Skip to main content
Erschienen in: European Archives of Psychiatry and Clinical Neuroscience 1/2017

04.07.2016 | Invited Review

Psychiatric disorders biochemical pathways unraveled by human brain proteomics

verfasst von: Verônica M. Saia-Cereda, Juliana S. Cassoli, Daniel Martins-de-Souza, Juliana M. Nascimento

Erschienen in: European Archives of Psychiatry and Clinical Neuroscience | Ausgabe 1/2017

Einloggen, um Zugang zu erhalten

Abstract

Approximately 25 % of the world population is affected by a mental disorder at some point in their life. Yet, only in the mid-twentieth century a biological cause has been proposed for these diseases. Since then, several studies have been conducted toward a better comprehension of those disorders, and although a strong genetic influence was revealed, the role of these genes in disease mechanism is still unclear. This led most recent studies to focus on the molecular basis of mental disorders. One line of investigation that has risen in the post-genomic era is proteomics, due to its power of revealing proteins and biochemical pathways associated with biological systems. Therefore, this review compiled and analyzed data of differentially expressed proteins, which were found in postmortem brain studies of the three most prevalent psychiatric diseases: schizophrenia, bipolar disorder and major depressive disorders. Overviewing both the proteomic methods used in postmortem brain studies, the most consistent metabolic pathways found altered in these diseases. We have unraveled those disorders share about 21 % of proteins affected, and though most are related to energy metabolism pathways deregulation, the main differences found are 14-3-3-mediated signaling in schizophrenia, mitochondrial dysfunction in bipolar disorder and oxidative phosphorylation in depression.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
5.
Zurück zum Zitat Nock MK, Hwang I, Sampson NA, Kessler RC (2010) Mental disorders, comorbidity and suicidal behavior: results from the National Comorbidity Survey Replication. Mol Psychiatry 15:868–876. doi:10.1038/mp.2009.29 PubMedCrossRef Nock MK, Hwang I, Sampson NA, Kessler RC (2010) Mental disorders, comorbidity and suicidal behavior: results from the National Comorbidity Survey Replication. Mol Psychiatry 15:868–876. doi:10.​1038/​mp.​2009.​29 PubMedCrossRef
8.
Zurück zum Zitat To S, Zepf R, Woods AG (2005) The symptoms, neurobiology, and current pharmacological treatment of depression. J Neurosci Nurs 32:102–107 To S, Zepf R, Woods AG (2005) The symptoms, neurobiology, and current pharmacological treatment of depression. J Neurosci Nurs 32:102–107
11.
Zurück zum Zitat Trivedi MH, Rush AJ, Wisniewski SR et al (2006) Factors associated with health-related quality of life among outpatients with major depressive disorder: a STAR* D report. J Clin Psychiatry 67:185–195PubMedCrossRef Trivedi MH, Rush AJ, Wisniewski SR et al (2006) Factors associated with health-related quality of life among outpatients with major depressive disorder: a STAR* D report. J Clin Psychiatry 67:185–195PubMedCrossRef
17.
Zurück zum Zitat Hegarty JD, Baldessarini RJ, Oepen G (1994) One hundred years of schizophrenia. Am J Psychiatry 151:1409–1416PubMedCrossRef Hegarty JD, Baldessarini RJ, Oepen G (1994) One hundred years of schizophrenia. Am J Psychiatry 151:1409–1416PubMedCrossRef
21.
23.
Zurück zum Zitat Maj M (2003) The effect of lithium in bipolar disorder: a review of recent research evidence. Bipolar Disord 5:180–188PubMedCrossRef Maj M (2003) The effect of lithium in bipolar disorder: a review of recent research evidence. Bipolar Disord 5:180–188PubMedCrossRef
29.
