PHOSPHOTRIESTERASE DECREASES PARAOXON TOXICITY IN MICE

被引:19
作者
KALISTEKORHONEN, E
YLITALO, P
HANNINEN, O
RAUSHEL, FM
机构
[1] UNIV KUOPIO,DEPT PHYSIOL,SF-70211 KUOPIO,FINLAND
[2] UNIV TAMPERE,DEPT CLIN SCI,SF-33101 TAMPERE,FINLAND
[3] TEXAS A&M UNIV SYST,DEPT CHEM & BIOCHEM,COLL STN,TX 77843
[4] TEXAS A&M UNIV SYST,DEPT BIOPHYS,COLL STN,TX 77843
关键词
D O I
10.1006/taap.1993.1154
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effect of phosphotriesterase (PTE) on the ip toxicity of paraoxon was studied in mice. The PTE preparation (0.1 ml; paraoxon-hydrolyzing activity, 1.5 μmol/min) was given iv. Cholinesterase activities were measured 2 hr after paraoxon administration. The PTE treatment, given 10 min before paraoxon, did not protect serum cholinesterase (ChE) against the inhibiting effect of paraoxon, but it clearly prevented the decrease of the brain ChE activity. In PTE-nontreated animals ChE was reduced by 60% at the paraoxon dose of 0.5 mg/kg, whereas in PTE-treated mice a significant reduction was not seen until a paraoxon dose of 2.0 mg/kg. The iv injection of PTE did prevent the decrease in brain CItE activity by paraoxon, when it was administered before or immediately after the paraoxon. PTE, injected 15 min after paraoxon, resulted in a minor protection in the brain ChE activities. The iv injection of PTE increased the serum paraoxon-hydrolyzing activity up to 5.1-fold. When the same amounts of PTE were administered ip, im, or sc the increases in the hydrolyzing activities were 4.7-, 2.5-, and 1.8-fold, respectively. The activities returned to the normal level within 24 hr after the PTE. The elimination half-life of the activity of PTE administered iv was approximately 5.5 hr. In conclusion, PTE substantially prevents the toxicity of paraoxon in mice by hydrolyzing paraoxon in circulation. © 1993 Academic Press. All rights reserved.
引用
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页码:275 / 278
页数:4
相关论文
共 11 条
[1]   A PURIFIED RECOMBINANT ORGANOPHOSPHORUS ACID ANHYDRASE PROTECTS MICE AGAINST SOMAN [J].
BROOMFIELD, CA .
PHARMACOLOGY & TOXICOLOGY, 1992, 70 (01) :65-66
[2]   SERUM PARAOXONASE AND ITS INFLUENCE ON PARAOXON AND CHLORPYRIFOS-OXON TOXICITY IN RATS [J].
COSTA, LG ;
MCDONALD, BE ;
MURPHY, SD ;
OMENN, GS ;
RICHTER, RJ ;
MOTULSKY, AG ;
FURLONG, CE .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1990, 103 (01) :66-76
[3]   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
[4]  
DUMAS DP, 1989, BIOTECHNOL APPL BIOC, V11, P235
[5]   INACTIVATION OF ORGANOPHOSPHORUS NERVE AGENTS BY THE PHOSPHOTRIESTERASE FROM PSEUDOMONAS-DIMINUTA [J].
DUMAS, DP ;
DURST, HD ;
LANDIS, WG ;
RAUSHEL, FM ;
WILD, JR .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1990, 277 (01) :155-159
[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]   INHIBITION OF CHOLINESTERASES BY DFP AND INDUCTION OF ORGANOPHOSPHATE-DETOXICATING ENZYMES IN RATS [J].
KALISTEKORHONEN, E ;
TORRONEN, R ;
YLITALO, P ;
HANNINEN, O .
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM, 1990, 21 (04) :527-533
[8]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265
[9]   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
[10]  
RAVEH L, 1992, BIOCHEM PHARMACOL, V44, P389