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Diabetes, Vol 46, Issue 12 2022-2028, Copyright © 1997 by American Diabetes Association
Diet-induced muscle insulin resistance in rats is ameliorated by acute dietary lipid withdrawal or a single bout of exercise: parallel relationship between insulin stimulation of glucose uptake and suppression of long-chain fatty acyl-CoA
ND Oakes, KS Bell, SM Furler, S Camilleri, AK Saha, NB Ruderman, DJ Chisholm and EW Kraegen
Garvan Institute of Medical Research, St. Vincent's Hospital, Sydney, NSW, Austalia. n.oakes@garvan.unsw.edu.au
Chronic high-fat feeding in rats induces profound whole-body insulin
resistance, mainly due to effects in oxidative skeletal muscle. The
mechanisms of this reaction remain unclear, but local lipid availability
has been implicated. The aim of this study was to examine the influence of
three short-term physiological manipulations intended to lower muscle lipid
availability on insulin sensitivity in high-fat-fed rats. Adult male Wistar
rats fed a high-fat diet for 3 weeks were divided into four groups the day
before the study: one group was fed the normal daily high-fat meal (FM);
another group was fed an isocaloric low-fat high-glucose meal (GM); a third
group was fasted overnight (NM); and a fourth group underwent a single bout
of exercise (2-h swim), then were fed the normal high-fat meal (EX). In
vivo insulin action was assessed using the hyperinsulinemic glucose clamp
(plasma insulin 745 pmol/l, glucose 7.2 mmol/l). Prior exercise, a single
low-fat meal, or fasting all significantly increased insulin-stimulated
glucose utilization, estimated at either the whole-body level (P < 0.01
vs. FM) or in red quadriceps muscle (EX 18.2, GM 28.1, and NM 19.3 vs. FM
12.6 +/- 1.1 micromol x 100 g(-1) x min(-1); P < 0.05), as well as
increased insulin suppressibility of muscle total long-chain fatty acyl-CoA
(LC-CoA), the metabolically available form of fatty acid (EX 24.0, GM 15.5,
and NM 30.6 vs. FM 45.4 nmol/g; P < 0.05). There was a strong inverse
correlation between glucose uptake and LC-CoA in red quadriceps during the
clamp (r = -0.7, P = 0.001). Muscle triglyceride was significantly reduced
by short-term dietary lipid withdrawal (GM -22 and NM -24% vs. FM; P <
0.01), but not prior exercise. We concluded that muscle insulin resistance
induced by high-fat feeding is readily ameliorated by three independent,
short-term physiological manipulations. The data suggest that insulin
resistance is an important factor in the elevated muscle lipid availability
induced by chronic high-fat feeding.

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Copyright © 1997 by the American Diabetes Association.
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