Nociceptin receptor and ligand in Alzheimer's disease:Implications for psychiatric symptoms and circadianregulation

Abstract

BackgroundNociceptin (N/OFQ) and its receptor OPRL1 play crucial roles in emotional processing, reward-related behaviors, learning, and neurotransmitter regulation, but their involvement in Alzheimers disease (AD) pathology remains poorly understood. This study investigated possible relationships between prepronociceptin (PNOC) and OPRL1 expression and psychiatric symptoms in AD, utilizing Natural Language Processing (NLP) to assess Research Domain Criteria (RDoC) domains. MethodsPost-mortem brain tissue from the dorsal anterior cingulate gyrus (BA32) was analyzed in 61 donors across different Braak and Braak (B&B) stages. RNA expression of PNOC and OPRL1 was quantified and correlated with RDoC scores derived from medical records using NLP. Sex-stratified analyses, circadian rhythmicity analysis, and cell-type specific expression patterns were examined. ResultsBoth genes showed significant downregulation in AD cases (PNOC: p = 0.024; OPRL1: p < 0.001), with notable sex differences. Men displayed higher post-mortem PNOC (Cohens d = -0.482) and OPRL1 (Cohens d = -0.237) expression compared to women. In adjusted models controlling for B&B stage and post-mortem interval, PNOC expression significantly correlated with dimensional scores of positive valence ({beta} = -0.38, p = 0.035) and arousal regulatory systems ({beta} = -0.43, p = 0.015) derived from a text classification algorithm applied to medical records. OPRL1 showed disrupted circadian rhythmicity in AD cases (p = 0.151 vs. p = 0.020 in controls). ConclusionsThese findings suggest distinct roles for PNOC and OPRL1 in AD pathology, with PNOC primarily associated with psychiatric symptoms and OPRL1 showing disrupted circadian regulation. Sex-specific expression patterns further indicate the need for personalized therapeutic approaches targeting the nociceptin system.