3,247 results match your criteria: "Max-Planck Institute of Psychiatry[Affiliation]"

An integrated transcriptomic cell atlas of human neural organoids.

Nature

November 2024

Department of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland.

Human neural organoids, generated from pluripotent stem cells in vitro, are useful tools to study human brain development, evolution and disease. However, it is unclear which parts of the human brain are covered by existing protocols, and it has been difficult to quantitatively assess organoid variation and fidelity. Here we integrate 36 single-cell transcriptomic datasets spanning 26 protocols into one integrated human neural organoid cell atlas totalling more than 1.

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Article Synopsis
  • Robust annotation of compounds is essential in metabolomics, and the INADEQUATE NMR experiment is a powerful yet underused tool for structural elucidation due to the lack of community platforms integrating it with other NMR methods.
  • * PyINETA is introduced as an open-source platform that automates the use of INADEQUATE for structural analysis, integrates it with the C-resolved experiment (C-JRES), and maintains a transparent annotation pipeline.
  • * Evaluation of PyINETA in a mouse study demonstrated its capability to track the distribution of C-labeled amino acids across different tissues, revealing specific metabolite enrichment in organs like the liver and spleen.*
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Background: The hippocampal formation represents a key region in the pathophysiology of schizophrenia. Aerobic exercise poses a promising add-on treatment to potentially counteract structural impairments of the hippocampal formation and associated symptomatic burden. However, current evidence regarding exercise effects on the hippocampal formation in schizophrenia is largely heterogeneous.

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The microRNA profile of brain-derived extracellular vesicles: A promising step forward in developing pharmacodynamic biomarkers for psychiatric disorders.

Eur Neuropsychopharmacol

January 2025

Institute of Psychiatric Phenomics and Genomics (IPPG), LMU University Hospital, LMU Munich, Munich 80336, Germany; Department of Psychiatry and Behavioral Sciences, Norton College of Medicine, SUNY Upstate Medical University, Syracuse, NY, USA; Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

MicroRNAs (miRNAs) have the potential to affect drug metabolism, and some drugs affect cellular miRNA expression. miRNAs are found inside extracellular vesicles (EVs), and the profile of these EV-miRNAs can change across different diseases and disease states. Consequently, in recent years EV-miRNAs have attracted increasing attention as possible non-invasive biomarkers.

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Placental epigenetic signatures of maternal distress in glucocorticoid-related genes and newborn outcomes: A study of Spanish primiparous women.

Eur Neuropsychopharmacol

January 2025

Department of Evolutionary Biology, Ecology and Environmental Sciences, Faculty of Biology, University of Barcelona, Barcelona, Spain; Biomedicine Institute of the University of Barcelona (IBUB), Barcelona, Spain; Health Institut Carlos III, Network Centre for Biomedical Research in Mental Health (CIBER of Mental Health, CIBERSAM), Madrid, Spain. Electronic address:

Article Synopsis
  • Maternal stress during pregnancy can influence the health of offspring, raising the risk for neuropsychiatric disorders through changes in placental DNA methylation.
  • The study examined the effects of maternal stress on DNA methylation of cortisol-regulating genes (NR3C1, FKBP5, HSD11B2) using placental samples from 45 mother-infant pairs divided by stress exposure levels.
  • Results indicated that higher maternal cortisol in early pregnancy was linked to specific DNA methylation changes in the NR3C1 and FKBP5 genes, but no direct connection to newborn neurodevelopment was established, underscoring the need for more research on placental epigenetics.
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Neurocognitive dysfunction in adolescents with recent onset major depressive disorder: a cross-sectional comparative study.

Eur Child Adolesc Psychiatry

November 2024

Clinic for Child and Adolescent Psychiatry, Psychotherapy and Psychosomatic Medicine, University Hospital Muenster, Schmeddingstrasse 50, 48149, Muenster, Germany.

The aim of this study was to examine the neurocognitive deficits associated with the first episode of major depressive disorder (recent onset depression, ROD) in adolescents as compared to adult patients. Cross-sectional neurocognitive data from the baseline assessments of the PRONIA study with N = 650 (55.31% females) were analyzed.

