The DOI matches its Crossref record; 86 of the 86 references it cites were found in a registry or an index.
Evidence for a viscerotopic sensory representation in the cortex and thalamus in the rat
Abstract
The functional organization of the insular cortex was studied by recording neuronal responses to visceral sensory stimuli. Horseradish peroxidase (HRP) was then iontophoresed at the recording sites to identify afferents from the ventrobasal thalamus to specific visceroceptive sites in the insular cortex. The relationship of the ventrobasal thalamus to the insular cortex and to brainstem relay nuclei for the ascending visceral projections was then examined by using the axonal transport of HRP, wheat germ agglutinin conjugated to HRP (WGA‐HRP), and fluorescent dyes. Of a total of 55 neurons that were tested for responses to visceral sensory stimuli, 33 units responded to atleast one visceral sensory modality: 6 received gastric mechanoreceptor input, 8 responded to taste inputs, 13 were activated by arterial chemoreceptors and/or showed respiratory related activity, and 6 responded to cardiovascular baroreceptor stimulation. On the basis of its cytoarchitecture and connections with the thalamus, the insular cortex was divided into a dorsal granular area, an intermediate dysgranular region, and a ventral agranular strip. Taste‐responsive neurons were located anteriorly, primarily in the dysgranular region, whereas unit responses to general visceral modalities were distributed dorsally and posteriorly in the granular insular cortex. Gastric mechanoreceptor‐responsive units were situated more dorsally and anteriorly in the granular insular cortex, while cardiopulmonary inputs were located more ventrally and posteriorly. Injections of HRP into the gustatory insular cortex resulted in retrograde labeling of neurons in the parvicellular part of the ventroposterior medial thalamic nucleus (VPMpc). Injections into the general visceral insular cortex retrogradely labeled neurons lateral to VPMpc in the ventroposterior lateral parvicellular thalamic nucleus (VPLpc). Injections of HRP, WGA‐HRP, and fluorescent dyes into VPMpc and VPLpc verified that their projection to the insular cortex is topographically organized. In the same experiments, retrogradely labeled neurons in the parabrachial nucleus identified the likely subnuclei within this nucleus for relay of visceral sensory information to the thalamus. Injections of WGA‐HRP into the parabrachial nucleus demonstrated that its projection to the ventrobasal thalamus is also topographically organized. These results demonstrate the relationship of general visceral and special visceral (taste) representations in the insular cortex. The ascending pathway for visceral sensory information appears to be viscerotopically organized at all levels of the neuraxis, including the insular cortex.
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
“The gustatory and visceral pathway (involving GU/VISC cortical areas and VPMpc/VPLpc nuclei)55,108”
From A mesoscale connectome of the mouse brain (2014) · cites this paper as [55]
Citations
Cites
Emson, P. C., Heffher, R. R., & Pearson, J. (1984) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-198409000-00010 · Cited by 1,651
Ricardo, J. A., & Koh, E. T. (1978) · Brain Research · doi:10.1016/0006-8993(78)91125-3 · Cited by 1,362
The 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
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-citationBiological and biochemical bases of behavior
Harlow, H. F., & Woolsey, C. N. (1958) · University of Wisconsin Press eBooks · Cited by 1,185
Subnuclear organization of the efferent connections of the parabrachial nucleus in the rat
Fulwiler, C., & Saper, C. B. (1984) · Brain Research Reviews · doi:10.1016/0165-0173(84)90012-2 · Cited by 1,057
Self-citationTaste pathways to hypothalamus and amygdala
Norgren, R. (1976) · The Journal of Comparative Neurology · doi:10.1002/cne.901660103 · Cited by 761
