Brain FNDC5/Irisin Expression in Patients and Mouse Models of Major Depression DOI Creative Commons
Ricardo A. S. Lima-Filho,

Juliana S. Fortuna,

Danielle Cozachenco

et al.

eNeuro, Journal Year: 2023, Volume and Issue: 10(2), P. ENEURO.0256 - 22.2023

Published: Jan. 25, 2023

Major depressive disorder (MDD) is a major cause of disability in adults. MDD both comorbidity and risk factor for Alzheimer's disease (AD), regular physical exercise has been associated with reduced incidence severity AD. Irisin an exercise-induced myokine derived from proteolytic processing fibronectin type III domain-containing protein 5 (FNDC5). FNDC5/irisin the brains AD patients mouse models. However, whether brain expression altered depression remains elusive. Here, we investigate changes

Language: Английский

Major depressive disorder: hypothesis, mechanism, prevention and treatment DOI Creative Commons
Lulu Cui,

Shu Li,

Siman Wang

et al.

Signal Transduction and Targeted Therapy, Journal Year: 2024, Volume and Issue: 9(1)

Published: Feb. 9, 2024

Abstract Worldwide, the incidence of major depressive disorder (MDD) is increasing annually, resulting in greater economic and social burdens. Moreover, pathological mechanisms MDD underlying effects pharmacological treatments for are complex unclear, additional diagnostic therapeutic strategies still needed. The currently widely accepted theories pathogenesis include neurotransmitter receptor hypothesis, hypothalamic-pituitary-adrenal (HPA) axis cytokine neuroplasticity hypothesis systemic influence but these cannot completely explain mechanism MDD. Even it hard to adopt only one reveal MDD, thus recent years, great progress has been made elucidating roles multiple organ interactions identifying novel approaches multitarget modulatory strategies, further revealing disease features Furthermore, some newly discovered potential targets studied antidepressants have attracted widespread attention, reagents even approved clinical treatment methods such as phototherapy acupuncture effective improvement symptoms. In this work, we comprehensively summarize latest research on diagnosis preventive medicines, well related trials.

Language: Английский

Citations

266

Regional, circuit and network heterogeneity of brain abnormalities in psychiatric disorders DOI Creative Commons
Ashlea Segal, Linden Parkes, Kevin Aquino

et al.

Nature Neuroscience, Journal Year: 2023, Volume and Issue: 26(9), P. 1613 - 1629

Published: Aug. 14, 2023

The substantial individual heterogeneity that characterizes people with mental illness is often ignored by classical case-control research, which relies on group mean comparisons. Here we present a comprehensive, multiscale characterization of the gray matter volume (GMV) differences in 1,294 cases diagnosed one six conditions (attention-deficit/hyperactivity disorder, autism spectrum bipolar depression, obsessive-compulsive disorder and schizophrenia) 1,465 matched controls. Normative models indicated person-specific deviations from population expectations for regional GMV were highly heterogeneous, affecting same area <7% diagnosis. However, these embedded within common functional circuits networks up to 56% cases. salience-ventral attention system was implicated transdiagnostically, other systems selectively involved schizophrenia attention-deficit/hyperactivity disorder. Phenotypic between assigned diagnosis may thus arise heterogeneous localization specific deviations, whereas phenotypic similarities be attributable dysfunction networks.

Language: Английский

Citations

115

Toward a Better Understanding of the Mechanisms and Pathophysiology of Anhedonia: Are We Ready for Translation? DOI
Diego A. Pizzagalli

American Journal of Psychiatry, Journal Year: 2022, Volume and Issue: 179(7), P. 458 - 469

