Evidence map›Paper›PMID 39825014›Full record

ArticleMolecular psychiatry2025

Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia.

Daria Chestnykh, Christiane Mühle, Fabian Schumacher, Liubov S Kalinichenko, Stefan Löber, Peter Gmeiner, Christian Alzheimer, Stephan von Hörsten, Burkhard Kleuser, Steffen Uebe and 7 more

Abstract read
In one paragraph

Article in Molecular psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Sphingolipids in Emotional Well-Being.Journal of neurochemistry · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Daria ChestnykhDepartment of Psychiatry and Psychotherapy, University Clinic, Friedrich-Alexander-University of Erlangen-Nuremberg, Erlangen, Germany.
Christiane MühleDepartment of Psychiatry and Psychotherapy, University Clinic, Friedrich-Alexander-University of Erlangen-Nuremberg, Erlangen, Germany.ORCID 0000-0001-7517-9154
Fabian SchumacherInstitute of Pharmacy, Freie Universität Berlin, Berlin, Germany.ORCID 0000-0001-8703-3275
Liubov S KalinichenkoDepartment of Psychiatry and Psychotherapy, University Clinic, Friedrich-Alexander-University of Erlangen-Nuremberg, Erlangen, Germany.
Stefan LöberDepartment of Chemistry and Pharmacy, Medicinal Chemistry, Friedrich-Alexander-Universität Erlangen-Nürnberg, Nikolaus-Fiebiger-Str. 10, 91058, Erlangen, Germany.
Peter GmeinerDepartment of Chemistry and Pharmacy, Medicinal Chemistry, Friedrich-Alexander-Universität Erlangen-Nürnberg, Nikolaus-Fiebiger-Str. 10, 91058, Erlangen, Germany.
Christian AlzheimerInstitute of Physiology and Pathophysiology, Friedrich-Alexander-University of Erlangen-Nuremberg, 91054, Erlangen, Germany.
Stephan von HörstenDepartment of Experimental Therapy, Preclinical Experimental Center, Friedrich-Alexander-University of Erlangen-Nuremberg, Erlangen, Germany.ORCID 0000-0001-6409-0664
Burkhard KleuserInstitute of Pharmacy, Freie Universität Berlin, Berlin, Germany.
Steffen UebeInstitute of Human Genetics, Friedrich Alexander University of Erlangen-Nuremberg, Erlangen, Germany.
Arif B EkiciInstitute of Human Genetics, Friedrich Alexander University of Erlangen-Nuremberg, Erlangen, Germany.ORCID 0000-0001-6099-7066
Erich GulbinsDepartment of Molecular Biology, University of Duisburg-Essen, 45147, Essen, Germany.
Johannes KornhuberDepartment of Psychiatry and Psychotherapy, University Clinic, Friedrich-Alexander-University of Erlangen-Nuremberg, Erlangen, Germany.ORCID 0000-0002-8096-3987
Hee Kyung JinKNU Alzheimer's Disease Research Institute, Kyungpook National University, Daegu, 41566, South Korea.
Jae-Sung BaeKNU Alzheimer's Disease Research Institute, Kyungpook National University, Daegu, 41566, South Korea.ORCID 0000-0002-8270-0072
Anbarasu LourdusamyAcademic Unit for Translational Medical Sciences, School of Medicine, University of Nottingham, Nottingham, NG7 2UH, UK.ORCID 0000-0002-1978-6301
Christian P MüllerDepartment of Psychiatry and Psychotherapy, University Clinic, Friedrich-Alexander-University of Erlangen-Nuremberg, Erlangen, Germany. Christian.Mueller@uk-erlangen.de.ORCID 0000-0002-5325-9900

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) 270949263/GRK2162/1Deutsche Forschungsgemeinschaft (German Research Foundation) AL 294/10-2Deutsche Forschungsgemeinschaft (German Research Foundation) GRK2162/2Deutsche Forschungsgemeinschaft (German Research Foundation) KO 947/17-2
6 · The paper itself

Abstract

Schizophrenia is a chronic and severe mental disorder. It is currently treated with antipsychotic drugs (APD). However, APD's work only in a limited number of patients and may have cognition impairing side effects. A growing body of evidence points out the potential involvement of abnormal sphingolipid metabolism in the pathophysiology of schizophrenia. Here, an analysis of human gene polymorphisms and brain gene expression in schizophrenia patients identified an association of SMPD1 and SMPD3 genes coding for acid- (ASM) and neutral sphingomyelinase-2 (NSM). In a rat model of psychosis using amphetamine hypersensitization, we found a locally restricted increase of ASM activity in the prefrontal cortex (PFC). Short-term haloperidol (HAL) treatment reversed behavioral symptoms and the ASM activity. A sphingolipidomic analysis confirmed an altered ceramide metabolism in the PFC during psychosis. Targeting enhanced ASM activity in a psychotic-like state with the ASM inhibitor KARI201 reversed psychotic like behavior and associated changes in the sphingolipidome. While effective HAL treatment led to locomotor decline and cognitive impairments, KARI201 did not. An RNA sequencing analysis of the PFC suggested a dysregulation of numerous schizophrenia related genes including Olig1, Fgfr1, Gpr17, Gna12, Abca2, Sox1, Dpm2, and Rab2a in the rat model of psychosis. HAL and KARI201 antipsychotic effects were associated with targeting expression of other schizophrenia associated genes like Col6a3, Slc22a8, and Bmal1, or Nr2f6a, respectively, but none affecting expression of sphingolipid regulating genes. Our data provide new insight into a potentially pathogenic mechanism of schizophrenia and suggest a new pharmaco-treatment strategy with reduced side effects.

Indexed as

Antipsychotic AgentsSchizophreniaSphingomyelin PhosphodiesteraseAdultAnimalsBrainDisease Models, AnimalFemaleHaloperidolHumansMalePrefrontal CortexRatsRats, Sprague-DawleySphingolipidsAntipsychotic AgentsHaloperidolSMPD1 protein, humanSMPD3 protein, humanSphingolipidsSphingomyelin Phosphodiesterase

Identifiers

PMID39825014
PMCPMC12185314

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.