Welker, C. (1971) · Brain Research · doi:10.1016/s0006-8993(71)80004-5 · Cited by 744
Loewy, A. D., & Burton, H. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901810211 · Cited by 718
de Olmos, J. S., Hardy, H., & Heimer, L. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901810202 · Cited by 712
Flagged first, then by citations
Research works printed but not linked: 12
- Burton H., 1983, Somatosensory Integration in the Thalamus, 17
- Cechetto D. F., 1985, Organization of visceral sensory neurons in the insular cortex in the rat, Fed. Proc., 44, 1028
- Cechetto D. F., 1985, Relationship of visceral afferents and limbic connections in the insular cortex in the rat, Soc. Neurosci. Abstr., 11, 827
- Dell P., 1952, Correlations entre le systeme vegetatif et le systeme de la vie de relations. Mesencephale, diencephale et cortex cerebral, J. Physiol. (Paris), 44, 471
- Dell P., 1951, Projections thalamiques corticales et cerebelleuses des afferences viscerales vagales, C. R. Soc. Biol. (Paris), 145, 1084
- Emmers R., 1966, Separate cortical receiving areas for gustatory and tongue tactile afferents in the rat, Anat. Rec., 154, 460
- Kaada B. R., 1951, Somato‐motor, autonomic and electrocorticographic responses to electrical stimulation of ‘rhinencephalic’ and other structures in primates, cat and dog, Acta Physiol. Scand. [Suppl.], 83, 1
- Mraovitch S., 1982, Direct projections to autonomic centers of forebrain and brain stem from a cortical vasopressor area in rat, Soc. Neurosci. Abstr., 8, 77
- Norgren R., 1984, Handbook of Physiology—The Nervous System III, 1087
- Ranieri F., 1973, Splanchnic afferents arising from gastro‐intestinal and peritoneal mechanoreceptors, Exp. Brain Res., 16, 291
- Roberts T. S., 1963, I Insular and opercular cortex and its thalamic projection in Macaca mulatta, Schweiz. Arch. Neurol. Neurochir. Psychiatr., 92, 1
- Rose M., 1928, Die inselrinde des menschen und der tiere, J. Psychol. Neurol. (Leipzig), 37, 467
Cited by
Sorted by citations
Items 501–600 of 697
Yokota, T., Eguchi, K., & Hiraba, K. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq126 · Cited by 15
Cortical and Subcortical Projections from Granular Insular Cortex Receiving Orofacial Proprioception
Tsutsumi, Y., Tachibana, Y., Sato, F., Furuta, T., Ohara, H., Tomita, A., Fujita, M., Moritani, M., & Yoshida, A. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.07.047 · Cited by 15
Trifunovic, R., & Reilly, S. (2002) · Brain Research Bulletin · doi:10.1016/s0361-9230(02)00766-9 · Cited by 15
Hanamori, T. (2005) · Brain Research · doi:10.1016/j.brainres.2005.02.034 · Cited by 15
Functional brain mapping in patients with chronic back pain shows age-related differences
Baran, T. M., Lin, F. V., & Geha, P. (2021) · Pain · doi:10.1097/j.pain.0000000000002534 · Cited by 13
Nausea-induced suppression of feeding is mediated by central amygdala Dlk1-expressing neurons
Ding, W., Weltzien, H., Peters, C., & Klein, R. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.113990 · Cited by 14
Morphology and connectivity of parabrachial and cortical inputs to gustatory thalamus in rats
Holtz, S. L., Fu, A., Loflin, W., Corson, J. A., & Erişir, A. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23673 · Cited by 14
A capital role for the brain’s insula in the diverse fibromyalgia-associated symptoms
Paepe, B. D., Smet, J., Baeken, C., Oosterwijck, J. V., & Meeus, M. (2020) · Medical Hypotheses · doi:10.1016/j.mehy.2020.110077 · Cited by 15
Columnar organization of mechanoreceptive neurons in the cortical taste area in the rat
Wang, X., & Ogawa, H. (2002) · Experimental Brain Research · doi:10.1007/s00221-002-1228-0 · Cited by 14
Hanamori, T., Kunitake, T., Kato, K., & Kannan, H. (1997) · Chemical Senses · doi:10.1093/chemse/22.4.399 · Cited by 14
Saleh, T. M., Connell, B. J., & Allen, G. V. (1999) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1999.276.6.r1780 · Cited by 14
Cardiac Manifestations of Acute Neurological Lesions
