Literature DB >> 23782997

Effects of alternate-day fasting on high-fat diet-induced insulin resistance in rat skeletal muscle.

Kazuhiko Higashida1, Eri Fujimoto, Mitsuru Higuchi, Shin Terada.   

Abstract

AIMS: The purpose of this study was to investigate the effects of alternate-day fasting (ADF) on insulin-stimulated glucose transport activity in skeletal muscle in rats fed a high-fat diet. MAIN
METHODS: Male Wistar rats were placed on a high-fat diet (n=24) or standard chow diet (Chow, n=12) for 10weeks. Rats fed the high-fat diet were separated into two groups after 4weeks. One group was subjected to ADF for the subsequent 6weeks (HF-ADF, n=12), and the other group was maintained on an ad libitum diet (HF-AL, n=12). After the 10-week dietary intervention, measurements of insulin-stimulated glucose uptake and insulin tolerance test (ITT) were performed. KEY
FINDINGS: Whereas the total intra-abdominal fat mass in the HF-AL group was significantly higher than in the Chow and HF-ADF groups, there was no significant difference between the Chow and HF-ADF groups. However, insulin-stimulated glucose uptake in skeletal muscles was significantly lower in both high-fat fed groups than in the Chow group. Muscle GLUT-4 protein content in HF-AL is significantly lower (~30%) than in Chow, and further reduction (~42%) was observed in the HF-ADF group rats. The HF-ADF and HF-AL group rats had less reduction in glycemia than did the Chow group rats during ITT. SIGNIFICANCE: ADF was unable to eliminate high-fat diet-induced muscle insulin resistance, despite a substantial decrease in total intra-abdominal fat mass. This might have resulted from a reduction in GLUT-4 protein in both HF-AL and HF-ADF rats compared to the Chow group.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Alternate-day fasting; GLUT-4; Insulin resistance; Intra-abdominal fat; Rat; Skeletal muscle

Mesh:

Substances:

Year:  2013        PMID: 23782997     DOI: 10.1016/j.lfs.2013.06.007

Source DB:  PubMed          Journal:  Life Sci        ISSN: 0024-3205            Impact factor:   5.037


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