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Updated: Jun 29, 2025

Assessing Pupil-linked Changes in Locus Coeruleus-mediated Arousal Elicited by Trigeminal Stimulation
Published on: November 26, 2019
Comparison of trigeminal lateralization with differing stimulants.
Tiffany Chen1, Nicolas S Poupore1, Michael C Shih1
1Department of Otolaryngology-Head and Neck Surgery Medical University of South Carolina Charleston South Carolina USA.
Trigeminal sensitivity varies across different transient receptor potential (TRP) receptors, as stimulant responses did not correlate. This suggests TRP receptor dysfunction may cause distinct patient symptoms, requiring further research.
Area of Science:
- Neuroscience
- Sensory Science
- Ophthalmology
Background:
- Trigeminal nerve stimulants activate specific receptors, influencing sensory perception.
- Variability in trigeminal sensitivity across different transient receptor potential (TRP) receptors is not well understood.
- Dysfunction of TRP receptors may lead to diverse patient symptoms.
Purpose of the Study:
- To investigate trigeminal sensitivity across different TRP receptors.
- To determine if trigeminal sensitivity is consistent across various stimulants.
- To explore correlations between trigeminal sensitivity, olfaction, and patient-reported outcomes.
Main Methods:
- Prospective cohort study with 50 participants across the olfactory spectrum.
- Trigeminal lateralization testing using eucalyptol, isothiocyanate (mustard oil), and acetic acid (vinegar).
- Olfaction testing with Sniffin' Sticks and measurement of patient-reported outcome measures (PROMs).
Main Results:
- Mean trigeminal lateralization scores: eucalyptol (16.18), mustard oil (14.94), vinegar (15.28).
- Eucalyptol correlated with olfactory threshold scores; acetic acid correlated with PROMs.
- No significant correlation found between lateralization scores of different stimulants or with age.
Conclusions:
- Trigeminal sensitivity is receptor-specific, with no cross-correlation observed between tested stimulants.
- Findings suggest that sensitivity to one TRP receptor type may not predict sensitivity to others.
- Further research with TRPV1 and TRPA1 agonists is recommended to validate these findings.
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