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PPARα signaling is activated by cocoa in mouse liver

机译:PPARα信号传导被小鼠肝脏中的可可激活

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In this study we evaluated in mouse liver the effects of cocoa on PPARα signaling. To this aim, mouse diet was supplemented with 10%, w/w, cocoa for one and two weeks. We quantified the expression of PPARα target genes and PPARα gene level and some parameters related to PPARα activation (hepatosomatic index, peroxisomal β-oxidation system and catalase activity). Moreover, we evaluated antioxidant capacity of cocoa by detecting the expression of CAT and SOD1 genes (known to be involved in oxidative balance) and hypolipidemic properties on serum triglycerides. We made a parallel treatment with 0.025%, w/w, ciprofibrate, a well-known PPARα activator, to quantify signal modulation by cocoa. It is known that PPARα activation by ciprofibrate is mediated by direct binding to the receptor and strongly induces expression of target genes. Our results show that cocoa weakly up-regulates PPARα target genes as a consequence of the modulation of the PPARα gene level and does not improve the triglyceride profile in blood. Finally, cocoa increased SOD1 gene expression suggesting an antioxidant effect.
机译:在这项研究中,我们评估了小鼠肝脏中可可粉对PPARα信号传导的影响。为了这个目的,在小鼠饮食中补充了10%w / w的可可粉一两周。我们定量了PPARα靶基因的表达和PPARα基因的水平以及一些与PPARα活化有关的参数(肝体指数,过氧化物酶体β-氧化系统和过氧化氢酶活性)。此外,我们通过检测CAT和SOD1基因的表达(已知参与氧化平衡)和血清甘油三酯的降血脂特性来评估可可的抗氧化能力。我们用0.025%w / w环丙贝特(一种众所周知的PPARα活化剂)进行了平行处理,以量化可可粉对信号的调制。已知环丙贝特对PPARα的激活是通过直接与受体结合而介导的,并强烈诱导靶基因的表达。我们的研究结果表明,由于可调节的P​​PARα基因水平,可可微弱地上调了PPARα靶基因,并没有改善血液中的甘油三酸酯谱。最后,可可增加了SOD1基因的表达,表明具有抗氧化作用。

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