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Periodized low protein-high carbohydrate diet confers potent, but transient, metabolic improvements.

Molecular metabolism
November 1, 2018
Zhencheng Li et al. (9 authors)
Journal ArticleResearch Support, Non-U.S. Gov'tAnimal Study
Study Details

Study Goal

The researchers aimed to evaluate the metabolic benefits of a periodized low protein-high carbohydrate diet (pLPHC) in mice and explore its interactions with exercise training.

Results Summary

pLPHC conferred metabolic benefits similar to chronic LPHC, including increased FGF21, adaptive thermogenesis, obesity protection, and improved insulin sensitivity, though benefits were transient and fluctuated with diet cycles. Exercise training improved weight maintenance but impaired the FGF21 response to pLPHC, while repeated cycles enhanced this response.

Population

Mice

Effective Dosage

14-day cycles of LPHC (5% energy from protein) alternating with 14-day control diet

Duration

Up to 4 months

Interactions

Interaction with exercise training noted

Extracted Claims (14)
InterventionDirectionEndpointPopulationDosageImpactClaim #
Chronic ad libitum low protein-high carbohydrate diet (LPHC)
increase
health- and life-span
mice
-
increases
#1
pLPHC
increase
metabolic benefits
mice
-
conferred metabolic benefits similar to chronic LPHC
#2
pLPHC
increase
FGF21
mice
-
increased
#3
pLPHC
increase
adaptive thermogenesis
mice
-
increased
#4
pLPHC
decrease
obesity
mice
-
obesity-protection
#5
pLPHC
increase
total energy intake
mice
-
increased
#6
pLPHC
increase
insulin sensitivity
mice
-
improved
#7
pLPHC
no change
improved insulin sensitivity
mice
-
showed large fluctuations between diet periods
#8
switching back to control diet
decrease
improved insulin sensitivity
mice
14 days
was lost within 14 days
#9
Parallel exercise training
increase
weight maintenance
mice
-
improved
#10
Parallel exercise training
decrease
FGF21 response to pLPHC
mice
-
impaired
#11
repeated pLPHC cycles
increase
FGF21 response
mice
-
progressively augmented
#12
FGF21 suppression by exercise
neutral
Nupr1 mRNA in liver
mice
-
correlated tightly with
#13
potentiation by repeated cycles
neutral
Nupr1 mRNA in liver
mice
-
correlated tightly with
#14
Abstract

OBJECTIVE: Chronic ad libitum low protein-high carbohydrate diet (LPHC) increases health- and life-span in mice. A periodized (p) LPHC regimen would be a more practical long-term human lifestyle intervention, but the metabolic benefits of pLPHC are not known. Also, the interactions between LPHC diet and exercise training have not been investigated. Presently, we aimed to provide proof-of-concept data in mice of the efficacy of pLPHC and to explore the potential interactions with concurrent exercise training. METHODS: A detailed phenotypic and molecular characterization of mice undergoing different durations of 14 d LPHC (5 E% protein)/14 d control diet cycles for up to 4 months with or without concurrent access to activity wheels allowing voluntary exercise training. RESULTS: pLPHC conferred metabolic benefits similar to chronic LPHC, including increased FGF21 and adaptive thermogenesis, obesity-protection despite increased total energy intake and improved insulin sensitivity. The improved insulin sensitivity showed large fluctuations between diet periods and was lost within 14 days of switching back to control diet. Parallel exercise training improved weight maintenance but impaired the FGF21 response to pLPHC whereas repeated pLPHC cycles progressively augmented this response. Both the FGF21 suppression by exercise and potentiation by repeated cycles correlated tightly with Nupr1 mRNA in liver, suggesting dependence on liver integrated stress response. CONCLUSION: These results suggest that pLPHC may be a viable strategy to promote human health but also highlight the transient nature of the benefits and that the interaction with other lifestyle-interventions such as exercise training warrants consideration.

Medical Subject Headings (MeSH)
AnimalsBody WeightDietDiet, High-Protein Low-CarbohydrateDietary CarbohydratesDietary ProteinsEnergy IntakeFemaleFibroblast Growth FactorsGlucoseInsulin ResistanceLiverMiceMice, Inbred C57BLObesityProof of Concept Study
Study Links
Quality Scores
SafetyNot Assessed
Efficacy75/10
Quality80/10
Citation Metrics
Total Citations12
Citations/Year1.7
Relative Citation Ratio0.49
NIH Percentile26.4%
Research Impact Scores
APT Score0.25
Weight Score1.54
Normalized Score0.66
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