The realm of psychiatric therapeutics is witnessing a transformative evolution as researchers delve into the translational pathways of oxytocin therapy, targeting schizophrenia’s most stubborn challenge: its negative symptoms. Schizophrenia, a complex neuropsychiatric disorder characterized by disturbances in thought, perception, and behavior, has long resisted effective treatment for certain debilitating aspects—particularly those negative symptom domains such as social withdrawal, anhedonia, and apathy. Among emerging interventions, oxytocin, a neuropeptide classically recognized for its role in social bonding and affiliation, is capturing scientific attention for its potential to unravel these clinical mysteries.

At the crux of this innovative approach is the intersection of neurohormonal modulation and neural circuit dynamics. Oxytocin’s modulation of social and emotional processing pathways offers a mechanistic foothold in the enigmatic pathophysiology underlying negative symptoms. Recent translational research studies have pioneered the exploration of how exogenous oxytocin administration can influence synaptic plasticity, neurotransmitter release, and neuronal connectivity within the corticolimbic circuitry—areas critically affected in schizophrenia. This represents a promising avenue to not merely ameliorate symptoms pharmacologically but to potentially restore disrupted neural mechanisms.

The translational challenge, however, lies in bridging preclinical models and clinical applications. Schizophrenia’s heterogeneity demands nuanced approaches that consider symptom-specific neurobiological substrates. The negative symptom dimension, often overshadowed by positive symptoms such as hallucinations and delusions, has evaded adequate therapeutic strategies largely due to its complex neurobiological basis. Oxytocin’s ability to interact with systems governing social cognition and motivation hints at a groundbreaking modality designed to target these deficits directly.

At the molecular level, oxytocin receptors distributed across key brain regions including the prefrontal cortex, amygdala, and hippocampus mediate its diverse effects. These areas are integral to emotional regulation and motivational drives, which are profoundly impaired in schizophrenia’s negative symptomatology. By engaging these receptors, oxytocin signaling can modulate glutamatergic and dopaminergic neurotransmission, both of which are pivotal in schizophrenia pathophysiology. This fine-tuning of neurotransmitter networks holds potential for reversing synaptic abnormalities associated with diminished social engagement.

Advancements in neuroimaging technologies have provided invaluable insights into oxytocin’s functional impact on brain activity patterns. Functional MRI studies reveal that oxytocin administration enhances connectivity within neural circuits responsible for social cognition, empathy, and reward processing. These findings crystallize the potential for oxytocin to recalibrate dysfunctional brain networks and reestablish functional integration, thereby alleviating symptoms that severely impair patients’ quality of life and societal integration.

One cannot overlook the translational complexity posed by oxytocin’s pharmacokinetics and delivery mechanisms. Oxytocin’s short half-life and poor blood-brain barrier penetrability necessitate innovative delivery strategies to achieve therapeutically relevant central nervous system concentrations. Intranasal administration has emerged as a preferred route, enabling direct transport to the brain and circumventing peripheral degradation. Yet, optimizing dosing regimens and treatment duration requires ongoing systematic investigation to maximize clinical benefits.

Behavioral outcomes also underscore the promise of oxytocin therapy in schizophrenia. Clinical trials report improvements in social functioning and motivation, correlating with enhanced neural activity in relevant brain regions. These functional gains transcend symptomatic relief, fostering real-world benefits such as improved interpersonal relationships and increased participation in therapeutic milieus. Consequently, oxytocin-based interventions could represent a paradigm shift from symptom management towards holistic rehabilitation.

Genetic and epigenetic considerations add another dimension to the therapeutic landscape. Individual variability in oxytocin receptor gene expression and epigenetic modifications may influence treatment responsiveness. Recognizing these genetic underpinnings can facilitate personalized medicine approaches, tailoring oxytocin therapy to individuals more likely to benefit based on biomarker profiles. Integrating genetic screening into clinical trials may accelerate precision psychiatry efforts.

Moreover, the interplay between oxytocin and other neuropeptides or neurotransmitter systems warrants deep exploration. Synergistic effects between oxytocin and serotonin or dopamine systems could potentiate therapeutic outcomes. Such interactions illuminate the need for combinatorial treatment strategies that harness multiple molecular pathways, thereby offering a comprehensive assault on schizophrenia’s multifaceted nature.