Ko, N., & Zaroff, J. G. (2008) · Elsevier eBooks · doi:10.1016/b978-044306707-5.50013-4 · Cited by 14
Hayama, T., & Ogawa, H. (2001) · Neuroscience Letters · doi:10.1016/s0304-3940(01)01707-4 · Cited by 14
Ichiyama, R. M., Waldrop, T. G., & Iwamoto, G. A. (2004) · Brain Research · doi:10.1016/j.brainres.2004.02.034 · Cited by 14
Cortical unit responses to chemical stimulation of the oral cavity in the rat
Kosar, E., & Schwartz, G. J. (1990) · Brain Research · doi:10.1016/0006-8993(90)90459-o · Cited by 14
Harrigan, T., Bureau, Y. R. J., Persinger, M. A., & Parker, G. H. (1994) · Life Sciences · doi:10.1016/0024-3205(94)90156-2 · Cited by 14
Adachi, K., Fujita, S., Yoshida, A., Sakagami, H., Koshikawa, N., & Kobayashi, M. (2012) · The Journal of Comparative Neurology · doi:10.1002/cne.23246 · Cited by 13
Pritchard, T. C. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374236-0.10033-1 · Cited by 12
Pehl, Wendl, Kaess, & Pfeiffer (1998) · Alimentary Pharmacology & Therapeutics · doi:10.1046/j.1365-2036.1998.00398.x · Cited by 13
Kim, Y. W., Kim, H. S., & An, Y. (2013) · Chinese Medical Journal · doi:10.3760/cma.j.issn.0366-6999.20121243 · Cited by 13
El lado negativo de las emociones: la adicción a drogas de abuso
Abarca, M. C., Cerić, F., & Torrealba, F. (2008) · Revista de Neurología · doi:10.33588/rn.4709.2008259 · Cited by 13
Central Taste Anatomy and Physiology of Rodents and Primates
Pritchard, T. C., & Lorenzo, P. M. D. (2015) · Wiley eBooks · doi:10.1002/9781118971758.ch32 · Cited by 13
King, M. S. (2018) · Brain Research · doi:10.1016/j.brainres.2018.01.018 · Cited by 12
Animal Models of Gastrointestinal Problems in Parkinson's Disease
Greene, J. G. (2011) · Journal of Parkinson s Disease · doi:10.3233/jpd-2011-11033 · Cited by 13
Mao, L., Cho, Y. K., & Li, C. (2008) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00802.2007 · Cited by 12
Cortical Determinants of Goal-Directed Behavior
Coutureau, É., & Parkes, S. L. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812098-9.00008-5 · Cited by 12
Neuropathology and Cardiovascular Regulation
Cechetto, D. F. (2000) · Humana Press eBooks · doi:10.1007/978-1-59259-713-0_4 · Cited by 12
Self-citationYoshimura, H., Kato, N., Sugai, T., Segami, N., & Onoda, N. (2003) · Developmental Brain Research · doi:10.1016/s0165-3806(03)00160-3 · Cited by 12
Saleh, T. M. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00979-7 · Cited by 12
Saper, C. B., Loewy, A. D., & Swanson, L. W. (2016) · Brain Research · doi:10.1016/j.brainres.2016.01.010 · Cited by 12
Self-citationBaker, J. R., & Kimpinski, K. (2019) · The Cerebellum · doi:10.1007/s12311-019-01076-8 · Cited by 11
Feng, N., Gao, M. J., Wu, J., Yang, G., Piao, R., & Liu, P. (2021) · Quantitative Imaging in Medicine and Surgery · doi:10.21037/qims-20-1103 · Cited by 11
Binks, A. P. (2022) · Handbook of clinical neurology · doi:10.1016/b978-0-323-91534-2.00008-4 · Cited by 13
The role of the insular cortex in the control of visceral functions
Александров, В. Г., & Aleksandrova, N. P. (2015) · Human Physiology · doi:10.1134/s0362119715050023 · Cited by 11
Acute stress-induced increases in thalamic CRH mRNA are blocked by repeated stress exposure
Hsu, D. T., Lombardo, K. A., Bakshi, V. P., Balachandran, J. S., Roseboom, P. H., & Kalin, N. H. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02807-4 · Cited by 11
Medial parabrachial nucleus neurons modulate d-fenfluramine-induced anorexia through 5HT2C receptors
Trifunovic, R., & Reilly, S. (2005) · Brain Research · doi:10.1016/j.brainres.2005.10.092 · Cited by 11
Hanamori, T. (2009) · Brain Research · doi:10.1016/j.brainres.2009.04.024 · Cited by 11
Butcher, K., & Cechetto, D. F. (1998) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-76-7-8-737 · Cited by 11
Self-citationGarcía, R., Zafra, M. A., & Puerto, A. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.11.008 · Cited by 10
Taste-potentiated odor aversion learning in rats with lesions of the insular cortex
Lin, J.-Y., Roman, C., & Reilly, S. (2009) · Brain Research · doi:10.1016/j.brainres.2009.08.051 · Cited by 10
