Metabolic and psychiatric effects of acyl coenzyme A binding protein (ACBP)

dc.contributor.authorJoseph, Adrien
dc.contributor.authorBravo San Pedro, José Manuel
dc.contributor.authorKroemer, Guido
dc.date.accessioned2025-12-15T11:18:22Z
dc.date.available2025-12-15T11:18:22Z
dc.date.issued2020
dc.description.abstractAcyl coenzyme A binding protein (ACBP), also known as diazepam binding inhibitor (DBI) is a multifunctional protein with an intracellular action (as ACBP), as well as with an extracellular role (as DBI). The plasma levels of soluble ACBP/DBI are elevated in human obesity and reduced in anorexia nervosa. Accumulating evidence indicates that genetic or antibody-mediated neutralization of ACBP/DBI has anorexigenic effects, thus inhibiting food intake and inducing lipo-catabolic reactions in mice. A number of anorexiants have been withdrawn from clinical development because of their side effects including an increase in depression and suicide. For this reason, we investigated the psychiatric impact of ACBP/DBI in mouse models and patient cohorts. Intravenously (i.v.) injected ACBP/DBI protein conserved its orexigenic function when the protein was mutated to abolish acyl coenzyme A binding, but lost its appetite-stimulatory effect in mice bearing a mutation in the γ2 subunit of the γ-aminobutyric acid (GABA) A receptor (GABAAR). ACBP/DBI neutralization by intraperitoneal (i.p.) injection of a specific mAb blunted excessive food intake in starved and leptin-deficient mice, but not in ghrelin-treated animals. Neither i.v. nor i.p. injected anti-ACBP/DBI antibody affected the behavior of mice in the dark-light box and open-field test. In contrast, ACBP/DBI increased immobility in the forced swim test, while anti-ACBP/DBI antibody counteracted this sign of depression. In patients diagnosed with therapy-resistant bipolar disorder or schizophrenia, ACBP/DBI similarly correlated with body mass index (BMI), not with the psychiatric diagnosis. Patients with high levels of ACBP/DBI were at risk of dyslipidemia and this effect was independent from BMI, as indicated by multivariate analysis. In summary, it appears that ACBP/DBI neutralization has no negative impact on mood and that human depression is not associated with alterations in ACBP/DBI concentrations.
dc.description.departmentDepto. de Fisiología
dc.description.facultyFac. de Medicina
dc.description.refereedTRUE
dc.description.statuspub
dc.identifier.citationJoseph A, Moriceau S, Sica V, Anagnostopoulos G, Pol J, Martins I, Lafarge A, Maiuri MC, Leboyer M, Loftus J, Bellivier F, Belzeaux R, Berna F, Etain B, Capdevielle D, Courtet P, Dubertret C, Dubreucq J, D’Amato T, Fond G, Gard S, Llorca P-M, Mallet J, Misdrahi D, Olie E, Passerieux C, Polosan M, Roux P, Samalin L, Schürhoff F, Schwan R, Magnan C, Oury F, Bravo-San Pedro JM, Kroemer G; FACE-SZ and FACE-BD groups. Metabolic and psychiatric effects of acyl coenzyme A binding protein (ACBP)/diazepam binding inhibitor (DBI). Cell death & disease. 2020;11:502.
dc.identifier.doi10.1038/s41419-020-2716-5
dc.identifier.issn2041-4889
dc.identifier.officialurlhttps://doi.org/10.1038/s41419-020-2716-5
dc.identifier.pmid32632162
dc.identifier.relatedurlhttps://www.nature.com/articles/s41419-020-2716-5
dc.identifier.relatedurlhttps://pmc.ncbi.nlm.nih.gov/articles/PMC7338362/
dc.identifier.urihttps://hdl.handle.net/20.500.14352/128940
dc.issue.number7
dc.journal.titleCell Death and Disease
dc.language.isoeng
dc.page.initial502
dc.publisherSpringer
dc.rights.accessRightsopen access
dc.subject.ucmCiencias Biomédicas
dc.subject.ucmMedicina
dc.subject.unesco32 Ciencias Médicas
dc.titleMetabolic and psychiatric effects of acyl coenzyme A binding protein (ACBP)
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number11
dspace.entity.typePublication
relation.isAuthorOfPublication9ba7067d-d334-47dd-8c68-451c794165a2
relation.isAuthorOfPublication.latestForDiscovery9ba7067d-d334-47dd-8c68-451c794165a2

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