Mood Stabilizers in Psychiatric Disorders and Mechanisms Learnt from in Vitro Model Systems
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The Effects of P75 and Sorcs2 on Neuronal Function and Structure
The Effects of Zn2+ on the Binding of the BDNF Prodomain with SorCS2 on Neuronal Function and Structure: Implications for Learning and Memory Caroline Pennacchio Briarcliff High School http://www.newscientist.com/data/images/ns/cms/teaser/blog/201211/f0049969_lead.jpg Introduction • Neurons -> Brain • Hippocampus = Control Center • Neural connections -> Brain-Derived Neurotrophic Factor (BDNF) Introduction Review of Literature Research Questions/Hypotheses Methods Bibliography Ligands • Regulate cell proliferation, differentiation • Axon and dendrite growth, synaptogenesis, and synaptic function and plasticity (Reichardt, 2006, Lu, B, Pang, PT, Woo. N.H., 2005, Minichiello L, 2009) http://www.mdpi.com/ijms/ijms-13-13713/article_deploy/html/images/ijms-13-13713f1-1024.png Introduction Review of Literature Research Questions/Hypotheses Methods Bibliography Pro-Neurotrophins • Proteolytically cleaved in trans-Golgi by furin or in secretory granules by pro-protein contervases ] • Extracellular cleavages created in mature domain formation show how to control synaptic functions of neurotrophins (Lu, 2003) • proBDNF regulates hippocampal structure, synaptic transmission, and plasticity (Yang et al., 2014) https://www.researchgate.net/profile/Jay_Pundavela/publication/269520194/figure/fig1/Fig-1-Binding-of-neurotrophins- • Induce apoptotic signaling (Nykjaer et al. 2004; Teng et al. 2005; Jansen et al. and-proneurotrophins-to-Trk-receptors-and-p75NTR-NGF_small.png 2007; Willnow et al. 2008; Yano et al. 2009) Introduction Review of Literature -
Is Microvascular Abnormality a New Endophenotype In
Psychiatria Danubina, 2015; Vol. 27, No. 3, pp 225-229 Mini review © Medicinska naklada - Zagreb, Croatia IS MICROVASCULAR ABNORMALITY A NEW ENDOPHENOTYPE IN SCHIZOPHRENIA? Ladislav Hosak1, Khurum Hakeem2, Marjan Raad2 & Jan Studnicka3 1Department of Psychiatry, Charles University in Prague, School of Medicine in Hradec Kralove and University Hospital Hradec Kralove, Czech Republic 2Charles University in Prague, School of Medicine in Hradec Kralove, Czech Republic 3Department of Ophthalmology, Charles University in Prague, School of Medicine in Hradec Kralove and University Hospital Hradec Kralove, Czech Republic received: 9.7.2015; revised: 28.8.2015; accepted: 4.9.2015 SUMMARY Background: A new method of assessment of microvascular abnormality in living schizophrenic subjects via retinal imaging was described by Meier et al. (2013). The principal aim of this review is to summarise the relevant knowledge and suggest further avenues of research into this topic. Subject and methods: On 20th April 2015, we carried out a search using the computer database system PubMed by using keywords „microvascular AND schizophrenia“. Results: Out of the 17 articles found, only seven were relevant. They are generally consistent with the hypothesis of microvas- cular pathology and brain inflammation as part of the pathogenesis in schizophrenia. It is important to stress that all studies of brain microvasculature in schizophrenia to date have been post mortem findings, apart from the work by Meier et al. (2013) which is related to retinal imaging in living subjects. Conclusions: Based on the literature, we suggest the following research and clinical avenues: Firstly, to assess whether microvascular abnormality found via retinal imaging, fulfils the criteria for the schizophrenia endophenotype. -
Alcohol Sensitivity As an Endophenotype of Alcohol Use Disorder: Exploring Its Translational Utility Between Rodents and Humans
