کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1919323 | 1535627 | 2012 | 7 صفحه PDF | دانلود رایگان |
It has been proposed that Shc proteins may influence aging by regulating insulin signaling and energy metabolism. Evidence suggests that deletion of p66Shc could partially attenuate weight gain on a high fat diet by increasing energy expenditure. However, the impact of p66Shc on the metabolic response to calorie restriction (CR) has not been determined. Thus, we used indirect respiration calorimetry to determine the impact of CR on energy expenditure (EE) and substrate utilization (RQ) in 18mo p66Shc(−/−) and wild-type (WT) mice. Calorimetry measurements were completed at baseline and following 3 d of 40% CR and 2 mo of 26% CR. There was no difference (P > 0.10) in EE and RQ between gentoypes, regardless of how EE data was normalized. Both p66Shc(−/−) and WT mice showed decreases (P < 0.001) in EE normalized for body weight at 2 mo of CR. However, the response to 3 d of CR was different between genotypes with only the p66Shc(−/−) showing a decrease (P < 0.001) in 24 h EE expressed per mouse or normalized for body weight. The results indicate that p66Shc does not significantly influence EE in 18mo mice at baseline or 2 mo of CR, although it may play a role in the EE response to very acute CR.
► Energy expenditure was studied in p66Shc(−/−) and wild-type mice.
► Energy expenditure was measured under ad libitum and calorie restricted conditions.
► Energy expenditure was decreased in p66Shc(−/−) mice at 3 d of calorie restriction.
► Respiratory quotient was not altered in the p66Shc(−/−) mice.
► p66Shc may play a role in the energetic response to calorie restriction.
Journal: Mechanisms of Ageing and Development - Volume 133, Issue 6, June 2012, Pages 414–420