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Dietary fat modifies mitochondrial and plasma membrane apoptotic signaling in skeletal muscle of calorierestricted mice

机译:饮食脂肪改变了卡路里受限小鼠骨骼肌线粒体和质膜的凋亡信号

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Calorie restriction decreases skeletal muscle apoptosis, and this phenomenon has been mechanistically linked to its protective action against sarcopenia of aging. Alterations in lipid composition of membranes have been related with the beneficial effects of calorie restriction. However, no study has been designed to date to elucidate if different dietary fat sources with calorie restriction modify apoptotic signaling in skeletal muscle. We show that a 6-month calorie restriction decreased the activity of the plasma membrane neutral sphingomyelinase, although caspase-8/10 activity was not altered, in young adult mice. Lipid hydroperoxides, Bax levels, and cytochrome c and AIF release/accumulation into the cytosol were also decreased, although caspase-9 activity was unchanged. No alterations in caspase-3 and apoptotic index (DNA fragmentation) were observed, but calorie restriction improved structural features of gastrocnemius fibers by increasing cross-sectional area and decreasing circularity of fibers in cross sections. Changing dietary fat with calorie restriction produced substantial alterations of apoptotic signaling. Fish oil augmented the protective effect of calorie restriction decreasing plasma membrane neutral sphingomyelinase, Bax levels, caspase-8/10, and -9 activities, while increasing levels of the antioxidant coenzyme Q at the plasma membrane, and potentiating the increase of crosssectional area and the decrease of fiber circularity in cross sections. Many of these changes were not found when we used lard. Our data support that dietary fish oil with calorie restriction produces a cellular anti-apoptotic environment in skeletal muscle with a downregulation of components involved in the initial stages of apoptosis engagement, both at the plasma membrane and the mitochondria.
机译:热量限制会减少骨骼肌细胞的凋亡,并且这种现象在机械上与其对衰老的肌肉减少症的保护作用有关。膜脂质组成的变化与热量限制的有益作用有关。然而,迄今为止,尚未进行任何研究来阐明具有卡路里限制的不同饮食脂肪来源是否会改变骨骼肌的凋亡信号。我们显示,在成年小鼠中,6个月的卡路里限制降低了质膜中性鞘磷脂酶的活性,尽管caspase-8 / 10活性没有改变。脂质过氧化氢,Bax水平以及细胞色素c和AIF在细胞质中的释放/积累也降低了,尽管caspase-9活性没有变化。没有观察到caspase-3和凋亡指数(DNA片段化)的改变,但是热量限制通过增加横截面积和减少横截面中纤维的圆度来改善腓肠肌纤维的结构特征。通过限制卡路里来改变饮食脂肪会导致凋亡信号的实质性改变。鱼油增强了热量限制的保护作用,降低了质膜中性鞘磷脂酶,Bax水平,caspase-8 / 10和-9活性,同时增加了质膜上抗氧化剂辅酶Q的水平,并增强了横截面积和横截面中纤维圆度的降低。当我们使用猪油时,并没有发现其中许多变化。我们的数据支持饮食限制卡路里的鱼油在骨骼肌中产生细胞抗凋亡环境,并降低质膜和线粒体细胞凋亡参与初始阶段所涉及的成分。

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