Cited by 589Regulation of Appetite and ObesityBiochemical Analysis and Sensing TechniquesNeurotransmitter Receptor Influence on Behavior

The DOI matches its Crossref record; 27 of the 28 references it cites were found in a registry or an index.

The taste reactivity test. II. Mimetic responses to gustatory stimuli in chronic thalamic and chronic decerebrate rats

Grill, Harvey J., Norgren, Ralph·1978·Brain Research

DOI 10.1016/0006-8993(78)90569-3

Open this paper in CoChat — free account

Abstract

The taste reactivity test described in the preceding paper was used to begin determining the capacity of brain stem structures to execute and regulate ingestive behavior. Both chronic thalamic and chronic decerebrate rat preparations were examined repeatedly, and their gustatory mimetic responses compared through frame-by-frame videotape analysis with the responses of neurologically normal controls. In response to orally injected taste stimuli, chronic decerebrate rats executed the same mimetic response components, and very similar response sequences observed in intact rats. In contrast, all taste stimuli elicited a quinine-like rejection sequence from chronic thalamic rats. In thalamic rats mimetic responses associated with ingestion were completely absent. Based on the similarities in the ingestion and rejection responses of decerebrate and intact rats, it appears that discriminative responses to taste result from integrative mechanisms complete within, or caudal to, the midbrain. Since decerebrate rats have the capacity to execute both ingestion and rejection response sequences, neural mechanisms rostral to the midbrain in some way suppress ingestion and/or releaser ejection responses in the thalamic preparation.

Integrity signals

Registry

Crossref · 10.1016/0006-8993(78)90569-3

Cites

27 of 27 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

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 Integrative Action of the Nervous System.
Sherrington, C. (1907) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-190734120-00021 · Cited by 4,136
The Integrative Action of the Nervous System
Smith, W. (1907) · Nature · doi:10.1038/076122a0 · Cited by 2,112
Adipsia and Aphagia after 6‐Hydroxydopamine Induced Degeneration of the Nigro‐striatal Dopamine System
Ungerstedt, U. (1971) · Acta Physiologica Scandinavica · doi:10.1111/j.1365-201x.1971.tb11001.x · Cited by 1,294
The taste reactivity test. I. Mimetic responses to gustatory stimuli in neurologically normal rats
Grill, H. J., & Norgren, R. (1978) · Brain Research · doi:10.1016/0006-8993(78)90568-1 · Cited by 1,220
Self-citation
Hypothalamic control of food intake in rats and cats.
Anand, B. K., & Brobeck, J. R. (1951) · PubMed · Cited by 1,197
The lateral hypothalamic syndrome: Recovery of feeding and drinking after lateral hypothalamic lesions.
Teitelbaum, P., & Epstein, A. N. (1962) · Psychological Review · doi:10.1037/h0039285 · Cited by 884
Animal Behaviour: A Synthesis of Ethology and Comparative Psychology
Cullen, J. M., & Hinde, R. A. (1968) · Journal of Animal Ecology · doi:10.2307/3093 · Cited by 846
Taste pathways to hypothalamus and amygdala
Norgren, R. (1976) · The Journal of Comparative Neurology · doi:10.1002/cne.901660103 · Cited by 761
Self-citation
Mechanism of the development of obesity in animals with hypothalamic lesions.
Brobeck, J. R. (1946) · Physiological Reviews · doi:10.1152/physrev.1946.26.4.541 · Cited by 488
A Golgi study of the descending medial forebrain bundle
Millhouse, O. E. (1969) · Brain Research · doi:10.1016/0006-8993(69)90161-9 · Cited by 345

Show all 28 references

Research works printed but not linked: 3

Bard, 1939, Central nervous mechanisms for emotional behavioral patterns in animals, Res. Publ. Ass. nerv. mes., 19, 190
Grill, 1975, Sucrose as an aversive stimulus, Neurosci. Abstr., 1, 525
Jackson, 1898, Relations of different divisions of the central nervous system to one another and to parts of the body, Lancet, 1, 79

