TOXIC EFFECT OF CHLORINATED AND PYRETHROID PESTICIDES
TOXIC EFFECT OF CHLORINATED AND PYRETHROID PESTICIDES
批准号:
3249645
负责人:
FUMIO MATSUMURA
金额:
$12.22万
依托单位国家:
美国
项目类别:
财政年份:
1977
资助国家:
美国
项目状态:
已结题
起止时间:
1977-12-20 至 1987-01-31
关键词:
adenosinetriphosphatase cardiotoxin cell cell interaction chlordane chlorohydrocarbon insecticide cytochrome P450 detoxification dichlorodiphenyltrichloroethane environmental toxicology gel electrophoresis halobiphenyl /halotriphenyl compound hepatotoxin insecticide biological effect liver cells liver function mirex /kepone neurotoxins neurotransmitters pesticide interaction pyrethroid radiotracer saltwater environment scintillation spectrometry
中文摘要
在本研究项目中,我们建议研究氯化物的毒性效应,
和拟除虫菊酯类农药主要是钙调节过程
神经系统,肝脏和心脏 主要实验动物
使用的是大鼠,但小鼠,豚鼠,仓鼠和一些
还将使用无脊椎动物物种。 主要研究的化合物有
滴滴涕、毒杀芬、氯氰菊酯、狄氏剂、艾氏剂、萘甲草胺、环氧化萘甲草胺、
丙烯菊酯、氯菊酯、氰戊菊酯、氯氰菊酯和溴氰菊酯。 在
肝脏的情况下,主要重点将放在长期
这些化学物质对肝细胞钙转运功能的影响。
同时也研究了它们对间隙结的影响
已知其受钙浓度控制,
功能协调发展的 这些农药对细胞间的影响程度
识别和通信将被确定。 的情况
神经系统,我们计划研究它们对各种钙的影响,
调节系统,如钠钙交换,特别是部分
与ATP利用率有关,对Ca-Mg ATP酶的影响。 在后一种情况下
与钙调素相互作用的变化以及
将检查释放和神经分泌。 至于环二性型
氯化农药,我们计划研究它们对GABA-氯化物的影响,
渠道系统。 将特别强调对下列问题的研究:
苦毒素受体 该项目还将涵盖以下领域:
农药对心脏生化的影响,特别是与其
影响钙调节。
英文摘要
In this research project we propose to study toxic effects of chlorinated
and pyrethroid pesticides mainly on calcium regulating processes in the
nervous system, the liver and the heart. The main experimental animals to
be used is the rat, but the mouse, the guinea pig, the hamster and some
inverterbrate species will also be used. The compounds mainly studied are
DDT, toxaphene, chlordane, dieldrin aldrin, neptachlor, neptachlor epoxide,
allethrin, permethrin, fenvalerate cypermetnrin and decamethrin. In the
case of the liver, the major emphasis will be placed on the long term
effects of these chemicals on calcium transport functions of hepatocytes.
Also an effort will be made to study their effects on the gap-junction
which is known to be controlled by calcium concentration for its
functions. The extents of the influence of these pesticides on cell-cell
recognition and communication will be determined. In the case of the
nervous system, we plan to study their influence on various calcium
regulating systems such as Na-Ca exchange, particularly the portion
relating to ATP utilization, and on Ca-Mg ATPase. In the latter case
changes in its interaction with calmodulin as well as in transmitter
release, and neurosecretion will be examined. As for cyclodience-type
chlorinated presticides we plan to examine their effects on GABA-chloride
channel systems. A particular emphasis will be placed on the studies on
the picrotoxinin receptor. This project will also cover the area of
pesticide effects on cardiac biochemistry especially as related to their
influence on calcium regulation.
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