Literature DB >> 30954559

Targeted lipidomics reveal derangement of ceramides in major depression and bipolar disorder.

Nathalie Brunkhorst-Kanaan1, Katharina Klatt-Schreiner2, Juliane Hackel2, Katrin Schröter1, Sandra Trautmann2, Lisa Hahnefeld2, Sabine Wicker3, Andreas Reif1, Dominique Thomas2, Gerd Geisslinger4, Sarah Kittel-Schneider1, Irmgard Tegeder5.   

Abstract

Changes of sphingolipid metabolism were suggested to contribute to the patho-etiology of major depression (MD) and bipolar disorder (BD). In a pilot study we assessed if lipid allostasis manifested in pathological plasma concentrations of bioactive lipids i.e. endocannabinoids, sphingolipids, ceramides, and lysophosphatidic acids.
METHODS: Targeted and untargeted lipidomic analyses were performed according to GLP guidelines in 67 patients with unipolar or bipolar disorders (20-67 years, 36 male, 31 female) and 405 healthy controls (18-79 years, 142 m, 263 f), who were matched according to gender, age and body mass index. Multivariate analyses were used to identify major components, which accounted for the variance between groups and were able to predict group membership.
RESULTS: Differences between MD and BP patients versus controls mainly originated from ceramides and their hexosyl-metabolites (C16Cer, C18Cer, C20Cer, C22Cer, C24Cer and C24:1Cer; C24:1GluCer, C24LacCer), which were strongly increased, particularly in male patients. Ceramide levels were neither associated with the current episode, nor with the therapeutic improvement of the Montgomery Åsberg Depression Rating Scale (MARDS). However, long-chain ceramides were linearly associated with age, stronger in patients than controls, and with high plasma levels of diacyl- and triacylglycerols. Patients receiving antidepressants had higher ceramide levels than patients not taking these drugs. There was no such association with lithium or antipsychotics except for olanzapine.
CONCLUSION: Our data suggest that high plasma ceramides in patients with major depression and bipolar disorder are indicative of a high metabolic burden, likely aggravated by certain medications.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Bipolar disorder; Ceramides; Lipidome; Major depression; Tandem mass spectrometry

Mesh:

Substances:

Year:  2019        PMID: 30954559     DOI: 10.1016/j.metabol.2019.04.002

Source DB:  PubMed          Journal:  Metabolism        ISSN: 0026-0495            Impact factor:   8.694


  26 in total

1.  High-Fat Diet and Short-Term Unpredictable Stress Increase Long-Chain Ceramides Without Enhancing Behavioral Despair.

Authors:  Lubriel Sambolín-Escobales; Lizmarie Tirado-Castro; Cristina Suarez; Dariangelly Pacheco-Cruz; Wilfred Fonseca-Ferrer; Pragney Deme; Norman Haughey; Gladys Chompre; James T Porter
Journal:  Front Mol Biosci       Date:  2022-05-04

2.  Endogenous cortisol excess confers a unique lipid signature and metabolic network.

Authors:  Arturo Vega-Beyhart; Marta Iruarrizaga; Adriana Pané; Guillermo García-Eguren; Oriol Giró; Laura Boswell; Gloria Aranda; Vanesa Flores; Gregori Casals; Cristina Alonso; Mireia Mora; Irene Halperin; Francesc Carmona; Joaquim Enseñat; Oscar Vidal; Ting Hu; Gemma Rojo; Ramon Gomis; Felicia A Hanzu
Journal:  J Mol Med (Berl)       Date:  2021-04-21       Impact factor: 4.599

3.  Autophagy activation, lipotoxicity and lysosomal membrane permeabilization synergize to promote pimozide- and loperamide-induced glioma cell death.

Authors:  Nina Meyer; Lisa Henkel; Benedikt Linder; Svenja Zielke; Georg Tascher; Sandra Trautmann; Gerd Geisslinger; Christian Münch; Simone Fulda; Irmgard Tegeder; Donat Kögel
Journal:  Autophagy       Date:  2021-01-19       Impact factor: 16.016

4.  Activation of sphingosine-1-phosphate receptor subtype 1 in the central nervous system contributes to morphine-induced hyperalgesia and antinociceptive tolerance in rodents.

Authors:  Timothy M Doyle; Kali Janes; Zhoumou Chen; Peter M Grace; Emanuela Esposito; Salvatore Cuzzocrea; Tally M Largent-Milnes; William L Neumann; Linda R Watkins; Sarah Spiegel; Todd W Vanderah; Daniela Salvemini
Journal:  Pain       Date:  2020-09-01       Impact factor: 7.926

5.  Secretory Acid Sphingomyelinase in the Serum of Medicated Patients Predicts the Prospective Course of Depression.

Authors:  Christiane Mühle; Claudia Johanna Wagner; Katharina Färber; Tanja Richter-Schmidinger; Erich Gulbins; Bernd Lenz; Johannes Kornhuber
Journal:  J Clin Med       Date:  2019-06-13       Impact factor: 4.241

6.  Anxiety and Depression Are Related to Higher Activity of Sphingolipid Metabolizing Enzymes in the Rat Brain.

Authors:  Iulia Zoicas; Christiane Mühle; Anna K Schmidtner; Erich Gulbins; Inga D Neumann; Johannes Kornhuber
Journal:  Cells       Date:  2020-05-17       Impact factor: 6.600

7.  The Forebrain-Specific Overexpression of Acid Sphingomyelinase Induces Depressive-Like Symptoms in Mice.

Authors:  Iulia Zoicas; Fabian Schumacher; Burkhard Kleuser; Martin Reichel; Erich Gulbins; Anna Fejtova; Johannes Kornhuber; Cosima Rhein
Journal:  Cells       Date:  2020-05-18       Impact factor: 6.600

8.  Shorter Chain Triglycerides Are Negatively Associated with Symptom Improvement in Schizophrenia.

Authors:  Anna Tkachev; Elena Stekolshchikova; Nickolay Anikanov; Svetlana Zozulya; Aleksandra Barkhatova; Tatiana Klyushnik; Daria Petrova
Journal:  Biomolecules       Date:  2021-05-11

9.  mRNA Expression of SMPD1 Encoding Acid Sphingomyelinase Decreases upon Antidepressant Treatment.

Authors:  Cosima Rhein; Iulia Zoicas; Lena M Marx; Stefanie Zeitler; Tobias Hepp; Claudia von Zimmermann; Christiane Mühle; Tanja Richter-Schmidinger; Bernd Lenz; Yesim Erim; Martin Reichel; Erich Gulbins; Johannes Kornhuber
Journal:  Int J Mol Sci       Date:  2021-05-27       Impact factor: 5.923

10.  Serum Metabolic Profiling of Late-Pregnant Women With Antenatal Depressive Symptoms.

Authors:  Qiang Mao; Tian Tian; Jing Chen; Xunyi Guo; Xueli Zhang; Tao Zou
Journal:  Front Psychiatry       Date:  2021-07-08       Impact factor: 4.157

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