衰老雌性小鼠骨骼肌中的酶能力保持得更好,底物转运蛋白水平更高。

Kenya Takahashi, Yu Kitaoka, Hideo Hatta
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摘要

本研究调查了成年(5 个月大)、中年(12 个月大)和高龄(24 个月大)小鼠骨骼肌中高能磷酸酶、糖酵解酶和线粒体酶活性以及代谢物转运蛋白水平的性别差异。腓肠肌糖原含量随着年龄的增长而增加,与性别无关,但只有高龄雌性小鼠的腓肠肌甘油三酯水平有所增加。衰老会降低雌雄小鼠跖肌和比目鱼肌的肌酸激酶和腺苷酸激酶活性,但雌性小鼠不会。不分性别,足底肌和比目鱼肌的磷酸果激酶和乳酸脱氢酶(LDH)活性都有所下降。此外,与老年雄性小鼠相比,老年雌性小鼠足底肌肉中的己糖激酶活性和比目鱼肌中的乳酸脱氢酶活性下降的程度更大。老年雌性小鼠足底肌肉中的线粒体酶活性增加,但雄性小鼠的线粒体酶活性没有变化。在雌雄老化小鼠的足底肌和比目鱼肌中,葡萄糖转运体 4 的蛋白质含量和脂肪酸转运酶/分化簇 36 的蛋白质含量都有所增加,其中雌性小鼠的含量明显更高。这些发现表明,尽管脂质代谢发生了改变,但雌性小鼠在衰老过程中具有更好的能力来维持骨骼肌中代谢酶的活性和更高水平的代谢物转运蛋白。我们的数据为研究肌肉新陈代谢提供了一个基础,因为年龄依赖性新陈代谢紊乱和疾病对雌性和雄性的影响是不同的。
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Better maintenance of enzymatic capacity and higher levels of substrate transporter proteins in skeletal muscle of aging female mice.

This study investigated sex-specific differences in high-energy phosphate, glycolytic, and mitochondrial enzyme activities and also metabolite transporter protein levels in the skeletal muscles of adult (5 months old), middle-aged (12 months old), and advanced-aged (24 months old) mice. While gastrocnemius glycogen content increased with age regardless of sex, gastrocnemius triglyceride levels increased only in advanced-aged female mice. Aging decreased creatine kinase and adenylate kinase activities in the plantaris muscle of both sexes and in the soleus muscle of male mice but not in female mice. Irrespective of sex, phosphofructokinase and lactate dehydrogenase (LDH) activities decreased in the plantaris and soleus muscles. Additionally, hexokinase activity in the plantaris muscle and LDH activity in the soleus muscle decreased to a greater extent in aged male mice compared with those in aged female mice. Mitochondrial enzyme activities increased in the plantaris muscle of aged female mice but did not change in male mice. The protein content of the glucose transporter 4 in the aged plantaris muscle and fatty acid translocase/cluster of differentiation 36 increased in the aged plantaris and soleus muscles of both sexes, with a significantly higher content in female mice. These findings suggest that females possess a better ability to maintain metabolic enzyme activity and higher levels of metabolite transport proteins in skeletal muscle during aging, despite alterations in lipid metabolism. Our data provide a basis for studying muscle metabolism in the context of age-dependent metabolic perturbations and diseases that affect females and males differently.

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