SLOW ACCUMULATION OF ACETYLCHOLINESTERASE IN RAT-BRAIN DURING ENZYME-INHIBITION BY REPEATED DOSING WITH CHLORPYRIFOS

被引:39
作者
CHIAPPA, S [1 ]
PADILLA, S [1 ]
KOENIGSBERGER, C [1 ]
MOSER, V [1 ]
BRIMIJOIN, S [1 ]
机构
[1] US EPA,HLTH EFFECTS RES LAB,DIV NEUROTOXICOL,RES TRIANGLE PK,NC 27711
关键词
CHLORPYRIFOS; ACETYLCHOLINESTERASE GENE EXPRESSION; RAT BRAIN; ORGANOPHOSPHATE;
D O I
10.1016/0006-2952(95)00004-J
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
When given to rats, O,O'-diethyl-O-[3,5,6-trichloro-2-pyridyl]-phosphorothionate (chlorpyrifos), a common insecticide, causes an unusually lengthy dose-dependent fall in the activity of brain acetylcholinesterase (AChE; EC 3.1.1.7). To determine whether the slow recovery involves impaired AChE synthesis, experiments were designed to measure AChE activity, immunoreactive AChE protein (AChE-IR) and AChE mRNA. Male, Long-Evans rats, maintained at 350 +/- 5 g, were dosed (s.c.) weekly for 4 weeks with 0, 15, 30, or 60 mg/kg chlorpyrifos in peanut oil. Brain tissue was harvested 1, 3, 5, 7 and 9 weeks after treatment began. AChE activity was measured by Ellman assay, and AChE-IR was estimated by two-site ELISA using monoclonal antibodies to rat brain AChE. While AChE activity fell significantly at all times and doses, AChE-IR increased at 3 and 5 weeks in the two higher dosage groups. Larger increases of AChE-IR were observed after chlorpyrifos was administered for 4 weeks by the oral route. Northern blots quantified with reference to cyclophilin were consistent with stable levels of AChE mRNA. Overall, it appears that chronically reduced brain AChE activity after chlorpyrifos reflects sustained enzyme inhibition, not loss of enzyme protein or suppression of AChE message.
引用
收藏
页码:955 / 963
页数:9
相关论文
共 34 条
[1]   A LOTUS 1-2-3-BASED SYSTEM FOR RECORDING AND MAINTAINING BODY-WEIGHT OF LABORATORY-ANIMALS [J].
ALI, JS ;
OLSZYK, VB ;
DUNN, DD ;
LEE, KLA ;
KENDALL, SM ;
RHODERICK, RR ;
BUSHNELL, PJ .
BEHAVIOR RESEARCH METHODS INSTRUMENTS & COMPUTERS, 1992, 24 (01) :82-87
[2]  
Aspelin kL, 1992, PESTICIDES IND SALES
[3]   STOP-FLOW - NEW TECHNIQUE FOR MEASURING AXONAL-TRANSPORT, AND ITS APPLICATION TO TRANSPORT OF DOPAMINE-BETA-HYDROXYLASE [J].
BRIMIJOIN, S .
JOURNAL OF NEUROBIOLOGY, 1975, 6 (04) :379-394
[4]   2-SITE IMMUNOASSAY FOR ACETYLCHOLINESTERASE IN BRAIN, NERVE, AND MUSCLE [J].
BRIMIJOIN, S ;
HAMMOND, P ;
RAKONCZAY, Z .
JOURNAL OF NEUROCHEMISTRY, 1987, 49 (02) :555-562
[5]  
BUSHNELL PJ, 1993, J PHARMACOL EXP THER, V266, P1007
[6]   INHIBITION OF HUMAN-SERUM COMPLEMENT ACTIVITY BY DIISOPROPYLFLUOROPHOSPHATE AND SELECTED ANTICHOLINESTERASE INSECTICIDES [J].
CASALE, GP ;
BAVARI, S ;
CONNOLLY, JJ .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1989, 12 (03) :460-468
[7]   AN INVESTIGATION OF ACETYLCHOLINESTERASE INHIBITION AND AGING AND CHOLINE-ACETYLTRANSFERASE ACTIVITY FOLLOWING A HIGH-LEVEL ACUTE EXPOSURE TO PARAOXON [J].
CHAMBERS, HW ;
CHAMBERS, JE .
PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 1989, 33 (02) :125-131
[8]   INHIBITION PATTERNS OF BRAIN ACETYLCHOLINESTERASE AND HEPATIC AND PLASMA ALIESTERASES FOLLOWING EXPOSURES TO 3 PHOSPHOROTHIONATE INSECTICIDES AND THEIR OXONS IN RATS [J].
CHAMBERS, JE ;
CARR, RL .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1993, 21 (01) :111-119
[9]   TIME COURSE OF INHIBITION OF ACETYLCHOLINESTERASE AND ALIESTERASES FOLLOWING PARATHION AND PARAOXON EXPOSURES IN RATS [J].
CHAMBERS, JE ;
CHAMBERS, HW .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1990, 103 (03) :420-429
[10]   RECOVERY OF ACETYLCHOLINESTERASE IN CULTURED CHICK-EMBRYO MUSCLE TREATED WITH PARAOXON [J].
CISSON, CM ;
WILSON, BW .
BIOCHEMICAL PHARMACOLOGY, 1977, 26 (21) :1955-1960