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A premammillary lateral hypothalamic nuclear complex responds to hedonic but not aversive tastes in the male rat

https://doi.org/10.1007/s00429-015-1038-3
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Organization of projections from the basomedial nucleus of the amygdala: A PHAL study in the rat
inferredcites →https://doi.org/10.1002/(sici)1096-9861(19970707)383:3<245::aid-cne1>3.0.co;2-3openalex-snapshot
Organization of efferent projections from the parabrachial area to the hypothalamus: aPhaseolus vulgaris-leucoagglutinin study in the rat
inferredcites →https://doi.org/10.1002/cne.11036openalex-snapshot
Axonal projections from the parasubthalamic nucleus
inferredcites →https://doi.org/10.1002/cne.20618openalex-snapshot
Calcitonin gene-related peptide-containing pathways in the rat forebrain
inferredcites →https://doi.org/10.1002/cne.22789openalex-snapshot
The lateral hypothalamic parvalbumin‐immunoreactive (PV1) nucleus in rodents
inferredcites →https://doi.org/10.1002/cne.23145openalex-snapshot
Neuroanatomy of melanocortin‐4 receptor pathway in the lateral hypothalamic area
inferredcites →https://doi.org/10.1002/cne.902770303openalex-snapshot
Efferent connections of the substantia innominata in the rat
inferredcites →https://doi.org/10.1002/cne.903030303openalex-snapshot
Autonomic responses and efferent pathways from the insular cortex in the rat
inferredcites →https://doi.org/10.1002/cne.903060309openalex-snapshot
Olfactory projections to the hypothalamus
inferredcites →https://doi.org/10.1002/cne.903160304openalex-snapshot
Distribution of substance P‐immunoreactive elements in the preoptic area and the hypothalamus of the rat
inferredcites →https://doi.org/10.1002/cne.903310305openalex-snapshot
Comparative localization of mRNAs encoding two forms of glutamic acid decarboxylase with nonradioactive in situ hybridization methods
inferredcites →https://doi.org/10.1016/0006-8993(89)90805-6openalex-snapshot
Response properties of lateral hypothalamic neurons during ingestive behavior with special reference to licking of various taste solutions
inferredcites →https://doi.org/10.1016/0166-2236(87)90017-8openalex-snapshot
The rat brain in stereotaxic coordinates (2nd edn)
inferredcites →https://doi.org/10.1016/0166-2236(93)90187-qopenalex-snapshot
Brain maps: structure of the rat brain
inferredcites →https://doi.org/10.1016/0301-0082(93)90012-hopenalex-snapshot
Anatomy and physiology of central galanin-containing pathways
inferredcites →https://doi.org/10.1016/0304-3940(92)90035-6openalex-snapshot
Immunoreactivities for antisera to three putative neuropeptides of the rat melanin-concentrating hormone precursor are coexpressed in neurons of the rat lateral dorsal hypothalamus
inferredcites →https://doi.org/10.1016/0306-4522(90)90091-hopenalex-snapshot
Calbindin D-28k and parvalbumin in the rat nervous system
inferredcites →https://doi.org/10.1016/0891-0618(95)00083-6openalex-snapshot
Cajal's nucleus of the stria medullaris: Characterization by in situ hybridization and immunohistochemistry for enkephalin
inferredcites →https://doi.org/10.1016/b978-0-12-369497-3.10008-1openalex-snapshot
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inferredcites →https://doi.org/10.1016/c2009-0-63235-9openalex-snapshot
The Rat Brain in Stereotaxic Coordinates
inferredcites →https://doi.org/10.1016/j.brainres.2011.05.026openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.cmet.2011.06.016openalex-snapshot
Leptin Action via Neurotensin Neurons Controls Orexin, the Mesolimbic Dopamine System and Energy Balance
inferredcites →https://doi.org/10.1016/j.jchemneu.2011.05.003openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.neulet.2005.06.066openalex-snapshot
Comparison of melanin-concentrating hormone and hypocretin/orexin mRNA expression patterns in a new parceling scheme of the lateral hypothalamic zone
inferredcites →https://doi.org/10.1016/j.neulet.2009.10.047openalex-snapshot
Comparison of melanin-concentrating hormone and hypocretin/orexin peptide expression patterns in a current parceling scheme of the lateral hypothalamic zone
inferredcites →https://doi.org/10.1016/j.neulet.2014.02.028openalex-snapshot
Coaxiality of Foxb1- and parvalbumin-expressing neurons in the lateral hypothalamic PV1-nucleus
inferredcites →https://doi.org/10.1016/j.neuroscience.2004.10.020openalex-snapshot
Functional mapping of the prosencephalic systems involved in organizing predatory behavior in rats
inferredcites →https://doi.org/10.1016/j.neuroscience.2014.11.026openalex-snapshot
Appetitive associative learning recruits a distinct network with cortical, striatal, and hypothalamic regions
inferredcites →https://doi.org/10.1016/s0006-8993(99)01336-0openalex-snapshot
Distribution of orexin neurons in the adult rat brain
inferredcites →https://doi.org/10.1016/s0092-8674(00)80949-6openalex-snapshot
Orexins and Orexin Receptors: A Family of Hypothalamic Neuropeptides and G Protein-Coupled Receptors that Regulate Feeding Behavior
inferredcites →https://doi.org/10.1016/s0165-0173(97)00008-8openalex-snapshot
Chemoarchitecture of the rat lateral septal nucleus 1Published on the World Wide Web on 2 June 1997. 1
inferredcites →https://doi.org/10.1016/s0306-4522(03)00146-5openalex-snapshot
Diencephalic neurons producing melanin-concentrating hormone are influenced by local and multiple extra-hypothalamic tachykininergic projections through the neurokinin 3 receptor
inferredcites →https://doi.org/10.1016/s0361-9230(03)00170-9openalex-snapshot
Role of the central amygdaloid nucleus in shaping the discharge of gustatory neurons in the rat parabrachial nucleus
inferredcites →https://doi.org/10.1016/s0896-6273(02)00969-8openalex-snapshot
The Need to Feed
inferredcites →https://doi.org/10.1038/380243a0openalex-snapshot
A role for melanin-concentrating hormone in the central regulation of feeding behaviour
inferredcites →https://doi.org/10.1038/nature12596openalex-snapshot
Genetic identification of a neural circuit that suppresses appetite
inferredcites →https://doi.org/10.1038/nn.2739openalex-snapshot
AGRP neurons are sufficient to orchestrate feeding behavior rapidly and without training
inferredcites →https://doi.org/10.1046/j.0953-816x.2001.01640.xopenalex-snapshot
Projections from the nociceptive area of the central nucleus of the amygdala to the forebrain: a PHA‐L study in the rat
inferredcites →https://doi.org/10.1073/pnas.84.3.881openalex-snapshot
Three rat preprotachykinin mRNAs encode the neuropeptides substance P and neurokinin A.
