0143-4179(83)90049-5 · Cited by 28,959
AChE-stained horizontal sections of the rat brain in stereotaxic coordinates
Paxinos, G., WATSON, C. R. R., & Emson, P. C. (1980) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(80)90021-7 · Cited by 4,501
Bardo, M. T., & Hammer, R. P. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90226-e · Cited by 3,229
Brain maps: structure of the rat brain
Guillery, R. W. (1993) · Trends in Neurosciences · doi:10.1016/0166-2236(93)90187-q · Cited by 1,669
Swanson, L. W., & Hartman, B. K. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901630406 · Cited by 1,475
Ricardo, J. A., & Koh, E. T. (1978) · Brain Research · doi:10.1016/0006-8993(78)91125-3 · Cited by 1,362
Limbic system mechanisms of stress regulation: Hypothalamo-pituitary-adrenocortical axis
Herman, J. P., Ostrander, M. M., Mueller, N. K., & Figueiredo, H. (2005) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2005.08.006 · Cited by 1,322
Efferent connections of the parabrachial nucleus in the rat
Saper, C. B., & Loewy, A. D. (1980) · Brain Research · doi:10.1016/0006-8993(80)91117-8 · Cited by 1,217
Self-citationDirect hypothalamo-autonomic connections
Saper, C. B., Loewy, A. D., Swanson, L. W., & Cowan, W. M. (1976) · Brain Research · doi:10.1016/0006-8993(76)90738-1 · Cited by 1,199
Self-citationCoexpression of Agrp and NPY in fasting-activated hypothalamic neurons
Hahn, T. M., Breininger, J. F., Baskin, D. G., & Schwartz, M. W. (1998) · Nature Neuroscience · doi:10.1038/1082 · Cited by 1,164
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Hsu, D. T., Kirouac, G. J., Zubieta, J.-K., & Bhatnagar, S. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00073 · Cited by 238
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Daniel, S., & Rainnie, D. G. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.178 · Cited by 224
Geerling, J. C., & Loewy, A. D. (2009) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.90399.2008 · Cited by 184
Self-citationPantazopoulos, H., Markota, M., Jaquet, F., Ghosh, D., Wallin, A., Santos, A., Caterson, B., & Berretta, S. (2015) · Translational Psychiatry · doi:10.1038/tp.2014.128 · Cited by 153
Pardo‐Bellver, C., Cádiz‐Moretti, B., Novejarque, A., Martínez‐Garciá, F., & Lanuza, E. (2012) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2012.00033 · Cited by 166
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Schmitt, O., Usunoff, K. G., Lazarov, N., Itzev, D. E., Eipert, P., Rolfs, A., & Wree, A. (2011) · Brain Structure and Function · doi:10.1007/s00429-011-0343-8 · Cited by 69
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Johnson, S. B., Emmons, E. B., Anderson, R. M., Glanz, R. M., Romig‐Martin, S. A., Narayanan, N. S., LaLumiere, R. T., & Radley, J. J. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1185-16.2016 · Cited by 71
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Gómez-Sánchez, E. P. (2011) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2011.02.001 · Cited by 52
Crestani, C. C., Alves, F. H., Corrêa, F. M. D. A., Guimarães, F. S., & Joca, S. R. L. (2010) · Behavioral and Brain Functions · doi:10.1186/1744-9081-6-30 · Cited by 52
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Sartor, G. C., & Aston‐Jones, G. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08277.x · Cited by 48
Radley, J. J. (2012) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2012.00007 · Cited by 48
Freire, R. C. R., Cabrera-Abreu, C., & Milev, R. V. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-32-9705-0_18 · Cited by 50
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
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Osacká, J., Ghosal, S., Packard, B. A., Ulrich‐Lai, Y. M., & Herman, J. P. (2015) · Stress · doi:10.3109/10253890.2015.1013531 · Cited by 42
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Murck, H., Adolf, C., Schneider, A., Schlageter, L., Heinrich, D. A., Ritzel, K., Sturm, L., Quinkler, M. O., Beuschlein, F., Reincke, M., et al. (2021) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2021.02.064 · Cited by 26
Stein, M. K., & Loewy, A. D. (2010) · Brain Research · doi:10.1016/j.brainres.2010.08.085 · Cited by 26
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Fox, M. E., Bucher, E. S., Johnson, J. A., & Wightman, R. M. (2016) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.6b00210 · Cited by 11
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Self-citationAdolescent rat circadian activity is modulated by psychostimulants
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Ciriello, J., Caverson, M. M., & Li, Z.-S. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.09.032 · Cited by 12
Binks, A. P. (2022) · Handbook of clinical neurology · doi:10.1016/b978-0-323-91534-2.00008-4 · Cited by 13
