Hazardous effect of organophosphate compound, dichlorvos in transgenic Drosophila melanogaster (hsp70-lacZ):: Induction of hsp70, anti-oxidant enzymes and inhibition of acetylcholinesterase

被引:51
作者
Gupta, SC [1 ]
Siddique, HR [1 ]
Saxena, DK [1 ]
Chowdhuri, DK [1 ]
机构
[1] Ind Toxicol Res Ctr, Embryotoxicol Sect, Lucknow 226001, Uttar Pradesh, India
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2005年 / 1725卷 / 01期
关键词
dichlorvos; hsp70; SOD; CAT; LPO; AchE; transgenic Drosophila;
D O I
10.1016/j.bbagen.2005.04.033
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
We tested a working hypothesis that stress genes and anti-oxidant enzyme machinery are induced by the organophosphate compound dichlorvos in a non-target organism. Third instar larvae of Drosophila melanogaster transgenic for hsp70 were exposed to 0. 1 to 100.0 ppb dichlorvos and 5.0 MM CUSO4 (an inducer of oxidative stress and stress genes) and hsp70, and activities of acetylcholinesterase (AchE), superoxide dismutase (SOD), catalase (CAT) and lipid peroxidation (LPO) product were measured. The study was further extended to examine tissue damage, if any, under such conditions. A concentration- and time-dependent increase in hsp70 and antioxidant enzymes was observed in the exposed organism as compared to control. A comparison of stress gene expression with SOD, CAT activities and LPO product under similar experimental conditions revealed that induction of hsp70 precedes the anti-oxidant enzyme activities in the exposed organism. Further, concomitant with a significant inhibition of AChE activity, significant induction of hsp70 was observed following chemical exposure. Mild tissue damage was observed in the larvae exposed to 10.0 ppb dichlorvos for 48 It when hsp70 expression reaches plateau. Dichlorvos at 0.1 ppb dietary concentration did not evoke significant hsp70 expression, anti-oxidant enzymes and LPO and AchE inhibition in the exposed organism, and thereby, was found to be non-hazardous to D. melanogaster. Conversely, 1.0 ppb of the test chemical stimulated a significant induction of hsp70 and anti-oxidant enzymes and significant inhibition of AchE; hence this concentration of test chemical was hazardous to the organism. The present study suggests that (a) both stress genes and anti-oxidant enzymes are stimulated as indices of cellular defense against xenobiotic hazard in D. melanogaster with hsp70 being proposed as first-tier bio-indicator of cellular hazard, (b) 0.1 ppb of the test chemical may be regarded as No Observed Adverse Effect Level (NOAEL), and 1.0 ppb dichlorvos as Low Observed Adverse Effect Level (LOAEL). (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:81 / 92
页数:12
相关论文
共 71 条
[61]  
2
[62]  
*US DEP HHS, 1997, TOX PROF DICHL AG TO
[63]   HSP70 - NUCLEAR CONCENTRATION DURING ENVIRONMENTAL-STRESS AND CYTOPLASMIC STORAGE DURING RECOVERY [J].
VELAZQUEZ, JM ;
LINDQUIST, S .
CELL, 1984, 36 (03) :655-662
[64]   Ethylazinphos interaction with membrane lipid organization induces increase of proton permeability and impairment of mitochondrial bioenergetic functions [J].
Videira, RA ;
Antunes-Madeira, MC ;
Madeira, VMC .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2001, 175 (03) :209-216
[65]   The effect of the insecticide dichlorvos on esterase activity extracted from the psocids, Liposcelis bostrychophila and L-entomophila -: art. no. 23 [J].
Wang, JJ ;
Cheng, WX ;
Ding, W ;
Zhao, ZM .
JOURNAL OF INSECT SCIENCE, 2004, 4
[66]  
*WHO, 1979, IARC MON EV CARC RIS, V20
[67]  
YAMANO T, 1992, TOXICOLOGY, V76, P69, DOI 10.1016/0300-483X(92)90019-B
[68]   Dissociation of DDVP-induced DNA strand breaks from oxidative damage in isolated rat hepatocytes [J].
Yamano, T .
TOXICOLOGY, 1996, 108 (1-2) :49-56
[69]   Biochemical changes in primary culture of skeletal muscle cells following dimethoate exposure [J].
Yang, DR ;
Lu, XF ;
Zhang, WG ;
He, FS .
TOXICOLOGY, 2002, 174 (02) :79-85
[70]   Co-expression of human chaperone Hsp70 and Hsdj or Hsp40 co-factor increases solubility of overexpressed target proteins in insect cells [J].
Yokoyama, N ;
Hirata, M ;
Ohtsuka, K ;
Nishiyama, Y ;
Fujii, K ;
Fujita, M ;
Kuzushima, K ;
Kiyono, T ;
Tsurumi, T .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2000, 1493 (1-2) :119-124