Despite encouraging preliminary results, challenges remain in standardizing oxytocin treatment protocols and managing placebo effects, which are particularly pronounced in psychiatric interventions. Identifying objective biomarkers to quantify therapeutic response could mitigate these challenges, enhancing the robustness of clinical trial outcomes. Advances in biomarker discovery, including neuroimaging and peripheral assays, represent critical adjuncts to validating oxytocin’s clinical utility.

Ethical considerations also surface in deploying a neuropeptide with such profound effects on social cognition and behavior. Long-term implications of modulating the oxytocinergic system necessitate rigorous safety profiling and monitoring to preempt adverse effects or unintended alterations in personality traits. Ensuring informed consent and transparent communication with patients is paramount as this innovative therapy advances from experimental phases to broader clinical practice.

Looking ahead, integration of oxytocin therapy into multidisciplinary treatment regimens could redefine schizophrenia care. Combining pharmacological interventions with psychosocial therapies may amplify benefits, nurturing neuroplastic changes through behavioral reinforcement. Such holistic strategies align with contemporary models of psychiatric rehabilitation emphasizing functional recovery and social reintegration.

The translational journey of oxytocin therapy epitomizes the intersection of basic neuroscience and clinical innovation. It underscores the imperative to dissect neural mechanisms with precision and translate these insights into tangible patient outcomes. As researchers continue to elucidate the molecular and circuit-level effects of oxytocin, the therapeutic horizon for schizophrenia’s negative symptoms appears increasingly promising.

In summation, the exploration of oxytocin as a therapeutic agent in schizophrenia exemplifies a pioneering frontier in psychiatric research. Bridging symptom domains with neural mechanisms offers nuanced understanding and targeted intervention strategies. While further research is essential to refine and validate this approach, the current trajectory heralds a potential leap forward in addressing one of schizophrenia’s most refractory symptom clusters.

The implications extend beyond schizophrenia, as insights gained from oxytocin therapy may inform novel treatments for a spectrum of neuropsychiatric disorders characterized by social and motivational deficits. This body of work contributes not only to psychiatric therapeutics but profoundly enriches our comprehension of human social neuroscience and neurochemical modulation.

As clinical trials progress and translational frameworks evolve, the promise of oxytocin as a cornerstone of next-generation schizophrenia therapy stands as a beacon of hope, illuminating pathways to improved cognition, social engagement, and ultimately, better lives for those affected by this challenging disorder.

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Subject of Research: Oxytocin therapy targeting negative symptoms in schizophrenia by exploring neural mechanisms and translational pathways.

Article Title: Translational pathways of oxytocin therapy in schizophrenia: bridging negative symptom domains and neural mechanisms.

Article References:
Ji, L., Wang, X., Li, Y. et al. Translational pathways of oxytocin therapy in schizophrenia: bridging negative symptom domains and neural mechanisms. Transl Psychiatry (2026). https://doi.org/10.1038/s41398-026-04145-9

Image Credits: AI Generated

DOI: https://doi.org/10.1038/s41398-026-04145-9

In an intriguing breakthrough, a recent longitudinal study reveals a compelling link between gut microbiota metabolites and the efficacy of cognitive behavioral therapy (CBT) in treating social anxiety disorder (SAD). Published in Translational Psychiatry in June 2026, the research sheds new light on the biological underpinnings of anxiety disorders and opens promising avenues for integrative treatment strategies that transcend purely psychological interventions.

Social anxiety disorder, characterized by intense fear and avoidance of social situations, has traditionally been viewed through the lens of neurobiology and psychological processes. However, mounting evidence over the past decade identifies the gut-brain axis as a pivotal player in mental health. This latest study deepens that understanding by examining specific metabolites—short-chain fatty acids (SCFAs)—in the plasma of individuals diagnosed with SAD, before and after undergoing CBT.

Short-chain fatty acids, namely propionic, butyric, isobutyric, and valeric acids, are metabolites produced predominantly through the fermentation of dietary fibers by gut bacteria. These molecules do not merely exist as metabolic byproducts; emerging science indicates they hold critical roles in modulating immune response, inflammation, and even neural signaling pathways. This study anchors these biochemical insights to psychological outcomes, offering empirical data linking SCFA levels with social anxiety symptomatology.

