SUICIDE INHIBITION OF MONOAMINE OXIDASE-A AND OXIDASE-B BY (-)-DEPRENYL - A COMPUTER-AIDED SOLUTION FOR DETERMINING INHIBITION SPECIFICITY

被引:3
作者
BATKE, J [1 ]
GAAL, J [1 ]
机构
[1] CHINOIN CHEM & PHARMACEUT WORKS LTD, BUDAPEST, HUNGARY
关键词
D O I
10.1016/0006-2952(93)90543-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
An analytical solution to the differential equations describing the kinetics of the suicide inhibition of a two-enzyme system has been derived and the modelling of suicide inhibition of the monoamine oxidases A and B (MAO A and B. EC 1.4.3.4) by a quasi-selective agent, (-)-deprenyl, is presented as an example. A new parameter, the specificity index is defined and used in a model which describes the specific and non-specific binding of (-)-deprenyl to MAO B and MAO A, respectively. This type of analysis may be of therapeutic value by indicating optimal dosage of quasi-selective MAO B inhibitors for the treatment of Parkinson's disease.
引用
收藏
页码:597 / 602
页数:6
相关论文
共 18 条
[1]  
DELLACORTE L, 1977, BIOCHEM PHARMACOL, V26, P407
[2]   INTERACTIONS OF MONOAMINE-OXIDASE WITH SUBSTRATES AND INHIBITORS [J].
DOSTERT, PL ;
BENEDETTI, MS ;
TIPTON, KF .
MEDICINAL RESEARCH REVIEWS, 1989, 9 (01) :45-89
[3]  
ELIZAN TS, 1993, INHIBITORS MONOAMINE, P277
[4]   THE NATURE OF THE INHIBITION OF RAT-LIVER MONOAMINE-OXIDASE TYPE-A AND TYPE-B BY THE ACETYLENIC INHIBITORS CLORGYLINE, L-DEPRENYL AND PARGYLINE [J].
FOWLER, CJ ;
MANTLE, TJ ;
TIPTON, KF .
BIOCHEMICAL PHARMACOLOGY, 1982, 31 (22) :3555-3561
[5]   DETERMINATION OF MONOAMINE-OXIDASE CONCENTRATIONS IN RAT-LIVER BY INHIBITOR BINDING [J].
GOMEZ, N ;
UNZETA, M ;
TIPTON, KF ;
ANDERSON, MC ;
OCARROLL, AM .
BIOCHEMICAL PHARMACOLOGY, 1986, 35 (24) :4467-4472
[6]   TRANSIENTS AND RELAXATION KINETICS OF ENZYME REACTIONS [J].
GUTFREUND, H .
ANNUAL REVIEW OF BIOCHEMISTRY, 1971, 40 :315-+
[7]  
HEIKKILA RE, 1984, NATURE, V311, P467, DOI 10.1038/311467a0
[8]  
Knoll J, 1972, Adv Biochem Psychopharmacol, V5, P393
[9]  
KOPIN IJ, 1988, MT SINAI J MED, V55, P43
[10]   CHRONIC PARKINSONISM IN HUMANS DUE TO A PRODUCT OF MEPERIDINE-ANALOG SYNTHESIS [J].
LANGSTON, JW ;
BALLARD, P ;
TETRUD, JW ;
IRWIN, I .
SCIENCE, 1983, 219 (4587) :979-980