Degradation of hyaluronic acid by photosensitized riboflavin in vitro. Modulation of the effect by transition metals, radical quenchers, and metal chelators

被引:47
作者
Frati, E
Khatib, AM
Front, P
Panasyuk, A
Aprile, F
Mitrovic, DR
机构
[1] LARIBOISERE HOSP,INSERM U349,PARIS,FRANCE
[2] INST RHEUMATOL,SIENA,ITALY
[3] AMS,INST RHEUMATOL,MOSCOW,RUSSIA
关键词
hyaluronic acid; riboflavin; transition metals; radical quenchers; metal chelators; reactive oxygen species;
D O I
10.1016/S0891-5849(96)00525-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The effect of photoexcited riboflavin (RF) on the viscosity of hyaluronic acid (HA) solutions has been investigated. UV irradiation of RF causes under aerobic conditions fragmentation of HA and a decrease in the viscosity of its solutions. A decrease of HA viscosity occurs in PO4-buffered solutions and is accelerated by high pH, Fe2+ (but much less so by Fe3+), certain metal chelators, and horseradish peroxidase (HRP); it is partially inhibited by catalase and less so by superoxide dismutase (SOD). The reactivity of the system was completely blocked by Tris, ethanol, aspirin, d-manitol, dimethylthiourea (DMTU), dimethylsulfoxide (DMSO), and sodium azide. These results indicate that the most likely chemical species involved in the reaction is the hydroxyl radical. Singlet oxygen (O-1(2)) generation is suggested by the ability of NaN3 and DMSO to completely inhibit the reactivity of the system. These two agents, however, may also interact with OH. radical, as well and suppress the reactivity of the system. H2O2 and O-2(radical anion) seem also to be produced in significant amounts, because catalase and SOD partially block the reactivity of the system. The effect of HRP may be due to hydrogen subtraction from HA and H2O2 reduction to water. Photoexcitation of RF may potentially occur in vitro and in vivo in the organs and tissues that are permeable to light, such as the eye or skin, and damage HA and other cell-matrix components causing inflammation and accelerating aging. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:1139 / 1144
页数:6
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