Sorted by citations

Items 301–400 of 589

Pavlovian conditioning of the cephalic phase of gastric acid secretion in the rat
Weingarten, H. P., & Powley, T. L. (1981) · Physiology & Behavior · doi:10.1016/0031-9384(81)90260-2 · Cited by 21
Orbicularis oculi muscle activation during swallowing in humans
Erteki̇n, C., Eryaşar, G., Gürgör, N., Arıcı, Ş., Seçıl, Y., & Kurt, T. (2012) · Experimental Brain Research · doi:10.1007/s00221-012-3290-6 · Cited by 20
Unconditioned oromotor taste reactivity elicited by sucrose and quinine is unaffected by extensive bilateral damage to the gustatory zone of the insular cortex in rats
King, C. T., Hashimoto, K., Blonde, G. D., & Spector, A. C. (2014) · Brain Research · doi:10.1016/j.brainres.2014.12.035 · Cited by 20
Terminal field specificity of forebrain efferent axons to the pontine parabrachial nucleus and medullary reticular formation
Zhang, C., Kang, Y., & Lundy, R. F. (2010) · Brain Research · doi:10.1016/j.brainres.2010.10.086 · Cited by 20
Electrical stimulation of the insular cortex induces flavor-preferences in rats
Cubero, I., & Puerto, A. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02516-6 · Cited by 20
Preference and aversion for deterrent chemicals in two species of Peromyscus mouse
Glendinning, J. I. (1993) · Physiology & Behavior · doi:10.1016/0031-9384(93)90056-l · Cited by 20
Behavioral plasticity, serial order, and the motor program
MacKay, D. G. (1981) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00000625 · Cited by 20
Gustatory Neural Coding
Smith, D. V., & Scott, T. R. (2003) · CRC Press eBooks · doi:10.1201/9780203911457-40 · Cited by 20
Morphine inhibition of parabrachial taste units reversed by naloxone
Hermann, G. E., & Novin, D. (1980) · Brain Research Bulletin · doi:10.1016/0361-9230(80)90246-4 · Cited by 20
Development of Coordinated Movement: Dynamic, Relational and Multileveled Perspectives
Fentress, J. C. (1986) · Springer eBooks · doi:10.1007/978-94-009-4460-2_6 · Cited by 19
Energy Balance, Ingestive Behavior, and Reproductive Success
Schneider, J. E., & Watts, A. G. (2002) · Elsevier eBooks · doi:10.1016/b978-012532104-4/50009-3 · Cited by 18
Gustatory Pathways in Fish and Mammals
Whitehead, M. C., & Finger, T. E. (2008) · Elsevier eBooks · doi:10.1016/b978-012370880-9.00082-7 · Cited by 19
Hypoglossal motor nerve activity elicited by taste and thermal stimuli applied to the tongue in rats
Yamamoto, T., Fujiwara, T., Matsuo, R., & Kawamura, Y. (1982) · Brain Research · doi:10.1016/0006-8993(82)90773-9 · Cited by 19
Chorda tympani and vagus nerve convergence onto caudal brain stem neurons in the rat
Bereiter, D. A., Berthoud, H. R., & Jeanrenaud, B. (1981) · Brain Research Bulletin · doi:10.1016/0361-9230(81)90017-4 · Cited by 19
Conditioned activation of fetal behavior
Smotherman, W. P., & Robinson, S. R. (1991) · Physiology & Behavior · doi:10.1016/0031-9384(91)90500-n · Cited by 19
The Neuroscience of Pleasure. Focus on “Ventral Pallidum Firing Codes Hedonic Reward: When a Bad Taste Turns Good”
Wheeler, R. A., & Carelli, R. M. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00727.2006 · Cited by 18
Restoration of quinine‐stimulated fos‐immunoreactive neurons in the central nucleus of the amygdala and gustatory cortex following reinnervation or cross‐reinnervation of the lingual taste nerves in rats
King, C. T., Garcea, M., & Spector, A. C. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23546 · Cited by 18
A functionalistic approach to feeding.
Bolles, R. C. (1990) · American Psychological Association eBooks · doi:10.1037/10075-020 · Cited by 18
Gustatory functions of the nucleus tractus solitarius in the rabbit
Schwartzbaum, J. S., & Lorenzo, P. M. D. (1982) · Brain Research Bulletin · doi:10.1016/0361-9230(82)90061-2 · Cited by 18
Problems of concept and vocabulary in the anhedonia hypothesis
Neill, D. B. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00010542 · Cited by 18
The impact of a junk-food diet during development on ‘wanting’ and ‘liking’
