Long chain analogs of physostigmine as potential drugs for Alzheimer's disease: new insights into the mechanism of action in the inhibition of acetylcholinesterase

被引:55
作者
Perola, E
Cellai, L
Lamba, D
Filocamo, L
Brufani, M
机构
[1] CNR, Ist Strutturist Chim Giordano Giacomello, I-00016 Monterotondo Staz, Rome, Italy
[2] Univ Rome La Sapienza, Dipartimento Sci Biochim A Rossi Fanelli, I-00185 Rome, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY | 1997年 / 1343卷 / 01期
关键词
acetylcholinesterase; inhibition kinetics; physostigmine analog; inhibition mechanism; reactivation time;
D O I
10.1016/S0167-4838(97)00133-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Heptylphysostigmine is in advanced clinical trial as a drug for Alzheimer's disease. 8-Morpholinooctylphysostigmine and 8-(cis-2,6-dimethylmorpholino)octylphysostigmine are currently undergoing pre-clinical evaluation. The mechanism of action of these compounds in the inhibition of acetylcholinesterase has been investigated. All the examined compounds display non competitive-like kinetics of inhibition. There are no reversible components in the observed inhibition: the whole inhibitory effect is due to the time-dependent pseudo-irreversible carbamylation of the active site. Yet the observed time course of the inhibition does not match a simple second order kinetics. An influence of the quaternary structure of the enzyme on the more complex kinetics of carbamylation is hypothesized. Reactivation experiments on the inhibited enzyme show long lasting inhibitory effects for these compounds. The higher duration of the anticholinesterase effect of the morpholino derivatives compared to heptylphysostigmine should provide the basis for their higher therapeutic potential. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:41 / 50
页数:10
相关论文
共 16 条
[1]  
Aldridge WN, 1972, FRONTIERS BIOL, V26
[2]   SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF NEW ACETYLCHOLINESTERASE INHIBITORS - MORPHOLINOALKYLCARBAMOYLOXYESEROLINE DERIVATIVES [J].
ALISI, MA ;
BRUFANI, M ;
FILOCAMO, L ;
GOSTOLI, G ;
LICANDRO, E ;
CESTA, MC ;
LAPPA, S ;
MARCHESINI, D ;
PAGELLA, P .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1995, 5 (18) :2077-2080
[3]   THE CHOLINERGIC HYPOTHESIS OF GERIATRIC MEMORY DYSFUNCTION [J].
BARTUS, RT ;
DEAN, RL ;
BEER, B ;
LIPPA, AS .
SCIENCE, 1982, 217 (4558) :408-417
[4]  
Brufani Mario, 1997, Drugs of the Future, V22, P397
[5]   Cation-pi interactions in chemistry and biology: A new view of benzene, Phe, Tyr, and Trp [J].
Dougherty, DA .
SCIENCE, 1996, 271 (5246) :163-168
[6]   A NEW AND RAPID COLORIMETRIC DETERMINATION OF ACETYLCHOLINESTERASE ACTIVITY [J].
ELLMAN, GL ;
COURTNEY, KD ;
ANDRES, V ;
FEATHERSTONE, RM .
BIOCHEMICAL PHARMACOLOGY, 1961, 7 (02) :88-&
[7]   A CONTROLLED TRIAL OF TACRINE IN ALZHEIMERS-DISEASE [J].
FARLOW, M ;
GRACON, SI ;
HERSHEY, LA ;
LEWIS, KW ;
SADOWSKY, CH ;
DOLANURENO, J .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1992, 268 (18) :2523-2529
[8]   PHARMACOKINETICS AND PHARMACODYNAMICS OF PHYSOSTIGMINE AFTER INTRAVENOUS ADMINISTRATION IN BEAGLE DOGS [J].
GIACOBINI, E ;
SOMANI, S ;
MCILHANY, M ;
DOWNEN, M ;
HALLAK, M .
NEUROPHARMACOLOGY, 1987, 26 (7B) :831-836
[9]   QUATERNARY LIGAND-BINDING TO AROMATIC RESIDUES IN THE ACTIVE-SITE GORGE OF ACETYLCHOLINESTERASE [J].
HAREL, M ;
SCHALK, I ;
EHRETSABATIER, L ;
BOUET, F ;
GOELDNER, M ;
HIRTH, C ;
AXELSEN, PH ;
SILMAN, I ;
SUSSMAN, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (19) :9031-9035
[10]   RELATIONSHIP BETWEEN PHARMACOKINETICS AND PHARMACODYNAMICS OF EPTASTIGMINE IN YOUNG HEALTHY-VOLUNTEERS [J].
IMBIMBO, BP ;
LICINI, M ;
SCHETTINO, M ;
MOSCA, A ;
ONELLI, E ;
ZECCA, L ;
GIUSTINA, A .
JOURNAL OF CLINICAL PHARMACOLOGY, 1995, 35 (03) :285-290