EFFECT OF DILTIAZEM ON PLASMA-CONCENTRATIONS OF OXYPURINES AND URIC-ACID

Citation
Pkf. Yeung et al., EFFECT OF DILTIAZEM ON PLASMA-CONCENTRATIONS OF OXYPURINES AND URIC-ACID, Therapeutic drug monitoring, 19(3), 1997, pp. 286-291
Citations number
38
Categorie Soggetti
Pharmacology & Pharmacy","Public, Environmental & Occupation Heath",Toxicology,Biology
Journal title
ISSN journal
01634356
Volume
19
Issue
3
Year of publication
1997
Pages
286 - 291
Database
ISI
SICI code
0163-4356(1997)19:3<286:EODOPO>2.0.ZU;2-8
Abstract
To determine the clinical effect of diltiazem on the metabolism of ade nosine, and its importance in ischemic heart disease, arterial plasma concentrations of the purine metabolites were determined in 21 healthy volunteers (10 female and 11 male) and 19 patients with effort-angina (8 female and 11 male) before, during, and immediately after standard treadmill exercise feats conducted before and after they had taken 60 mg diltiazem (Cardizem; Hoechst Marion Roussel, Laval, QC, Canada) fo ur times a day for 1 week. The results showed that the cardiac patient s had significantly lower mean plasma concentrations of uric acid (46. 82 +/- 25.51 versus 95.47 +/- 35.41 mu g/ml, p < 0.05), inosine (0.25 +/- 0.19 versus 0.84 +/- 0.17 mu g/ml, p < 0.05), and hypoxanthine (0. 18 +/- 0.35 versus 0.50 +/- 0.27 mu g/ml, p < 0.05), Diltiazem decreas ed the mean resting plasma concentrations of uric acid in patients (ur ic acid 43.47 +/- 22.26 versus 46.82 +/- 25.51 mu g/ml, p < 0.05) and healthy volunteers (uric acid 85.68 +/- 26.71 versus 95.47 +/- 35.41 m u g/ml, p < 0.05). There was no statistically significant change in th e plasma concentrations of the purine metabolites during exercise (p > 0.05). Female subjects had significantly lower plasma concentrations of uric acid than males (patients, 34.87 +/- 26.93 versus 55.78 +/- 21 .25 mu g/ml healthy volunteers, 84.79 +/- 32.07 versus 104.22 +/- 37.0 5 mu g/ml; p < 0.05 for both). Results of the study suggest that norma l therapeutic doses of diltiazem may modulate the metabolism of adenos ine and that some of the purine metabolites may be useful markers for specific types of ischemic heart disease.