Baldassini W A, Ramsey J J, Hagopian K, Lanna D P D
Department of Animal Science, "Luiz de Queiroz" College of Agriculture (ESALQ), University of São Paulo (USP), Piracicaba, São Paulo, Brazil.
Veterinary Medicine, Molecular Biosciences, University of California-Davis (UC DAVIS), Davis, CA, USA.
Cell Biochem Funct. 2017 Dec;35(8):527-537. doi: 10.1002/cbf.3310.
The purpose of this study was to determine if Shc proteins influence the metabolic response to acute (7 days) feeding of a high-fat diet (HFD). To this end, whole animal energy expenditure (EE) and substrate oxidation were measured in the Shc knockout (ShcKO) and wild-type (WT) mice fed a control or HFD. The activities of enzymes of glycolysis, the citric acid cycle, electron transport chain (ETC), and β-oxidation were also investigated in liver and skeletal muscle of ShcKO and WT animals. The study showed that ShcKO increases (P < .05) EE adjusted for either total body weight or lean mass. This change in EE could contribute to decreases in weight gain in ShcKO versus WT mice fed an HFD. Thus, our results indicate that Shc proteins should be considered as potential targets for developing interventions to mitigate weight gain on HFD by stimulating EE. Although decreased levels of Shc proteins influenced the activity of some enzymes in response to high-fat feeding (eg, increasing the activity of acyl-CoA dehydrogenase), it did not produce concerted changes in enzymes of glycolysis, citric acid cycle, or the ETC. The physiological significance of observed changes in select enzyme activities remains to be determined.
We report higher EE in ShcKO versus WT mice when consuming the HFD. Although decreased levels of Shc proteins influenced the activity of a central enzyme of β-oxidation in response to high-fat feeding, it did not produce concerted changes in enzymes of glycolysis, citric acid cycle, or the ETC. Thus, an increase in EE in response to consumption of an HFD may be a mechanism that leads to decreased weight gain previously reported in ShcKO mice with long-term consumption of an HFD.
本研究的目的是确定Shc蛋白是否影响对高脂饮食(HFD)急性(7天)喂养的代谢反应。为此,在喂食对照饮食或HFD的Shc基因敲除(ShcKO)小鼠和野生型(WT)小鼠中测量了全动物能量消耗(EE)和底物氧化。还研究了ShcKO和WT动物肝脏和骨骼肌中糖酵解、柠檬酸循环、电子传递链(ETC)和β-氧化酶的活性。研究表明,根据总体重或瘦体重调整后,ShcKO的EE增加(P<0.05)。与喂食HFD的WT小鼠相比,EE的这种变化可能导致ShcKO小鼠体重增加减少。因此,我们的结果表明,Shc蛋白应被视为开发干预措施的潜在靶点,以通过刺激EE减轻HFD导致的体重增加。尽管Shc蛋白水平降低影响了一些酶对高脂喂养的反应活性(例如,增加了酰基辅酶A脱氢酶的活性),但它并未在糖酵解、柠檬酸循环或ETC的酶中产生协同变化。所选酶活性观察到的变化的生理意义仍有待确定。
我们报告,在食用HFD时,ShcKO小鼠的EE高于WT小鼠。尽管Shc蛋白水平降低影响了一种β-氧化中心酶对高脂喂养的反应活性,但它并未在糖酵解、柠檬酸循环或ETC的酶中产生协同变化。因此,对HFD摄入的EE增加可能是一种机制,导致先前报道的长期食用HFD的ShcKO小鼠体重增加减少。