Panacea Index Logo

Command Palette

Search for a command to run...

Impairment of fat oxidation under high- vs. low-glycemic index diet occurs before the development of an obese phenotype.

American journal of physiology. Endocrinology and metabolism
February 1, 2010
F Isken et al. (6 authors)
Comparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tAnimal Study
Study Details

Study Goal

The researchers aimed to determine the long-term effects and mechanisms of high vs. low glycemic index (GI) diets on fat mass, insulin resistance, and metabolic flexibility in obesity-prone mice.

Results Summary

Mice on a high-GI diet showed rapid increases in body fat, liver fat, and reduced glucose clearance, along with impaired metabolic flexibility. Early impaired fatty acid oxidation preceded these changes, suggesting a causal role.

Population

Male C57BL/6J mice (obesity-prone)

Effective Dosage

Not specified (isoenergetic and macronutrient-matched diets differing only in starch type)

Duration

20 weeks (long-term) and 6 weeks (short-term)

Interactions

None mentioned

Extracted Claims (15)
InterventionDirectionEndpointPopulationDosageImpactClaim #
high glycemic index (GI) diet
increase
fat mass
obesity-prone C57BL/6J mice
-
increases
#1
high glycemic index (GI) diet
increase
insulin resistance
obesity-prone C57BL/6J mice
-
increases
#2
high GI diet
increase
body fat mass
mice
-
showed a rapid-onset (from week 5) marked increase
#3
high GI diet
increase
liver fat
mice
-
showed a rapid-onset (from week 5) marked increase
#4
high GI diet
increase
lipogenesis
mice
-
gene expression profile in liver consistent with elevated
#5
long-term high-GI diet
decrease
glucose clearance following a glucose load
mice
-
significantly reduced
#6
long-term high-GI diet
decrease
carbohydrate oxidation in the postprandial state
mice
-
led to a delayed switch
#7
long-term high-GI diet
decrease
fat oxidation in the postprandial state
mice
-
led to a delayed switch
#8
long-term high-GI diet
decrease
metabolic flexibility
mice
-
indicating reduced
#9
short-term high- vs. low-GI exposure
no change
carbohydrate oxidation
-
-
no difference
#10
high-GI intervention
decrease
fatty acid oxidation
-
-
significantly blunted
#11
long-term high-GI feeding
increase
obese phenotype
obesity-prone C57BL/6J mice
-
resulted in
#12
long-term high-GI feeding
increase
insulin-resistant phenotype
obesity-prone C57BL/6J mice
-
resulted in
#13
long-term high-GI feeding
increase
metabolically inflexible phenotype
obesity-prone C57BL/6J mice
-
resulted in
#14
high-GI intervention
decrease
fatty acid oxidation
-
-
Early onset and significantly impaired
#15
Abstract

Exposure to high vs. low glycemic index (GI) diets increases fat mass and insulin resistance in obesity-prone C57BL/6J mice. However, the longer-term effects and potentially involved mechanisms are largely unknown. We exposed four groups of male C57BL/6J mice (n = 10 per group) to long-term (20 wk) or short-term (6 wk) isoenergetic and macronutrient matched diets only differing in starch type and as such GI. Body composition, liver fat, molecular factors of lipid metabolism, and markers of insulin sensitivity and metabolic flexibility were investigated in all four groups of mice. Mice fed the high GI diet showed a rapid-onset (from week 5) marked increase in body fat mass and liver fat, a gene expression profile in liver consistent with elevated lipogenesis, and, after long-term exposure, significantly reduced glucose clearance following a glucose load. The long-term high-GI diet also led to a delayed switch to both carbohydrate and fat oxidation in the postprandial state, indicating reduced metabolic flexibility. In contrast, no difference in carbohydrate oxidation was observed after short-term high- vs. low-GI exposure. However, fatty acid oxidation was significantly blunted as early as 3 wk after beginning of the high-GI intervention, at a time where most measured phenotypic markers including body fat mass were comparable between groups. Thus long-term high-GI feeding resulted in an obese, insulin-resistant, and metabolically inflexible phenotype in obesity-prone C57BL/6J mice. Early onset and significantly impaired fatty acid oxidation preceded these changes, thereby indicating a potentially causal involvement.

Medical Subject Headings (MeSH)
AdiposityAnalysis of VarianceAnimal FeedAnimalsBlood GlucoseDietary CarbohydratesDietary FatsFatty AcidsGene Expression ProfilingGlycemic IndexInsulin ResistanceLipid MetabolismLiverLongitudinal StudiesMaleMiceMice, Inbred C57BLObesityOxidation-ReductionStatistics, Nonparametric
Study Links
Quality Scores
SafetyNot Assessed
Efficacy85/10
Quality80/10
Citation Metrics
Total Citations73
Citations/Year4.9
Relative Citation Ratio2.18
NIH Percentile77.1%
Research Impact Scores
APT Score0.75
Weight Score0.68
Normalized Score0.70
Related Supplements