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REVIEW article

Front. Cell Dev. Biol.

Sec. Signaling

This article is part of the Research TopicNeural Signaling in Psychiatric Disorders: Mechanisms and InsightsView all 3 articles

From Synapse to System: Mechanistic Pathways of Neural Signaling Dysfunction in Psychiatric Disorders

Provisionally accepted
Rohan  GuptaRohan Gupta1*Niraj  Kumar JhaNiraj Kumar Jha1Naveen  KumarNaveen Kumar1Rupak  NagraikRupak Nagraik2Karthikeyan  RaviKarthikeyan Ravi3
  • 1Galgotias University, Greater Noida, India
  • 2Graphic Era Deemed to be University, Dehradun, India
  • 3Chettinad Hospital and Research Institute, Kanchipuram, India

The final, formatted version of the article will be published soon.

Psychiatric disorders are increasingly viewed as network-level brain diseases resulting from disruptions in neural signaling across various hierarchies, including molecular, synaptic, circuit, and systems levels. Evidence indicates that receptor dysregulation, abnormal intracellular pathways, and changes in ion channel activity lead to widespread network dysconnectivity, resulting in cognitive, emotional, and behavioral deficits. This review integrates advancements in genomics, transcriptomics, connectomics, and computational modeling to establish a framework for understanding signaling abnormalities in major psychiatric disorders. Further, this study investigates essential molecular and cellular processes such as synaptic plasticity, receptor-mediated communication, intracellular signaling cascades, and neuroimmune interactions, and connects these to disturbances in oscillatory dynamics, circuit architecture, and overall brain network organization. Additionally, neuroimaging and graph-theoretic studies consistently demonstrate an excitation–inhibition imbalance, atypical synaptic pruning, impaired oscillatory synchrony, and maladaptive connectivity within networks, including the default mode, salience, and fronto-limbic systems, across schizophrenia, depression, bipolar disorder, anxiety, and autism spectrum disorders. Moreover, genetic and epigenetic variations in signaling genes, such as CACNA1C, GRIN2B, and DISC1, along with developmental and environmental factors, contribute to network vulnerability and clinical heterogeneity. Emerging artificial intelligence and multimodal integration methods facilitate the identification of individualized "signaling fingerprints," which connect molecular perturbations to systems-level dysfunction. This research enhances precision psychiatry and guides targeted interventions based on neuromodulation, molecular mechanisms, and biomarkers.

Keywords: computational neuroscience, Network dysconnectivity, Neural signaling, precision psychiatry, psychiatric disorders

Received: 08 Dec 2025; Accepted: 23 Jan 2026.

Copyright: © 2026 Gupta, Jha, Kumar, Nagraik and Ravi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Rohan Gupta

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