brain sciences Review Alcohol Sensitivity as an Endophenotype of Alcohol Use Disorder: Exploring Its Translational Utility between Rodents and Humans Clarissa C. Parker 1,*, Ryan Lusk 2 and Laura M. Saba 2,* 1 Department of Psychology and Program in Neuroscience, Middlebury College, Middlebury, VT 05753, USA 2 Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA; [email protected] * Correspondence: [email protected] (C.C.P.); [email protected] (L.M.S.) Received: 3 September 2020; Accepted: 9 October 2020; Published: 13 October 2020 Abstract: Alcohol use disorder (AUD) is a complex, chronic, relapsing disorder with multiple interacting genetic and environmental influences. Numerous studies have verified the influence of genetics on AUD, yet the underlying biological pathways remain unknown. One strategy to interrogate complex diseases is the use of endophenotypes, which deconstruct current diagnostic categories into component traits that may be more amenable to genetic research. In this review, we explore how an endophenotype such as sensitivity to alcohol can be used in conjunction with rodent models to provide mechanistic insights into AUD. We evaluate three alcohol sensitivity endophenotypes (stimulation, intoxication, and aversion) for their translatability across human and rodent research by examining the underlying neurobiology and its relationship to consumption and AUD. We show examples in which results gleaned from rodents are successfully integrated with information from human studies to gain insight in the genetic underpinnings of AUD and AUD-related endophenotypes. Finally, we identify areas for future translational research that could greatly expand our knowledge of the biological and molecular aspects of the transition to AUD with the broad hope of finding better ways to treat this devastating disorder. -
Sorcs2 Deletion Leads to Altered Neuronal Lysosome Activity
bioRxiv preprint doi: https://doi.org/10.1101/2021.04.08.439000; this version posted April 10, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 SorCS2 deletion leads to altered neuronal lysosome activity 2 3 Sérgio Almeida1*, André M. Miranda2, Andrea E. Tóth1, Morten S. Nielsen1 and Tiago Gil Oliveira2 4 1 Department of Biomedicine, Aarhus University, Aarhus, Denmark 5 2 Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal 6 *Corresponding author: Sérgio Almeida, Department of Biomedicine, Aarhus University, Høegh- 7 Guldbergsgade 10, DK-8000C Aarhus, Denmark. Phone: +45 60511406. E-mail: [email protected] 8 9 10 11 12 13 Abstract 14 Vps10p domain receptors are important for regulating intracellular protein sorting within the central 15 nervous system and as such constitute risk factors for different brain pathologies. Here, we show that 16 removal of SorCS2 leads to altered lysosomal activity in mouse primary neurons. SorCS2-/- neurons show 17 elevated lysosomal markers such as LAMP1 and acidic hydrolases including cathepsin B and D. Despite 18 increased levels, SorCS2-/- neurons fail to degrade cathepsin specific substrates in a live context. SorCS2- 19 deficient mice present an increase in lysolipids, which may contribute to membrane permeabilization and 20 increased susceptibility to lysosomal stress. Our findings highlight SorCS2 as an important factor for a 21 balanced neuronal lysosome milieu. -
Discovering Imaging Endophenotypes for Major Depression
Molecular Psychiatry (2011) 16, 604–619 & 2011 Macmillan Publishers Limited All rights reserved 1359-4184/11 www.nature.com/mp PERSPECTIVE Discovering imaging endophenotypes for major depression G Hasler1 and G Northoff2 1Psychiatric University Hospital, University of Berne, Berne, Switzerland and 2University of Ottawa Institute of Mental Health Research, Ottawa, ON, Canada Psychiatry research lacks an in-depth understanding of mood disorders phenotypes, leading to limited success of genetics studies of major depressive disorder (MDD). The dramatic progress in safe and affordable magnetic resonance-based imaging methods has the potential to identify subtle abnormalities of neural structures, connectivity and function in mood disordered subjects. This review paper presents strategies to improve the phenotypic definition of MDD by proposing imaging endophenotypes derived from magnetic resonance spectroscopy measures, such as cortical gamma-amino butyric acid (GABA) and glutamate/glutamine concentrations, and from measures of resting-state activity and functional connectivity. The proposed endophenotypes are