growth/size/body
• 1.6-fold
|
mortality/aging
homeostasis/metabolism
N |
• mitochondrial fatty acid oxidation and triglyceride hydrolutic activities in skeletal muscle are normal
• mice exhibit normal insulin sensitivity
|
• in cardiac muscle
|
• during the light and dark phase
|
• glucose clearance is enhanced
|
• in fasted mice
• in re-fed mice
|
• in re-fed mice
|
• exercised mice fail to exhibit a decrease in the skeletal muscle indicating a defect in skeletal muscle triglyceride catabolism compared with control mice
|
• 43-fold in the cardiac muscle of non-fasted mice
• 15-fold in the cardiac muscle of fasted mice
|
• in non-exercised and exercised mice
|
• in exercised mice
|
• moderate in fasted mice
|
• marked accumulation of triglycerides in skeletal muscle
• exercised mice fail to exhibit a decrease in skeletal muscle compared with control mice
|
• mild increase in LPA acyltransferase activity
|
• in cardiac muscle
• however, in vitro triglyceride hydrolytic activity in skeletal muscle is normal
|
cardiovascular system
• 43-fold in the cardiac muscle of non-fasted mice
• 15-fold in the cardiac muscle of fasted mice
|
• 1.6-fold
|
• septal and posterial wall thickening
|
• increased 6.7-fold
• however, glucose uptake in skeletal muscle, liver and adipose tissue is normal
|
• left ventricle
|
muscle
• 43-fold in the cardiac muscle of non-fasted mice
• 15-fold in the cardiac muscle of fasted mice
|
• increased 6.7-fold
• however, glucose uptake in skeletal muscle, liver and adipose tissue is normal
|
• left ventricle
|
• marked accumulation of triglycerides in skeletal muscle
• exercised mice fail to exhibit a decrease in skeletal muscle compared with control mice
|
liver/biliary system
• moderate in fasted mice
|
cellular
• increased 6.7-fold
• however, glucose uptake in skeletal muscle, liver and adipose tissue is normal
|