At the heart of this investigation is the observation that plasma concentrations of several SCFAs significantly increased over a two-year period in SAD patients who received effective CBT. More specifically, patients exhibited a marked elevation in propionic, butyric, isobutyric, and valeric acids following therapeutic intervention. This longitudinal design underscores the potential for sustained biological changes associated with psychosocial treatments, pointing toward a dynamic interplay between mind, gut microbiome, and metabolic environment.

Perhaps the most striking finding of this study is the comparatively lower baseline plasma concentration of isobutyric acid among SAD patients relative to matched healthy controls prior to the onset of therapy. This difference suggests that isobutyric acid levels could serve as a biomarker for social anxiety, or at least indicate a gut microbial dysbiosis associated with the disorder. The implications are profound, hinting that SCFAs might not only reflect but also contribute to the pathophysiology of social anxiety.

The study’s methodology ensured robust longitudinal tracking of SCFA plasma concentrations, employing advanced biochemical assays to quantify these metabolites with high specificity and sensitivity. Participants were carefully matched to controls, minimizing confounding variables and enabling precise attribution of changes to CBT rather than extraneous factors. Through these rigorous controls, causality is suggested rather than mere correlation.

From a mechanistic standpoint, SCFAs influence the central nervous system by crossing the blood-brain barrier and interacting with various receptors and pathways. For instance, butyric acid is known to act as a histone deacetylase inhibitor, modulating gene expression and neuroplasticity. This epigenetic effect could explain how psychological treatment triggers neurobiological shifts mediated by microbial metabolites, thereby enhancing therapeutic outcomes at a molecular level.

Additionally, SCFAs modulate systemic inflammation, an increasingly recognized factor in psychiatric disorders. Chronic inflammation can exacerbate anxiety symptoms, and elevated SCFA levels may counteract this by promoting anti-inflammatory cytokine production. The dynamic rise in SCFAs post-CBT suggests that psychosocial interventions might indirectly attenuate inflammatory burden via microbiota-dependent pathways.

This integration of microbiome science with psychotherapy heralds a paradigm shift. Traditionally, mental health treatments focus on neurotransmitters and cognitive restructuring, but the recognition that gut-derived metabolites can mediate treatment responses invites a more holistic approach. Future protocols may incorporate dietary modifications, probiotics, or microbiota-targeted therapies alongside CBT to amplify benefit.

Moreover, the identification of isobutyric acid as differentially expressed before treatment paves the way for predictive diagnostics. Plasma SCFA profiling could inform personalized therapeutic plans, identifying individuals with SAD more likely to respond favorably to CBT or requiring adjunctive biological interventions. Such precision psychiatry approaches will revolutionize mental health care delivery.

The study’s findings also raise questions about bidirectional causality: does social anxiety modulate gut microbiota composition and function, or do microbial metabolites predispose individuals to anxiety states? While this research advances understanding, disentangling cause and effect remains an important quest demanding further longitudinal and interventional studies with integrated microbiome sequencing and metabolomics.

Clinical translation of these insights will require interdisciplinary collaboration among psychiatrists, microbiologists, neuroscientists, and nutritionists. Investigating the impact of targeted prebiotics or SCFA supplementation concurrent with CBT may offer a mechanistic leverage point to enhance remission rates and cognitive rehabilitation outcomes in SAD patients.

Importantly, this research exemplifies how a psychosocial intervention like CBT extends beyond cognitive restructuring to evoke tangible biological changes. Coupling psychological and biochemical metrics provides a richer, multisystem perspective of therapeutic success, moving psychiatry towards a more integrative science-based discipline.

In sum, the identification of increased plasma SCFA concentrations in response to CBT among social anxiety patients represents a landmark contribution. It substantiates the gut-brain axis as a critical substrate through which mental health interventions exert their efficacy and highlights novel molecular targets for next-generation therapeutics.

As global prevalence of social anxiety and related disorders rises, innovations that blend psychological and biological treatments hold promise for reducing suffering and morbidity. This pioneering study lays the groundwork for a new frontier in psychiatry—one where microbial metabolites might one day be routinely monitored and modulated to maximize mental wellness.

The translational impact of these findings cannot be overstated. By harnessing the microbiota’s biochemical repertoire, clinicians may soon customize therapy regimens for SAD that not only reshape thinking patterns but also recalibrate the microbiome-metabolome axis, culminating in lasting recovery and resilience.