discussed regarding specificity, mood state-independence, heritability, familiarity, clinical relevance and possible associations with candidate genes. By improving phenotypic definitions, the discovery of new imaging endophenotypes will increase the power of candidate gene and genome-wide associations studies. It will also help to develop and evaluate novel therapeutic treatments and enable clinicians to apply individually tailored therapeutic approaches. Finally, improvements of the phenotypic definition of MDD based on neuroimaging measures will contribute to a new classification system of mood disorders based on etiology and pathophysiology. Molecular Psychiatry (2011) 16, 604–619; doi:10.1038/mp.2011.23 Keywords: affective disorders; genetics; intermediate phenotype; MRI; MRS; neuroimaging Twin and family studies have demonstrated that 31–42% (2) An endophenotype is heritable. -
Obituary Johan Schioldann
Obituary Johan Schioldann To cite this version: Johan Schioldann. Obituary. History of Psychiatry, SAGE Publications, 2006, 17 (2), pp.247-252. 10.1177/0957154X06061602. hal-00570850 HAL Id: hal-00570850 https://hal.archives-ouvertes.fr/hal-00570850 Submitted on 1 Mar 2011 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. HPY 17(2) Schou obituary 2/5/06 09:21 Page 1 History of Psychiatry, 17(2): 247–252 Copyright © 2006 SAGE Publications (London, Thousand Oaks, CA and New Delhi) www.sagepublications.com [200606] DOI: 10.1177/0957154X06061602 Obituary Mogens Abelin Schou (1918–2005) – half a century with lithium JOHAN SCHIOLDANN* Mogens Schou, the most prominent of the pioneers of modern lithium therapy, passed away on 29 September 2005. He was 86 years old. A couple of days before, he had returned home from an IGSLI (International Group for the Study of Lithium-Treated Patients) meeting in Poland. He succumbed to pneumonia, having managed to finish a last manuscript just hours before. Schou was born in Copenhagen in 1918. His father, Hans Jacob Schou, an influential figure in Danish psychiatry, adopted the notion of a biological basis of affective disorders from his countryman, Carl Lange, one of the early era lithium pioneers (Schioldann, 2001), and established a research laboratory to study the possible biochemical and physiological changes in manic-depressive illness (Schou, 2005). -
Recent Efforts to Dissect the Genetic Basis of Alcohol Use and Abuse
Title: Recent efforts to dissect the genetic basis of alcohol use and abuse Authors: Sandra Sanchez-Roige, PhD1, Abraham A. Palmer, PhD1,2, Toni-Kim Clarke, PhD3 Affiliations: 1 Department of Psychiatry, University of California San Diego, La Jolla, CA, 92093, USA, 2 Institute for Genomic Medicine, University of California San Diego, La Jolla, CA, 92093, USA, 3 Division of Psychiatry, University of Edinburgh, Edinburgh, UK Correspondence: Sandra Sanchez-Roige, Ph.D. Department of Psychiatry, University of California San Diego, La Jolla, CA, 92093, USA. E-mail: [email protected] Short Title: Alcohol genetics Keywords: alcoholism; alcohol consumption; AUDIT; alcohol-metabolizing genes; Genome- wide association studies; Genetics Word count: 3,981 1 Abstract (202 words) Alcohol use disorders (AUD) are defined by several symptom criteria, which can be further dissected at the genetic level. Over the past several years, our understanding of the genetic factors influencing alcohol use and abuse has progressed tremendously; hundreds of loci have now been implicated in different aspects of alcohol use. Previously known associations with alcohol metabolizing enzymes (ADH1B, ALDH2) have been definitively replicated. Additionally, novel associations with loci containing the genes KLB, GCKR, CRHR1 and CADM2 have been reported. Downstream analyses have leveraged these genetic findings to reveal important relationships between alcohol use behaviors and both physical and mental health. AUD and aspects of alcohol misuse have been shown to overlap strongly with psychiatric disorders, whereas aspects of alcohol consumption have shown stronger links to metabolism. These results demonstrate that the genetic architecture of alcohol consumption only partially overlaps with the genetics of clinically defined AUD. -