Zurück zum Zitat Klose J, Kobalz U (1995) Two-dimensional electrophoresis of proteins: an updated protocol and implications for a functional analysis of the genome. Electrophoresis 16:1034–1059PubMedCrossRef Klose J, Kobalz U (1995) Two-dimensional electrophoresis of proteins: an updated protocol and implications for a functional analysis of the genome. Electrophoresis 16:1034–1059PubMedCrossRef
32.
Zurück zum Zitat Kislinger T, Emili A (2003) Going global: protein expression profiling using shotgun mass spectrometry. Curr Opin Mol Ther 5:285–293PubMed Kislinger T, Emili A (2003) Going global: protein expression profiling using shotgun mass spectrometry. Curr Opin Mol Ther 5:285–293PubMed
35.
Zurück zum Zitat Rinas A, Jones LM (2014) Fast photochemical oxidation of proteins coupled to multidimensional protein identification technology (MudPIT): expanding footprinting strategies to complex systems. J Am Soc Mass Spectrom 26:540–546. doi:10.1007/s13361-014-1017-6 PubMedCrossRef Rinas A, Jones LM (2014) Fast photochemical oxidation of proteins coupled to multidimensional protein identification technology (MudPIT): expanding footprinting strategies to complex systems. J Am Soc Mass Spectrom 26:540–546. doi:10.​1007/​s13361-014-1017-6 PubMedCrossRef
37.
Zurück zum Zitat Pernikářová V, Bouchal P (2015) Targeted proteomics of solid cancers: from quantification of known biomarkers towards reading the digital proteome maps. Expert Rev Proteomics 9450:1–17. doi:10.1586/14789450.2015.1094381 Pernikářová V, Bouchal P (2015) Targeted proteomics of solid cancers: from quantification of known biomarkers towards reading the digital proteome maps. Expert Rev Proteomics 9450:1–17. doi:10.​1586/​14789450.​2015.​1094381
38.
Zurück zum Zitat Gygi SP, Rist B, Gerber SA et al (1999) Quantitative analysis of complex protein mixtures using isotope-coded affinity tags. Nat Biotechnol 17:994–999. doi:10.1038/13690 PubMedCrossRef Gygi SP, Rist B, Gerber SA et al (1999) Quantitative analysis of complex protein mixtures using isotope-coded affinity tags. Nat Biotechnol 17:994–999. doi:10.​1038/​13690 PubMedCrossRef
45.
Zurück zum Zitat Lu P, Vogel C, Wang R et al (2007) Absolute protein expression profiling estimates the relative contributions of transcriptional and translational regulation. Nat Biotechnol 25:117–124. doi:10.1038/nbt1270 PubMedCrossRef Lu P, Vogel C, Wang R et al (2007) Absolute protein expression profiling estimates the relative contributions of transcriptional and translational regulation. Nat Biotechnol 25:117–124. doi:10.​1038/​nbt1270 PubMedCrossRef
46.
47.
Zurück zum Zitat Ishihama Y (2005) Exponentially modified protein abundance index (emPAI) for estimation of absolute protein amount in proteomics by the number of sequenced peptides per protein. Mol Cell Proteomics 4:1265–1272. doi:10.1074/mcp.M500061-MCP200 PubMedCrossRef Ishihama Y (2005) Exponentially modified protein abundance index (emPAI) for estimation of absolute protein amount in proteomics by the number of sequenced peptides per protein. Mol Cell Proteomics 4:1265–1272. doi:10.​1074/​mcp.​M500061-MCP200 PubMedCrossRef
49.
Zurück zum Zitat Chelius D, Bondarenko P (2002) Quantitative profiling of proteins in complex mixtures using liquid chromatography and mass spectrometry. J Proteome Res 1:317–323PubMedCrossRef Chelius D, Bondarenko P (2002) Quantitative profiling of proteins in complex mixtures using liquid chromatography and mass spectrometry. J Proteome Res 1:317–323PubMedCrossRef
59.
