JN AJP: Gastrointestinal and Liver Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 78: 920-938, 1997;
0022-3077/97 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Halsell, C. B.
Right arrow Articles by Travers, S. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Halsell, C. B.
Right arrow Articles by Travers, S. P.

The Journal of Neurophysiology Vol. 78 No. 2 August 1997, pp. 920-938
Copyright ©1997 The American Physiological Society

Anterior and Posterior Oral Cavity Responsive Neurons Are Differentially Distributed Among Parabrachial Subnuclei in Rat

Christopher B. Halsell and Susan P. Travers

Section of Oral Biology, The Ohio State University, Columbus, Ohio 43210

Halsell, Christopher B. and Susan P. Travers. Anterior and posterior oral cavity responsive neurons are differentially distributed among parabrachial subnuclei in rat. J. Neurophysiol. 78: 920-938, 1997. The responses of single parabrachial nucleus (PBN) neurons were recorded extracellularly to characterize their sensitivity to stimulation of individual gustatory receptor subpopulations (G neurons, n = 75) or mechanical stimulation of defined oral regions (M neurons, n = 54) then localized to morphologically defined PBN subdivisions. Convergence from separate oral regions onto single neurons occurred frequently for both G and M neurons, but converging influences were more potent when they arose from nearby locations confined to the anterior (AO) or posterior oral cavity (PO). A greater number of G neurons responded optimally to stimulation of AO than to PO receptor subpopulations, and these AO-best G neurons had higher spontaneous and evoked response rates but were less likely to receive convergent input than PO-best G neurons. In contrast, proportions, response rates, and convergence patterns of AO- and PO-best M neurons were more comparable. The differential sensitivity of taste receptor subpopulations was reflected in PBN responses. AO stimulation with NaCl elicited larger responses than PO stimulation; the converse was true for QHCl stimulation. Within the AO, NaCl elicited a larger response when applied to the anterior tongue than to the nasoincisor duct. Hierarchical cluster analysis of chemosensitive response profiles suggested two groups of PBN G neurons. One group was composed of neurons optimally responsive to NaCl (N cluster); the other to HCl (H cluster). Most N- and H-cluster neurons were AO-best. Although they were more heterogenous, all but one of the remaining G neurons were unique in responding best or second-best to quinine and so were designated as quinine sensitive (Q+). Twice as many Q+ neurons were PO- compared with AO-best. M neurons were scattered across PBN subdivisions, but G neurons were concentrated in two pairs of subdivisions. The central medial and ventral lateral subdivisions contained both G and M neurons but were dominated by AO-best N-cluster G neurons. The distribution of G neurons in these subdivisions appeared similar to distributions in most previous studies of PBN gustatory neurons. In contrast to earlier studies, however, the external medial and external lateral-inner subdivisions also contained G neurons, intermingled with a comparable population of M neurons. Unlike cells in the central medial and ventral lateral subnuclei, nearly every neuron in the external subnuclei was PO best, and only one was an N-cluster cell. In conclusion, the present study supports a functional distinction between sensory input from the AO and PO at the pontine level, which may represent an organizing principle throughout the gustatory neuraxis. Furthermore, two morphologically distinct pontine regions containing orosensory neurons are described.




This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
T. Suwabe and R. M. Bradley
Characteristics of Rostral Solitary Tract Nucleus Neurons With Identified Afferent Connections That Project to the Parabrachial Nucleus in Rats
J Neurophysiol, July 1, 2009; 102(1): 546 - 555.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
L. C. Geran and S. P. Travers
Bitter-Responsive Gustatory Neurons in the Rat Parabrachial Nucleus
J Neurophysiol, March 1, 2009; 101(3): 1598 - 1612.
[Abstract] [Full Text] [PDF]


Home page
Chem SensesHome page
J. W. Biondolillo, L. A. Williams, and M. S. King
Blocking Glutamate Receptors in the Waist Area of the Parabrachial Nucleus Decreases Taste Reactivity Behaviors in Conscious Rats
Chem Senses, March 1, 2009; 34(3): 221 - 230.
[Abstract] [Full Text] [PDF]


