Striatal cue-reactivity and neurotransmitter function in gambling disorder

Bellmunt-Gil, Albert and Majuri, Joonas and Nummenmaa, Lauri and Helin, Semi and Forsback, Sarita and Rajander, Johan and Kaasinen, Valtteri and Joutsa, Juho (2025) Striatal cue-reactivity and neurotransmitter function in gambling disorder. JOURNAL OF BEHAVIORAL ADDICTIONS, 14 (2). pp. 997-1009. ISSN 2062-5871

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Abstract

Background Abnormal striatal cue reactivity is one of the neurobiological hallmarks of substance use disorders (SUDs). Cue reactivity is associated with relapse, prompting efforts to target its underlying mechanisms with therapeutic interventions. However, the neural correlates of cue reactivity in behavioral addictions, such as gambling disorder (GD), remain poorly understood. Here we investigated striatal cue reactivity and its associations with neurotransmitters in individuals with GD using multimodal neuroimaging. Methods Thirteen subjects with GD and 16 healthy controls (HC) underwent fMRI using a block-design consisting of three different types of visual stimuli: gambling-related, erotic, and neutral videos. The subjects also underwent brain PET imaging with three radiotracers to assess dopamine ([18F]FDOPA), opioid ([11C]carfentanil) and serotonin ([11C]MADAM) function. Results GD subjects showed a significantly greater BOLD response in the dorsal striatum compared to HC when viewing gambling-related versus neutral videos (pFWE<0.05). Enhanced cue-reactivity was specific to gambling, as there were no significant differences between the groups with natural reward cues (erotic vs. neutral videos). The dorsal and ventral striatum BOLD responses to gambling videos were coupled in HC (r = 0.7, p = 0.003) but not in GD (r = −0.1, p = 0.75; group difference p = 0.008). In GD, dorsal striatal BOLD response to gambling cues correlated with [11C]carfentanil, but not with [18F]FDOPA or [11C]MADAM, binding (r = 0.8, p < 0.001). Conclusions GD is characterized by increased gambling cue-induced activity in the dorsal striatum, which is linked to mu-opioid receptor availability. The findings highlight the potential role of the mu-opioid system in mediating cue-reactivity in behavioral addictions.

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