PENTOXIFYLLINE - A HYDROXYL RADICAL SCAVENGER

Citation
Jp. Freitas et Pm. Filipe, PENTOXIFYLLINE - A HYDROXYL RADICAL SCAVENGER, Biological trace element research, 47(1-3), 1995, pp. 307-311
Citations number
9
Categorie Soggetti
Biology
ISSN journal
01634984
Volume
47
Issue
1-3
Year of publication
1995
Pages
307 - 311
Database
ISI
SICI code
0163-4984(1995)47:1-3<307:P-AHRS>2.0.ZU;2-I
Abstract
Pentoxifylline (PTX), a tri-substituted purine and xanthine derivative , has been used for several years to improve microcirculation because of its hemorheological properties. PTX has also antifibrotic and anti- inflammatory effects. We studied the reaction of PTX with the hydroxyl radical and superoxide anion. Hydroxyl radical was generated by a mix ture of ascorbic acid, H2O2 and Fe (III)-EDTA. We evaluated the iron-d ependent degradation of deoxyribose, mediated by hydroxyl radical, in the presence of different concentrations of PTX (from 0.05 to 3 mM), m easuring the degradation products of deoxyribose that react with 2-thi obarbituric acid (TEA). The reaction of PTX with hydroxyl radical occu rred with a rate constant of (1.1 +/- 0.2) x 10(10) M(-1)/s. These res ults support the properties of PTX as a hydroxyl radical scavenger. So me authors verified that PTX decreases the release of superoxide anion from activated neutrophils. We studied the effect of PTX as a scaveng er of superoxide generated in vitro by a hypoxanthine-xanthine oxidase system. PTX was not a superoxide anion scavenger in this system.