Wyss M, Wallimann T
Swiss Federal Institute of Technology, ETH Hönggerberg, Zürich.
Mol Cell Biochem. 1994 Apr-May;133-134:51-66. doi: 10.1007/BF01267947.
Currently, considerable research activities are focussing on biochemical, physiological and pathological aspects of the creatine kinase (CK)-phosphorylcreatine (PCr)-creatine (Cr) system (for reviews see [1,2]), but only little effort is directed towards a thorough investigation of Cr metabolism as a whole. However, a detailed knowledge of Cr metabolism is essential for a deeper understanding of bioenergetics in general and, for example, of the effects of muscular dystrophies, atrophies, CK deficiencies (e.g. in transgenic animals) or Cr analogues on the energy metabolism of the tissues involved. Therefore, the present article provides a short overview on the reactions and enzymes involved in Cr biosynthesis and degradation, on the organization and regulation of Cr metabolism within the body, as well as on the metabolic consequences of 3-guanidinopropionate (GPA) feeding which is known to induce a Cr deficiency in muscle. In addition, the phenotype of muscles depleted of Cr and PCr by GPA feeding is put into context with recent investigations on the muscle phenotype of 'gene knockout' mice deficient in the cytosolic muscle-type M-CK.
目前,大量的研究活动聚焦于肌酸激酶(CK)-磷酸肌酸(PCr)-肌酸(Cr)系统的生化、生理及病理方面(综述见[1,2]),但针对Cr代谢整体的深入研究却很少。然而,全面了解Cr代谢对于深入理解生物能量学,以及例如肌肉萎缩症、萎缩、CK缺乏(如在转基因动物中)或Cr类似物对相关组织能量代谢的影响至关重要。因此,本文简要概述了Cr生物合成和降解所涉及的反应及酶、体内Cr代谢的组织和调节,以及已知会导致肌肉中Cr缺乏的3-胍基丙酸(GPA)喂养的代谢后果。此外,通过GPA喂养使肌肉中Cr和PCr耗尽后的表型,与近期对缺乏胞质肌肉型M-CK的“基因敲除”小鼠肌肉表型的研究联系起来。