# Mapping Fos-immunoreactive neurons activated by intra-oral infusion of quinine, sucrose or water throughout the brain of B6 mice

**Authors:** Michael S. King, Lianyi Lu, Max L. Fletcher, John D. Boughter

PMC · DOI: 10.1007/s00429-026-03095-8 · Brain Structure & Function · 2026-03-21

## TL;DR

This study maps brain regions in mice activated by bitter, sweet, or water taste stimuli, revealing distinct neural clusters for each.

## Contribution

The study identifies specific brain regions and clusters of neurons activated by quinine, sucrose, or water in mice.

## Key findings

- Quinine and sucrose activated more neurons than water in the parabrachial nucleus and amygdala.
- Quinine uniquely activated the central lateral PBN and parvocellular reticular formation.
- Cluster analysis revealed distinct neural populations responding to quinine, sucrose, or both.

## Abstract

Fos immunohistochemistry was used to identify neurons in taste-related brain areas throughout the B6 mouse brain activated by intra-oral (IO) infusion of 3.0 mM quinine hydrochloride (Q), 1.0 M sucrose (S) or filtered water (W). IO infusion of Q and S elicited more Fos-immunoreactive (Fos-IR) neurons than W in the central medial (CM) and dorsomedial (DM) subareas of the parabrachial nucleus (PBN) and the central medial (CeM) amygdala (ps < 0.05). Infusion of Q led to more Fos expression than W in the central lateral (CL) PBN and the parvocellular reticular formation (PCRT; ps < 0.05). The only area where IO infusion of Q and S elicited a different number of Fos-IR neurons was the PCRT which responded more to Q (p < 0.05). Cluster analysis of the number of Fos-IR neurons in all 29 taste-related nuclei and subareas examined revealed that populations of neurons distributed among these brain regions respond best to Q, S or both Q and S. Specifically, the Q-best cluster included more posterior structures like the nucleus of the solitary tract, RT and part of the PBN. The S-best cluster included more anterior structures like the bed nucleus of the stria terminalis, nucleus accumbens and orbitofrontal cortex. And, the cluster of areas that responded better to Q and S than W included the amygdala, gustatory and piriform cortices and a few PBN subareas. Therefore, the data suggest that collections of neurons among taste-responsive brain areas are important for distinguishing Q and S from water as well as identifying the specific tastant.

## Linked entities

- **Chemicals:** quinine hydrochloride (PubChem CID 91558), sucrose (PubChem CID 5988), water (PubChem CID 962)

## Full-text entities

- **Genes:** Fos (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 314322] {aka c-fos}, Calca (calcitonin/calcitonin-related polypeptide, alpha) [NCBI Gene 12310] {aka CA, CGRP-1, CGRP1, Calc, Calc1, Cgrp}, Satb2 (special AT-rich sequence binding protein 2) [NCBI Gene 212712] {aka BAP002, mKIAA1034}, Fos (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 14281] {aka D12Rfj1, c-fos, cFos}
- **Diseases:** bitter (MESH:D013651)
- **Chemicals:** 3, 3'-diaminobenzidine (MESH:D015100), Q (MESH:D005973), CV (-), silane (MESH:D012821), glycerol (MESH:D005990), cocaine (MESH:D003042), paraformaldehyde (MESH:C003043), DAB (MESH:C000469), quinine (MESH:D011803), H2O2 (MESH:D006861), PB (MESH:D007854), W (MESH:D014414), xylazine (MESH:D014991), phosphate (MESH:D010710), water (MESH:D014867), cresyl violet (MESH:C028911), dopamine (MESH:D004298), sugars (MESH:D000073893), NaCl (MESH:D012965), HCl (MESH:D006851), S (MESH:D013455), sucrose (MESH:D013395)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13005817/full.md

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Source: https://tomesphere.com/paper/PMC13005817