Zurück zum Zitat Schilling B, MacLean B, Held JM et al (2015) Multiplexed, scheduled, high-resolution parallel reaction monitoring on a full scan QqTOF instrument with integrated data-dependent and targeted mass spectrometric workflows. Anal Chem 87:10222–10229. doi:10.1021/acs.analchem.5b02983 PubMedCrossRef Schilling B, MacLean B, Held JM et al (2015) Multiplexed, scheduled, high-resolution parallel reaction monitoring on a full scan QqTOF instrument with integrated data-dependent and targeted mass spectrometric workflows. Anal Chem 87:10222–10229. doi:10.​1021/​acs.​analchem.​5b02983 PubMedCrossRef
64.
Zurück zum Zitat Khan SS, Smith MS, Reda D et al (2004) Multiplex bead array assays for detection of soluble cytokines : comparisons of sensitivity and quantitative values among kits from multiple manufacturers. Cytometry B Clin Cytom 39:35–39. doi:10.1002/cyto.b.20021 CrossRef Khan SS, Smith MS, Reda D et al (2004) Multiplex bead array assays for detection of soluble cytokines : comparisons of sensitivity and quantitative values among kits from multiple manufacturers. Cytometry B Clin Cytom 39:35–39. doi:10.​1002/​cyto.​b.​20021 CrossRef
66.
Zurück zum Zitat Nechansky A, Grunt S, Roitt IM, Kircheis R (2008) Comparison of the calibration standards of three commercially available multiplex kits for human cytokine measurement to WHO standards reveals striking differences. Biomark Insights 43:227–235 Nechansky A, Grunt S, Roitt IM, Kircheis R (2008) Comparison of the calibration standards of three commercially available multiplex kits for human cytokine measurement to WHO standards reveals striking differences. Biomark Insights 43:227–235
69.
Zurück zum Zitat Beasley CL, Pennington K, Behan A et al (2006) Proteomic analysis of the anterior cingulate cortex in the major psychiatric disorders: evidence for disease-associated changes. Proteomics 6:3414–3425. doi:10.1002/pmic.200500069 PubMedCrossRef Beasley CL, Pennington K, Behan A et al (2006) Proteomic analysis of the anterior cingulate cortex in the major psychiatric disorders: evidence for disease-associated changes. Proteomics 6:3414–3425. doi:10.​1002/​pmic.​200500069 PubMedCrossRef
71.
72.
Zurück zum Zitat Martins-De-Souza D, Gattaz WF, Schmitt A et al (2009) Prefrontal cortex shotgun proteome analysis reveals altered calcium homeostasis and immune system imbalance in schizophrenia. Eur Arch Psychiatry Clin Neurosci 259:151–163. doi:10.1007/s00406-008-0847-2 PubMedCrossRef Martins-De-Souza D, Gattaz WF, Schmitt A et al (2009) Prefrontal cortex shotgun proteome analysis reveals altered calcium homeostasis and immune system imbalance in schizophrenia. Eur Arch Psychiatry Clin Neurosci 259:151–163. doi:10.​1007/​s00406-008-0847-2 PubMedCrossRef
73.
Zurück zum Zitat Saia-Cereda VM, Cassoli JS, Schmitt A et al (2015) Proteomics of the corpus callosum unravel pivotal players in the dysfunction of cell signaling, structure, and myelination in schizophrenia brains. Eur Arch Psychiatry Clin Neurosci 265:601–612. doi:10.1007/s00406-015-0621-1 PubMedCrossRef Saia-Cereda VM, Cassoli JS, Schmitt A et al (2015) Proteomics of the corpus callosum unravel pivotal players in the dysfunction of cell signaling, structure, and myelination in schizophrenia brains. Eur Arch Psychiatry Clin Neurosci 265:601–612. doi:10.​1007/​s00406-015-0621-1 PubMedCrossRef
74.
