Literature DB >> 11751472

Gustatory projections from the nucleus of the solitary tract to the parabrachial nuclei in the hamster.

Young K Cho1, Cheng-Shu Li, David V Smith.   

Abstract

Taste-responsive cells in the nucleus of the solitary tract (NST) either project to the parabrachial nuclei (PbN) of the pons, through which taste information is transmitted to forebrain gustatory nuclei, or give rise to axons terminating locally within the medulla. Numerous anatomical studies clearly demonstrate a substantial projection from the rostral NST, where most taste-responsive cells are found, to the PbN. In contrast, previous electrophysiological studies in the rat have shown that only a small proportion (21-45%) of taste-responsive NST cells are antidromically activated from the PbN, suggesting that less than half the cells recorded from the NST are actually involved in forebrain processing of gustatory information. In the present experiment we investigated the projections from the NST to the PbN electrophysiologically in urethane anesthetized hamsters. Responses of 101 single neurons in the rostral NST were recorded extracellularly following lingual stimulation with 32 mM NaCl, sucrose and quinine hydrochloride (QHCl) and 3.2 mM citric acid. The taste-responsive region of the PbN was identified electrophysiologically and stimulated with a concentric bipolar electrode to antidromically activate each NST cell. Of the 101 taste-responsive NST cells, 81 (80.2%) were antidromically activated from the ipsilateral PbN. The mean firing rates to taste stimulation and the spontaneous activity of these projection neurons were significantly greater than those of non-projecting cells. Every sucrose-best neuron in the sample projected to the PbN. The mean conduction velocity of the 23 QHCl-best neurons was significantly lower than that of the other 58 PbN projection neurons, suggesting that the most QHCl-responsive cells are a subset of smaller neurons. These data show that a large majority of NST cells responsive to taste stimulation of the anterior tongue project to the gustatory subdivisions of the PbN and that these cells have the most robust responses to gustatory stimulation.

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Year:  2002        PMID: 11751472     DOI: 10.1093/chemse/27.1.81

Source DB:  PubMed          Journal:  Chem Senses        ISSN: 0379-864X            Impact factor:   3.160


  18 in total

1.  Glucagon-like Peptide-1 receptor signaling in the lateral parabrachial nucleus contributes to the control of food intake and motivation to feed.

Authors:  Amber L Alhadeff; John-Paul Baird; Jennifer C Swick; Matthew R Hayes; Harvey J Grill
Journal:  Neuropsychopharmacology       Date:  2014-03-26       Impact factor: 7.853

2.  Characteristics of rostral solitary tract nucleus neurons with identified afferent connections that project to the parabrachial nucleus in rats.

Authors:  Takeshi Suwabe; Robert M Bradley
Journal:  J Neurophysiol       Date:  2009-05-13       Impact factor: 2.714

3.  Gustatory neural circuitry in the hamster brain stem.

Authors:  Young K Cho; Cheng-Shu Li
Journal:  J Neurophysiol       Date:  2008-06-04       Impact factor: 2.714

4.  Activation of delta-opioid receptors reduces excitatory input to putative gustatory cells within the nucleus of the solitary tract.

Authors:  Mingyan Zhu; Young K Cho; Cheng-Shu Li
Journal:  J Neurophysiol       Date:  2008-11-19       Impact factor: 2.714

5.  Elucidation of the anatomy of a satiety network: Focus on connectivity of the parabrachial nucleus in the adult rat.

Authors:  Györgyi Zséli; Barbara Vida; Anais Martinez; Ronald M Lechan; Arshad M Khan; Csaba Fekete
Journal:  J Comp Neurol       Date:  2016-05-05       Impact factor: 3.215

6.  Licking and gaping elicited by microstimulation of the nucleus of the solitary tract.

Authors:  Nicole R Kinzeler; Susan P Travers
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2008-05-21       Impact factor: 3.619

7.  Descending projections from the nucleus accumbens shell excite activity of taste-responsive neurons in the nucleus of the solitary tract in the hamster.

Authors:  Cheng-Shu Li; Da-Peng Lu; Young K Cho
Journal:  J Neurophysiol       Date:  2015-03-04       Impact factor: 2.714

8.  A computational analysis of signal fidelity in the rostral nucleus of the solitary tract.

Authors:  Alison Boxwell; David Terman; Marion Frank; Yuchio Yanagawa; Joseph B Travers
Journal:  J Neurophysiol       Date:  2017-11-01       Impact factor: 2.714

9.  Endogenous central amygdala mu-opioid receptor signaling promotes sodium appetite in mice.

Authors:  Craig M Smith; Lesley L Walker; Tanawan Leeboonngam; Michael J McKinley; Derek A Denton; Andrew J Lawrence
Journal:  Proc Natl Acad Sci U S A       Date:  2016-11-14       Impact factor: 11.205

10.  Cocaine- and amphetamine-regulated transcript peptide immunoreactivity in the brain of the CCK-1 receptor deficient obese OLETF rat.

Authors:  Hajnalka Abraham; Mihai Covasa; Andras Hajnal
Journal:  Exp Brain Res       Date:  2009-06-17       Impact factor: 1.972

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