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Age Dependent Modification of the Metabolic Profile of the Tibialis Anterior Muscle Fibers in C57BL/6J Mice

机译:C57BL / 6J小鼠胫前肌纤维代谢谱的年龄依赖性修饰

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摘要

Skeletal muscle aging is accompanied by mass reduction and functional decline, as a result of multiple factors, such as protein expression, morphology of organelles, metabolic equilibria, and neural communication. Skeletal muscles are formed by multiple fibers that express different Myosin Heavy Chains (MyHCs) and have different metabolic properties and different blood supply, with the purpose to adapt their contraction to the functional need. The fine interplay between the different fibers composing a muscle and its architectural organization determine its functional properties. Immunohistochemical and histochemical analyses of the skeletal muscle tissue, besides evidencing morphological characteristics, allow for the precise determination of protein expression and metabolic properties, providing essential information at the single-fiber level. Aiming to gain further knowledge on the influence of aging on skeletal muscles, we investigated the expression of the MyHCs, the Succinate Dehydrogenase (SDH) activity, and the presence of capillaries and Tubular Aggregates (TAs) in the tibialis anterior muscles of physiologically aging C57BL/6J mice aged 8 (adult), 18 (middle aged), and 24 months (old). We observed an increase of type-IIB fast-contracting fibers, an increase of the oxidative capacity of type-IIX and -IIA fibers, a general decrease of the capillarization, and the onset of TAs in type-IIB fibers. These data suggest that aging entails a selective modification of the muscle fiber profiles.
机译:由于多种因素,例如蛋白质表达,细胞器形态,代谢平衡和神经沟通,骨骼肌衰老伴随着质量减少和功能下降。骨骼肌由表达不同肌球蛋白重链(MyHCs),具有不同代谢特性和血液供应的多种纤维形成,目的是使它们的收缩适应功能需求。组成肌肉的不同纤维及其结构组织之间的良好相互作用决定了其功能特性。骨骼肌组织的免疫组织化学和组织化学分析除了可以证明形态特征外,还可以精确确定蛋白质的表达和代谢特性,从而在单纤维水平上提供必要的信息。为了进一步了解衰老对骨骼肌的影响,我们研究了在生理上衰老的C57BL胫骨前肌中MyHCs的表达,琥珀酸脱氢酶(SDH)活性以及毛细血管和小管聚集体(TAs)的存在。 / 6J小鼠分别为8岁(成年),18岁(中年)和24个月(大)。我们观察到IIB型快速收缩纤维的增加,IIX型和-IIA型纤维的氧化能力的增加,毛细作用的普遍减少以及IIB型纤维中TA的出现。这些数据表明,衰老需要选择性地改变肌肉纤维的轮廓。

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