Lesser, E. N., Arroyo-Ramirez, A., Mi, S. J., & Robinson, M. J. F. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.09.041 · Cited by 17
Genetic control of oromotor phenotypes: A survey of licking and ingestive behaviors in highly diverse strains of mice
John, S. J. S., Lu, L., Williams, R. W., Saputra, J. M., & Boughter, J. D. (2017) · Physiology & Behavior · doi:10.1016/j.physbeh.2017.04.007 · Cited by 17
Salt Appetite, and the Influence of Opioids
Smith, C. M., & Lawrence, A. J. (2017) · Neurochemical Research · doi:10.1007/s11064-017-2336-3 · Cited by 18
Archaeology of mind
Panksepp, J. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00013054 · Cited by 19
Central Taste Anatomy and Neurophysiology
Scott, T. R., & Rolls, E. T. (2003) · CRC Press eBooks · doi:10.1201/9780203911457.ch33 · Cited by 17
A search for the cortical gustatory area in the hamster
Yamamoto, T., & Kitamura, R. (1990) · Brain Research · doi:10.1016/0006-8993(90)91382-q · Cited by 17
THE VERTEBRATE PHYLOGENY, NEURAL CODE, AND INTEGRATIVE PROCESSES OF TASTE
Pfaffmann, C. (1978) · Elsevier eBooks · doi:10.1016/b978-0-12-161906-0.50008-9 · Cited by 17
Gustatory and olfactory contributions to alcohol consumption in rats
Morrow, N. S., Kiefer, S. W., & Metzler, C. W. (1993) · Alcohol · doi:10.1016/0741-8329(93)90003-7 · Cited by 17
DORSOMEDIAL HINDBRAIN PARTICIPATION IN CONTROL OF FOOD INTAKE
Ritter, R. C., & Edwards, G. L. (1986) · Elsevier eBooks · doi:10.1016/b978-0-12-589060-1.50010-9 · Cited by 17
Licking and gaping elicited by microstimulation of the nucleus of the solitary tract
Kinzeler, N. R., & Travers, S. P. (2008) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00189.2008 · Cited by 16
Sucrose and Non-nutritive Sweeteners Can Suppress the Bitterness of Vegetables Independent of PTC Taster Phenotype
Wilkie, L. M., Phillips, E. D. C., & Wadhera, D. (2013) · Chemosensory Perception · doi:10.1007/s12078-013-9151-2 · Cited by 16
Presence of TSH receptors in discrete areas of the hypothalamus and caudal brainstem with relevance for feeding controls—Support for functional significance
Burgos, J., Iresjö, B., Wärnåker, S., & Smedh, U. (2016) · Brain Research · doi:10.1016/j.brainres.2016.04.007 · Cited by 16
The behavioral function of dopamine
Beninger, R. J. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00010402 · Cited by 16
Towards a Neuroscience of Well-Being: Implications of Insights from Pleasure Research
Berridge, K. C., & Kringelbach, M. L. (2013) · Happiness studies book series · doi:10.1007/978-94-007-6609-9_7 · Cited by 16
The Neural Code and Integrative Processes of Taste
Smith, D. V., & Vogt, M. B. (1997) · Elsevier eBooks · doi:10.1016/b978-012161958-9/50003-8 · Cited by 16
Mechanisms of Chemosensory Transduction in Taste Cells
Akabas, M. H. (1990) · International review of neurobiology · doi:10.1016/s0074-7742(08)60585-1 · Cited by 16
CAUDAL BRAINSTEM CONTRIBUTIONS TO THE INTEGRATED NEURAL CONTROL OF ENERGY HOMEOSTASIS
Grill, H. J. (1986) · Elsevier eBooks · doi:10.1016/b978-0-12-589060-1.50009-2 · Cited by 16
Self-citation
Towards Modeling Anhedonia and Its Treatment in Zebrafish
de Abreu, M. S., Costa, F. V., Giacomini, A. C. V. V., Demin, K. A., Zabegalov, K. N., Maslov, G. O., Kositsyn, Y. M., Petersen, E. V., Strekalova, T., Rosemberg, D. B., et al. (2021) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyab092 · Cited by 20
μ-Opioid modulation in the rostral solitary nucleus and reticular formation alters taste reactivity: evidence for a suppressive effect on consummatory behavior
Kinzeler, N. R., & Travers, S. P. (2011) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00142.2011 · Cited by 15
Greater Superficial Petrosal Nerve Transection in Rats does not Change Unconditioned Licking Responses to Putatively Sweet Taste Stimuli
Jiang, E., Blonde, G. D., Garcea, M., & Spector, A. C. (2008) · Chemical Senses · doi:10.1093/chemse/bjn039 · Cited by 15
