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The cessation of regular exercise and dieting causes rapid adiposity rebound and glucose intolerance in young male rats, findings that are abolished by the glucocorticoid receptor antagonist Mifepristone (LB759)

2014· article· en· W1567782537 on OpenAlexafffund
Trevor Teich, Jacklyn A. Pivovarov, Jacqueline L. Beaudry, Hazel Hunt, Joseph K. Belanoff, Michael C. Riddell

Bibliographic record

VenueThe FASEB Journal · 2014
Typearticle
Languageen
FieldMedicine
TopicHormonal Regulation and Hypertension
Canadian institutionsLunenfeld-Tanenbaum Research InstituteYork University
FundersNatural Sciences and Engineering Research Council of Canada
KeywordsEndocrinologyInternal medicineMifepristoneMedicineDietingAntiglucocorticoidAntagonistGlucocorticoidGlucocorticoid receptorWeight lossReceptorObesityBiology

Abstract

fetched live from OpenAlex

A rapid deterioration of whole‐body insulin sensitivity and visceral fat mass rebound occurs following cessation of regular exercise in humans and rodents. Both dieting and daily exercise have been shown to increase intracellular visceral fat exposure to glucocorticoids (GCs) via up‐regulation of the pre‐receptor enzyme 11β‐hydroxysteroid dehydrogenase type 1 (11β‐HSD1), a phenomenon that may predispose animals to rapid fat rebound. We hypothesized that sustained elevations of GC exposure in visceral fat, upon removal of regular exercise and caloric restriction (CR), may influence this detrimental metabolic response. Thus, we tested the efficacy of Mifepristone, a potent but non‐selective GC receptor antagonist, on limiting adiposity rebound and preserving whole‐body insulin sensitivity following cessation of daily exercise and CR. Using young male Sprague‐Dawley rats, we provided 20g/day of standard rodent chow and access to voluntary running wheels for 3 weeks followed by locking of the wheels and reintroduction to ad libitum feeding either with or without Mifepristone (80 mg/kg/day) via oral gavage for 1 week. Additional Sedentary and Control Runner groups, who were also calorie restricted (20 g/day), were used as pre‐wheel lock comparisons (n= 8‐10 per group). Cessation of daily running and CR resulted in a 6.5‐fold increase in HOMA‐IR and a 2‐fold increase in glucose AUC during an oral glucose tolerance test in Placebo vs. Control Runners (p<0.05). Mifepristone treatment abolished both of these impairments. Mifepristone also attenuated visceral fat mass rebound in epididymal depots by 14% vs. Placebo and significantly reduced perirenal fat mass rebound by 55% vs. Placebo (p<0.05). Control Runners demonstrated a 5‐fold increase in 11β‐HSD1 protein content in epididymal fat vs. Sedentary and a similar increase remained in the Placebo group one week following cessation of exercise and CR vs. Sedentary (p<0.05). Daily Mifepristone significantly reduced 11β‐HSD1 vs. Control Runners and Placebo groups (p<0.05). These findings suggest that elevations in GC action following regular exercise and dieting promote rapid deterioration in metabolic control in healthy organisms and that this deterioration can be inhibited by a GC receptor antagonist. Grant Funding Source : Supported by NSERC and Corcept Therapeutics

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.008

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0010.000
Science and technology studies0.0000.001
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0020.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.012
GPT teacher head0.234
Teacher spread0.222 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2014
Admission routes2
Has abstractyes

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