Evidence map›Paper›PMID 28451885›Full record

ArticleMolecular neurobiology2018

Impact of High-Fat Diet and Early Stress on Depressive-Like Behavior and Hippocampal Plasticity in Adult Male Rats.

Danusa Mar Arcego, Ana Paula Toniazzo, Rachel Krolow, Carine Lampert, Carolina Berlitz, Emily Dos Santos Garcia, Fabrício do Couto Nicola, Juliana Bender Hoppe, Mariana Maier Gaelzer, Caroline Peres Klein and 2 more

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

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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

12 authors.

Danusa Mar ArcegoPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica/Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, UFRGS, Ramiro Barcelos, 2600 (Anexo) Lab. 37., Porto Alegre, RS, 90035-003, Brazil. danusa.arcego@gmail.com.
Ana Paula ToniazzoPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica/Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, UFRGS, Ramiro Barcelos, 2600 (Anexo) Lab. 37., Porto Alegre, RS, 90035-003, Brazil.
Rachel KrolowPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica/Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, UFRGS, Ramiro Barcelos, 2600 (Anexo) Lab. 37., Porto Alegre, RS, 90035-003, Brazil.
Carine LampertPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica/Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, UFRGS, Ramiro Barcelos, 2600 (Anexo) Lab. 37., Porto Alegre, RS, 90035-003, Brazil.
Carolina BerlitzPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica/Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, UFRGS, Ramiro Barcelos, 2600 (Anexo) Lab. 37., Porto Alegre, RS, 90035-003, Brazil.
Emily Dos Santos GarciaPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica/Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, UFRGS, Ramiro Barcelos, 2600 (Anexo) Lab. 37., Porto Alegre, RS, 90035-003, Brazil.
Fabrício do Couto NicolaPrograma de Pós-Graduação em Neurociências, Instituto de Ciências Básicas da Saúde, UFRGS, Porto Alegre, RS, Brazil.
Juliana Bender HoppePrograma de Pós-Graduação em Ciências Biológicas: Bioquímica/Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, UFRGS, Ramiro Barcelos, 2600 (Anexo) Lab. 37., Porto Alegre, RS, 90035-003, Brazil.
Mariana Maier GaelzerPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica/Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, UFRGS, Ramiro Barcelos, 2600 (Anexo) Lab. 37., Porto Alegre, RS, 90035-003, Brazil.
Caroline Peres KleinPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica/Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, UFRGS, Ramiro Barcelos, 2600 (Anexo) Lab. 37., Porto Alegre, RS, 90035-003, Brazil.
Camilla LazzarettiPrograma de Pós-Graduação em Neurociências, Instituto de Ciências Básicas da Saúde, UFRGS, Porto Alegre, RS, Brazil.
Carla DalmazPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica/Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, UFRGS, Ramiro Barcelos, 2600 (Anexo) Lab. 37., Porto Alegre, RS, 90035-003, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During development, the brain goes through fundamental processes, including organization of neural networks and plasticity. Environmental interventions may change initial brain programming, leading to long-lasting effects and altering the susceptibility to psychopathologies, including depression disorder. It is known that depression is a psychiatric disorder with a high prevalence worldwide, including high rates among adolescents. In this study, we evaluated whether social isolation in the prepubertal period and chronic use of high-fat diet (HFD) may induce depressive-like behavior in male adult rats. We also investigated hippocampal plasticity markers and neurotransmitter systems. We found both social isolation and HFD induced a depressive-like behavior in the forced swimming task. Moreover, chronic HFD reduced synaptic markers in hippocampus, demonstrated by reductions in βIII-tubulin (neuronal marker), PSD-95, SNAP-25, and neurotrophin-3. The HFD group also presented decreased glutamatergic and GABAergic receptors subunits. On the other hand, stress affected hippocampal brain-derived neurotrophic factor (BDNF) signaling pathways, and increased expression of subunit of the NMDA receptor (NR2A). Both factors (stress and diet) decreased GR in the hippocampus without affecting plasma corticosterone at basal levels. Interactions between early stress and HFD access were observed only in the BNDF receptor (tropomyosin receptor kinase B; TrkB) and synaptophysin. In summary, these findings showed that a brief social isolation and chronic HFD, during a sensitive developmental period, cause depressive-like behavior in adulthood. The mechanisms underlying these behavioral effects may involve changes in the levels of synaptic proteins in hippocampus: HFD consumption appears to affect synaptic markers, while social isolation affected BDNF signaling more significantly.

Indexed as

Behavior, AnimalNeuronal PlasticityAnimalsBiomarkersDepressionDiet, High-Fatgamma-Aminobutyric AcidGlutamic AcidHippocampusMaleModels, BiologicalRats, WistarReceptors, GlucocorticoidSexual MaturationSocial IsolationStress, PsychologicalBiomarkersgamma-Aminobutyric AcidGlutamic AcidReceptors, GlucocorticoidSucroseBDNFEarly life environmentEmotional responsesHigh-calorie dietsPrepubertal periodSocial isolation

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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.