It is well known that troglitazone and voluntary running have the capacity to improve
insulin resistance. The purpose of this study was to evaluate the combination effect
of troglitazone and voluntary running on insulin action. Female rats aged 7 weeks
were divided into high-fat diet (HF), high-fat diet + troglitazone (0.3 % in diet;
Tg), high-fat diet + voluntary running (for 3 wks; Tr), high-fat diet + troglitazone
+ voluntary running (Tg-Tr), and control (C) groups. A sequential euglycemic clamp
experiment with two different insulin infusion rates of 3.0 (L-clamp) and 30.0 mU/kg
BW/min (H-clamp) was performed on these rats after an overnight fast. Blood glucose
concentrations were kept at fasting levels by periodic adjustment of the intravenous
glucose infusion rate during the clamp experiment. Glucose infusion rates (GIRs) calculated
from 60 to 90, 150 to 180 min were regarded as an index of whole body insulin action.
After the clamp experiment, we determined the amount of glycogen content in the gastrocnemius
muscle. Fat feeding markedly reduced GIRs in both L- and H- clamp experiments compared
with C. Troglitazone treatment did not improve high-fat induced insulin resistance.
In both L- and H-clamp experiments, GIRs were increased by voluntary running compared
with HF, and reached the same levels as in C. GIRs of Tg-Tr were not greater than
those of Tr. Glycogen content in gastrocnemius muscle showed the same trend as the
results for GIRs. Therefore, the combination effect of troglitazone and voluntary
running on insulin action was not found, but the effect of voluntary running was shown
in fat-induced insulin resistance.
Key words:
Thiazolidinediones - Euglycemic Clamp - Glycogen
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Y. Sato
Research Center of Health, Physical Fitness and Sports
Nagoya University, Furo-cho
Chikusa-ku, Nagoya 464-8601
Japan
Phone: Phone:+ 81 (52) 789-3962
Fax: Fax:+ 81 (52) 789-3957
Email: E-mail:ysato@med.nagoya-u.ac.jp