TY - JOUR
T1 - Calorie restriction initiated at middle age improved glucose tolerance without affecting age-related impairments of insulin signaling in rat skeletal muscle
AU - Park, Seongjoon
AU - Komatsu, Toshimitsu
AU - Hayashi, Hiroko
AU - Yamaza, Haruyoshi
AU - Chiba, Takuya
AU - Higami, Yoshikazu
AU - Kuramoto, Kazunao
AU - Shimokawa, Isao
N1 - Funding Information:
The present study was supported by a Grant-in Aid for Scientific Research (B) (2) from Japan Society for the Promotion of Science (Grant No. 15390128). We are grateful to the staff at Biomedical Research Center at Center for Frontier Life Sciences, Nagasaki University for their technical assistance and animal care. We also thank Yutaka Araki and Yuko Moriyama for technical assistance.
PY - 2006/9
Y1 - 2006/9
N2 - Calorie restriction (CR) may affect glucose tolerance via modulation of the insulin action in skeletal muscle. The present study investigated the effect of CR initiated at middle age in rats bearing glucose intolerance, in comparison with CR at a younger age. Male F344 rats at 2.5 and 18 months (mo) of age were fed ad libitum (AL) or 30% CR diets for 4-4.5 mo, subjected to glucose tolerance testing, and then sacrificed 15 min after intraperitoneal glucose or saline injection to evaluate glucose-stimulated insulin response and subsequent activation of insulin signaling molecules. The protein abundance of phosphorylated (p) insulin receptors, p-Akt, and p-atypical PKC and the membrane fraction of glucose transporter 4 in quadriceps femoris muscle (QFM) were analyzed by EIA or immunoblotting. CR initiated either at young or middle age improved glucose tolerance with a lower serum insulin response to glucose. However, middle-aged CR did not improve aging-related impairments in insulin signaling in QFM. The present results emphasized the possibilities of CR activation of an insulin-independent mechanism in skeletal muscle and also of the involvement of non-muscle tissues in glucose uptake.
AB - Calorie restriction (CR) may affect glucose tolerance via modulation of the insulin action in skeletal muscle. The present study investigated the effect of CR initiated at middle age in rats bearing glucose intolerance, in comparison with CR at a younger age. Male F344 rats at 2.5 and 18 months (mo) of age were fed ad libitum (AL) or 30% CR diets for 4-4.5 mo, subjected to glucose tolerance testing, and then sacrificed 15 min after intraperitoneal glucose or saline injection to evaluate glucose-stimulated insulin response and subsequent activation of insulin signaling molecules. The protein abundance of phosphorylated (p) insulin receptors, p-Akt, and p-atypical PKC and the membrane fraction of glucose transporter 4 in quadriceps femoris muscle (QFM) were analyzed by EIA or immunoblotting. CR initiated either at young or middle age improved glucose tolerance with a lower serum insulin response to glucose. However, middle-aged CR did not improve aging-related impairments in insulin signaling in QFM. The present results emphasized the possibilities of CR activation of an insulin-independent mechanism in skeletal muscle and also of the involvement of non-muscle tissues in glucose uptake.
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U2 - 10.1016/j.exger.2006.06.055
DO - 10.1016/j.exger.2006.06.055
M3 - Article
C2 - 16920310
AN - SCOPUS:33749684748
SN - 0531-5565
VL - 41
SP - 837
EP - 845
JO - Experimental Gerontology
JF - Experimental Gerontology
IS - 9
ER -