The ability of gustatory stimuli to modify the cardiac sympathetic and vagus nerve activities
Yonemura, K., Takei, M., Kunitake, T., & Ishiko, N. (1989) · Neuroscience Letters · doi:10.1016/0304-3940(89)90144-4 · Cited by 15
Behavioral effects of neuroleptics: Performance deficits, reward deficits or both?
Ettenberg, A. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00010414 · Cited by 15
Curt Richter: a life in the laboratory
Rozin, P., & Schulkin, J. (2005) · Choice Reviews Online · doi:10.5860/choice.43-1551 · Cited by 15
Differential Effects of Electrical Stimulation of the Central Amygdala and Lateral Hypothalamus on Fos-immunoreactive Neurons in the Gustatory Brainstem and Taste Reactivity Behaviors in Conscious Rats
Riley, C., & King, M. S. (2013) · Chemical Senses · doi:10.1093/chemse/bjt039 · Cited by 14
Heterogeneity of neuronal responses in the nucleus of the solitary tract suggests sensorimotor integration in the neural code for taste
Denman, A. J., Sammons, J. D., Victor, J. D., & Lorenzo, P. M. D. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00578.2018 · Cited by 14
Rat palatability, pharmacodynamics effect and bioavailability of mefenamic acid formulations utilizing hot-melt extrusion technology
Alshehri, S., Shakeel, F., Elzayat, E. M., Meanazel, O. T. A., Altamimi, M. A., Shazly, G. A., Kazi, M., Almutairy, B. K., Alsulays, B. B., Alshetaili, A., et al. (2019) · Drug Development and Industrial Pharmacy · doi:10.1080/03639045.2019.1645161 · Cited by 14
Effects of a glucagon-like peptide-1 analog on appetitive and consummatory behavior for rewarding and aversive gustatory stimuli in rats
Douton, J. E., Norgren, R., & Grigson, P. S. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.113279 · Cited by 14
Self-citation
Operant control of the pattern of licking in rats
Hernández-Mesa, N., Mamedov, Z., & Bureš, J. (1985) · Experimental Brain Research · doi:10.1007/bf00238959 · Cited by 14
Elimination of lordosis in decerebrate female rats: Observations from acute and chronic preparations
Kow, L., Grill, H. J., & Pfaff, D. W. (1978) · Physiology & Behavior · doi:10.1016/0031-9384(78)90069-0 · Cited by 14
Self-citation
Gustatory Control of Food Selection
Scott, T. R. (1990) · Handbook of behavioral neurobiology · doi:10.1007/978-1-4613-0577-4_10 · Cited by 14
Glucose-monitoring neurons in the mediodorsal prefrontal cortex
Nagy, B., Szabó, I., Papp, S., Takács, G., Szalay, C., & Karádi, Z. (2012) · Brain Research · doi:10.1016/j.brainres.2012.01.025 · Cited by 13
Applications of taste reactivity to the study of the neural-hormonal controls of ingestive behavior
Flynn, F. W. (1995) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(94)00025-v · Cited by 13
Reflex Topography in the Nucleus of the Solitary Tract
Travers, S. P. (2005) · Chemical Senses · doi:10.1093/chemse/bjh173 · Cited by 13
Once is too much: Early development of the opponent process in taste reactivity behavior is associated with later escalation of cocaine self-administration in rats
Colechio, E. M., Alexander, D. N., Imperio, C. G., Jackson, K., & Grigson, P. S. (2017) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2017.09.002 · Cited by 14
Effects of GABA on Acutely Isolated Neurons from the Gustatory Zone of the Rat Nucleus of the Solitary Tract
Du, J., & Bradley, R. M. (1998) · Chemical Senses · doi:10.1093/chemse/23.6.683 · Cited by 13
Processing information about flavour
Holley, A. (2006) · Elsevier eBooks · doi:10.1533/9781845691400.1.36 · Cited by 14
Oral habituation in rat pups is in the brainstem
Swithers, S. E., Mishu, K. R., & HALL, W. G. (1992) · Physiology & Behavior · doi:10.1016/0031-9384(92)90189-9 · Cited by 13
d-fenfluramine's effects on normal ingestion assessed with taste reactivity measures
Gray, R. W., & Cooper, S. J. (1996) · Physiology & Behavior · doi:10.1016/0031-9384(95)02177-9 · Cited by 13
Hunger and Energy Homeostasis
Woods, S. C., & Seeley, R. J. (2002) · Wiley eBooks · doi:10.1002/0471214426.pas0315 · Cited by 12
Neurolepsis: Anhedonia or blunting of emotional reactivity?