Altered Brain Network Connectivity As a Potential Endophenotype Of
www.nature.com/scientificreports OPEN Altered Brain Network Connectivity as a Potential Endophenotype of Schizophrenia Received: 25 January 2017 Peng Li1, Teng-Teng Fan1, Rong-Jiang Zhao3, Ying Han4, Le Shi1,4, Hong-Qiang Sun1, Accepted: 2 June 2017 Si-Jing Chen1, Jie Shi4, Xiao Lin1,2 & Lin Lu1,2,4 Published: xx xx xxxx Abnormal functional brain connectivity could be considered an endophenotype of psychosis in schizophrenia. Identifying candidate endophenotypes may serve as a tool for elucidating its biological and neural mechanisms. The present study investigated the similarities and differences of features of brain network connectivity between patients and their first-degree relatives. Independent component analysis was conducted on imaging data collected from 34 healthy controls, 33 schizophrenia patients, and 30 unaffected first-degree relatives. The correlation between functional connectivity with neurocognitive performance and clinical symptoms were calculated. Abnormalities of between- network connectivity largely overlapped in patients and first-degree relatives, but the extent of such abnormalities was relatively minor in relatives. Negative connectivity between language networks and executive control networks was impaired in schizophrenia patients and their first-degree relatives, and this decreased connectivity was correlated with performance in language processing. Similar impairments were found in high-visual network and executive network coupling, and this decreased connection was correlated with the severity of positive symptoms in patients. The results indicated that abnormal functional connectivity within and between perceptual systems (i.e., high-visual and language) and executive control networks was related to the generic risk of schizophrenia, which makes it a potential endophenotype for schizophrenia. Schizophrenia is one of the most complex and heterogeneous mental disorders. -
Anhedonia and Deficits in Positive Emotional Experience In
ANHEDONIA AND DEFICITS IN POSITIVE EMOTIONAL EXPERIENCE IN INDIVIDUALS WITH GENETIC LIABILITY FOR SCHIZOPHRENIA A Dissertation Presented to The Faculty of the Graduate School At the University of Missouri In Partial Fulfillment Of the Requirements for the Degree Doctor of Philosophy By Anna R. Docherty Dr. John G. Kerns, Dissertation Supervisor MAY 2013 The undersigned, appointed by the dean of the Graduate School, have examined the dissertation entitled ANHEDONIA AND DEFICITS IN POSITIVE EMOTIONAL EXPERIENCE IN INDIVIDUALS WITH GENETIC LIABILITY FOR SCHIZOPHRENIA Presented by Anna Docherty A candidate for the degree of Doctor of Philosophy of Psychology And hereby certify that, in their opinion, it is worthy of acceptance. Professor John Kerns Professor Denis McCarthy Professor Bruce Bartholow Professor Judith Miles ACKNOWLEDGEMENTS I would like to express my deepest gratitude to John Kerns, my advisor, mentor, and dissertation committee chair. He has provided excellent guidance and support during my doctoral training. I am also grateful to my dissertation committee members, Drs. Denis McCarthy, Bruce Bartholow, and Judith Miles. Each member has provided strong mentorship and support throughout the development of this program of research, and their expertise has greatly enhanced this dissertation. Drs. Scott Sponheim, Phil Wood, Deborah Levy, and Daniel Weinberger have provided exceptional mentorship, resources, and technical support during the process of research design, data collection, and data analysis. I am grateful to the participants, -
No Evidence for Physical Anhedonia As a Candidate Symptom Or an Endophenotype in Bipolar Affective Disorder