Home page
Chem SensesHome page
K. Hashimoto, K. Obata, and H. Ogawa
Characterization of Parabrachial Subnuclei in Mice with Regard to Salt Tastants: Possible Independence of Taste Relay from Visceral Processing
Chem Senses, March 1, 2009; 34(3): 253 - 267.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
N. R. Kinzeler and S. P. Travers
Licking and gaping elicited by microstimulation of the nucleus of the solitary tract
Am J Physiol Regulatory Integrative Comp Physiol, August 1, 2008; 295(2): R436 - R448.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
C. T. King, M. Garcea, D. S. Stolzenberg, and A. C. Spector
Experimentally cross-wired lingual taste nerves can restore normal unconditioned gaping behavior in response to quinine stimulation
Am J Physiol Regulatory Integrative Comp Physiol, March 1, 2008; 294(3): R738 - R747.
[Abstract] [Full Text] [PDF]


Home page
Chem SensesHome page
J. M. Morganti, A. K. Odegard, and M. S. King
The Number and Location of Fos-like Immunoreactive Neurons in the Central Gustatory System Following Electrical Stimulation of the Parabrachial Nucleus in Conscious Rats
Chem Senses, July 1, 2007; 32(6): 543 - 555.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
L. C. Geran and S. P. Travers
Single Neurons in the Nucleus of the Solitary Tract Respond Selectively to Bitter Taste Stimuli
J Neurophysiol, November 1, 2006; 96(5): 2513 - 2527.
[Abstract] [Full Text] [PDF]


Home page
Behav Cogn Neurosci RevHome page
A. C. Spector and S. P. Travers
The representation of taste quality in the Mammalian nervous system.
Behav Cogn Neurosci Rev, September 1, 2005; 4(3): 143 - 191.
[Abstract] [PDF]


Home page
J. Neurophysiol.Home page
J. V. Verhagen, B. K. Giza, and T. R. Scott
Responses to Taste Stimulation in the Ventroposteromedial Nucleus of the Thalamus in Rats
J Neurophysiol, January 1, 2003; 89(1): 265 - 275.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
S. P. Travers
Quinine and citric acid elicit distinctive Fos-like immunoreactivity in the rat nucleus of the solitary tract
Am J Physiol Regulatory Integrative Comp Physiol, June 1, 2002; 282(6): R1798 - R1810.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
J.-P. Baird, J. B. Travers, and S. P. Travers
Parametric analysis of gastric distension responses in the parabrachial nucleus
Am J Physiol Regulatory Integrative Comp Physiol, November 1, 2001; 281(5): R1568 - R1580.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
J.-P. Baird, S. P. Travers, and J. B. Travers
Integration of gastric distension and gustatory responses in the parabrachial nucleus
Am J Physiol Regulatory Integrative Comp Physiol, November 1, 2001; 281(5): R1581 - R1593.
[Abstract] [Full Text] [PDF]


Home page
Chem SensesHome page
B. Cerf-Ducastel, P.-F. Van de Moortele, P. MacLeod, D. Le Bihan, and A. Faurion
Interaction of Gustatory and Lingual Somatosensory Perceptions at the Cortical Level in the Human: a Functional Magnetic Resonance Imaging Study
Chem Senses, May 1, 2001; 26(4): 371 - 383.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
Z. Chen, S. P. Travers, and J. B. Travers
Muscimol infusions in the brain stem reticular formation reversibly block ingestion in the awake rat
Am J Physiol Regulatory Integrative Comp Physiol, April 1, 2001; 280(4): R1085 - R1094.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
A. Blomqvist, E.-T. Zhang, and A. D. Craig
Cytoarchitectonic and immunohistochemical characterization of a specific pain and temperature relay, the posterior portion of the ventral medial nucleus, in the human thalamus
Brain, March 1, 2000; 123(3): 601 - 619.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
J. B. Travers, K. Urbanek, and H. J. Grill
Fos-like immunoreactivity in the brain stem following oral quinine stimulation in decerebrate rats
Am J Physiol Regulatory Integrative Comp Physiol, August 1, 1999; 277(2): R384 - R394.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
S. J. St. John and A. C. Spector
Behavioral Discrimination between Quinine and KCl Is Dependent on Input from the Seventh Cranial Nerve: Implications for the Functional Roles of the Gustatory Nerves in Rats
J. Neurosci., June 1, 1998; 18(11): 4353 - 4362.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online