• 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

通过给予去铁胺逆转铝诱导的行为缺陷。

Reversal of an aluminum-induced behavioral deficit by administration of deferoxamine.

作者信息

Connor D J, Harrell L E, Jope R S

机构信息

University of Alabama, Birmingham.

出版信息

Behav Neurosci. 1989 Aug;103(4):779-83. doi: 10.1037//0735-7044.103.4.779.

DOI:10.1037//0735-7044.103.4.779
PMID:2765182
Abstract

Administration of aluminum sulfate in the drinking water of male Sprague-Dawley rats for 30 days resulted in a reduction in the number of days to reach extinction criterion on a passive avoidance task (38% control level). The behavioral deficit was not due to nonspecific effects caused by lower fluid consumption. Partial reversal of the deficit was produced by discontinuing aluminum treatment 2 weeks prior to testing (p less than .05). Injection of the aluminum chelator deferoxamine returned the performance of the aluminum-treated animals to control levels in a dose-dependent manner but had no effect on control animals. No differences in open-field activity were evident across groups. These results indicate that the behavioral impairment is a specific, reversible, toxic effect of the aluminum administration.

摘要

给雄性斯普拉格-道利大鼠的饮用水中添加硫酸铝30天,结果显示在被动回避任务中达到消退标准所需的天数减少(为对照组水平的38%)。行为缺陷并非因液体摄入量减少导致的非特异性影响所致。在测试前2周停止铝处理可使缺陷部分逆转(p小于0.05)。注射铝螯合剂去铁胺可使经铝处理的动物的表现以剂量依赖的方式恢复到对照组水平,但对对照动物没有影响。各组之间在旷场活动方面没有明显差异。这些结果表明,行为损伤是铝给药的一种特异性、可逆的毒性作用。

相似文献

1
Reversal of an aluminum-induced behavioral deficit by administration of deferoxamine.通过给予去铁胺逆转铝诱导的行为缺陷。
Behav Neurosci. 1989 Aug;103(4):779-83. doi: 10.1037//0735-7044.103.4.779.
2
Concurrent exposure to aluminum and stress during pregnancy in rats: Effects on postnatal development and behavior of the offspring.大鼠孕期同时暴露于铝和应激:对后代出生后发育及行为的影响。
Neurotoxicol Teratol. 2005 Jul-Aug;27(4):565-74. doi: 10.1016/j.ntt.2005.06.014.
3
Neurotoxicity induced by prenatal aluminum exposure in rats.
Neurotoxicology. 1996 Summer;17(2):459-69.
4
Rivastigmine reverses aluminum-induced behavioral changes in rats.雷瓦司他汀可逆转铝诱导的大鼠行为改变。
Eur J Pharmacol. 2011 Jun 1;659(2-3):169-76. doi: 10.1016/j.ejphar.2011.03.011. Epub 2011 Mar 31.
5
Chronic, oral aluminum administration to rats: cognition and cholinergic parameters.
Pharmacol Biochem Behav. 1988 Oct;31(2):467-74. doi: 10.1016/0091-3057(88)90375-9.
6
Influence of age on aluminum-induced neurobehavioral effects and morphological changes in rat brain.
Neurotoxicology. 2002 Dec;23(6):775-81. doi: 10.1016/S0161-813X(02)00008-6.
7
Effects of amphetamine and haloperidol on avoidance behavior and exploratory activity.
Eur J Pharmacol. 1978 Dec 15;53(1):103-7. doi: 10.1016/0014-2999(78)90272-8.
8
[Effects of aluminum on amino acid neurotransmitters in hippocampus of rats].[铝对大鼠海马中氨基酸神经递质的影响]
Zhonghua Yu Fang Yi Xue Za Zhi. 2001 Nov;35(6):397-400.
9
Effects of perinatal methylphenidate (MPH) treatment on postweaning behaviors of male and female Sprague-Dawley rats.围产期哌甲酯(MPH)治疗对雄性和雌性斯普拉格-道利大鼠断奶后行为的影响。
Neurotoxicol Teratol. 2015 Jan-Feb;47:125-36. doi: 10.1016/j.ntt.2014.12.002. Epub 2014 Dec 13.
10
Cysteamine and pantethine effects on passive avoidance behavior, shuttle box learning, open-field activity, striatal catecholamines and somatostatin.半胱胺和泛硫乙胺对被动回避行为、穿梭箱学习、旷场活动、纹状体儿茶酚胺和生长抑素的影响。
Arch Int Pharmacodyn Ther. 1989 May-Jun;299:14-27.

引用本文的文献

1
Understanding Aspects of Aluminum Exposure in Alzheimer's Disease Development.了解阿尔茨海默病发展过程中铝暴露的相关方面。
Brain Pathol. 2016 Mar;26(2):139-54. doi: 10.1111/bpa.12333. Epub 2015 Dec 8.
2
Quercetin protects against chronic aluminum-induced oxidative stress and ensuing biochemical, cholinergic, and neurobehavioral impairments in rats.槲皮素可预防大鼠慢性铝诱导的氧化应激及随后的生化、胆碱能和神经行为损伤。
Neurotox Res. 2013 May;23(4):336-57. doi: 10.1007/s12640-012-9351-6. Epub 2012 Aug 24.
3
Evidence for centrophenoxine as a protective drug in aluminium induced behavioral and biochemical alteration in rat brain.
关于脑复新作为一种保护药物,对铝诱导的大鼠脑行为和生化改变的作用的证据。
Mol Cell Biochem. 2006 Oct;290(1-2):33-42. doi: 10.1007/s11010-006-9125-7. Epub 2006 Sep 13.