Zurück zum Zitat Martins-De-Souza D, Gattaz WF, Schmitt A et al (2009) Alterations in oligodendrocyte proteins, calcium homeostasis and new potential markers in schizophrenia anterior temporal lobe are revealed by shotgun proteome analysis. J Neural Transm 116:275–289. doi:10.1007/s00702-008-0156-y PubMedCrossRef Martins-De-Souza D, Gattaz WF, Schmitt A et al (2009) Alterations in oligodendrocyte proteins, calcium homeostasis and new potential markers in schizophrenia anterior temporal lobe are revealed by shotgun proteome analysis. J Neural Transm 116:275–289. doi:10.​1007/​s00702-008-0156-y PubMedCrossRef
75.
Zurück zum Zitat Martins-de-Souza D, Gattaz WF, Schmitt A et al (2009) Proteomic analysis of dorsolateral prefrontal cortex indicates the involvement of cytoskeleton, oligodendrocyte, energy metabolism and new potential markers in schizophrenia. J Psychiatr Res 43:978–986. doi:10.1016/j.jpsychires.2008.11.006 PubMedCrossRef Martins-de-Souza D, Gattaz WF, Schmitt A et al (2009) Proteomic analysis of dorsolateral prefrontal cortex indicates the involvement of cytoskeleton, oligodendrocyte, energy metabolism and new potential markers in schizophrenia. J Psychiatr Res 43:978–986. doi:10.​1016/​j.​jpsychires.​2008.​11.​006 PubMedCrossRef
78.
79.
Zurück zum Zitat Johnston-Wilson NL, Sims CD, Hofmann JP et al (2000) Disease-specific alterations in frontal cortex brain proteins in schizophrenia, bipolar disorder, and major depressive disorder. The Stanley Neuropathology Consortium. Mol Psychiatry 5:142–149. doi:10.1038/sj.mp.4000696 PubMedCrossRef Johnston-Wilson NL, Sims CD, Hofmann JP et al (2000) Disease-specific alterations in frontal cortex brain proteins in schizophrenia, bipolar disorder, and major depressive disorder. The Stanley Neuropathology Consortium. Mol Psychiatry 5:142–149. doi:10.​1038/​sj.​mp.​4000696 PubMedCrossRef
80.
Zurück zum Zitat Prabakaran S, Swatton JE, Ryan MM et al (2004) Mitochondrial dysfunction in schizophrenia: evidence for compromised brain metabolism and oxidative stress. Mol Psychiatry 9(684–697):643. doi:10.1038/sj.mp.4001532 CrossRef Prabakaran S, Swatton JE, Ryan MM et al (2004) Mitochondrial dysfunction in schizophrenia: evidence for compromised brain metabolism and oxidative stress. Mol Psychiatry 9(684–697):643. doi:10.​1038/​sj.​mp.​4001532 CrossRef
81.
82.
Zurück zum Zitat Pennington K, Beasley CL, Dicker P et al (2008) Prominent synaptic and metabolic abnormalities revealed by proteomic analysis of the dorsolateral prefrontal cortex in schizophrenia and bipolar disorder. Mol Psychiatry 13:1102–1117. doi:10.1038/sj.mp.4002098 PubMedCrossRef Pennington K, Beasley CL, Dicker P et al (2008) Prominent synaptic and metabolic abnormalities revealed by proteomic analysis of the dorsolateral prefrontal cortex in schizophrenia and bipolar disorder. Mol Psychiatry 13:1102–1117. doi:10.​1038/​sj.​mp.​4002098 PubMedCrossRef
84.
Zurück zum Zitat Wesseling H, Gottschalk MG, Bahn S (2014) Targeted multiplexed selected reaction monitoring analysis evaluates protein expression changes of molecular risk factors for major psychiatric disorders. Int J Neuropsychopharmacol 18:pyu015. doi:10.1093/ijnp/pyu015 PubMedPubMedCentralCrossRef Wesseling H, Gottschalk MG, Bahn S (2014) Targeted multiplexed selected reaction monitoring analysis evaluates protein expression changes of molecular risk factors for major psychiatric disorders. Int J Neuropsychopharmacol 18:pyu015. doi:10.​1093/​ijnp/​pyu015 PubMedPubMedCentralCrossRef
86.