Published: July 1, 2022

Anhedonia—the loss of pleasure or lack reactivity to pleasurable stimuli—remains a formidable treatment challenge across neuropsychiatric disorders. In major depressive disorder, anhedonia has been linked poor disease course, worse response psychological, pharmacological, and neurostimulation treatments, increased suicide risk. Moreover, although some neural abnormalities normalize after successful treatment, several persist—for example, blunted activation the ventral striatum reward-related cues reduced functional connectivity involving striatum. Critically, these have also identified in unaffected, never-depressed children parents with disorder found prospectively predict first onset depression. Thus, may be promising targets for prevention. Despite appreciation clinical importance its underlying mechanisms, important gaps remain. this overview, author summarizes extant knowledge about pathophysiology anhedonia, which provide road map toward novel prevention strategies, then highlights priorities facilitate clinically meaningful breakthroughs. These include need 1) appropriately controlled trials, especially those embracing an experimental therapeutics approach probe target engagement; 2) preclinical models relevant stronger translational value; 3) scales that incorporate neuroscientific advances our understanding anhedonia. The concludes by highlighting future directions, emphasizing integrated, collaborative, cross-species, multilevel tackling anhedonic phenotypes.

Language: Английский

Citations

103

Canalization and plasticity in psychopathology DOI Creative Commons

Robin Carhart‐Harris,

Shamil Chandaria,

David Erritzøe

et al.

Neuropharmacology, Journal Year: 2022, Volume and Issue: 226, P. 109398 - 109398

Published: Dec. 27, 2022

This theoretical article revives a classical bridging construct, canalization, to describe new model of general factor psychopathology. To achieve this, we have distinguished between two types plasticity, an early one that call 'TEMP' for 'Temperature or Entropy Mediated Plasticity', and another, 'canalization', which is close Hebbian plasticity. These forms plasticity can be most easily by their relationship 'precision' inverse variance; TEMP relates increased variance decreased precision, whereas the opposite true canalization. also subsumes learning rate, (Ising) temperature entropy. Dictionary definitions 'plasticity' it as property being shaped molded; better match this. Importantly, propose 'pathological' phenotypes develop via mechanisms canalization defensive response adversity associated distress dysphoria. Our states entrenches in psychopathology, narrowing phenotypic state-space agent develops expertise pathology. We suggest - combined with gently guiding psychological support counter address questions whether when adaptive versus maladaptive, furnish our references basic human neuroscience, offer concrete experiments measures test its main hypotheses implications. part Special Issue on "National Institutes Health Psilocybin Research Speaker Series".

Language: Английский

Citations

71

The pathogenesis of depression: roles of connexin 43-based gap junctions and inflammation DOI
Hong Jiang, Meng Zhang,

Xin-Mu Li

et al.

European Journal of Pharmacology, Journal Year: 2025, Volume and Issue: 989, P. 177260 - 177260

Published: Jan. 9, 2025

Language: Английский

Citations

2

Depression Recognition Using Daily Wearable-Derived Physiological Data DOI Creative Commons
Xinyu Shui, Hao Xu, Shuping Tan

et al.

Sensors, Journal Year: 2025, Volume and Issue: 25(2), P. 567 - 567

Published: Jan. 19, 2025

The objective identification of depression using physiological data has emerged as a significant research focus within the field psychiatry. advancement wearable measurement devices opened new avenues for individuals with in everyday-life contexts. Compared to other methods, wearables offer potential continuous, unobtrusive monitoring, which can capture subtle changes indicative depressive states. present study leverages multimodal wristband collect from fifty-eight participants clinically diagnosed during their normal daytime activities over six hours. Data collected include pulse wave, skin conductance, and triaxial acceleration. For comparison, we also utilized matched healthy controls publicly available dataset, same equivalent durations. Our aim was identify through analysis measurements derived daily life scenarios. We extracted static features such mean, variance, skewness, kurtosis indicators like heart rate, acceleration, well autoregressive coefficients these signals reflecting temporal dynamics. Utilizing Random Forest algorithm, distinguished non-depressive varying classification accuracies on aggregated 6 h, 2 30 min, 5 min segments, 90.0%, 84.7%, 80.1%, 76.0%, respectively. results demonstrate feasibility wearable-derived recognition. achieved suggest that this approach could be integrated into clinical settings early detection monitoring symptoms. Future work will explore methods personalized interventions real-time offering promising avenue enhancing mental health care integration technology.