The Architecture of Somatosensory Cortex
Zilles, K., & Palomero‐Gallagher, N. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.24128-x · Cited by 11
Haghir, H., Kuckertz, A., Zhao, L., Hami, J., & Palomero‐Gallagher, N. (2023) · Brain Structure and Function · doi:10.1007/s00429-023-02654-7 · Cited by 10
Lin, J.-Y., Roman, C., & Reilly, S. (2009) · Brain Research · doi:10.1016/j.brainres.2009.07.033 · Cited by 10
Yamada, D., Koppensteiner, P., Odagiri, S., Eguchi, M., Yamaguchi, S., Yamada, T., Katagiri, H., Wada, K., & Sekiguchi, M. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00366 · Cited by 10
Bernanke, A., Burnette, E. M., Murphy, J., Hernandez, N., Zimmerman, S., Walker, Q. D., Wander, R., Sette, S., Reavis, Z. W., Francis, R., et al. (2021) · PLoS ONE · doi:10.1371/journal.pone.0260577 · Cited by 10
Baroreceptor activity impacts upon controlled but not automatic distractor processing
Pramme, L., Schächinger, H., & Frings, C. (2015) · Biological Psychology · doi:10.1016/j.biopsycho.2015.06.006 · Cited by 11
Uezono, S., Yamada, Y., Kato, T., Abe, H., & Yamamoto, N. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23675 · Cited by 10
Morganti, J. M., Odegard, A. K., & King, M. S. (2007) · Chemical Senses · doi:10.1093/chemse/bjm023 · Cited by 10
Lu, C., Chang, F., & Hsieh, J. (2005) · Gastroenterology · doi:10.1053/j.gastro.2005.03.057 · Cited by 10
The insula mediates the effects of glucocorticoids in anxiety
Bahamonde, T., Quintana-Donoso, D., Linsambarth, S., Jerez-Baraona, J. M., Peña, F., Tamburini, G., Verdugo, D. A., Lemunao-Inostroza, Y., Ogaz, F., Díaz-Galarce, R., et al. (2023) · Neuropharmacology · doi:10.1016/j.neuropharm.2023.109620 · Cited by 9
Belém-Filho, I. J. A., de Godoy, A. C. V., Busnardo, C., Frias, A. T., Zangrossi, H., Borges, B. D. B., Herval, A. C. F., Corrêa, F. M. D. A., Crestani, C. C., & Alves, F. H. F. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110404 · Cited by 9
Autonomic Functions of the Prefrontal Cortex
Александров, В. Г., Кокурина, Т. Н., Рыбакова, Г. И., & Tumanova, T. S. (2021) · Human Physiology · doi:10.1134/s0362119721050029 · Cited by 9
Brain-wide connectivity map of mouse thermosensory cortices
Bokiniec, P., Whitmire, C. J., Leva, T. M., & Poulet, J. F. A. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac386 · Cited by 9
Stereotyped goal-directed manifold dynamics in the insular cortex
Talpir, I., & Livneh, Y. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114027 · Cited by 10
Information processing in brainstem bitter taste-relaying neurons defined by genetic tracing
Sugita, M., Yamamoto, K., Hirono, C., & Shiba, Y. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.06.032 · Cited by 9
Toyoda, H. (2018) · Journal of Oral Biosciences · doi:10.1016/j.job.2018.12.001 · Cited by 9
The Mysterious Island: Insula and Its Dual Function in Sleep and Wakefulness
Levichkina, E. V., Busygina, I. I., Pigareva, M. L., & Pigarev, I. N. (2021) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2020.592660 · Cited by 9
Role of the lateral hypothalamus in submandibular salivary secretion during feeding in rats
Matsuo, R., Kobashi, M., Mitoh, Y., & Fujita, M. (2014) · Brain Research · doi:10.1016/j.brainres.2014.11.026 · Cited by 9
Changes in properties of neuronal responses in two cortical taste areas in rats of various ages
Ogawa, H., Hasegawa, K., Ohgushi, M., & Murayama, N. (1994) · Neuroscience Research · doi:10.1016/0168-0102(94)90082-5 · Cited by 9
Callosal connections of the cortical taste area in rats
Hayama, T., & Ogawa, H. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02941-9 · Cited by 9
Binstock, T. (2001) · Medical Hypotheses · doi:10.1054/mehy.2001.1440 · Cited by 9
Tsutsumi, Y., Mizuno, Y., Haque, T., Sato, F., Furuta, T., Oka, A., Moritani, M., Bae, Y. C., Yamashiro, T., Tachibana, Y., et al. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02228-5 · Cited by 8