Zurück zum Zitat Gottschalk MG, Wesseling H, Guest PC, Bahn S (2015) Proteomic enrichment analysis of psychotic and affective disorders reveals common signatures in presynaptic glutamatergic signaling and energy. Metabolism. doi:10.1093/ijnp/pyu019 Gottschalk MG, Wesseling H, Guest PC, Bahn S (2015) Proteomic enrichment analysis of psychotic and affective disorders reveals common signatures in presynaptic glutamatergic signaling and energy. Metabolism. doi:10.​1093/​ijnp/​pyu019
90.
Zurück zum Zitat Möller HJ (2003) Bipolar disorder and schizophrenia: distinct illnesses or a continuum? J Clin Psychiatry 64:23–27PubMed Möller HJ (2003) Bipolar disorder and schizophrenia: distinct illnesses or a continuum? J Clin Psychiatry 64:23–27PubMed
93.
Zurück zum Zitat Davis KL, Stewart DG, Friedman JI, Buchsbaum M, Harvey PD, Hof PR, Haroutunian V (2003) White matter changes in schizophrenia: evidence for myelin-related dysfunction. Arch Gen Psychiatry 60(5):443–456PubMedCrossRef Davis KL, Stewart DG, Friedman JI, Buchsbaum M, Harvey PD, Hof PR, Haroutunian V (2003) White matter changes in schizophrenia: evidence for myelin-related dysfunction. Arch Gen Psychiatry 60(5):443–456PubMedCrossRef
95.
Zurück zum Zitat Flynn SW, Lang DJ, MacKay AL et al (2003) Abnormalities of myelination in schizophrenia detected in vivo with MRI, and post-mortem with analysis of oligodendrocyte proteins. Mol Psychiatry 8:811–820. doi:10.1038/sj.mp.4001337 PubMedCrossRef Flynn SW, Lang DJ, MacKay AL et al (2003) Abnormalities of myelination in schizophrenia detected in vivo with MRI, and post-mortem with analysis of oligodendrocyte proteins. Mol Psychiatry 8:811–820. doi:10.​1038/​sj.​mp.​4001337 PubMedCrossRef
97.
Zurück zum Zitat Deloulme JC, Raponi E, Gentil BJ et al (2004) Nuclear expression of S100B in oligodendrocyte progenitor cells correlates with differentiation toward the oligodendroglial lineage and modulates oligodendrocytes maturation. Mol Cell Neurosci 27:453–465. doi:10.1016/j.mcn.2004.07.008 PubMedCrossRef Deloulme JC, Raponi E, Gentil BJ et al (2004) Nuclear expression of S100B in oligodendrocyte progenitor cells correlates with differentiation toward the oligodendroglial lineage and modulates oligodendrocytes maturation. Mol Cell Neurosci 27:453–465. doi:10.​1016/​j.​mcn.​2004.​07.​008 PubMedCrossRef
101.
Zurück zum Zitat Tkachev D, Mimmack ML, Ryan MM et al (2003) Oligodendrocyte dysfunction in schizophrenia and bipolar disorder. Lancet 362:798–805PubMedCrossRef Tkachev D, Mimmack ML, Ryan MM et al (2003) Oligodendrocyte dysfunction in schizophrenia and bipolar disorder. Lancet 362:798–805PubMedCrossRef
103.
Zurück zum Zitat Aston C, Jiang L, Sokolov BP (2005) Transcriptional profiling reveals evidence for signaling and oligodendroglial abnormalities in the temporal cortex from patients with major depressive disorder. Mol Psychiatry 10:309–322. doi:10.1038/sj.mp.4001565 PubMedCrossRef Aston C, Jiang L, Sokolov BP (2005) Transcriptional profiling reveals evidence for signaling and oligodendroglial abnormalities in the temporal cortex from patients with major depressive disorder. Mol Psychiatry 10:309–322. doi:10.​1038/​sj.​mp.​4001565 PubMedCrossRef
104.