Language: Английский

Citations

2

Brain Serotonin Release Is Reduced in Patients With Depression: A [11C]Cimbi-36 Positron Emission Tomography Study With a d-Amphetamine Challenge DOI Creative Commons
David Erritzøe, Beata R. Godlewska, Gaia Rizzo

et al.

Biological Psychiatry, Journal Year: 2022, Volume and Issue: 93(12), P. 1089 - 1098

Published: Oct. 29, 2022

Language: Английский

Citations

51

Rapid neuroplasticity changes and response to intravenous ketamine: a randomized controlled trial in treatment-resistant depression DOI Creative Commons
Jared M. Kopelman, Timothy A. Keller, Benjamin Panny

et al.

Translational Psychiatry, Journal Year: 2023, Volume and Issue: 13(1)

Published: May 9, 2023

Intravenous ketamine is posited to rapidly reverse depression by enhancing neuroplasticity. In human patients, we quantified gray matter microstructural changes on a rapid (24-h) timescale within key regions where neuroplasticity enhancements post-ketamine have been implicated in animal models. this study, 98 unipolar depressed adults who failed at least one antidepressant medication were randomized 2:1 single infusion of intravenous (0.5 mg/kg) or vehicle (saline) and completed diffusion tensor imaging (DTI) assessments pre-infusion baseline 24-h post-infusion. DTI mean diffusivity (DTI-MD), putative marker matter, was calculated for 7 interest (left right BA10, amygdala, hippocampus; ventral Anterior Cingulate Cortex) compared clinical response measured with the Montgomery-Asberg Depression Rating Scale (MADRS) Quick Inventory Depressive Symptoms-Self-Report (QIDS-SR). Individual differences DTI-MD change (greater decrease from post-infusion, indicative more enhancement) associated larger improvements scores across several regions. left BA10 these relationships driven primarily group (group * interaction effects: p = 0.016-0.082). associations generalized both arms (p 0.007). hippocampus, MADRS only, effects observed opposite direction, such that inversely arm specifically 0.032-0.06). The acute may be mediated, part, quantifiable DTI.

Language: Английский

Citations

32

Time-course of the tDCS antidepressant effect: An individual participant data meta-analysis DOI Creative Commons
Stevan Nikolin, Adriano H. Moffa, Laís B. Razza

et al.

Progress in Neuro-Psychopharmacology and Biological Psychiatry, Journal Year: 2023, Volume and Issue: 125, P. 110752 - 110752

Published: March 16, 2023

Language: Английский

Citations

29

Chronic psychosocial stress triggers microglial‐/macrophage‐induced inflammatory responses leading to neuronal dysfunction and depressive‐related behavior DOI
Alexandros G. Kokkosis, Miguel Madeira,

Zachary Hage

et al.

Glia, Journal Year: 2023, Volume and Issue: 72(1), P. 111 - 132

Published: Sept. 7, 2023

Abstract Chronic environmental stress and traumatic social experiences induce maladaptive behavioral changes is a risk factor for major depressive disorder (MDD) various anxiety‐related psychiatric disorders. Clinical studies animal models of chronic have reported that symptom severity correlated with innate immune responses upregulation neuroinflammatory cytokine signaling in brain areas implicated mood regulation (mPFC; medial Prefrontal Cortex). Despite increasing evidence implicating impairments neuroplasticity synaptic deficits into the pathophysiology stress‐related mental disorders, how microglia may modulate neuronal homeostasis response to has not been defined. Here, using repeated defeat (RSDS) mouse model we demonstrate microglial‐induced inflammatory are regulating plasticity associated psychosocial stress. Specifically, show induces rapid activation proliferation as well macrophage infiltration mPFC, these processes spatially related activation. Moreover, report significant association microglial susceptibility or resilience In addition, find exposure exacerbates phagocytosis elements plasticity. Importantly, by utilizing two different CSF1R inhibitors (the penetrant PLX5622 non‐penetrant PLX73086) highlight crucial role (and secondarily macrophages) catalyzing pathological manifestations linked mPFC resulting usually depression.

Language: Английский

Citations

26