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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Linking proteomic alterations in schizophrenia hippocampus to NMDAr hypofunction in human neurons and oligodendrocytes

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Author(s):
Zuccoli, Giuliana S. [1] ; Reis-de-Oliveira, Guilherme [1] ; Garbes, Bruna [2] ; Falkai, Peter [3] ; Schmitt, Andrea [3] ; Nakaya, I, Helder ; Martins-de-Souza, Daniel [1, 4, 5, 6]
Total Authors: 7
Affiliation:
[1] Univ Campinas UNICAMP, Inst Biol, Dept Biochem & Tissue Biol, Lab Neuroprote, Campinas - Brazil
[2] I, Univ Sao Paulo, Sch Pharmaceut Sci, Dept Clin & Toxicol Anal, Sao Paulo - Brazil
[3] Ludwig Maximillian Univ Munich LMU, Dept Psychiat & Psychotherapy, Munich - Germany
[4] Conselho Nacl Desenvolvimento Cient & Tecnol, Inst Nacl Biomarcadores Neuropsiquiatria INBION, Sao Paulo - Brazil
[5] DOr Inst Res & Educ IDOR, Sao Paulo - Brazil
[6] Univ Estadual Campinas, Expt Med Res Cluster EMRC, Campinas - Brazil
Total Affiliations: 6
Document type: Journal article
Source: EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE; v. 271, n. 8, p. 1579-1586, DEC 2021.
Web of Science Citations: 0
Abstract

Glutamatergic neurotransmission dysfunction and the early involvement of the hippocampus have been proposed to be important aspects of the pathophysiology of schizophrenia. Here, we performed proteomic analysis of hippocampus postmortem samples from schizophrenia patients as well as neural cells-neurons and oligodendrocytes-treated with MK-801, an NMDA receptor antagonist. There were similarities in processes such as oxidative stress and apoptotic process when comparing hippocampus samples with MK-801-treated neurons, and in proteins synthesis when comparing hippocampus samples with MK-801-treated oligodendrocytes. This reveals that studying the effects of glutamatergic dysfunction in different neural cells can contribute to a better understanding of what it is observed in schizophrenia patients' postmortem brains. (AU)

FAPESP's process: 18/01410-1 - Evaluating the effects of clozapine on immune system cells
Grantee:Guilherme Reis-De-Oliveira
Support Opportunities: Scholarships in Brazil - Doctorate (Direct)
FAPESP's process: 17/25588-1 - From the basic understanding to clinical biomarkers to schizophrenia: a neuroproteomics-centered multidisciplinary study
Grantee:Daniel Martins-de-Souza
Support Opportunities: Research Projects - Thematic Grants
FAPESP's process: 13/08216-2 - CRID - Center for Research in Inflammatory Diseases
Grantee:Fernando de Queiroz Cunha
Support Opportunities: Research Grants - Research, Innovation and Dissemination Centers - RIDC
FAPESP's process: 19/00098-7 - Multi-User Equipment approved in grant 2017/25588-1: cromatógrafo Acquity UPLC I-Class
Grantee:Daniel Martins-de-Souza
Support Opportunities: Multi-user Equipment Program
FAPESP's process: 12/19278-6 - Systems biology of long non-coding RNAs
Grantee:Helder Takashi Imoto Nakaya
Support Opportunities: Research Grants - Young Investigators Grants
FAPESP's process: 17/50137-3 - Long noncoding RNA interplay with the host microbiome may determine mucosal influenza vaccine immunogenicity
Grantee:Helder Takashi Imoto Nakaya
Support Opportunities: Regular Research Grants
FAPESP's process: 18/14666-4 - Influence of the endocannabinoid system on the energetic profile of neural cells during neurodevelopment: implications in Schizophrenia
Grantee:Giuliana da Silva Zuccoli
Support Opportunities: Scholarships in Brazil - Doctorate