Rech, R. H. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00010578 · Cited by 13
Hedonic arousal, memory, and motivation
Katz, L. D. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0001044x · Cited by 13
LiCl-induced sickness modulates rat gustatory cortical responses
Stone, B. T., Lin, J.-Y., Mahmood, A., Sanford, A. J., & Katz, D. B. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001537 · Cited by 12
Temporal and qualitative dynamics of conditioned taste aversions in C57BL/6J and DBA/2J mice self-administering LiCl
Glatt, A. R., John, S. J. S., Lu, L., & Boughter, J. D. (2015) · Physiology & Behavior · doi:10.1016/j.physbeh.2015.10.033 · Cited by 12
Salt appetite: its neuroendocrine basis.
Stellar, E. (1993) · PubMed · Cited by 12
The Many Flavors of Temporal Coding in Gustatory Cortex
Katz, D. B. (2005) · Chemical Senses · doi:10.1093/chemse/bjh123 · Cited by 12
THE CENTRAL GUSTATORY AND VISCERAL AFFERENT SYSTEMS ARISING FROM THE NUCLEUS OF THE SOLITARY TRACT
Norgren, R. (1981) · Elsevier eBooks · doi:10.1016/b978-0-08-027337-2.50045-6 · Cited by 12
Self-citation
Physiological state tunes mesolimbic signaling: lessons from sodium appetite and inspiration from Randall R. Sakai
Fortin, S. M., & Roitman, M. F. (2017) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.11.021 · Cited by 11
Behavioral Analysis of Taste Function in Rodent Models
John, S. J. S., & Spector, A. C. (2008) · Elsevier eBooks · doi:10.1016/b978-012370880-9.00096-7 · Cited by 11
Subjective perception of cocaine reward in mice assessed by a single exposure place preference (sePP) paradigm
Runegaard, A. H., Jensen, K. L., Dencker, D., Wörtwein, G., & Gether, U. (2017) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2017.07.010 · Cited by 10
Neural Isolation of the Olfactory Bulbs Severely Impairs Taste-Guided Behavior to Normally Preferred, But Not Avoided, Stimuli
Inui‐Yamamoto, C., Blonde, G. D., Schmid, F., Mariotti, L., Campora, M., Inui, T., Schier, L. A., & Spector, A. C. (2020) · eNeuro · doi:10.1523/eneuro.0026-20.2020 · Cited by 11
Evaluation of Flavor Effects on Oral Nicotine Liking and/or Disliking Using the Taste Reactivity Test in Rats
Bağdaş, D., Rupprecht, L. E., Nunes, E. J., Schillinger, E. S., Immanuel, J. J., & Addy, N. (2021) · Nicotine & Tobacco Research · doi:10.1093/ntr/ntab241 · Cited by 11
Oral behaviour following forebrain ablations in Gallus Domesticus
Gentle, M. J. (1981) · Behavioural Processes · doi:10.1016/0376-6357(81)90030-9 · Cited by 11
Behavior Manifestations Indicative of Hedonics and Intensity in Chemosensory Experience
Steiner, J. (1994) · Springer eBooks · doi:10.1007/978-4-431-68355-1_110 · Cited by 11
The ontogeny of independent ingestion in mice: Or, why won't infant mice feed?
HALL, W. G., & Browde, J. A. (1986) · Developmental Psychobiology · doi:10.1002/dev.420190307 · Cited by 11
Motivational modulation of taste
Norgren, R., Grigson, P. S., Hajnal, A. S., & Lundy, R. F. (2003) · International Congress Series · doi:10.1016/s0531-5131(03)01064-1 · Cited by 11
Self-citation
Stimulation of Specific Regions of the Parabrachial Nucleus Elicits Ingestive Oromotor Behaviors in Conscious Rats.
Galvin, K. E., King, C. T., & King, M. S. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.1.163 · Cited by 11
Dopamine neurons, reward and behavior
German, D. C. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00010438 · Cited by 11
VMH Procainization abolishes cephalic phase insulin response
Berthoud, H. R., Bereiter, D. A., & Jeanrenaud, B. (1980) · Brain Research Bulletin · doi:10.1016/0361-9230(80)90241-5 · Cited by 11
Dopamine and the limits of behavioral reduction – or why aren't all schizophrenics fat and happy?
Katz, R. J. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00010451 · Cited by 11
Hypotheses of neuroleptic action: Levels of progress
Wise, R. A. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00010621 · Cited by 11
