• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

联合方法研究沙林中毒及其治疗后大鼠大脑中乙酰胆碱酯酶活性的变化。

Combined approach to demonstrate acetylcholinesterase activity changes in the rat brain following tabun intoxication and its treatment.

机构信息

Department of Toxicology, Faculty of Military Health Sciences, University of Defence, Hradec Kralove, Czech Republic.

出版信息

Toxicol Mech Methods. 2012 Jan;22(1):60-6. doi: 10.3109/15376516.2011.596231. Epub 2011 Aug 19.

DOI:10.3109/15376516.2011.596231
PMID:21851296
Abstract

Reactivation effects of K203 and currently available oximes (obidoxime, HI-6) in combination with atropine on acetylcholinesterase activities in the brain parts of rats poisoned with tabun were studied. The activity was determined by quantitative histochemical and biochemical methods correlating between them very well. The tabun-induced changes in acetylcholinsterase activity as well as in reactivation potency of reactivators used were different in various parts of the brain. Pontomedullar area seems to be important for observed changes following tabun intoxication and its treatment. From the oximes studied, the reactivation effect of K203 was comparable with obidoxime; HI-6 was ineffective. Combination of bio- and histochemical methods allow fine differentiation among the action of different oximes following tabun poisoning.

摘要

研究了 K203 与目前可用的肟类化合物(obidoxime、HI-6)与阿托品联合对塔崩中毒大鼠脑部分乙酰胆碱酯酶活性的复活作用。通过定量组织化学和生化方法进行了活性测定,两种方法之间相关性很好。塔崩引起的乙酰胆碱酯酶活性变化以及所使用的复活剂的复活能力在大脑的不同部位是不同的。桥脑髓质区域似乎对观察到的塔崩中毒及其治疗后的变化很重要。在所研究的肟类化合物中,K203 的复活作用与 obidoxime相当;HI-6 无效。生物化学和组织化学方法的结合可以精细地区分不同肟类化合物在塔崩中毒后的作用。

相似文献

1
Combined approach to demonstrate acetylcholinesterase activity changes in the rat brain following tabun intoxication and its treatment.联合方法研究沙林中毒及其治疗后大鼠大脑中乙酰胆碱酯酶活性的变化。
Toxicol Mech Methods. 2012 Jan;22(1):60-6. doi: 10.3109/15376516.2011.596231. Epub 2011 Aug 19.
2
A comparison of tabun-inhibited rat brain acetylcholinesterase reactivation by three oximes (HI-6, obidoxime, and K048) in vivo detected by biochemical and histochemical techniques.三种肟类化合物(HI-6、双解磷和 K048)对塔崩抑制的大鼠脑乙酰胆碱酯酶的体内重活化作用的比较:生化和组织化学技术检测。
J Enzyme Inhib Med Chem. 2010 Dec;25(6):790-7. doi: 10.3109/14756360903433373.
3
An evaluation of therapeutic and reactivating effects of newly developed oximes (K156, K203) and commonly used oximes (obidoxime, trimedoxime, HI-6) in tabun-poisoned rats and mice.对新开发的肟类化合物(K156、K203)和常用肟类化合物(双复磷、氧磷定、HI-6)对塔崩中毒大鼠和小鼠的治疗及复活作用的评估。
Toxicology. 2008 Jan 20;243(3):311-6. doi: 10.1016/j.tox.2007.10.015. Epub 2007 Oct 26.
4
A comparison of neuroprotective efficacy of the oxime K203 and its fluorinated analogue (KR-22836) with obidoxime in Tabun-poisoned rats.在沙林中毒大鼠中肟 K203 及其氟代类似物(KR-22836)与 obidoxime 的神经保护疗效比较。
Basic Clin Pharmacol Toxicol. 2010 Nov;107(5):861-7. doi: 10.1111/j.1742-7843.2010.00588.x.
5
An evaluation of reactivating and therapeutic efficacy of newly developed oximes (K206, K269) and commonly used oximes (obidoxime, HI-6) in cyclosarin-poisoned rats and mice.新开发的肟类化合物(K206、K269)和常用肟类化合物(双复磷、HI-6)对环沙林中毒大鼠和小鼠的复活及治疗效果评估。
Clin Toxicol (Phila). 2009 Jan;47(1):72-6. doi: 10.1080/15563650802043652.
6
Tabun-inhibited rat tissue and blood cholinesterases and their reactivation with the combination of trimedoxime and HI-6 in vivo.体内三羟肟酸和双羟肟酸联合对敌敌畏抑制的大鼠组织和血液胆碱酯酶的复能作用。
Chem Biol Interact. 2010 Sep 6;187(1-3):287-90. doi: 10.1016/j.cbi.2010.02.009. Epub 2010 Feb 16.
7
A comparison of the potency of newly developed oximes (K074, K075) and commonly used oximes (obidoxime, HI-6) to counteract tabun-induced neurotoxicity in rats.新开发的肟类化合物(K074、K075)与常用肟类化合物(双复磷、HI-6)对大鼠体内塔崩诱导的神经毒性的解毒效力比较。
Toxicology. 2007 Jan 5;229(1-2):136-44. doi: 10.1016/j.tox.2006.10.009. Epub 2006 Oct 20.
8
A comparison of the potency of newly developed oximes (K027, K048) and commonly used oximes (obidoxime, HI-6) to counteract tabun-induced neurotoxicity in rats.新开发的肟类化合物(K027、K048)与常用肟类化合物(双复磷、HI-6)对抗大鼠中塔崩诱导的神经毒性效力的比较。
J Appl Toxicol. 2006 Jul-Aug;26(4):309-16. doi: 10.1002/jat.1137.
9
In vitro and in vivo evaluation of pyridinium oximes: mode of interaction with acetylcholinesterase, effect on tabun- and soman-poisoned mice and their cytotoxicity.吡啶肟类化合物的体外和体内评价:与乙酰胆碱酯酶的相互作用模式、对塔崩和梭曼中毒小鼠的影响及其细胞毒性。
Toxicology. 2006 Feb 15;219(1-3):85-96. doi: 10.1016/j.tox.2005.11.003. Epub 2005 Dec 5.
10
A comparison of reactivating and therapeutic efficacy of the oxime K203 and its fluorinated analog (KR-22836) with currently available oximes (obidoxime, trimedoxime, HI-6) against tabun in rats and mice.对沙林在大鼠和小鼠体内肟类化合物 K203 及其氟化类似物(KR-22836)与目前市售肟类化合物(obidoxime、trimedoxime、HI-6)的复活和治疗效果进行比较。
J Enzyme Inhib Med Chem. 2010 Aug;25(4):480-4. doi: 10.3109/14756360903257918.