108.
Zurück zum Zitat Wang Q, Wang Y, Ji W et al (2015) SNAP25 is associated with schizophrenia and major depressive disorder in the Han Chinese population. J Clin Psychiatry 76:76–82. doi:10.4088/JCP.13m08962 CrossRef Wang Q, Wang Y, Ji W et al (2015) SNAP25 is associated with schizophrenia and major depressive disorder in the Han Chinese population. J Clin Psychiatry 76:76–82. doi:10.​4088/​JCP.​13m08962 CrossRef
109.
Zurück zum Zitat Biewenga JE, Schrama LH, Gispen WH (1996) Presynaptic phosphoprotein B-50/GAP-43 in neuronal and synaptic plasticity. Acta Biochim Pol 43:327–338PubMed Biewenga JE, Schrama LH, Gispen WH (1996) Presynaptic phosphoprotein B-50/GAP-43 in neuronal and synaptic plasticity. Acta Biochim Pol 43:327–338PubMed
110.
Zurück zum Zitat Suzuki T, Mitake S, Okumura-Noji K et al (1997) Excitable membranes and synaptic transmission: postsynaptic mechanisms. Localization of alpha-internexin in the postsynaptic density of the rat brain. Brain Res 765:74–80PubMedCrossRef Suzuki T, Mitake S, Okumura-Noji K et al (1997) Excitable membranes and synaptic transmission: postsynaptic mechanisms. Localization of alpha-internexin in the postsynaptic density of the rat brain. Brain Res 765:74–80PubMedCrossRef
111.
Zurück zum Zitat O’Dushlaine C, Rossin L, Lee PH et al (2015) Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nat Neurosci 18:199–209. doi:10.1038/nn.3922 CrossRef O’Dushlaine C, Rossin L, Lee PH et al (2015) Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nat Neurosci 18:199–209. doi:10.​1038/​nn.​3922 CrossRef
112.
Zurück zum Zitat Lee SH (2013) Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet. doi:10.1038/ng.2711 Lee SH (2013) Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet. doi:10.​1038/​ng.​2711
113.
117.
Zurück zum Zitat Bell R, Munro J, Russ C et al (2000) Systematic screening of the 14-3-3 eta (eta) chain gene for polymorphic variants and case-control analysis in schizophrenia. Am J Med Genet 96:736–743PubMedCrossRef Bell R, Munro J, Russ C et al (2000) Systematic screening of the 14-3-3 eta (eta) chain gene for polymorphic variants and case-control analysis in schizophrenia. Am J Med Genet 96:736–743PubMedCrossRef
119.
Zurück zum Zitat Schubert KO, Föcking M, Cotter DR (2015) Proteomic pathway analysis of the hippocampus in schizophrenia and bipolar affective disorder implicates 14-3-3 signaling, aryl hydrocarbon receptor signaling, and glucose metabolism: potential roles in GABAergic interneuron pathology. Schizophr Res. doi:10.1016/j.schres.2015.02.002 PubMed Schubert KO, Föcking M, Cotter DR (2015) Proteomic pathway analysis of the hippocampus in schizophrenia and bipolar affective disorder implicates 14-3-3 signaling, aryl hydrocarbon receptor signaling, and glucose metabolism: potential roles in GABAergic interneuron pathology. Schizophr Res. doi:10.​1016/​j.​schres.​2015.​02.​002 PubMed
120.
123.
Zurück zum Zitat Ruce MIC, Asile IONV, Asile MAV, Îlcea ALMAV (2015) c-abl and YWHAZ gene expression in gastric cancer. Rom J Morphol Embryol 56:717–723 Ruce MIC, Asile IONV, Asile MAV, Îlcea ALMAV (2015) c-abl and YWHAZ gene expression in gastric cancer. Rom J Morphol Embryol 56:717–723
125.
