Evidence map›Paper›PMID 34121997›Full record

ArticleFrontiers in neuroscience2021

High Fructose Corn Syrup-Moderate Fat Diet Potentiates Anxio-Depressive Behavior and Alters Ventral Striatal Neuronal Signaling.

Ayanabha Chakraborti, Christopher Graham, Sophie Chehade, Bijal Vashi, Alan Umfress, Pradeep Kurup, Benjamin Vickers, H Alexander Chen, Rahul Telange, Taylor Berryhill and 9 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

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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

19 authors at 1 institution in 1 country.

Ayanabha ChakrabortiDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
Christopher GrahamDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
Sophie ChehadeDepartment of Biology, University of Alabama at Birmingham, Birmingham, AL, United States.
Bijal VashiDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
Alan UmfressDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
Pradeep KurupDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
Benjamin VickersDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
H Alexander ChenDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
Rahul TelangeDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
Taylor BerryhillDepartment of Pharmacology, University of Alabama at Birmingham Medical Center, Birmingham, AL, United States.
William Van Der PolCenter for Clinical and Translational Science, University of Alabama at Birmingham, Birmingham, AL, United States.
Mickie PowellDepartment of Biology, University of Alabama at Birmingham, Birmingham, AL, United States.
Stephen BarnesDepartment of Pharmacology, University of Alabama at Birmingham Medical Center, Birmingham, AL, United States.
Casey MorrowDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL, United States.
Daniel L SmithDepartment of Nutrition Sciences, University of Alabama at Birmingham, Birmingham, AL, United States.
M Shahid MukhtarDepartment of Biology, University of Alabama at Birmingham, Birmingham, AL, United States.
Stephen WattsDepartment of Biology, University of Alabama at Birmingham, Birmingham, AL, United States.
Gregory KennedyDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
James BibbDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
University of Alabama at Birmingham · US

Funding

Yale/NIDA Neuroproteomics Research CenterP30DA018343 · NIDA · YALE UNIVERSITY · PI ANGUS C. NAIRN, Kenneth Robert WILLIAMS · 2004 to 2026
$37.1M
Why is the prevalence of obesity so high in U.S. Southern States? Regional predictors of BMI and obesity treatment response.P30DK056336 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BARBARA A GOWER · 2000 to 2026
$31.9M
UAB Center for Clinical and Translational Science (CCTS)UL1TR001417 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KIMBERLY, ROBERT P. · 2015 to 2018
$31.4M
University of Alabama at Birmingham's Diabetes Research CenterP30DK079626 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BARBARA A GOWER · 2013 to 2026
$19.5M
Sex hormones and arthritis in a long lived animal modelP30AG050886 · NIA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Jianhua Zhang · 2015 to 2026
$11.3M
Excitatory and Metabotopic Regulation of PKA in Stress and ResilienceR01MH116896 · NIMH · UNIVERSITY OF ARIZONA · PI BIBB, JAMES A · 2019 to 2022
$1.5M
NCATS NIH HHS UL1 TR001417NIA NIH HHS P30 AG050886NIDA NIH HHS P30 DA018343NIDDK NIH HHS P30 DK056336NIDDK NIH HHS P30 DK079626NIMH NIH HHS R01 MH116896
6 · The paper itself

Abstract

The neurobiological mechanisms that mediate psychiatric comorbidities associated with metabolic disorders such as obesity, metabolic syndrome and diabetes remain obscure. High fructose corn syrup (HFCS) is widely used in beverages and is often included in food products with moderate or high fat content that have been linked to many serious health issues including diabetes and obesity. However, the impact of such foods on the brain has not been fully characterized. Here, we evaluated the effects of long-term consumption of a HFCS-Moderate Fat diet (HFCS-MFD) on behavior, neuronal signal transduction, gut microbiota, and serum metabolomic profile in mice to better understand how its consumption and resulting obesity and metabolic alterations relate to behavioral dysfunction. Mice fed HFCS-MFD for 16 weeks displayed enhanced anxiogenesis, increased behavioral despair, and impaired social interactions. Furthermore, the HFCS-MFD induced gut microbiota dysbiosis and lowered serum levels of serotonin and its tryptophan-based precursors. Importantly, the HFCS-MFD altered neuronal signaling in the ventral striatum including reduced inhibitory phosphorylation of glycogen synthase kinase 3β (GSK3β), increased expression of ΔFosB, increased Cdk5-dependent phosphorylation of DARPP-32, and reduced PKA-dependent phosphorylation of the GluR1 subunit of the AMPA receptor. These findings suggest that HFCS-MFD-induced changes in the gut microbiota and neuroactive metabolites may contribute to maladaptive alterations in ventral striatal function that underlie neurobehavioral impairment. While future studies are essential to further evaluate the interplay between these factors in obesity and metabolic syndrome-associated behavioral comorbidities, these data underscore the important role of peripheral-CNS interactions in diet-induced behavioral and brain function. This study also highlights the clinical need to address neurobehavioral comorbidities associated with obesity and metabolic syndrome.

Indexed as

anxietydepressiondiethigh fructose corn syrup (HFCS)nucleus accumbensserotonintryptophan

Identifiers

PMID34121997
PMCPMC8187874
OpenAlexW3165593362

What OpenQuestion holds

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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.