- Gut-derived succinate associates with compulsive-like behaviour and distinguishes OCD patients from controls (AUC 0.73), correlating with prefrontal cortex activity.
- Succinate disrupts dmPFC glutamatergic neurons via dual pathways: microglial SUCNR1 engagement and vagal afferent signalling mediated by 5-HT4 receptors.
- Pharmacological modulation of succinate metabolism, including succinate dehydrogenase inhibition, ameliorates compulsive-like behaviour in Hoxb8-/- OCD-model mice and offers druggable targets.
Adv Sci (Weinh). 2026 Sep 27:e77836. doi: 10.1002/advs.77836. Online ahead of print.
ABSTRACT
Emerging evidence indicates that gut microbiota influences host physiology and behavior through the microbiota-gut-brain axis, potentially contributing to the pathogenesis of obsessive-compulsive disorder (OCD). Our preliminary research demonstrated that mice colonized with fecal microbiota from OCD patients developed compulsive-like behaviors, associated with a significant increase in the microbial metabolite succinate. However, the mechanisms linking succinate to compulsive-like behavior remain to be fully elucidated. Here, we demonstrate that succinate is associated with significant compulsive-like behaviors. Succinate is associated with disruptions of glutamatergic neurons within the dorsal medial prefrontal cortex (dmPFC), and we characterize dual pathways linked to the behavioral abnormality: both by dmPFC microglial engagement via the succinate cognate receptor SUCNR1, and by gut-to brain signaling conveyed through vagal afferents and the 5-HT4 receptor. Pharmacological modulation of the succinate metabolism pathway through succinate dehydrogenase inhibition ameliorates compulsive-like behavior in Hoxb8-/- OCD-model mice. Circulating succinate levels significantly distinguish OCD patients from healthy controls with an AUC of 0.73, and correlate with prefrontal cortex activity on functional imaging. Collectively, our study delineates a gut-brain axis implicating succinate in central nervous system dysregulation associated compulsive-like behavior, elucidates novel immunometabolism and neural circuit mechanisms underlying OCD pathogenesis, and identifies druggable targets for potential precise interventions.
PMID:42801575 | DOI:10.1002/advs.77836
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