127.
Zurück zum Zitat Coyle JT, Schwarcz R (2013) Mind glue. Arch Gen Psychiatry 57:90–93CrossRef Coyle JT, Schwarcz R (2013) Mind glue. Arch Gen Psychiatry 57:90–93CrossRef
133.
138.
Zurück zum Zitat Du J, Machado-Vieira R, Khairova R (2011) Synaptic plasticity in the pathophysiology and treatment of bipolar disorder. Curr Top Behav Neurosci. doi:10.1007/7854 PubMed Du J, Machado-Vieira R, Khairova R (2011) Synaptic plasticity in the pathophysiology and treatment of bipolar disorder. Curr Top Behav Neurosci. doi:10.​1007/​7854 PubMed
139.
Zurück zum Zitat Che M, Wang R, Wang H, Zheng XFS (2015) Expanding roles of superoxide dismutases in cell regulation and cancer. Drug Discov Today 21:1–7 Che M, Wang R, Wang H, Zheng XFS (2015) Expanding roles of superoxide dismutases in cell regulation and cancer. Drug Discov Today 21:1–7
140.
Zurück zum Zitat Tsang CK, Liu Y, Thomas J et al (2014) Superoxide dismutase 1 acts as a nuclear transcription factor to regulate oxidative stress resistance. Nat Commun 5:1–11. doi:10.1038/ncomms4446 CrossRef Tsang CK, Liu Y, Thomas J et al (2014) Superoxide dismutase 1 acts as a nuclear transcription factor to regulate oxidative stress resistance. Nat Commun 5:1–11. doi:10.​1038/​ncomms4446 CrossRef
141.
Zurück zum Zitat Coughlin JM, Ishizuka K, Kano SI et al (2013) Marked reduction of soluble superoxide dismutase-1 (SOD1) in cerebrospinal fluid of patients with recent-onset schizophrenia. Mol Psychiatry 18:10–11. doi:10.1038/mp.2012.6 PubMedCrossRef Coughlin JM, Ishizuka K, Kano SI et al (2013) Marked reduction of soluble superoxide dismutase-1 (SOD1) in cerebrospinal fluid of patients with recent-onset schizophrenia. Mol Psychiatry 18:10–11. doi:10.​1038/​mp.​2012.​6 PubMedCrossRef
142.
Zurück zum Zitat Gigante AD, Andreazza AC, Lafer B et al (2011) Decreased mRNA expression of uncoupling protein 2, a mitochondrial proton transporter, in post-mortem prefrontal cortex from patients with bipolar disorder and schizophrenia. Neurosci Lett 505:47–51. doi:10.1016/j.neulet.2011.09.064 PubMedCrossRef Gigante AD, Andreazza AC, Lafer B et al (2011) Decreased mRNA expression of uncoupling protein 2, a mitochondrial proton transporter, in post-mortem prefrontal cortex from patients with bipolar disorder and schizophrenia. Neurosci Lett 505:47–51. doi:10.​1016/​j.​neulet.​2011.​09.​064 PubMedCrossRef
151.
Zurück zum Zitat Martins-de-Souza D (2014) Proteomics, metabolomics, and protein interactomics in the characterization of the molecular features of major depressive disorder. Dialogues Clin Neurosci 16:63–73PubMedPubMedCentral Martins-de-Souza D (2014) Proteomics, metabolomics, and protein interactomics in the characterization of the molecular features of major depressive disorder. Dialogues Clin Neurosci 16:63–73PubMedPubMedCentral
153.
Zurück zum Zitat Sawai H, Takai-igarashi T, Tanaka H (2015) Identification of collaborative activities with oxidative phosphorylation in bipolar disorder. Bioinformation 11:207PubMedPubMedCentralCrossRef Sawai H, Takai-igarashi T, Tanaka H (2015) Identification of collaborative activities with oxidative phosphorylation in bipolar disorder. Bioinformation 11:207PubMedPubMedCentralCrossRef
154.
