# Effects of opioid blockade on taste perception across smoking status: an analysis of detection thresholds, intensity, and pleasantness

**Authors:** Justin J. Anker, Mustafa al’Absi

PMC · DOI: 10.1007/s00702-025-02937-9 · Journal of Neural Transmission · 2025-09-13

## TL;DR

This study explores how blocking opioids with naltrexone affects taste perception differently in smokers and non-smokers.

## Contribution

The study reveals nicotine's interaction with the opioid system affects taste intensity but not pleasure in smokers.

## Key findings

- Naltrexone reduced sweet, salty, and sour taste intensity in ad-lib smokers but not in non-smokers or withdrawal smokers.
- Taste pleasantness ratings were unaffected by naltrexone across all groups.
- No differences in sweet or bitter detection thresholds were observed between drug and smoking groups.

## Abstract

The endogenous opioid system (EOS) is a neuromodulator of taste, and nicotine can modify both EOS signaling and taste perception. Understanding how nicotine interacts with EOS-driven taste perception is important for dietary guidance and smoking-cessation strategies. In this study, we tested whether opioid blockade with naltrexone vs. placebo differentially affects taste thresholds, intensity, and pleasantness in non-smokers, ad-lib smokers, and smokers in short-term withdrawal. A mixed factorial design was used; with drug (placebo vs. naltrexone) as a within-subject factor and smoking status (non-smoker, ad-lib smoker, withdrawal/abstaining) as a between-subjects factor. Each participant attended two sessions, receiving a placebo in one session and naltrexone in the other (counterbalanced). During each session participants completed (1) a sweet and bitter detection threshold test, and (2) suprathreshold intensity and pleasantness ratings for sweet, salty, sour, umami, and water. Results indicated that neither sweet nor bitter detection thresholds differed by drug or smoking groups. Among ad-lib smokers, however, suprathreshold intensity for sweet, salty, and sour tastes was significantly decreased under naltrexone vs. placebo, whereas pleasantness ratings remained unchanged. No drug effect on either intensity or pleasantness was observed in non-smokers and withdrawal smokers. The study’s results indicate a nicotine-related interaction with the EOS that reduces sensory gain but does not impact hedonic evaluation regarding taste perception

## Linked entities

- **Chemicals:** naltrexone (PubChem CID 5360515), nicotine (PubChem CID 942)

## Full-text entities

- **Diseases:** taste or (MESH:D013651), enhanced (MESH:C564835), oral health disorders (OMIM:603663)
- **Chemicals:** quinine (MESH:D011803), nicotine (MESH:D009538), citric acid (MESH:D019343), Lib (-), dopamine (MESH:D004298), cortisol (MESH:D006854), Naltrexone (MESH:D009271), salt (MESH:D012492), Water (MESH:D014867), NaCl (MESH:D012965), sucrose (MESH:D013395), MSG (MESH:D012970), cotinine (MESH:D003367)
- **Species:** Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097]

## Full text

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## Figures

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## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12535516/full.md

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Source: https://tomesphere.com/paper/PMC12535516