Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Randomized Controlled Trial
. 2012 Apr;220(3):559-64.
doi: 10.1007/s00213-011-2503-1. Epub 2011 Sep 30.

Depot naltrexone decreases rewarding properties of sugar in patients with opioid dependence

Affiliations
Randomized Controlled Trial

Depot naltrexone decreases rewarding properties of sugar in patients with opioid dependence

Daniel D Langleben et al. Psychopharmacology (Berl). 2012 Apr.

Abstract

Background: Opioid neurotransmission mediates hedonic value of sweet tastants; their intake may be exaggerated by the consumption of exogenous opioids (e.g., opioid dependence). Sweet Taste Test (STT) is a validated quantitative instrument assessing taste perception and hedonic features of sugar (sucrose) using a randomized and double-blind administration at five different sucrose concentrations ranging from 0.05 to 0.83 M.

Methods: The STT and cue-induced craving procedure were administered to opioid-dependent patients (n = 15) before and 1 week after the injection of a long-acting depot naltrexone (XRNT) preparation.

Results: Analyses of covariance, employing sucrose concentration and its perceived taste as covariates, showed that XRNT therapy significantly reduced the self-reported hedonic and motivational characteristics of sucrose. Greater reductions in both these characteristics were associated with more diminution in the cue-induced opioid craving.

Conclusions: Opioid antagonism in opioid-dependent subjects leads to a smaller sweet taste reward, which, in turn, may be proportional to decreased opioid craving. These pilot results support the heuristic value of the STT as a potential marker of the XRNT treatment response and call for further inquiry into potential clinical applications of the test.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Examples of images used in the cue-induced craving procedure. The subjects visually processed images of heroin preparation or injection (a and c) and images of housework and office work (b and d), presented in a fixed and pseudorandom order. The two stimuli classes were matched for luminosity and semantic content. All images had uniform black background and none contained human faces (see the Text).
Figure 2
Figure 2
Subjective self-rating for the perceived taste of the drink (−5: very bitter; +5 very sweet) along with liking the taste of the drink (−5: not at all; +5: very much) and wanting to have more of the same drink (−5: not at all; +5: very much). The data were obtained pre- and on XRNT pharmacotherapy. Results across the three sampling points were averaged and expressed as mean ± standard deviation.

Similar articles

Cited by

References

    1. Arbisi PA, Billington CJ, Levine AS. The effect of naltrexone on taste detection and recognition threshold. Appetite. 1999;32:241–9. - PubMed
    1. Berridge KC. The debate over dopamine’s role in reward: the case for incentive salience. Psychopharmacology (Berl) 2007;191:391–431. - PubMed
    1. Berridge KC, Robinson TE. Parsing reward. Trends in Neurosciences. 2003;26:507–13. - PubMed
    1. Berridge KC, Robinson TE, Aldridge JW. Dissecting components of reward: ‘liking’, ‘wanting’, and learning. Curr Opin Pharmacol. 2009;9:65–73. - PMC - PubMed
    1. Berthoud HR. Neural systems controlling food intake and energy balance in the modern world. Current Opinion in Clinical Nutrition and Metabolic Care. 2003;6:615–20. - PubMed

Publication types

MeSH terms