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Reed, M. D., Hildebrand, D. G. C., Santangelo, G., Moffa, A., Pira, A. S., Rycyna, L., Radic, M., Price, K. E., Archbold, J., McConnell, K., et al. (2015) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2015.05.001 · Cited by 15
Pharmacology of the Bed Nucleus of the Stria Terminalis
Glangetas, C., & Georges, F. E. (2016) · Current Pharmacology Reports · doi:10.1007/s40495-016-0077-7 · Cited by 10
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Granjeiro, É. M., Gomes, F. V., Alves, F. H. F., Crestani, C. C., Corrêa, F. M. D. A., & Resstel, L. B. M. (2011) · Autonomic Neuroscience · doi:10.1016/j.autneu.2011.11.004 · Cited by 10
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Povysheva, N. V., Zheng, H., & Rinaman, L. (2021) · Neurobiology of Stress · doi:10.1016/j.ynstr.2021.100363 · Cited by 7
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Berry, S. C., Lawrence, A. D., Lancaster, T. M., Casella, C., Aggleton, J. P., & Postans, M. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119096 · Cited by 6
Asami, R., Ono, K., Nakanishi, O., & Inenaga, K. (2011) · Brain Research · doi:10.1016/j.brainres.2011.01.072 · Cited by 6
de Cerqueira, D. R., Ferreira, H. S., Moiteiro, A. L. B. B., & Fregoneze, J. B. (2016) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.05.003 · Cited by 8
Adolf, C., Murck, H., Sarkis, A., Schneider, H., Heinrich, D. A., Williams, T. A., Reincke, M., & Kunzel, H. E. (2022) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2022.09.008 · Cited by 5
Zhu, K., Tao, G., Huang, Z., Qu, W., & Wang, L. (2023) · European Journal of Neuroscience · doi:10.1111/ejn.16068 · Cited by 5
Lee, M. J., Burau, K. D., & Dafny, N. (2013) · Journal of Neural Transmission · doi:10.1007/s00702-012-0929-1 · Cited by 5
Öz, P., Yertutanol, F. D. K., Gözler, T., Özçetin, A., & Uzbay, T. I. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.01.056 · Cited by 5
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Nambu, Y., Horie, K., Kurganov, E., & Miyata, S. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.135732 · Cited by 4
Erkan, B., Hergünsel, Ö. B., Barut, O., Saygı, T., Koçak, B., Güngör, A., Yağmurlu, K., & Tanrıöver, N. (2024) · Journal of neurosurgery · doi:10.3171/2024.1.jns231541 · Cited by 3
Greiner, E. M., & Petrovich, G. D. (2024) · Brain Structure and Function · doi:10.1007/s00429-024-02791-7 · Cited by 3
Koob, G. F., Arends, M. A., McCracken, M. L., & Moal, M. L. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-816990-2.00001-6 · Cited by 4
Niu, Y., Camacho, M. C., Ravi, S., Wallroff, B., Hageman, J., Blackford, J. U., & Humphreys, K. L. (2025) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2025.101638 · Cited by 2
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Reda, A. J., Doss, D. J., Makhoul, G. S., Lerma, B. H. M., Johnson, G. W., Sainburg, L. E., Cavender, A. C., Sundrani, S. C., Liao, E., Roche, A., et al. (2025) · Neurology · doi:10.1212/wnl.0000000000214385 · Cited by 1
Velazquez-Hernandez, G., Miller, N. W., Curtis, V. R., Rivera-Pacheco, C. M., Lowe, S. M., Moy, S. S., Zannas, A. S., Pégard, N. C., Burgos-Robles, A., & Rodríguez-Romaguera, J. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.17.599379 · Cited by 1
Metadata
- Authors
- Shin, J., Geerling, J. C., & Loewy, A. D.
- Affiliations
- Washington University in St. Louis (US)
- Corresponding author
- Loewy, Arthur D.
- ORCID
- Geerling, Joel C.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 2008-10-29
- Volume
- 511
- Issue
- 5
- Pages
- 628-657
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- PMC
- PMC2748802
- OpenAlex
- W2033296244
- Cited by
- 115
- References
- 135
- Citations by year
- 2026: 3 · 2025: 4 · 2024: 6 · 2023: 2 · 2022: 6 · 2021: 5 · 2020: 8 · 2019: 4 · 2018: 4 · 2017: 1 · 2016: 9 · 2015: 7 · 2014: 12 · 2013: 13 · 2012: 9
- FWCI
- 2.88
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Heart, Lung, and Blood Institute (HL25449, R37HL025449, R01HL025449)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroscience of respiration and sleep
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Keywords
- nucleus tractus solitarius, sodium depletion, amygdala, paraventricular thalamus, hypothalamus, arcuate nucleus, perifornical area, brainstem, serotonin, catecholamines, hunger, stress, arousal, reward, retrograde tracing
- MeSH terms
- Afferent Pathways, Animals, Autonomic Nervous System, Axonal Transport, Brain Mapping, Brain Stem, Cholera Toxin, Immunohistochemistry, Limbic System, Male, Septal Nuclei, Biogenic Monoamines, Biomarkers, Prosencephalon, Rats, Sprague-Dawley, Autonomic Pathways, Neurotransmitter Agents, Rats
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