Zurück zum Zitat Wesseling H, Chan MK, Tsang TM et al (2013) A combined metabonomic and proteomic approach identifies frontal cortex changes in a chronic phencyclidine rat model in relation to human schizophrenia brain pathology. Neuropsychopharmacology 38:2532–2544. doi:10.1038/npp.2013.160 PubMedPubMedCentralCrossRef Wesseling H, Chan MK, Tsang TM et al (2013) A combined metabonomic and proteomic approach identifies frontal cortex changes in a chronic phencyclidine rat model in relation to human schizophrenia brain pathology. Neuropsychopharmacology 38:2532–2544. doi:10.​1038/​npp.​2013.​160 PubMedPubMedCentralCrossRef
155.
Zurück zum Zitat Zubenko GS, Hughes HB, Jordan RM et al (2014) Differential hippocampal gene expression and pathway analysis in an etiology-based mouse model of major depressive disorder. Am J Med Genet B Neuropsychiatr Genet 165B:457–466. doi:10.1002/ajmg.b.32257 PubMedCrossRef Zubenko GS, Hughes HB, Jordan RM et al (2014) Differential hippocampal gene expression and pathway analysis in an etiology-based mouse model of major depressive disorder. Am J Med Genet B Neuropsychiatr Genet 165B:457–466. doi:10.​1002/​ajmg.​b.​32257 PubMedCrossRef
158.
Zurück zum Zitat Martins-de-souza D, Cassoli JS, Nascimento JM (2015) The protein interactome of collapsing response mediator protein-2 (CRMP2/DPYSL2) reveals novel partner proteins in brain tissue. Clin Relevance 2:1–25. doi:10.1002/prca.201500004.This Martins-de-souza D, Cassoli JS, Nascimento JM (2015) The protein interactome of collapsing response mediator protein-2 (CRMP2/DPYSL2) reveals novel partner proteins in brain tissue. Clin Relevance 2:1–25. doi:10.​1002/​prca.​201500004.​This
159.
160.
Zurück zum Zitat Kessler RC, Aguilar-Gaxiola S, Alonso J et al (2011) The global burden of mental disorders: an update from the WHO World Mental Health (WMH) surveys. Epidemiol Psichiatr Soc 18:23–33. doi:10.1017/S1121189X00001421 CrossRef Kessler RC, Aguilar-Gaxiola S, Alonso J et al (2011) The global burden of mental disorders: an update from the WHO World Mental Health (WMH) surveys. Epidemiol Psichiatr Soc 18:23–33. doi:10.​1017/​S1121189X0000142​1 CrossRef
163.
Zurück zum Zitat Kessler R, Foster C, Saunders W, Stang P (1995) Social consequences of psychiatric disorders, I: educational attainment. Am J Psychiatry 152:1026–1032PubMedCrossRef Kessler R, Foster C, Saunders W, Stang P (1995) Social consequences of psychiatric disorders, I: educational attainment. Am J Psychiatry 152:1026–1032PubMedCrossRef
Metadaten
Titel
Psychiatric disorders biochemical pathways unraveled by human brain proteomics
verfasst von
Verônica M. Saia-Cereda
Juliana S. Cassoli
Daniel Martins-de-Souza
Juliana M. Nascimento
Publikationsdatum
04.07.2016
Verlag
Springer Berlin Heidelberg
Erschienen in
European Archives of Psychiatry and Clinical Neuroscience / Ausgabe 1/2017
Print ISSN: 0940-1334
Elektronische ISSN: 1433-8491
DOI
https://doi.org/10.1007/s00406-016-0709-2

Weitere Artikel der Ausgabe 1/2017

European Archives of Psychiatry and Clinical Neuroscience 1/2017 Zur Ausgabe

Update Psychiatrie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.