Hockwin O, Fink H, Glasmacher M
Z Alternsforsch. 1976;31(6):521-35.
Interpretation of factor analysis of 18 metabolic parameters of the bovine lens leads to the determination of the following criteria of lens metabolism: Factor 1: Biologic aging of the lens 33.9%; Factor 2: Glycolysis regulation 17.7%; Factor 3: Topography of lens metabolism 8.7%; Factor 4: Regulation of fructose breakdown 7.9%; Factor 5: Substrate depot 6.6%; Factor 6: Kinases 6.3%. These results could partly be experimentally verified. This interpretation of factor analysis has been an attempt to fit biochemical processes to formal statistical parameters. There was no indication that any of the variables under investigation were indendently responsible for the age dependend changes. However, the set-up made evident that rather complex biochemical influences of different intensity bring about the observed aging phenomena. It may be assumed that on or the other of these variables acts as a "triggering mechanism". Age related disturbances in the biochemical balance may be initiated by the glycolysis regulation factor, the importance of which is expressed by its high portion of 17%. Here changes in the ratio of reduced and oxydized coenzymes may act as a "triggering mechanism" (26, 30). Topography of lens metabolism, carbohydrate breakdown via metabolic pathways, the presence of substrate depots, and the internal regulation of the kinases are, according to their portion in factor loading, of about equal importance with respect to aging processes, however, factors 1 and 2, with a 50% portion, must be given precedence in any consideration. Factor 1, interpreted as "biological lens aging", yields about 1/3 of the information on the age influence on lens metabolism. This factor stands independent in being loaded by lens weight, which is the accepted age representative. However, lens weight means protein as well as the process of protein synthesis. It may be assumed that this factor represents a connective link between protein and carbohydrate metabolism, since it is well known that changes in protein belong to the most remarkable age disturbances (31,32), and that the quality of the proteins is dependent on the period of its synthesis (18,33).
对牛晶状体18种代谢参数进行因子分析的结果,确定了晶状体代谢的以下标准:因子1:晶状体生物老化,占33.9%;因子2:糖酵解调节,占17.7%;因子3:晶状体代谢的拓扑结构,占8.7%;因子4:果糖分解调节,占7.9%;因子5:底物储存,占6.6%;因子6:激酶,占6.3%。这些结果部分可以通过实验验证。这种对因子分析的解释是试图将生化过程与形式统计参数相拟合。没有迹象表明所研究的任何变量独立地导致了与年龄相关的变化。然而,研究结果表明,不同强度的相当复杂的生化影响导致了所观察到的老化现象。可以假设这些变量中的一个或另一个充当“触发机制”。与年龄相关的生化平衡紊乱可能由糖酵解调节因子引发,其重要性通过17%的高占比体现出来。这里还原型和氧化型辅酶比例的变化可能充当“触发机制”(参考文献26, 30)。就老化过程而言,根据其在因子负荷中的占比,晶状体代谢的拓扑结构、通过代谢途径的碳水化合物分解、底物储存的存在以及激酶的内部调节具有大致相同的重要性,然而,在任何考虑中,占比50%的因子1和因子2必须优先考虑。被解释为“晶状体生物老化”的因子1,提供了约1/3关于年龄对晶状体代谢影响的信息。该因子独立地由晶状体重量负荷,而晶状体重量是公认的年龄代表指标。然而,晶状体重量意味着蛋白质以及蛋白质合成过程。可以假设这个因子代表了蛋白质和碳水化合物代谢之间的联系环节,因为众所周知,蛋白质变化是最显著的年龄相关紊乱之一(参考文献31, 32),并且蛋白质的质量取决于其合成时期(参考文献18, 33)。