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NOise Reduction with DIstribution Corrected (NORDIC) principal component analysis (PCA) has been shown to selectively suppress thermal noise and improve the temporal signal-to-noise ratio (tSNR) in human functional magnetic resonance imaging (fMRI). However, the feasibility to improve data quality for rodent fMRI using NORDIC PCA remains uncertain. NORDIC PCA may also be particularly beneficial for improving topological brain mapping, as conventional mapping requires precise spatiotemporal signals from large datasets (ideally ~1 hour acquisition) for individual representations.

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Background: The brain and the intestinal microbiota are highly interconnected and especially vulnerable to disruptions in early life. Emerging evidence indicates that psychosocial adversity detrimentally impacts the intestinal microbiota, affecting both physical and mental health. This study aims to investigate the gut microbiome in young children in the immediate aftermath of maltreatment exposure.

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  • The co-chaperone FKBP51, linked to the FKBP5 gene, is a significant psychiatric risk factor for anxiety and depression, particularly affecting the stress response.
  • Corticotropin releasing hormone (CRH) is also important in regulating stress, and both FKBP51 and CRH work together to influence the hypothalamic-pituitary-adrenal (HPA) axis.
  • Research shows that mice lacking FKBP51 in CRH-expressing neurons display increased stress effects, emphasizing the need for specific research on different cell types to develop personalized approaches for improving stress resilience and mental health.
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  • Subcortical brain structures play a crucial role in various developmental and psychiatric disorders, and a study analyzed brain volumes in 74,898 individuals, identifying 254 genetic loci linked to these volumes, which accounted for up to 35% of variation.
  • The research included exploring gene expression in specific neural cell types, focusing on genes involved in intracellular signaling and processes related to brain aging.
  • The findings suggest that certain genetic variants not only influence brain volume but also have potential causal links to conditions like Parkinson’s disease and ADHD, highlighting the genetic basis for risks associated with neuropsychiatric disorders.
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Behavior is tightly synchronized with bodily physiology. Internal needs from the body drive behavior selection, while optimal behavior performance requires a coordinated physiological response. Internal state is dynamically represented by the nervous system to influence mood and emotion, and body-brain signals also direct responses to external sensory cues, enabling the organism to adapt and pursue its goals within an ever-changing environment.

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Multiomics Analysis of the Molecular Response to Glucocorticoids: Insights Into Shared Genetic Risk From Psychiatric to Medical Disorders.

Biol Psychiatry

October 2024

Department Genes and Environment, Max Planck Institute of Psychiatry, Munich, Germany; Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, Georgia. Electronic address:

Article Synopsis
  • The study explores how genetic variations affect gene expression and DNA methylation in response to glucocorticoid receptor activation, linking these changes to the risk of psychiatric and other diseases.
  • Researchers measured DNA methylation and gene expression in blood samples before and after treatment with dexamethasone, using genotype data to perform a comprehensive analysis of genetic influences.
  • Findings indicated that specific genetic variants affecting glucocorticoid responses are correlated with increased heritability and risks for various diseases, revealing insights not captured in standard baseline analyses.
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  • Researchers tried to create models to predict how well people with first episode psychosis (FEP) would do after treatment, but it was hard to tell if these predictions worked for different groups of patients.
  • They tested these models using patients from two big studies in Europe and found out that while the models were somewhat accurate, they didn't work as well when applied to patients from a different study.
  • The results showed that it’s really important to check and improve these prediction models with independent samples of patients to make them better and more reliable in the future.
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  • Subcortical brain structures play a crucial role in various disorders, and a study analyzed the genetic basis of brain volumes in nearly 75,000 individuals of European ancestry, revealing 254 loci linked to these volumes.
  • The research identified significant gene expression in neural cells, relating to brain aging and signaling, and found that polygenic scores could predict brain volumes across different ancestries.
  • The study highlights genetic connections between brain volumes and conditions like Parkinson's disease and ADHD, suggesting specific gene expression patterns could be involved in neuropsychiatric disorders.
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The dorsal midbrain comprises dorsal columns of the periaqueductal grey matter and corpora quadrigemina. These structures are rich in beta-endorphinergic and leu-enkephalinergic neurons and receive GABAergic inputs from substantia nigra pars reticulata. Although the inferior colliculus (IC) is mainly involved in the acoustic pathways, the electrical and chemical stimulation of central and pericentral nuclei of the IC elicits a vigorous defensive behaviour.

