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.
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收藏
页码:44 / 49
页数:6
相关论文
共 25 条
[11]   A NEW AND RAPID COLORIMETRIC DETERMINATION OF ACETYLCHOLINESTERASE ACTIVITY [J].
ELLMAN, GL ;
COURTNEY, KD ;
ANDRES, V ;
FEATHERSTONE, RM .
BIOCHEMICAL PHARMACOLOGY, 1961, 7 (02) :88-&
[13]   HI-6 THERAPY OF SOMAN AND TABUN POISONING IN PRIMATES AND RODENTS [J].
HAMILTON, MG ;
LUNDY, PM .
ARCHIVES OF TOXICOLOGY, 1989, 63 (02) :144-149
[14]  
Karczmar A.G., 1970, ANTICHOLINESTERASE A, P1
[15]   THE EFFECT OF CARBOXYLESTERASE INHIBITION ON INTERSPECIES DIFFERENCES IN SOMAN TOXICITY [J].
MAXWELL, DM ;
BRECHT, KM ;
ONEILL, BL .
TOXICOLOGY LETTERS, 1987, 39 (01) :35-42
[16]   PATHOLOGY OF NERVE AGENTS - PERSPECTIVES ON MEDICAL-MANAGEMENT [J].
MCLEOD, CG .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1985, 5 (06) :S10-S16
[17]   AUTOIMMUNE RESPONSE TO ACETYLCHOLINE RECEPTOR [J].
PATRICK, J ;
LINDSTROM, J .
SCIENCE, 1973, 180 (4088) :871-872
[18]   ACETYLCHOLINESTERASE PROPHYLAXIS AGAINST ORGANO-PHOSPHATE POISONING - QUANTITATIVE CORRELATION BETWEEN PROTECTION AND BLOOD-ENZYME LEVEL IN MICE [J].
RAVEH, L ;
ASHANI, Y ;
LEVY, D ;
DELAHOZ, D ;
WOLFE, AD ;
DOCTOR, BP .
BIOCHEMICAL PHARMACOLOGY, 1989, 38 (03) :529-534
[19]   PRIMATE MEMORY - RETENTION OF SERIAL LIST ITEMS BY A RHESUS-MONKEY [J].
SANDS, SF ;
WRIGHT, AA .
SCIENCE, 1980, 209 (4459) :938-940
[20]   MOLECULAR-CLONING AND CONSTRUCTION OF THE CODING REGION FOR HUMAN ACETYLCHOLINESTERASE REVEALS A G+C-RICH ATTENUATING STRUCTURE [J].
SOREQ, H ;
BENAZIZ, R ;
PRODY, CA ;
SEIDMAN, S ;
GNATT, A ;
NEVILLE, L ;
LIEMANHURWITZ, J ;
LEVLEHMAN, E ;
GINZBERG, D ;
LAPIDOTLIFSON, Y ;
ZAKUT, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (24) :9688-9692