Intrinsic membrane properties of pre-oromotor neurons in the intermediate zone of the medullary reticular formation
Venugopal, S., Boulant, J. A., Chen, Z., & Travers, J. B. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.03.036 · Cited by 10
Tamoxifen produces conditioned taste avoidance in male rats: An analysis of microstructural licking patterns and taste reactivity
Fudge, M. A., Kavaliers, M., Baird, J.-P., & Ossenkopp, K. (2009) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.06.009 · Cited by 10
Emotion, Feelings and Hedonics in the Human Brain
Kringelbach, M. L. (2024) · Routledge eBooks · doi:10.4324/9781003579557-5 · Cited by 10
Overt Attention toward Appetitive Cues Enhances Their Subjective Value, Independent of Orbitofrontal Cortex Activity
McGinty, V. B. (2019) · eNeuro · doi:10.1523/eneuro.0230-19.2019 · Cited by 13
Peripheral taste responses in genetically hypertensive rats
Formaker, B. K., & Hill, D. L. (1990) · Physiology & Behavior · doi:10.1016/0031-9384(90)90376-f · Cited by 10
The Number and Location of Fos-like Immunoreactive Neurons in the Central Gustatory System Following Electrical Stimulation of the Parabrachial Nucleus in Conscious Rats
Morganti, J. M., Odegard, A. K., & King, M. S. (2007) · Chemical Senses · doi:10.1093/chemse/bjm023 · Cited by 10
Neonatal ablations of the gustatory neocortex in the rat: Taste aversion learning and taste reactivity.
Kiefer, S. W., Cabral, R. J., & García, J. (1984) · Behavioral Neuroscience · doi:10.1037//0735-7044.98.5.804 · Cited by 10
Criteria for ruling out sedation as an interpretation of neuroleptic effects
Freed, W. J., & Zec, R. F. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00010426 · Cited by 10
Impact of vanilla flavor on nicotine taste, choice, intake, and seeking behaviors
Bağdaş, D., Zepei, A. M., Harris, L., Minanov, K., Jimenez, J. L., & Addy, N. (2024) · Psychopharmacology · doi:10.1007/s00213-024-06630-9 · Cited by 9
Effects of high fructose corn syrup on ethanol self-administration in rats
Ayoub, S. M., Minhas, M., Lapointe, T., Limebeer, C. L., Parker, L. A., & Leri, F. (2020) · Alcohol · doi:10.1016/j.alcohol.2020.05.003 · Cited by 9
Taste reactivity alterations after streptozotocin microinjection into the mediodorsal prefrontal cortex
Nagy, B., Takács, G., Szabó, I., Lénárd, L., & Karádi, Z. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.06.029 · Cited by 9
Ingestion analgesia occurs when a bad taste turns good.
Foo, H., & Mason, P. (2011) · Behavioral Neuroscience · doi:10.1037/a0025542 · 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
Energy Partitioning, Ingestive Behavior, and Reproductive Success
Schneider, J. E., & Watts, A. G. (2009) · Elsevier eBooks · doi:10.1016/b978-008088783-8.00006-1 · Cited by 9
Brainstem mechanisms underlying variations in the occurrence of experimentally elicited rhythmic oral movements in the rat
Thexton, A. J., Griffiths, C., & McGarrick, J. D. (1982) · Archives of Oral Biology · doi:10.1016/0003-9969(82)90151-0 · Cited by 9
Neuroleptic-induced anhedonia: Some psychopharmacological implications
Soubrié, P. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00010608 · Cited by 9
Attention, dopamine, and schizophrenia
Solomon, P. R., & Crider, A. B. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00010591 · Cited by 9
The anhedonia hypothesis of neuroleptic drug action: Basic and clinical considerations
Nemeroff, C. B., & Luttinger, D. A. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00010554 · Cited by 9
Animal Models to Investigate the Impact of Flavors on Nicotine Addiction and Dependence
Bağdaş, D., Kebede, N., Zepei, A. M., Harris, L., Minanov, K., Picciotto, M. R., & Addy, N. (2022) · Current Neuropharmacology · doi:10.2174/1570159x20666220524120231 · Cited by 8
Changes in sucrose and quinine taste reactivity patterns in infant rat pups after exposure to the other tastant
Suárez, A. B., Ifrán, M. C., Pautassi, R. M., & Kamenetzky, G. (2017) · Appetite · doi:10.1016/j.appet.2017.03.040 · Cited by 8