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CACNA1C, coding for the α1 subunit of L-type voltage-gated calcium channel (LTCC) Ca1.2, has been associated with multiple psychiatric disorders. Clinical studies have revealed alterations in behavior as well as in brain structure and function in CACNA1C risk allele carriers.

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Sex-specific association between schizophrenia polygenic risk and subclinical schizophrenia-related traits.

Prog Neuropsychopharmacol Biol Psychiatry

October 2024

Departament de Biologia Evolutiva, Ecologia i Ciències Ambientals, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain; Institut de Biomedicina de la Universitat de Barcelona (IBUB), Barcelona, Spain; Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Instituto de Salud Carlos III (ISCIII), Madrid, Spain. Electronic address:

Background: According to the dimensional view of psychiatric disorders, psychosis is expressed as a continuum in the general population. However, the investigation of the putative genetic aetiological continuity between its clinical and subclinical phenotypes has yielded mixed results. We aimed to replicate previous findings regarding the association of polygenic risk for schizophrenia with subclinical traits (i.

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Stress Molecular Signaling in Interaction With Cognition.

Biol Psychiatry

October 2024

Department of Psychiatry, McLean Hospital, Harvard Medical School, Belmont, Massachusetts; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.

Article Synopsis
  • Exposure to stressful life events can significantly increase the chances of developing psychiatric disorders, particularly affecting cognitive functions, which can be difficult to comprehend for both individuals and healthcare providers.
  • The review highlights the need to study specific brain areas (like the amygdala and hippocampus) to understand the structural and molecular changes induced by stress, which can persistently alter brain function.
  • It calls for more research into genetic risk factors and the use of advanced technologies to better comprehend how stress impacts various brain regions, aiming to improve prevention and treatment approaches for cognitive symptoms related to stress.
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The Tree Shrew Model of Parkinson Disease: A Cost-Effective Alternative to Nonhuman Primate Models.

Lab Invest

November 2024

National Research Facility for Phenotypic & Genetic Analysis of Model Animals (Primate Facility), Key Laboratory of Genetic Evolution & Animal Models, and National Resource Center for Nonhuman Primates, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, China; Key Laboratory of Animal Models and Human Disease Mechanisms of Yunnan Province, and KIZ/CUHK Joint Laboratory of Bioresources and Molecular Research in Common Diseases, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, China. Electronic address:

The surge in demand for experimental monkeys has led to a rapid increase in their costs. Consequently, there is a growing need for a cost-effective model of Parkinson disease (PD) that exhibits all core clinical and pathologic phenotypes. Evolutionarily, tree shrews (Tupaia belangeri) are closer to primates in comparison with rodents and could be an ideal species for modeling PD.

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Acute stress causes depressive-like reactions in the tail suspension (TST) and forced swim tests (FST) of mice. Similarly, inescapable foot shock is able to promote the development of anhedonia as indicated by decreased sucrose consumption of treated mice in the sucrose preference test (SPT). The astrocyte-specific deletion of the P2X7R by a conditional knockout strategy or its knockdown by the intracerebroventricular (i.

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Article Synopsis
  • - The study aimed to explore the genetic basis of major depressive disorder by analyzing symptoms across various clinical and community cohorts, acknowledging challenges like sample size differences and missing data patterns.
  • - Researchers performed genome-wide association studies using data from both diagnosed and undiagnosed participants, fitting models to understand the relationships between different depressive symptoms.
  • - Findings emphasized the relevance of symptom directionality (e.g., hypersomnia vs. insomnia) and the necessity of considering study design when analyzing genetic data related to depression.
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HDAC5 controls a hypothalamic STAT5b-TH axis, the sympathetic activation of ATP-consuming futile cycles and adult-onset obesity in male mice.

Mol Metab

December 2024

Research Unit NeuroBiology of Diabetes, Helmholtz Munich, Neuherberg, Germany; Institute for Diabetes and Obesity, Helmholtz Munich, Neuherberg, Germany; German Center for Diabetes Research (DZD), Neuherberg, Germany; Neurobiology of Diabetes, TUM School of Medicine & Health, Technische Universität München, München, Germany. Electronic address:

With age, metabolic perturbations accumulate to elevate our obesity burden. While age-onset obesity is mostly driven by a sedentary lifestyle and high calorie intake, genetic and epigenetic factors also play a role. Among these, members of the large histone deacetylase (HDAC) family are of particular importance as key metabolic determinants for healthy ageing, or metabolic dysfunction.

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