Department of Molecular Biosciences, School of Veterinary Medicine, University of California, Davis, CA 95616, USA.
Metabolism. 2012 Dec;61(12):1703-13. doi: 10.1016/j.metabol.2012.05.007. Epub 2012 Jun 7.
ShcKO mice have low body fat and resist weight gain on a high fat diet, indicating that Shc proteins may influence enzymes involved in β-oxidation. To investigate this idea, the activities of β-oxidation and ketone body metabolism enzymes were measured.
The activities of β-oxidation enzymes (acyl-CoA dehydrogenase, 3-hydroxyacyl-CoA dehydrogenase and ketoacyl-CoA thiolase) in liver and hindlimb skeletal muscle, ketolytic enzymes (acetoacetyl-CoA thiolase, β-hydroxybutyrate dehydrogenase and 3-oxoacid-CoA transferase) in skeletal muscle, and ketogenic enzymes (acetoacetyl-CoA thiolase and β-hydroxybutyrate dehydrogenase) in liver were measured from wild-type and ShcKO mice.
The activities of β-oxidation enzymes were increased (P<.05) in the ShcKO compared to wild-type mice in the fasted but not the fed state. In contrast, no uniform increases in the ketolytic enzyme activities were observed between ShcKO and wild-type mice. In liver, the activities of ketogenic enzymes were increased (P<.05) in ShcKO compared to wild-type mice in both the fed and fasted states. Levels of phosphorylated hormone sensitive lipase from adipocytes were also increased (P<.05) in fasted ShcKO mice.
These studies indicate that the low Shc levels in ShcKO mice result in increased liver and muscle β-oxidation enzyme activities in response to fasting and induce chronic increases in the activity of liver ketogenic enzymes. Decreases in the level of Shc proteins should be considered as possible contributors to the increase in activity of fatty acid oxidation enzymes in response to physiological conditions which increase reliance on fatty acids as a source of energy.
ShcKO 小鼠体脂含量低,高脂饮食时体重增加受到抑制,这表明 Shc 蛋白可能影响参与β-氧化的酶。为了验证这一观点,检测了β-氧化和酮体代谢酶的活性。
从野生型和 ShcKO 小鼠的肝脏和后肢骨骼肌中测量了β-氧化酶(酰基辅酶 A 脱氢酶、3-羟酰基辅酶 A 脱氢酶和酮酰基辅酶 A 硫解酶)、骨骼肌中的酮解酶(乙酰乙酰基辅酶 A 硫解酶、β-羟丁酸脱氢酶和 3-氧代酸辅酶 A 转移酶)以及肝脏中的生酮酶(乙酰乙酰基辅酶 A 硫解酶和β-羟丁酸脱氢酶)的活性。
与野生型小鼠相比,禁食但不进食状态下 ShcKO 小鼠的β-氧化酶活性增加(P<.05)。相比之下,ShcKO 与野生型小鼠之间的酮解酶活性并没有一致的增加。在肝脏中,禁食和进食状态下,ShcKO 小鼠的生酮酶活性均高于野生型小鼠(P<.05)。脂肪细胞中磷酸化激素敏感脂酶的水平在禁食 ShcKO 小鼠中也升高(P<.05)。
这些研究表明,ShcKO 小鼠中 Shc 水平降低导致禁食时肝脏和肌肉中β-氧化酶活性增加,并诱导肝脏生酮酶活性的慢性增加。Shc 蛋白水平的降低应被视为生理条件下增加脂肪酸氧化酶活性的可能原因,这些条件增加了对脂肪酸作为能量来源的依赖。