Liu Zhenqi, Barrett Eugene J
Division of Endocrinology and Metabolism, Department of Internal Medicine, and the General Clinical Research Center, University of Virginia Health Sciences Center, Charlottesville, Virginia 22908, USA.
Am J Physiol Endocrinol Metab. 2002 Dec;283(6):E1105-12. doi: 10.1152/ajpendo.00337.2002.
The body's protein mass not only provides architectural support for cells but also serves vital roles in maintaining their function and survival. The whole body protein pool, as well as that of individual tissues, is determined by the balance between the processes of protein synthesis and degradation. These in turn are regulated by interactions among hormonal, nutritional, neural, inflammatory, and other influences. Prolonged changes in either the synthetic or degradative processes (or both) that cause protein wasting increase morbidity and mortality. The application of tracer kinetic methods, combined with measurements of the activity of components of the cellular signaling pathways involved in protein synthesis and degradation, affords new insights into the regulation of both protein synthesis and breakdown in vivo. These insights, including those from studies of insulin, insulin-like growth factor I, growth hormone, and amino acid-mediated regulation of muscle and whole body protein turnover, provide opportunities to develop and test therapeutic approaches with promise to minimize or prevent these adverse health consequences.
人体的蛋白质不仅为细胞提供结构支持,还在维持细胞功能和存活方面发挥着至关重要的作用。全身蛋白质库以及各个组织的蛋白质库,是由蛋白质合成与降解过程之间的平衡所决定的。而这些过程又依次受到激素、营养、神经、炎症及其他因素相互作用的调节。合成或降解过程(或两者)的长期变化若导致蛋白质消耗,会增加发病率和死亡率。示踪动力学方法的应用,结合对参与蛋白质合成和降解的细胞信号通路成分活性的测量,为体内蛋白质合成和分解的调节提供了新的见解。这些见解,包括来自胰岛素、胰岛素样生长因子I、生长激素以及氨基酸介导的肌肉和全身蛋白质周转调节研究的见解,为开发和测试有望将这些不良健康后果降至最低或预防其发生的治疗方法提供了机会。