CLINICAL-PHARMACOLOGY OF REVERSIBLE MONOAMINE OXIDASE-A INHIBITORS

Citation
Pr. Bieck et al., CLINICAL-PHARMACOLOGY OF REVERSIBLE MONOAMINE OXIDASE-A INHIBITORS, Clinical neuropharmacology, 16, 1993, pp. 190000034-190000041
Citations number
11
Categorie Soggetti
Pharmacology & Pharmacy",Neurosciences
Journal title
ISSN journal
03625664
Volume
16
Year of publication
1993
Supplement
2
Pages
190000034 - 190000041
Database
ISI
SICI code
0362-5664(1993)16:<190000034:CORMOI>2.0.ZU;2-E
Abstract
Traditional monoamine oxidase inhibitors (MA01s) have long been associ ated with tyramine-related hypertension-the cheese effect. Despite the ir undoubted clinical efficacy, this problem has restricted their use. New, selective, and reversible MAO-A inhibitors-which act only on the A isoenzyme-appear not to have this effect. Our investigations of the se drugs, exemplified by brofaromine, have shown a reduced and more ra pidly reversed tyramine pressor sensitivity. Moreover, we were unable to detect any clinically significant food interaction, following inges tion of a quantity of cheese containing sufficient tyramine to increas e systolic blood pressure by at least 30 mm Hg. These results confirm the improved safety of brofaromine, and other drugs in this class, whe n compared with classic MA01s.