# Decreased Responsiveness to Chemical Itch in Old Mice

**Authors:** Qiaofeng Zhao, Mitsutoshi Tominaga, Sumika Toyama, Kotaro Honda, Eriko Komiya, Yayoi Kamata, Hang Ma, Kenji Takamori

PMC · DOI: 10.3390/cells14120889 · Cells · 2025-06-12

## TL;DR

Older mice show reduced sensitivity to chemical itch due to changes in nerve function and signaling molecules.

## Contribution

This study reveals age-related impairments in chemical itch perception through behavioral, cellular, and molecular analyses in mice.

## Key findings

- Old mice showed reduced scratching behavior after pruritogen injections.
- Neuronal responses to histamine and chloroquine were diminished in old mice.
- TRPV1 and Cav3.2 expression was reduced in dorsal root ganglia neurons of old mice.

## Abstract

Aging is associated with altered itch perception, potentially due to changes in neuronal function and pruriceptive signaling. The underlying mechanisms, however, remain unclear. We investigated age-related differences in itch sensitivity at behavioral, cellular, and molecular levels. Young and old mice were intradermally injected with various pruritogens, including small molecules (histamine, chloroquine, and serotonin) and peptides (BAM8–22, AY-NH2, and SLIGRL-NH2). Scratching behavior and mechanical itch sensitivity were assessed, and calcium imaging was used to evaluate sensory neuron responses in the dorsal root ganglia. Additionally, immunofluorescence staining was performed to analyze the expression of TRPV1 and Cav3.2. Old mice exhibited reduced scratching behavior following injections, and their neuronal responses to histamine and chloroquine were diminished. Although all treated groups showed increased mechanical alloknesis, the effect was less pronounced in old animals. The expression of TRPV1 and Cav3.2 was also reduced in dorsal root ganglia neurons of old mice. These findings suggest that aging impairs both functional responsiveness and molecular signaling in sensory neurons, contributing to reduced chemical itch sensitivity in aged individuals.

## Linked entities

- **Proteins:** TRPV1 (transient receptor potential cation channel subfamily V member 1), CACNA1H (calcium voltage-gated channel subunit alpha1 H)
- **Chemicals:** histamine (PubChem CID 774), chloroquine (PubChem CID 2719), serotonin (PubChem CID 5202), BAM8–22 (PubChem CID 16158367), AY-NH2 (PubChem CID 9987061), SLIGRL-NH2 (PubChem CID 9831050)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Cacna1h (calcium channel, voltage-dependent, T type, alpha 1H subunit) [NCBI Gene 58226] {aka Cav3.2, MNCb-1209, alpha13.2}, Trpv1 (transient receptor potential cation channel, subfamily V, member 1) [NCBI Gene 193034] {aka OTRPC1, TRPV1alpha, TRPV1beta, VR-1, Vr1}
- **Diseases:** itch (MESH:D011537)
- **Chemicals:** serotonin (MESH:D012701), AY-NH2 (-), chloroquine (MESH:D002738), calcium (MESH:D002118), histamine (MESH:D006632), BAM8-22 (MESH:C571042), SLIGRL-NH2 (MESH:C112356)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12190969/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12190969/full.md

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Source: https://tomesphere.com/paper/PMC12190969