No evidence for physical anhedonia as a candidate symptom or an endophenotype in bipolar affective disorder. Bruno Etain, Isabelle Roy, Chantal Henry, Angela Rousseva, Franck Schurhoff, Marion Leboyer, Frank Bellivier To cite this version: Bruno Etain, Isabelle Roy, Chantal Henry, Angela Rousseva, Franck Schurhoff, et al.. No evidence for physical anhedonia as a candidate symptom or an endophenotype in bipolar affective disorder.. Bipolar Disorders, Wiley, 2007, 9 (7), pp.706-12. 10.1111/j.1399-5618.2007.00413.x. inserm-00133082 HAL Id: inserm-00133082 https://www.hal.inserm.fr/inserm-00133082 Submitted on 28 Sep 2009 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Physical anhedonia and bipolar disorder - #BDI5O746 No evidence for physical anhedonia being a candidate symptom or an endophenotype in bipolar affective disorder. Bruno ETAIN, MD 1,2, Isabelle ROY, MD 1,2, Chantal HENRY, MD, PhD 3, Angela ROUSSEVA, MD 1,2, Franck SCHURHOFF, MD 1,2, Marion LEBOYER, MD, PhD 1,2, Frank BELLIVIER, MD, PhD 1,2. 1. AP-HP, Hopital Albert Chenevier, Département Hospitalo-universitaire de Psychiatrie ; Université Paris XII ; 94010 Créteil ; France 2. INSERM U513, Faculté de Médecine, 94000 Créteil, France 3. -
Chicken Linkage Disequilibrium Is Much More Complex Over Much Longer Distance Than Previously Appreciated
Look Over the Horizon - Chicken Linkage Disequilibrium is Much More Complex Over Much Longer Distance than Previously Appreciated Ehud Lipkin ( [email protected] ) Hebrew University of Jerusalem Janet E. Fulton Hy-Line (United States) Jacqueline Smith University of Edinburgh David W. Burt University of Edinburgh Morris Soller Hebrew University of Jerusalem Research Article Keywords: Chicken, long-range linkage disequilibrium, QTL, F6, LD blocks Posted Date: June 17th, 2021 DOI: https://doi.org/10.21203/rs.3.rs-598396/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/23 Abstract Background Appreciable Linkage Disequilibrium (LD) is commonly found between pairs of loci close to one another, decreasing rapidly with distance between the loci. This provides the basis studies to map Quantitative Trait Loci Regions (QTLRs), where it is custom to assume that the closest sites to a signicant markers are the prime candidate to be the causative mutation. Nevertheless, Long-Range LD (LRLD) can also be found among well-separated sites. LD blocks are runs of genomic sites all having appreciable LD with one another. High LD and LRLD are often separated by genomic sites with which they have practically no LD. Thus, not only can LD be found among distant loci, but also its pattern may be complex, comprised of fragmented blocks. Here, chicken LRLD and LD blocks, and their relationship with previously described Marek’s Disease (MD) QTLRs, were studied in an F6 population from a full-sib advanced intercross line, and in eight commercial pure layer lines. -
The Transition from Primary Colorectal Cancer to Isolated Peritoneal Malignancy
medRxiv preprint doi: https://doi.org/10.1101/2020.02.24.20027318; this version posted February 25, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license . The transition from primary colorectal cancer to isolated peritoneal malignancy is associated with a hypermutant, hypermethylated state Sally Hallam1, Joanne Stockton1, Claire Bryer1, Celina Whalley1, Valerie Pestinger1, Haney Youssef1, Andrew D Beggs1 1 = Surgical Research Laboratory, Institute of Cancer & Genomic Science, University of Birmingham, B15 2TT. Correspondence to: Andrew Beggs, [email protected] KEYWORDS: Colorectal cancer, peritoneal metastasis ABBREVIATIONS: Colorectal cancer (CRC), Colorectal peritoneal metastasis (CPM), Cytoreductive surgery and heated intraperitoneal chemotherapy (CRS & HIPEC), Disease free survival (DFS), Differentially methylated regions (DMR), Overall survival (OS), TableFormalin fixed paraffin embedded (FFPE), Hepatocellular carcinoma (HCC) ARTICLE CATEGORY: Research article NOTE: This preprint reports new research that has not been certified by peer review and should not be used to guide clinical practice. 1 medRxiv preprint doi: https://doi.org/10.1101/2020.02.24.20027318; this version posted February 25, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license . NOVELTY AND IMPACT: Colorectal peritoneal metastasis (CPM) are associated with limited and variable survival despite patient selection using known prognostic factors and optimal currently available treatments.