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The effect of ebselen on adenine nucleotide hydrolysis by platelets from adult rats.
- Source :
-
Chemico-biological interactions [Chem Biol Interact] 2004 Jun 30; Vol. 148 (1-2), pp. 93-9. - Publication Year :
- 2004
-
Abstract
- The extracellular hydrolysis of adenine nucleotides by intact rat blood platelets occurs by the action of a cascade of enzymes constituted by an NTPDase 3 (CD39, EC 3.6.1.5, apyrase) and a 5'-nucleotidase (CD73, EC 3.5.7.3), whose final product is adenosine. Ebselen is a seleno-organic compound that possesses low toxicity and exhibits antioxidant, anti-inflammatory, anti-atherosclerotic, and cytoprotective properties. The main objective of this study was to evaluate if the anti-inflammatory drug ebselen can modulate the extracellular adenine nucleotide hydrolysis by platelets from rats. Our results showed that ebselen, at final concentrations of 30 and 100 microM, inhibits in vitro ATP extracellular hydrolysis by 48 and 60%, respectively. Ebselen, at final concentrations of 100 and 130 microM, also inhibited the in vitro extracellular hydrolysis of ADP by 28 and 35%, respectively. However, this drug did not alter AMP hydrolysis by platelets in the appropriate assay conditions. Kinetic analysis showed that the inhibition of ADP and ATP hydrolysis by ebselen, in rat platelets, is of the uncompetitive type. The IC50 calculated from the results were 99 +/- 10 and 186 +/- 47 microM (mean +/- S.D., n = 3) for ATP and ADP hydrolysis, respectively.
- Subjects :
- Animals
Blood Platelets metabolism
Dose-Response Relationship, Drug
Hydrolysis
Inhibitory Concentration 50
Isoindoles
Male
Rats
Rats, Wistar
Adenosine Diphosphate metabolism
Adenosine Triphosphate metabolism
Anti-Inflammatory Agents, Non-Steroidal toxicity
Azoles toxicity
Blood Platelets drug effects
Organoselenium Compounds toxicity
Subjects
Details
- Language :
- English
- ISSN :
- 0009-2797
- Volume :
- 148
- Issue :
- 1-2
- Database :
- MEDLINE
- Journal :
- Chemico-biological interactions
- Publication Type :
- Academic Journal
- Accession number :
- 15223359
- Full Text :
- https://doi.org/10.1016/j.cbi.2004.04.003