inferredcites →https://doi.org/10.1093/cercor/bhn253openalex-snapshot
Proteomic Analysis Illuminates a Novel Structural Definition of the Claustrum and Insula
inferredcites →https://doi.org/10.1111/j.1460-9568.2010.07241.xopenalex-snapshot
The histaminergic tuberomammillary nucleus is critical for motivated arousal
inferredcites →https://doi.org/10.1111/j.1471-4159.2004.02776.xopenalex-snapshot
Characterization of subpopulations of neurons producing melanin‐concentrating hormone in the rat ventral diencephalon
inferredcites →https://doi.org/10.1126/science.1241812openalex-snapshot
The Inhibitory Circuit Architecture of the Lateral Hypothalamus Orchestrates Feeding
inferredcites →https://doi.org/10.1126/science.272.5267.1484openalex-snapshot
Structural Evidence for Functional Domains in the Rat Hippocampus
inferredcites →https://doi.org/10.1152/ajpendo.00643.2012openalex-snapshot
Leptin receptor neurons in the mouse hypothalamus are colocalized with the neuropeptide galanin and mediate anorexigenic leptin action
inferredcites →https://doi.org/10.1523/jneurosci.1902-05.2005openalex-snapshot
The Ventral Pallidum and Hedonic Reward: Neurochemical Maps of Sucrose “Liking” and Food Intake
inferredcites →https://doi.org/10.1523/jneurosci.22-19-08748.2002openalex-snapshot
Amygdalo-Hypothalamic Circuit Allows Learned Cues to Override Satiety and Promote Eating
inferredcites →https://doi.org/10.1523/jneurosci.3729-14.2015openalex-snapshot
Parabrachial Calcitonin Gene-Related Peptide Neurons Mediate Conditioned Taste Aversion

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/cne.23853openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cne.24470openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00429-016-1353-3openalex-snapshot
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Parasubthalamic and calbindin nuclei in the posterior lateral hypothalamus are the major hypothalamic targets for projections from the central and anterior basomedial nuclei of the amygdala
inferred← citeshttps://doi.org/10.1007/s00429-017-1501-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jchemneu.2022.102089openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neulet.2023.137245openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neuropharm.2021.108906openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neuroscience.2019.03.045openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.physbeh.2023.114333openalex-snapshot
Dissection of the bed nucleus of the stria terminalis neuronal subtypes in feeding regulation
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2025.111250openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/nn.4623openalex-snapshot
Central amygdala circuits modulate food consumption through a positive-valence mechanism
inferred← citeshttps://doi.org/10.1038/s41380-024-02653-yopenalex-snapshot
The parasubthalamic nucleus refeeding ensemble delays feeding initiation and hastens water drinking
inferred← citeshttps://doi.org/10.1038/s41467-023-37797-yopenalex-snapshot
Parasubthalamic calretinin neurons modulate wakefulness associated with exploration in male mice
inferred← citeshttps://doi.org/10.1038/s41467-025-58144-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1073/pnas.2004914117openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/2023.01.28.525750openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/2024.06.22.600182openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/2024.09.29.615708openalex-snapshot
Topographic organization of bidirectional connections between the cingulate region (infralimbic area and anterior cingulate area, dorsal part) and the interbrain (diencephalon) of the adult male rat
inferred← citeshttps://doi.org/10.1523/eneuro.0116-21.2021openalex-snapshot
Understanding the Significance of the Hypothalamic Nature of the Subthalamic Nucleus
inferred← citeshttps://doi.org/10.3389/fncir.2021.768125openalex-snapshot
Whole Brain Mapping of Neurons Innervating Extraorbital Lacrimal Glands in Mice and Rats of Both Genders
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inferred← citeshttps://doi.org/10.70675/96430ef5z0268z4e14za024z45e7fa53eda6openalex-snapshot
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inferred← citeshttps://doi.org/10.7554/elife.104643openalex-snapshot
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inferred← citeshttps://doi.org/10.7554/elife.104643.1openalex-snapshot
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inferred← citeshttps://doi.org/10.7554/elife.75470openalex-snapshot
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