Evidence map›Paper›PMID 25966970›Full record

ArticleMolecular neurobiology2016

Agmatine, by Improving Neuroplasticity Markers and Inducing Nrf2, Prevents Corticosterone-Induced Depressive-Like Behavior in Mice.

Andiara E Freitas, Javier Egea, Izaskun Buendia, Vanessa Gómez-Rangel, Esther Parada, Elisa Navarro, Ana Isabel Casas, Aneta Wojnicz, José Avendaño Ortiz, Antonio Cuadrado and 3 more

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

38 citing papers in PubMed, 105 citations in OpenAlex.

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  11. A novel murine model of mania.Molecular psychiatry · 2023
    Article
  12. An enriched environment improves long-term functional outcomes in mice after intracerebral hemorrhage by mechanisms that involve the Nrf2/BDNF/glutaminase pathway.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2023
    Article
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  18. Nrf2-BDNF-TrkB pathway contributes to cortical hemorrhage-induced depression, but not sex differences.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
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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

13 authors at 6 institutions in 4 countries.

Andiara E FreitasNina Ireland Laboratory of Developmental Neurobiology, Department of Psychiatry, University of California, San Francisco, San Francisco, CA, 94158, USA. andiaraef@gmail.com.
Javier EgeaDepartamento de Farmacología y Terapéutica and Instituto Teófilo Hernando. Facultad de Medicina, Universidad Autónoma de Madrid, 28029, Madrid, Spain.
Izaskun BuendiaDepartamento de Farmacología y Terapéutica and Instituto Teófilo Hernando. Facultad de Medicina, Universidad Autónoma de Madrid, 28029, Madrid, Spain.
Vanessa Gómez-RangelDepartamento de Farmacología y Terapéutica and Instituto Teófilo Hernando. Facultad de Medicina, Universidad Autónoma de Madrid, 28029, Madrid, Spain.
Esther ParadaDepartamento de Farmacología y Terapéutica and Instituto Teófilo Hernando. Facultad de Medicina, Universidad Autónoma de Madrid, 28029, Madrid, Spain.
Elisa NavarroDepartamento de Farmacología y Terapéutica and Instituto Teófilo Hernando. Facultad de Medicina, Universidad Autónoma de Madrid, 28029, Madrid, Spain.
Ana Isabel CasasDepartamento de Farmacología y Terapéutica and Instituto Teófilo Hernando. Facultad de Medicina, Universidad Autónoma de Madrid, 28029, Madrid, Spain.
Aneta WojniczInstituto de Investigación Sanitaria Hospital de la Princesa and Servicio de Farmacología Clínica, Hospital Universitario de la Princesa, Madrid, Spain.
José Avendaño OrtizInstituto de Investigación Sanitaria Hospital de la Princesa and Servicio de Farmacología Clínica, Hospital Universitario de la Princesa, Madrid, Spain.
Antonio CuadradoDepartamento de Bioquímica e Instituto de Investigaciones Biomédicas Alberto Sols UAM-CSIC, Centro de Investigación en Red Sobre Enfermedades Neurodegenerativas (CIBERNED), Facultad de Medicina, Universidad Autónoma de Madrid, Madrid, Spain.
Ana Ruiz-NuñoInstituto de Investigación Sanitaria Hospital de la Princesa and Servicio de Farmacología Clínica, Hospital Universitario de la Princesa, Madrid, Spain.
Ana Lúcia S RodriguesDepartment of Biochemistry, Center of Biological Sciences, Universidade Federal de Santa Catarina, Campus Universitário, Trindade 88040-900, Florianópolis, Santa Catarina, Brazil.
Manuela G LopezDepartamento de Farmacología y Terapéutica and Instituto Teófilo Hernando. Facultad de Medicina, Universidad Autónoma de Madrid, 28029, Madrid, Spain.
Hospital Universitario de La Princesa · ESBiomedical Research Networking Center on Neurodegenerative Diseases · ESMaastricht University · NLUniversidad Autónoma de Madrid · ESUniversidade Federal de Santa Catarina · BRUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Agmatine, an endogenous neuromodulator, is a potential candidate to constitute an adjuvant/monotherapy for the management of depression. A recent study by our group demonstrated that agmatine induces Nrf2 and protects against corticosterone effects in a hippocampal neuronal cell line. The present study is an extension of this previous study by assessing the antidepressant-like effect of agmatine in an animal model of depression induced by corticosterone in mice. Swiss mice were treated simultaneously with agmatine or imipramine at a dose of 0.1 mg/kg/day (p.o.) and corticosterone for 21 days and the daily administrations of experimental drugs were given immediately prior to corticosterone (20 mg/kg/day, p.o.) administrations. Wild-type C57BL/6 mice (Nrf2 (+/+)) and Nrf2 KO (Nrf2 (-/-)) were treated during 21 days with agmatine (0.1 mg/kg/day, p.o.) or vehicle. Twenty-four hours after the last treatments, the behavioral tests and biochemical assays were performed. Agmatine treatment for 21 days was able to abolish the corticosterone-induced depressive-like behavior and the alterations in the immunocontent of mature BDNF and synaptotagmin I, and in the serotonin and glutamate levels. Agmatine also abolished the corticosterone-induced changes in the morphology of astrocytes and microglia in CA1 region of hippocampus. In addition, agmatine treatment in control mice increased noradrenaline, serotonin, and dopamine levels, CREB phosphorylation, mature BDNF and synaptotagmin I immunocontents, and reduced pro-BDNF immunocontent in the hippocampus. Agmatine's ability to produce an antidepressant-like effect was abolished in Nrf2 (-/-) mice. The present results reinforce the participation of Nrf2 in the antidepressant-like effect produced by agmatine and expand literature data concerning its mechanisms of action.

Indexed as

Behavior, AnimalAgmatineAnhedoniaAnimalsAntidepressive AgentsAstrocytesBiomarkersCorticosteroneDepressionFemaleHippocampusImipramineMice, Inbred C57BLMicrogliaModels, BiologicalNeuronal PlasticityAgmatineAntidepressive AgentsBiomarkersCorticosteroneImipramineNeurotransmitter AgentsNF-E2-Related Factor 2AgmatineBDNFCorticosteroneDepressionNrf2

Identifiers

PMID25966970
OpenAlexW337699631

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.