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1.
Brain Res ; 1714: 99-110, 2019 07 01.
Article in English | MEDLINE | ID: mdl-30807736

ABSTRACT

This study investigated neural projections from the parabrachial nucleus (PBN), a gustatory and visceral processing area in the brainstem, to the ventral tegmental area (VTA) in the midbrain. The VTA contains a large population of dopaminergic neurons that have been shown to play a role in reward processing. Anterograde neural tracing methods were first used to confirm that a robust projection from the caudal PBN terminates in the dorsal VTA; this projection was larger on the contralateral side. In the next experiment, we combined dual retrograde tracing from the VTA and the gustatory ventral posteromedial thalamus (VPMpc) with taste-evoked Fos protein expression, which labels activated neurons. Mice were stimulated through an intraoral cannula with sucrose, quinine, or water, and PBN sections were processed for immunofluorescent detection of Fos and retrograde tracers. The distribution of tracer-labeled PBN neurons demonstrated that the populations of cells projecting to the VTA or VPMpc are largely independent. Quantification of cells double labeled for Fos and either tracer demonstrated that sucrose and quinine were effective in activating both pathways. These results indicate that information about both appetitive and aversive tastes is delivered to a key midbrain reward interface via direct projections from the PBN.


Subject(s)
Parabrachial Nucleus/metabolism , Taste/physiology , Ventral Tegmental Area/metabolism , Animals , Dopaminergic Neurons/metabolism , Female , Male , Mice , Mice, Inbred C57BL , Neural Pathways/physiology , Neurites/metabolism , Neurons/metabolism , Parabrachial Nucleus/physiology , Quinine/metabolism , Reward , Sugars/metabolism , Ventral Thalamic Nuclei/metabolism
2.
Chem Senses ; 40(5): 295-303, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25820205

ABSTRACT

Previous electrophysiological investigation shows that combinations of compounds classified by humans as umami-tasting, such as glutamate salts and 5'-ribonucleotides, elicit synergistic responses in neurons throughout the rodent taste system and produce a pattern that resembles responses to sweet compounds. The current study tested the hypothesis that a synergistic mixture of monopotassium glutamate (MPG) and inositol monophosphate (IMP) possesses perceptual similarity to sucrose in mice. We estimated behavioral similarity among these tastants and the individual umami compounds using a series of conditioned taste aversion (CTA) tests, a procedure that measures whether a CTA formed to one stimulus generalizes to another. Our primary finding was that a CTA to a synergistic mixture of MPG + IMP generalizes to sucrose, and vice-versa. This indicates umami synergistic mixtures are perceived as having a sweet, or at least sucrose-like, taste to mice. Considering other recent studies, our data argue strongly in favor of multiple receptor mechanisms for umami detection, and complexity in taste perception models for rodents.


Subject(s)
Glutamic Acid , Inositol Phosphates , Taste/physiology , Animals , Female , Glutamic Acid/administration & dosage , Inositol Phosphates/administration & dosage , Male , Mice , Mice, Inbred C57BL , Sucrose/administration & dosage
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