PROTECTION OF RHESUS-MONKEYS AGAINST SOMAN AND PREVENTION OF PERFORMANCE DECREMENT BY PRETREATMENT WITH ACETYLCHOLINESTERASE

被引:51
作者
MAXWELL, DM
CASTRO, CA
DELAHOZ, DM
GENTRY, MK
GOLD, MB
SOLANA, RP
WOLFE, AD
DOCTOR, BP
机构
[1] WALTER REED ARMY MED CTR,DIV BIOCHEM,WASHINGTON,DC 20307
[2] USA,MED INST CHEM DEF,DIV PHARMACOL,ABERDEEN PROVING GROUND,MD 21010
关键词
D O I
10.1016/0041-008X(92)90365-Y
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The ability of acetylcholinesterase from fetal bovine serum (FBS AChE) to protect against soman, a highly toxic organophosphorus (OP) compound, was tested in rhesus monkeys. Intravenous administration of FBS AChE produced a minimal behavioral effect on the serial probe recognition task, a sensitive test of cognitive function and short-term memory. Pharmaco-kinetic studies of injected FBS AChE indicated a plasma half-life of 40 hr for FBS AChE in monkeys. Both in vitro and in vivo titration of FBS AChE with soman produced a 1:1 stoichiometry between organophosphate-inhibited FBS AChE and the cumulative dose of the toxic stereoisomers of soman. Administration of FBS AChE protected monkeys against the lethal effects of up to 2.7 LD50 of soman and prevented any signs of organophosphate intoxication, e.g., excessive secretions, respiratory depression, muscle fasciculations, or convulsions. In addition, monkeys pretreated with FBS AChE were devoid of any behavioral incapacitation after soman challenge, as measured by the serial probe recognition task. Compared to the current multicomponent drug treatment against soman, which does not prevent the signs or the behavioral deficits resulting from OP intoxication, use of FBS AChE as a single pretreatment drug provides significantly effective protection against both the lethal and the behavioral effects of soman. © 1992.
引用
收藏
页码:44 / 49
页数:6
相关论文
共 25 条
[1]  
Abuchowsky A, 1981, ENZYMES DRUGS, P367
[2]  
ADAMS NL, 1976, EBTR76039 EDG ARSE T
[3]   ISOLATION, ANTICHOLINESTERASE PROPERTIES, AND ACUTE TOXICITY IN MICE OF THE 4 STEREOISOMERS OF THE NERVE AGENT SOMAN [J].
BENSCHOP, HP ;
KONINGS, CAG ;
VANGENDEREN, J ;
DEJONG, LPA .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1984, 72 (01) :61-74
[4]   DRUGS ACTING ON CENTRAL CHOLINERGIC MECHANISMS AND AFFECTING RESPIRATION [J].
BRIMBLECOMBE, RW .
PHARMACOLOGY & THERAPEUTICS PART B-GENERAL & SYSTEMATIC PHARMACOLOGY, 1977, 3 (01) :65-74
[5]  
Castro C.A., 1991, NEUROTOXICOLOGY LITT, V125, P125
[6]  
Castro CA, 1991, PHARM BIOCH BEHAV, V41, P159
[7]   A SIMPLIFIED PROCEDURE FOR THE PURIFICATION OF LARGE QUANTITIES OF FETAL BOVINE SERUM ACETYLCHOLINESTERASE [J].
DELAHOZ, D ;
DOCTOR, BP ;
RALSTON, JS ;
RUSH, RS ;
WOLFE, AD .
LIFE SCIENCES, 1986, 39 (03) :195-199
[8]   COMPLETE AMINO-ACID-SEQUENCE OF FETAL BOVINE SERUM ACETYLCHOLINESTERASE AND ITS COMPARISON IN VARIOUS REGIONS WITH OTHER CHOLINESTERASES [J].
DOCTOR, BP ;
CHAPMAN, TC ;
CHRISTNER, CE ;
DEAL, CD ;
DELAHOZ, DM ;
GENTRY, MK ;
OGERT, RA ;
RUSH, RS ;
SMYTH, KK ;
WOLFE, AD .
FEBS LETTERS, 1990, 266 (1-2) :123-127
[9]   ENZYMES AS PRETREATMENT DRUGS FOR ORGANOPHOSPHATE TOXICITY [J].
DOCTOR, BP ;
RAVEH, L ;
WOLFE, AD ;
MAXWELL, DM ;
ASHANI, Y .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1991, 15 (01) :123-128
[10]   PROGRESS IN MEDICAL DEFENSE AGAINST NERVE AGENTS [J].
DUNN, MA ;
SIDELL, FR .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1989, 262 (05) :649-652