Corticocortical connections of the rostral forelimb area in rats: a quantitative tract-tracing study
Urban, E. T. R., Hudson, H. M., Li, Y., Nishibe, M., Barbay, S., Guggenmos, D. J., & Nudo, R. J. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad530 · Cited by 8
Neuroanatomy of the nociceptive system: From nociceptors to brain networks
Motzkin, J. C., Basbaum, A. I., & Crowther, A. (2024) · International review of neurobiology · doi:10.1016/bs.irn.2024.10.008 · Cited by 11
Tolerance to repeated rewarding electrical stimulation of the insular cortex
Hurtado, M. M., García, R., & Puerto, A. (2015) · Brain Research · doi:10.1016/j.brainres.2015.11.001 · Cited by 8
Koza, Y., Aydın, N., Aydın, M. D., Koza, E. A., Bayram, E., Atalay, C., Altaş, E., Kürşad, H., & Kabalar, M. E. (2019) · World Neurosurgery · doi:10.1016/j.wneu.2019.06.005 · Cited by 8
CB1 cannabinoid receptor-mediated plasticity of GABAergic synapses in the mouse insular cortex
Toyoda, H. (2020) · Scientific Reports · doi:10.1038/s41598-020-64236-5 · Cited by 8
Ogawa, H. (2000) · Chemical Senses · doi:10.1093/chemse/25.4.351 · Cited by 8
Bortel, A. B., Longo, D., Guzman, P. D., Dubeau, F., Biagini, G., & Avoli, M. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07225.x · Cited by 8
Tiège, X. D., Legros, B., Beeck, M. O. D., Goldman, S., & Bogaert, P. V. (2008) · Journal of Neurosurgery Pediatrics · doi:10.3171/ped.2008.2.11.377 · Cited by 8
Künzle, H., Radtke‐Schuller, S., & von Stebut, B. (2002) · Brain Research Bulletin · doi:10.1016/s0361-9230(01)00784-5 · Cited by 8
Parabrachial nucleus neurons providing axons to both the thalamus and the spinal cord in the rat
Li, J., & Mizuno, N. (1997) · Brain Research · doi:10.1016/s0006-8993(96)01213-9 · Cited by 8
Schachter, S. C. (2004) · doi:10.1002/9780470752463.ch73 · Cited by 8
A role of CB1R in inducing θ-rhythm coordination between the gustatory and gastrointestinal insula
Kang, Y., Satō, H., Saito, M., Yin, D. X., Park, S. K., Oh, S. B., Bae, Y. C., & Toyoda, H. (2016) · Scientific Reports · doi:10.1038/srep32529 · Cited by 7
Oura, K., Akasaka, H., Ishizuka, N., Sato, Y., Kudo, M., Yamaguchi, T., Oura, M. Y., Itabashi, R., & Maeda, T. (2023) · PLoS ONE · doi:10.1371/journal.pone.0280661 · Cited by 7
Crossed Connections From Insular Cortex to the Contralateral Thalamus
Adeyelu, T. T., Gandhi, T., & Lee, C. C. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.710925 · Cited by 7
Plasticity in the Interoceptive System
Torrealba, F., Madrid, C., Contreras, M., & Gómez, K. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-62817-2_4 · Cited by 8
Hashimoto, T., Kitajo, K., Kajihara, T., Ueno, K., Suzuki, C., Asamizuya, T., & Iriki, A. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2014.12.057 · Cited by 14
Perirhinal cortex supports both taste neophobia and its attenuation
Ramos, J. M. J. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107264 · Cited by 7
Kadohisa, M., Shinohara, M., & Ogawa, H. (2000) · Experimental Brain Research · doi:10.1007/s002210000525 · Cited by 7
Ogawa, H., Ohgushi, M., Hasegawa, K., & Murayama, N. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90057-p · Cited by 7
Palchaudhuri, S., Lin, B.-X., Osypenko, D., Wu, J., Kochubey, O., & Schneggenburger, R. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115320 · Cited by 7
Organization of the central pain pathways
(2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511770579.003 · Cited by 6
Tracheal occlusion conditioning causes stress, anxiety and neural state changes in conscious rats
Pate, K. M., & Davenport, P. W. (2012) · Experimental Physiology · doi:10.1113/expphysiol.2012.068924 · Cited by 6
Behavioral Disassociation of Perceived Sweet Taste Intensity and Hedonically Positive Palatability
Fonseca, E., Sandoval-Herrera, V., Simon, S. A., & Gutiérrez, R. (2020) · eNeuro · doi:10.1523/eneuro.0268-20.2020 · Cited by 6
Medioventral part of the posterior thalamus in the mouse
Motomura, K., & Kosaka, T. (2011) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2011.07.004 · Cited by 6