Authors: Grill, H. J., & Norgren, R.
Affiliations: Rockefeller University (US)
ORCID: Grill, Harvey J.
Venue: Brain Research
Publisher: Elsevier BV
Published: 1978-03
Volume: 143
Issue: 2
Pages: 281-297
ISSN: 0006-8993 (ISSN-L)
DOI: 10.1016/0006-8993(78)90569-3
OpenAlex: W1989396341
Cited by: 588
References: 28
Citations by year: 2026: 3 · 2025: 15 · 2024: 4 · 2023: 4 · 2022: 6 · 2021: 9 · 2020: 12 · 2019: 14 · 2018: 7 · 2017: 5 · 2016: 16 · 2015: 17 · 2014: 18 · 2013: 11 · 2012: 15
FWCI: 11.50
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
www.elsevier.com/legal/tdmrep-license (tdm)
Locations: Brain Research (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
Health Sciences › Nursing › Nutrition and Dietetics › Biochemical Analysis and Sensing Techniques
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Keywords: taste reactivity, ingestion, taste aversion, thalamic lesions, decerebrate preparation, brainstem, midbrain, ingestive behavior, taste discrimination
MeSH terms: Animals, Decerebrate State, Dose-Response Relationship, Drug, Drinking Behavior, Hydrochloric Acid, Male, Methods, Mouth, Quinine, Sodium Chloride, Sucrose, Taste, Thalamus, Tongue, 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

The taste reactivity test. II. Mimetic responses to gustatory stimuli in chronic thalamic and chronic decerebrate rats

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks