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缺乏糖原合酶导致糖原积累和肌肉功能障碍。

Lack of Glycogenin Causes Glycogen Accumulation and Muscle Function Impairment.

机构信息

Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, Barcelona 08028, Spain.

Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, Barcelona 08028, Spain; Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Madrid 28029, Spain.

出版信息

Cell Metab. 2017 Jul 5;26(1):256-266.e4. doi: 10.1016/j.cmet.2017.06.008.

Abstract

Glycogenin is considered essential for glycogen synthesis, as it acts as a primer for the initiation of the polysaccharide chain. Against expectations, glycogenin-deficient mice (Gyg KO) accumulate high amounts of glycogen in striated muscle. Furthermore, this glycogen contains no covalently bound protein, thereby demonstrating that a protein primer is not strictly necessary for the synthesis of the polysaccharide in vivo. Strikingly, in spite of the higher glycogen content, Gyg KO mice showed lower resting energy expenditure and less resistance than control animals when subjected to endurance exercise. These observations can be attributed to a switch of oxidative myofibers toward glycolytic metabolism. Mice overexpressing glycogen synthase in the muscle showed similar alterations, thus indicating that this switch is caused by the excess of glycogen. These results may explain the muscular defects of GSD XV patients, who lack glycogenin-1 and show high glycogen accumulation in muscle.

摘要

糖原合酶是糖原合成所必需的,因为它作为多糖链起始的引物。出人意料的是,缺乏糖原合酶的小鼠(Gyg KO)在横纹肌中积累了大量的糖原。此外,这种糖原不含共价结合的蛋白质,从而证明了在体内合成多糖时不需要蛋白质引物。引人注目的是,尽管糖原含量较高,但与对照动物相比,Gyg KO 小鼠在进行耐力运动时的静息能量消耗更低,阻力更小。这些观察结果可以归因于氧化肌纤维向糖酵解代谢的转变。在肌肉中过表达糖原合酶的小鼠表现出类似的改变,因此表明这种转变是由糖原过量引起的。这些结果可以解释 GSD XV 患者的肌肉缺陷,他们缺乏糖原合酶-1,并且在肌肉中积累了大量的糖原。

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