Valachová Katarína, Kogan Grigorij, Gemeiner Peter, Soltés Ladislav
Institute of Experimental Pharmacology & Toxicology, Slovak Academy of Sciences, SK-84104 Bratislava, Slovakia.
Interdiscip Toxicol. 2010 Mar;3(1):26-34. doi: 10.2478/v10102-010-0001-7. Epub 2010 Mar 29.
The degradation of several high-molar-mass hyaluronan samples was investigated in the presence of ascorbic acid itself and further by an oxidative system composed of ascorbic acid plus transition metal ions, i.e. Fe(II) or Cu(II) ions. The latter oxidative system imitates conditions in a joint synovial fluid during early phase of acute joint inflammation and can be used as a model for monitoring oxidative degradation of hyaluronan under pathophysiological conditions. The system Cu(II) plus ascorbate (the Weissberger oxidative system) resulted in a more significant decrease of hyaluronan molar mass compared to the oxidative system Fe(II) plus ascorbate. Addition of manganese(II) chloride was found to decrease the rate of the oxidative damage of hyaluronan initiated by ascorbate itself and by the Weissberger system.
研究了在抗坏血酸自身存在的情况下,以及进一步通过由抗坏血酸加过渡金属离子(即Fe(II)或Cu(II)离子)组成的氧化体系,对几种高分子量透明质酸样品的降解情况。后一种氧化体系模拟了急性关节炎症早期关节滑液中的条件,可作为监测病理生理条件下透明质酸氧化降解的模型。与Fe(II)加抗坏血酸的氧化体系相比,Cu(II)加抗坏血酸盐(魏斯伯格氧化体系)导致透明质酸摩尔质量的下降更为显著。发现添加氯化锰可降低由抗坏血酸自身和魏斯伯格体系引发的透明质酸氧化损伤速率。