Ultimately, this convergence of psychology, microbiology, and metabolomics ushers in a visionary era—one where the key to treating complex mental health disorders lies in embracing the full spectrum of human biology, from mind to microbe and back again.

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Subject of Research: Plasma short-chain fatty acid concentrations in social anxiety disorder and their modulation after cognitive behavioral therapy

Article Title: Plasma short-chain fatty acid concentrations in social anxiety disorder and changes after cognitive behavioral therapy

Article References:
Cai, W., Stiernborg, M., Wolthon, A. et al. Plasma short-chain fatty acid concentrations in social anxiety disorder and changes after cognitive behavioral therapy. Transl Psychiatry 16, 295 (2026). https://doi.org/10.1038/s41398-026-04134-y

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DOI: 03 June 2026

Scientists may have found a completely new way to treat depression by targeting inflammation instead of brain chemistry. A small clinical trial led by researchers at the University of Bristol suggests that targeting the immune system could help people with depression who do not improve with standard antidepressant medications. The findings, published May 20 in [...]

In a striking advancement in the field of psychiatric research, scientists have unveiled compelling evidence suggesting that the way N-methyl-D-aspartate (NMDA) receptor antagonists influence negative affective biases in male rodents could dramatically enhance our ability to predict the clinical efficacy of therapeutic agents for major depressive disorder (MDD). This breakthrough emerges from an exhaustive preclinical study that delves deep into the nuanced neuropharmacological mechanisms underpinning depression and its treatment, potentially revolutionizing how new antidepressants are evaluated and optimized.

Major depressive disorder remains a global health challenge, with current pharmacotherapies failing to deliver significant relief for a substantial proportion of patients. Traditional antidepressant drug development is often hampered by the lack of reliable early-stage indicators that correlate strongly with clinical outcomes. This gap results in lengthy, costly trials with uncertain success rates. The new research spearheaded by Hinchcliffe, Kamenish, Bartlett, and colleagues offers a beacon of hope by identifying behavioral and neurochemical biomarkers in animal models that could prefigure drug efficacy in humans.

Central to the study is the role of NMDA receptor antagonists, a class of drugs that modulate glutamatergic neurotransmission, which has garnered attention due to rapid antidepressant effects observed with compounds such as ketamine. However, not all NMDA antagonists produce equal therapeutic benefits, prompting researchers to investigate the subtle differences in how these agents influence affective states, particularly negative biases—cognitive distortions that exaggerate negative thoughts and perceptions and are hallmark features of depression.

Using sophisticated behavioral paradigms, the researchers assessed male rat models exposed to different NMDA antagonists, measuring shifts in negative affective bias—a parameter reflective of mood and emotional processing. The variations in response were not only measurable but predictive: rats showing certain patterns of bias modification in response to specific NMDA antagonists corresponded to profiles of clinical success reported in human trials of these drugs.

The methodology employed was meticulous, involving chronic and acute dosing regimens, detailed behavioral assays such as the affective bias test, and expansive neurochemical analyses through brain region-specific assays. This integrative approach allowed the team to parse out the particular receptor subtype interactions and downstream signaling cascades that underlie the differential modulation of affective biases. Their findings underscore the heterogeneity of NMDA receptor function and its complex interplay with mood regulation circuits.

Interestingly, the data also highlighted sex-specific nuances. While this study primarily focused on male rats, it sets the stage for comparative analyses with females, aiming to address the sex dimorphism observed both in depression prevalence and treatment response. Understanding such biological variances is critical for tailoring personalized therapeutic strategies in psychiatry.

Beyond the biological insights, this research carries profound implications for drug development pipelines. Currently, the lack of robust, translational behavioral biomarkers impedes efficient prediction of an agent’s potential success in human depression. By leveraging the modulation patterns of negative affective biases in animal models, pharmaceutical development could adopt this framework as a preclinical screening tool, potentially accelerating the introduction of novel and more effective antidepressants.

Moreover, the study invites a reevaluation of the current clinical trial designs. Incorporating biomarkers derived from affective bias modulation could refine patient stratification, enhance endpoint sensitivity, and reduce placebo effects, which have notoriously plagued psychiatric trials. This precision approach would align with contemporary movements towards personalized medicine in mental health care.

