Freshage Research Group. Department of Physiology. Faculty of Medicine. University of Valencia, CIBERFES-ISCIII, INCLIVA, Valencia, Spain.
Freshage Research Group. Department Physiotherapy. University of Valencia, CIBERFES-ISCIII, INCLIVA, Valencia, Spain.
Biomed Pharmacother. 2019 Oct;118:109130. doi: 10.1016/j.biopha.2019.109130. Epub 2019 Jul 12.
The objective of this work was to determine the specific mechanisms by which resveratrol inhibits lipogenesis and stimulates lipolysis.
Twelve male mice were individually introduced into a metabolic cage for 24 h to measure basal metabolic rate, prior to intervention. They were randomly divided into two groups, resveratrol (RSV) and control (C), and administered resveratrol intraperitoneally or vehicle, respectively, for two consecutive days. After 24 h, the metabolic energy expenditure was again determined for 24 h, before mice were sacrificed. Protein and gene expression of different enzymes related to metabolism in the hepatic tissue, adipose tissue and gastrocnemius of mice were analyzed by RT-PCR, western blot or ELISA.
We report that resveratrol lowers the respiratory quotient in old mice and that this may be due to the activation of fatty acid mobilization from white adipose tissue (because hormone-activated lipase expression is increased) and fatty acid transport into mitochondria and eventual oxidation in muscle and liver (because transport enzymes and beta oxidation enzymes are also increased). Indeed, we have observed that resveratrol in vivo causes an increase in the expression and phosphorylation of AMPKα in liver, muscle and adipose tissue and an increase in the expression of acyl-CoA synthetase, of carnitine palmitoyl transferase 1 and of carnitine acylcarnitine translocase, all enzymes involved in lipid catabolism. On the other hand, the levels of acetyl-CoA carboxylase as well as those its product, i.e. malonyl CoA, are decreased.
We conclude that a controlled dose of resveratrol activates fatty acid mobilization and degradation and inhibits fatty acid synthesis in old mice. This is the first time that these effects of resveratrol in lipid metabolism in healthy old (non-obese) animals are reported.
本研究旨在确定白藜芦醇抑制脂肪生成和促进脂肪分解的具体机制。
将 12 只雄性小鼠分别放入代谢笼中,以测量基础代谢率,然后进行干预。这些小鼠被随机分为两组,即白藜芦醇(RSV)组和对照组(C),分别连续两天腹腔内给予白藜芦醇或载体。24 小时后,再次测量 24 小时的代谢能量消耗,然后处死小鼠。通过 RT-PCR、Western blot 或 ELISA 分析小鼠肝组织、脂肪组织和比目鱼肌中与代谢相关的不同酶的蛋白和基因表达。
我们报告称,白藜芦醇可降低老年小鼠的呼吸商,这可能是由于白色脂肪组织中脂肪酸动员的激活(因为激素激活的脂肪酶表达增加)以及脂肪酸向线粒体的转运和最终在肌肉和肝脏中的氧化(因为转运酶和β氧化酶也增加)。事实上,我们已经观察到,白藜芦醇在体内引起肝、肌肉和脂肪组织中 AMPKα 的表达和磷酸化增加,以及酰基辅酶 A 合成酶、肉碱棕榈酰转移酶 1 和肉碱酰基辅酶 A 转位酶的表达增加,所有这些酶都参与脂肪分解。另一方面,乙酰辅酶 A 羧化酶及其产物丙二酰辅酶 A 的水平降低。
我们得出结论,控制剂量的白藜芦醇可激活脂肪酸动员和降解,并抑制老年小鼠的脂肪酸合成。这是首次报道白藜芦醇在健康老年(非肥胖)动物的脂质代谢中的这些作用。