Evidence map›Paper›PMID 31881260›Full record

ArticleNeuroscience2021

High Fructose Diet Induces Sex-specific Modifications in Synaptic Respiration and Affective-like Behaviors in Rats.

Alix Kloster, Molly M Hyer, Samya Dyer, Charlie Salome-Sanchez, Gretchen N Neigh

Open access · greenAbstract read
In one paragraph

Article 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
1.4field-weighted citation impact, top 17% 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, 22 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

5 authors at 1 institution in 1 country.

Alix KlosterDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA 23298, United States.
Molly M HyerDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA 23298, United States.
Samya DyerDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA 23298, United States.
Charlie Salome-SanchezDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA 23298, United States.
Gretchen N NeighDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA 23298, United States. Electronic address: gretchen.mccandless@vcuhealth.org.
Virginia Commonwealth University · US

Funding

Virginia Commonwealth University IRADCAK12GM093857 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI DANIEL C BULLARD, John J Ryan · 2010 to 2026
$7.0M
Adult Implications of Chronic Adolescent Stress: Mediators and ModifiersR01NR014886 · NINR · VIRGINIA COMMONWEALTH UNIVERSITY · PI NEIGH, GRETCHEN N · 2014 to 2018
$2.1M
NIGMS NIH HHS K12 GM093857NINR NIH HHS R01 NR014886
6 · The paper itself

Abstract

The consequences of excessive fructose intake extend beyond those of metabolic disorder to changes in emotional regulation and cognitive function. Long-term consumption of fructose, particularly common when begun in adolescence, is more likely to lead to deleterious consequences than acute consumption. These long-term consequences manifest differently in males and females, suggesting a sex-divergent mechanism by which fructose can impair physiology and neural function. The purpose of the current project was to investigate a possible sex-specific mechanism by which elevated fructose consumption drives behavioral deficits and accompanying metabolic symptoms - specifically, synaptic mitochondrial function. Male and female rats were fed a high fructose diet beginning at weaning and maintained into adulthood. Measures of physiological health across the diet consumption period indicated that females were more likely to gain weight than males while both displayed increased circulating blood glucose. As adults, females fed the high fructose diet displayed increased floating behavior in the forced swim task while males exhibited increased exploratory behavior in the open field. Synaptic respiration was altered by diet in both females and males but the effect was sex-divergent - fructose-fed females had increased synaptic respiration while males showed a decrease. When exposed to an acute energetic challenge, the pattern was reversed. Taken together, these data indicate that diet-induced alterations to neural function and physiology are sex-specific and highlight the need to consider sex as a biological variable when treating metabolic disease. Furthermore, these data suggest that synaptic mitochondrial function may contribute directly to the behavioral consequences of elevated fructose consumption.

Indexed as

DietFructoseAnimalsBody WeightFemaleMaleRatsRespirationWeaningFructoseanxietydepressionfructosemetabolismmitochondriasex differences

Identifiers

PMID31881260
PMCPMC7311226
OpenAlexW2997796288

What OpenQuestion holds

Textmetadata
LicenceTDM
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.