The mechanistic revelations about NMDA receptor subtypes also open new therapeutic avenues. Beyond simply antagonizing NMDA receptors, drugs could be engineered to target specific receptor populations or signaling pathways implicated in adjusting negative affective bias, thereby maximizing efficacy while minimizing side effects. Such targeted pharmacology would represent a paradigm shift from broad-spectrum antidepressants to finely-tuned neuropsychiatric agents.

Critically, these findings shed light on the elusive neurobiology of negative affective biases themselves. Understanding how these cognitive-emotional distortions arise and can be pharmacologically adjusted not only informs drug discovery but also enriches cognitive and behavioral therapeutic approaches. This convergence of pharmacology and psychology could revolutionize comprehensive treatment regimens for depression.

While these preclinical findings are promising, translational hurdles remain. Confirmation in human subjects will be essential, necessitating biomarker development in clinical populations through neuroimaging and psychometric assessments aligned with affective bias paradigms. Nonetheless, this research charts a clear and innovative path forward.

In conclusion, the study by Hinchcliffe et al. marks a significant stride towards unraveling the complex neuropharmacology of depression and refining the toolkit for antidepressant development. By anchoring clinical prediction to the modulation of negative affective biases by NMDA antagonists, it offers a sophisticated biomarker framework that holds promise for transforming future therapeutic landscapes and improving millions of lives burdened by major depressive disorder.

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Subject of Research: Differences in NMDA antagonist modulation of negative affective biases and their predictive value for clinical efficacy in major depressive disorder.

Article Title: Differences in how NMDA antagonists modulate negative affective biases in male rats may serve as a predictor of clinical efficacy in major depressive disorder.

Article References: Hinchcliffe, J.K., Kamenish, K., Bartlett, J. et al. Differences in how NMDA antagonists modulate negative affective biases in male rats may serve as a predictor of clinical efficacy in major depressive disorder. Transl Psychiatry (2026). https://doi.org/10.1038/s41398-026-04133-z

Image Credits: AI Generated

DOI: https://doi.org/10.1038/s41398-026-04133-z

In a groundbreaking advancement poised to reshape our understanding of emotional regulation and pain processing, researchers have unveiled compelling evidence that activating the nociceptin/orphanin FQ receptor (NOP receptor) substantially dampens both behavioral and neural reactions to conditioned aversive stimuli. This revelation, detailed in a transformative study published in Translational Psychiatry, meticulously dissects the neurobiological pathways through which NOP receptor agonism modulates emotional and sensory responses, carving new avenues for therapeutic interventions targeting anxiety, trauma, and mood disorders.

The nociceptin/orphanin FQ peptide, an endogenous neuropeptide structurally related to opioids but distinct in function, binds selectively to the NOP receptor, a G protein-coupled receptor abundantly distributed across neural circuits implicated in emotion and pain regulation. Historically enigmatic in its role compared to classic opioid receptors, recent research has increasingly illuminated nociceptin’s unique capacity to fine-tune behavioral and physiological responses to stress and adverse environments. The current study expands this knowledge by providing an integrative examination of the receptor’s ability to attenuate the learned behavioral aversions and corresponding neural activity that arise from conditioned negative stimuli.

Through the deployment of precise pharmacological agonists targeting the NOP receptor, the investigative team embarked upon a multi-modal exploration, employing both behavioral assays in animal models and cutting-edge neuroimaging techniques in humans. Subjects exposed to stimuli previously paired with negative outcomes demonstrated reduced avoidance behaviors and diminished neural activation within key brain regions such as the amygdala, prefrontal cortex, and insular cortex following receptor activation. These findings elucidate how NOP receptor engagement effectively weakens the salience of threats that are internally represented through associative learning rather than immediate sensory input.

Critically, the attenuation of aversive responses does not imply a blunt suppression of sensation or cognition but rather a selective downregulation of maladaptive, conditioned fear responses. This nuanced modulation suggests potential for therapeutic application in conditions characterized by pathological fear conditioning, such as post-traumatic stress disorder (PTSD) and phobias, where heightened reactivity to environmental cues perpetuates chronic distress and dysfunction. By targeting the NOP receptor’s signaling cascades, it may be possible to recalibrate the brain’s emotional valence assignment without impairing overall sensory processing or cognitive flexibility.

