2609005319
  • Open Access
  • Review

Stress-Driven Brain Remodeling in Opioid Use Disorder: Toward a Neuroprogressive Model

  • Filippo Della Rocca 1,2,   
  • Icro Maremmani 1,3,*,   
  • Manuel Glauco Carbone 1,4 and 
  • Angelo Giovanni Icro Maremmani 1,3

Received: 15 June 2026 | Revised: 15 September 2026 | Accepted: 30 September 2026 | Published: 26 October 2026

Abstract

Background: Opioid use disorder (OUD) is classically understood through reward dysregulation, opponent processes, and allostatic adaptation, but these models only partly account for the persistent cognitive, affective, and stress-regulatory abnormalities observed in some individuals with long-standing OUD. Methods: This Perspective integrates human evidence from neuroendocrinology, neuroimaging, and neurocognitive research with mechanistic findings from preclinical opioid-exposure and withdrawal models. Throughout the revised framework, direct evidence in humans is distinguished from cross-species mechanistic inference. Results: Repeated opioid exposure induces neuroadaptations that initially compensate for persistent pharmacological perturbation. When exposure is prolonged and accompanied by recurrent intoxication-withdrawal cycling, these adaptations may become increasingly maladaptive and interact with repeated stress-system destabilization. Human studies document abnormalities in hypothalamic-pituitary-adrenal (HPA) axis regulation, brain structure and connectivity, and executive-cognitive functioning in OUD, whereas preclinical studies provide plausible mechanisms involving glucocorticoid and extrahypothalamic corticotropin-releasing factor (CRF) signaling, noradrenergic and dynorphin systems, synaptic plasticity, neuroimmune activation, and cellular stress. We propose a staged continuum from neuroadaptation to maladaptive brain remodeling and, potentially, neuroprogression. At the advanced end of this continuum, we describe a provisional neuroprogressive phenotype characterized by persistent multidomain dysfunction in stress regulation, cognitive-executive processing, affective regulation, and behavioral control beyond acute intoxication or withdrawal in a vulnerable subset of individuals with OUD. Conclusions: The proposed neuroprogressive model defines a testable hypothesis in which cumulative opioid exposure and recurrent withdrawal-related stress burden may contribute to persistent loss of adaptive capacity. Treatment-related stabilization and partial recovery are incorporated into the model, but disease-modifying effects of opioid agonist treatment remain to be demonstrated prospectively. Longitudinal multimodal studies are required to establish the existence, boundaries, prevalence, reversibility, and clinical utility of the proposed phenotype.

Graphical Abstract

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Della Rocca, F.; Maremmani, I.; Carbone, M. G.; Maremmani, A. G. I. Stress-Driven Brain Remodeling in Opioid Use Disorder: Toward a Neuroprogressive Model. Clinical Neuropsychopharmacology and Addiction 2026, 2 (4), 16. https://doi.org/10.53941/cna.2026.100016.
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