Evidence map›Paper›PMID 26171219›Full record

ArticlePharmacology research & perspectives2015

Antidepressant activity of fingolimod in mice.

Luigi di Nuzzo, Rosamaria Orlando, Cristina Tognoli, Paola Di Pietro, Giuseppe Bertini, Jessica Miele, Domenico Bucci, Marta Motolese, Sergio Scaccianoce, Alessandra Caruso and 6 more

Open access · goldAbstract read
In one paragraph

Article in Pharmacology research & perspectives, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.4field-weighted citation impact, top 11% of its field
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

25 citing papers in PubMed, 55 citations in OpenAlex.

  1. The influence of trait anxiety on performance in the CatWalk test.Frontiers in behavioral neuroscience · 2026
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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

16 authors at 5 institutions in 1 country.

Luigi di NuzzoDepartment of Physiology and Pharmacology, University Sapienza of Rome Rome, Italy.
Rosamaria OrlandoIRCCS Associazione Oasi Maria S.S., Institute for Research on Mental Retardation and Brain Aging Troina, Italy.
Cristina TognoliDepartment of Neurological and Movement Sciences, University of Verona Verona, Italy.
Paola Di PietroIRCCS Neuromed Pozzilli, Italy.
Giuseppe BertiniDepartment of Neurological and Movement Sciences, University of Verona Verona, Italy.
Jessica MieleDepartment of Physiology and Pharmacology, University Sapienza of Rome Rome, Italy.
Domenico BucciIRCCS Neuromed Pozzilli, Italy.
Marta MotoleseIRCCS Neuromed Pozzilli, Italy.
Sergio ScaccianoceDepartment of Physiology and Pharmacology, University Sapienza of Rome Rome, Italy.
Alessandra CarusoDepartment of Physiology and Pharmacology, University Sapienza of Rome Rome, Italy.
Gianluca MauroInstitute of Psychiatry, Catholic University of Sacred Heart Rome, Italy.
Carmine De LuciaDepartment of Physiology and Pharmacology, University Sapienza of Rome Rome, Italy.
Giuseppe BattagliaIRCCS Neuromed Pozzilli, Italy.
Valeria BrunoDepartment of Physiology and Pharmacology, University Sapienza of Rome Rome, Italy ; IRCCS Neuromed Pozzilli, Italy.
Paolo Francesco FabeneDepartment of Neurological and Movement Sciences, University of Verona Verona, Italy.
Ferdinando NicolettiDepartment of Physiology and Pharmacology, University Sapienza of Rome Rome, Italy ; IRCCS Neuromed Pozzilli, Italy.
Sapienza University of Rome · ITIstituto Neurologico Mediterraneo · ITUniversity of Verona · ITOasi Maria SS · ITUniversità Cattolica del Sacro Cuore · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent findings indicate that fingolimod, the first oral drug approved for the treatment of multiple sclerosis (MS), acts as a direct inhibitor of histone deacetylases (HDACs) and enhances the production of brain-derived neurotrophic factor (BDNF) in the CNS. Both mechanisms are relevant to the pathophysiology and treatment of major depression. We examined the antidepressant activity of fingolimod in mice subjected to chronic unpredictable stress (CUS), a model of reactive depression endowed with face and pharmacological validity. Chronic treatment with fingolimod (3 mg kg(-1), i.p., once a day for 4 weeks) reduced the immobility time in the forced swim test (FST) in a large proportion of CUS mice. This treatment also caused anxiogenic-like effects in the social interaction test without affecting anxiety-like behavior in the elevated plus maze or spatial learning in the water maze. CUS mice showed reduced BDNF levels and enhanced HDAC2 levels in the hippocampus. These changes were reversed by fingolimod exclusively in mice that showed a behavioral response to the drug in the FST. Fingolimod treatment also enhanced H3 histone K14-acetylation and adult neurogenesis in the hippocampus of CUS mice. Fingolimod did not affect most of the parameters we have tested in unstressed control mice. The antidepressant-like activity of fingolimod was confirmed in mice chronically treated with corticosterone. These findings show for the first time that fingolimod exerts antidepressant-like effect acting in a "disease-dependent" manner, and raise the interesting possibility that the drug could relieve depressive symptoms in MS patients independently of its disease-modifying effect on MS.

Indexed as

BDNFchronic stressdepressionfingolimodhippocampus

Identifiers

PMID26171219
PMCPMC4492751
OpenAlexW1543741818

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.