Neural circuit analyses revealed that nociceptin/orphanin FQ receptor agonism primarily affects glutamatergic and GABAergic neurotransmission within limbic and cortical hubs, thereby restoring inhibitory-excitatory balance disrupted by chronic stress or traumatic conditioning. The dynamic suppression of hyperactive neurons in the amygdala curtails the amplification of fear signals, while the concurrent enhancement of prefrontal regulatory control bolsters top-down inhibition. This dual mechanism fosters an environment conducive to extinction learning, wherein previously threatening stimuli lose their emotional charge, facilitating adaptive coping and resilience.

Furthermore, the study underscores the receptor’s influence on the hypothalamic-pituitary-adrenal (HPA) axis, a critical neuroendocrine system orchestrating the stress response. Agonism of the NOP receptor markedly attenuated cortisol release in response to conditioned stressors, highlighting a systemic role in calibrating both central and peripheral stress pathways. This holistic modulation potentiates the receptor’s candidacy as a molecular target for integrative treatment approaches aimed at mitigating stress-induced psychopathology.

At the molecular level, investigations revealed that NOP receptor activation initiates intracellular signaling via Gi/o protein coupling, resulting in decreased cyclic adenosine monophosphate (cAMP) production and subsequent attenuation of protein kinase A (PKA) activity. These downstream effects culminate in the modulation of gene expression patterns linked to synaptic plasticity, enabling long-term adaptation of neuronal circuits involved in aversive conditioning. The resultant epigenetic landscape adjustments may underlie sustained therapeutic benefits following receptor-targeted interventions.

Importantly, the favorable safety profile observed with NOP receptor agonists distinguishes them from traditional opioid-based treatments, which carry high risk for dependence, tolerance, and adverse side effects. Unlike mu-opioid receptor agonists, nociceptin’s engagement does not produce significant respiratory depression nor pronounced reward-motivated behaviors, presenting a promising alternative for managing affective disorders without compromising patient safety.

These findings emerge within a broader scientific context that increasingly recognizes the complexity of the brain’s neuromodulatory systems beyond classical neurotransmitters. The study’s integrative approach—melding behavioral neuroscience, pharmacology, neuroimaging, and endocrinology—exemplifies the cutting-edge methodologies driving contemporary psychopharmacological research. The identification of the NOP receptor as a pivotal modulator of learned emotional responses heralds a paradigm shift in therapeutic strategies targeting the neurobiology of fear and anxiety.

The translational implications are profound. Pharmaceutical development based on NOP receptor agonists could usher in a new class of anxiolytics and antidepressants capable of dismantling pathological fear memories with enhanced precision. Additionally, adjunctive use in cognitive-behavioral therapies might amplify treatment efficacy by biologically facilitating fear extinction and emotional recalibration.

While the study provides robust mechanistic insights, it also evokes crucial questions about the receptor’s role across diverse populations, comorbid conditions, and chronicity of symptoms. Longitudinal clinical trials will be vital to ascertain optimal dosing regimens, durability of therapeutic effects, and potential interactions with existing pharmacotherapies or psychotherapies. Moreover, given the receptor’s involvement in multiple physiological domains, expanding research into its systemic effects will enrich understanding of its full clinical utility.

In sum, the demonstration of nociceptin/orphanin FQ receptor agonism as a modulator capable of attenuating aversive behavioral and neural responses stands as a landmark in neuropsychopharmacology. By illuminating a previously underappreciated neuromodulatory axis, this work paves the way for innovative, targeted interventions against some of the most debilitating mental health challenges rooted in maladaptive fear conditioning. As science advances, the promise of harnessing the nociceptin system to foster emotional resilience and mental well-being moves ever closer to fruition.

Subject of Research: Nociceptin/orphanin FQ receptor agonism and its effects on conditioned aversive behavioral and neural responses

Article Title: Nociceptin/orphanin FQ receptor agonism attenuates behavioral and neural responses to conditioned aversive stimuli

Article References:
Hur, KH., Pizzagalli, D.A., Stover, J. et al. Nociceptin/orphanin FQ receptor agonism attenuates behavioral and neural responses to conditioned aversive stimuli. Transl Psychiatry (2026). https://doi.org/10.1038/s41398-026-04111-5

Image Credits: AI Generated

DOI: https://doi.org/10.1038/s41398-026-04111-5