Troponinerhöhung und EKG-Veränderungen bei Schlaganfall und Subarachnoidalblutung
Liman, T., & Endres, M. (2008) · Der Nervenarzt · doi:10.1007/s00115-008-2541-z · Cited by 6
Conditioned Taste Aversion Learning
Parker, L. A. (2014) · Wiley eBooks · doi:10.1002/9781118468135.ch5 · Cited by 7
The Paraventricular Hypothalamus: A Sorting Center for Visceral and Somatic Pain
Sun, L., & Duan, S. (2025) · Neuroscience Bulletin · doi:10.1007/s12264-025-01353-z · Cited by 5
Mechanisms of orofacial sensory processing in the rat insular cortex
Kobayashi, M. (2018) · Journal of Oral Biosciences · doi:10.1016/j.job.2018.04.002 · Cited by 5
Transcortical descending pathways through granular insular cortex conveying orofacial proprioception
Ikenoue, E., Akhter, F., Tsutsumi, Y., Sato, F., Ohara, H., Uchino, K., Furuta, T., Tachibana, Y., & Yoshida, A. (2018) · Brain Research · doi:10.1016/j.brainres.2018.02.033 · Cited by 5
Involvement of group II metabotropic glutamate receptors in stress-induced behavioural sensitization
Stam, R., de Lange, R. P. J., Graveland, H., Verhave, P. S., & Wiegant, V. M. (2007) · Psychopharmacology · doi:10.1007/s00213-006-0659-x · Cited by 5
Hanamori, T. (2003) · Chemical Senses · doi:10.1093/chemse/bjg064 · Cited by 5
Sucrose intensity coding and decision-making in rat gustatory corticesPreprint
Fonseca, E., de Lafuente, V., Simon, S. A., & Gutiérrez, R. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/391342 · Cited by 5
Brainstem sensing of multiple body signals during food consumptionPreprint
Essner, R. A., Ruda, K., Choh, H. J., Kucukdereli, H., Amsalem, O., Edelhaus, J., Grødem, S., Lensjø, K. K., Lever, T. E., & Andermann, M. L. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.28.651046 · Cited by 5
Tallon‐Baudry, C., Loescher, M., & Clément, A. (2026) · Trends in Neurosciences · doi:10.1016/j.tins.2026.01.005 · Cited by 8
Mathew, J., Galacgac, J., Smith, M. L., Du, P., & Çakmak, Y. Ö. (2025) · Neurogastroenterology & Motility · doi:10.1111/nmo.15009 · Cited by 4
Kida, I., Enmi, J., Iida, H., & Yoshioka, Y. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.01.017 · Cited by 4
Kaufman, J. A., & Jones, T. B. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-39632-5.00019-0 · Cited by 4
Ascending Pathways: Anatomy and Physiology
Lima, D. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-805408-6.00177-9 · Cited by 4
Metadata
- Authors
- Cechetto, D. F., & Saper, C. B.
- Affiliations
- University of Chicago (US)
- ORCID
- Saper, Clifford B.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1987-08
- Volume
- 262
- Issue
- 1
- Pages
- 27-45
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2086146474
- Semantic Scholar
- 582241cc5e047d61d8f2273fbee158378c2139c5
- Cited by
- 703
- References
- 86
- Citations by year
- 2026: 15 · 2025: 10 · 2024: 12 · 2023: 15 · 2022: 17 · 2021: 26 · 2020: 29 · 2019: 14 · 2018: 14 · 2017: 18 · 2016: 21 · 2015: 29 · 2014: 28 · 2013: 18 · 2012: 22
- FWCI
- 8.19
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- American Heart Association
- National Institute of Neurological Disorders and Stroke (NS18669, NS-22835)
- Topics
- Life Sciences › Neuroscience › Sensory Systems › Ion Channels and Receptors
- Life Sciences › Neuroscience › Cognitive Neuroscience › Tactile and Sensory Interactions
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Multisensory perception and integration
- Keywords
- insula, ventrobasal thalamus, taste cortex, parabrachial nucleus, gastric mechanoreceptors, arterial chemoreceptors, baroreceptors, topographic projection, retrograde tracing, axonal transport
- MeSH terms
- Action Potentials, Afferent Pathways, Animals, Brain Mapping, Brain Stem, Cerebral Cortex, Fluorescent Dyes, Horseradish Peroxidase, Male, Neurons, Afferent, Sensory Receptor Cells, Respiration, Thalamic Nuclei, Viscera, Wheat Germ Agglutinins, Wheat Germ Agglutinin-Horseradish Peroxidase Conjugate, 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