• 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

氯喹在大鼠微粒体膜中与转运ATP酶和乙酰胆碱酯酶在体内外的相互作用。

The interaction of chloroquine with transport ATPase and acetylcholine esterase in microsomal membranes of rat in vitro and in vivo.

作者信息

Mazumder B, Mukherjee S, NagDas S K, Sen P C

机构信息

Department of Chemistry, Bose Institute, Calcutta, India.

出版信息

Biochem Int. 1988 Jan;16(1):35-44.

PMID:2833266
Abstract

Chloroquine, an antimalarial drug has been found to inhibit Na+, K+-ATPase activity in vitro in the microsomal membranes of rat brain on time, temperature and concentration dependent manner. There have been stimulation of Na+,K+-ATPase, Ca+2-ATPase and acetylcholine esterase activities in vivo studies at lower concentration of drug or shorter period of treatment with the drug, whereas higher concentrations or longer periods of treatment lead to inhibition in the microsomal membranes of different organs.

摘要

氯喹,一种抗疟药物,已被发现在体外能以时间、温度和浓度依赖的方式抑制大鼠脑微粒体膜中的钠钾ATP酶活性。在体内研究中,较低浓度的药物或较短的治疗时间会刺激钠钾ATP酶、钙ATP酶和乙酰胆碱酯酶的活性,而较高浓度或较长时间的治疗则会导致不同器官微粒体膜中的酶活性受到抑制。

相似文献

1
The interaction of chloroquine with transport ATPase and acetylcholine esterase in microsomal membranes of rat in vitro and in vivo.氯喹在大鼠微粒体膜中与转运ATP酶和乙酰胆碱酯酶在体内外的相互作用。
Biochem Int. 1988 Jan;16(1):35-44.
2
The in vivo inhibition of transport enzyme activities by chloroquine in different organs of rat is reversible.氯喹对大鼠不同器官转运酶活性的体内抑制作用是可逆的。
Mol Cell Biochem. 1992 Dec 2;118(1):15-21. doi: 10.1007/BF00249690.
3
The chlorpromazine inhibition of transport ATPase and acetylcholinesterase activities in the microsomal membranes of rat in vitro and in vivo.
Mol Cell Biochem. 1990 Jun 1;95(1):13-20. doi: 10.1007/BF00219525.
4
The in vivo inhibition of transport enzyme activities in different organs of rat by chlorpromazine is reversible.氯丙嗪对大鼠不同器官转运酶活性的体内抑制作用是可逆的。
Biochem Int. 1991 Dec;25(5):951-61.
5
[Na, K-ATPase activity of the microsomal fraction of the rat brain exposed to insulin].[暴露于胰岛素的大鼠脑微粒体部分的钠钾ATP酶活性]
Biull Eksp Biol Med. 1985 Jan;99(1):31-3.
6
[Effect of mineralocorticoids on the Na, K-ATPase activity of the rat brain].[盐皮质激素对大鼠脑钠钾ATP酶活性的影响]
Biull Eksp Biol Med. 1986 Oct;102(10):434-6.
7
[Endogenous activators and inhibitors of Na, K-ATPase induced by acetylcholine].[乙酰胆碱诱导的钠钾ATP酶的内源性激活剂和抑制剂]
Biull Eksp Biol Med. 1983 Feb;95(2):40-2.
8
[Effect of gangliosides on Na-K-ATPase activity and the conformation of microsomal membranes].[神经节苷脂对钠钾-ATP酶活性及微粒体膜构象的影响]
Biull Eksp Biol Med. 1978 Dec;86(12):682-4.
9
The neuroprotective role of L-cysteine towards the effects of short-term exposure to lanthanum on the adult rat brain antioxidant status and the activities of acetylcholinesterase, (Na+,K+)- and Mg2+-ATPase.L-半胱氨酸对成年大鼠大脑抗氧化状态以及乙酰胆碱酯酶、(钠,钾)-ATP酶和镁离子-ATP酶活性的短期镧暴露影响的神经保护作用。
Biometals. 2009 Apr;22(2):329-35. doi: 10.1007/s10534-008-9169-0. Epub 2008 Oct 21.
10
Tissue Na+K+ activated adenosine triphosphatase in retinol deficient albino rats.维生素A缺乏的白化大鼠体内的组织钠钾激活三磷酸腺苷酶
Int J Vitam Nutr Res. 1992;62(4):285-90.

引用本文的文献

1
Cardiac effects and toxicity of chloroquine: a short update.氯喹的心脏效应和毒性:简短更新。
Int J Antimicrob Agents. 2020 Aug;56(2):106057. doi: 10.1016/j.ijantimicag.2020.106057. Epub 2020 Jun 19.
2
The effect of binding of chlorpromazine and chloroquine to ion transporting ATPases.氯丙嗪和氯喹与离子转运ATP酶结合的作用。
Mol Cell Biochem. 1999 Aug;198(1-2):179-85. doi: 10.1023/a:1006902031255.
3
The chlorpromazine inhibition of transport ATPase and acetylcholinesterase activities in the microsomal membranes of rat in vitro and in vivo.
Mol Cell Biochem. 1990 Jun 1;95(1):13-20. doi: 10.1007/BF00219525.
4
The in vivo inhibition of transport enzyme activities by chloroquine in different organs of rat is reversible.氯喹对大鼠不同器官转运酶活性的体内抑制作用是可逆的。
Mol Cell Biochem. 1992 Dec 2;118(1):15-21. doi: 10.1007/BF00249690.