• 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

[Influence of homologous n-alcanoic acids on the function properties of isolated skeletal muscles. III. Contractures by fatty acids and relations to the effects of caffeine].

作者信息

Kössler F, Küchler G

出版信息

Acta Biol Med Ger. 1977;36(7-8):1085-95.

PMID:306181
Abstract

The influences of octanoic, decanoic, and hexadencanoic acid were tested on the contracture capability of isolated skeletal muscle of frogs and rats. 1. 100 mM octanoic or 10mM decanoic acid induce contractures in skeletal mucles after 20-30 min of exposure. 2. The time of exposure necessary for induction of contractures is shortened by an increase of bath temperature, electrical stimulation or KCl-depolarization of muscles. 3. Simultaneous addition of fatty acid and caffeine (10 mM) effects a depression and a delay of the caffeine contracture. The contractures evoked by 5 mM caffeine are inhibited by lower concentrations of fatty acids (1 mM octaonoic acid, 0,1 mM hexadecanoic acid). 4. After the complete development of a caffeine (or fatty acid) contracture the muscle is not able to develop an identical contracture by a second application of the same drug, even after intermediate treatment during one or two hours in Ringer solution. If the contracture is interrupted one minute after the caffeine application by changing the solution, the tension returns quickly to the resting level. A subsequent addition of caffeine (10 mM) after about 10 minutes effects an identical contracture. Thus the effect of fatty acids on caffeine contracture may be studied on the same muscle which served as its own control. 5. As mechanisms involved in the development of fatty acid contractures and in the inhibition of caffeine contractures, interactions of free fatty acids and lipids of biological membranes are disucssed. Especially, there may be changes of the calcium affinity of cellular membranes.

摘要

相似文献

1
[Influence of homologous n-alcanoic acids on the function properties of isolated skeletal muscles. III. Contractures by fatty acids and relations to the effects of caffeine].
Acta Biol Med Ger. 1977;36(7-8):1085-95.
2
[Effect of homologous n-alkanoic acids on the function of isolated skeletal muscles. V. Relations between twitch, tetanus and contracture].[同系正链烷酸对离体骨骼肌功能的影响。V. 单收缩、强直收缩与挛缩之间的关系]
Acta Biol Med Ger. 1980;39(5):615-22.
3
[Influence of homologous n-alkanoic acids on functional properties of isolated skeletal muscles. I. Muscle contraction].[同源正构烷酸对离体骨骼肌功能特性的影响。I. 肌肉收缩]
Acta Biol Med Ger. 1976;35(10):1327-34.
4
[The action of homologous n-alkanols on functional properties of isolated skeletal muscles. 3. Alcohol and caffeine contractures].[同系正构烷醇对离体骨骼肌功能特性的作用。3. 酒精和咖啡因挛缩]
Acta Biol Med Ger. 1974;32(6):651-8.
5
Modulation of caffeine contractures in mammalian skeletal muscles by variation of extracellular potassium.通过改变细胞外钾离子浓度对哺乳动物骨骼肌中咖啡因挛缩的调节作用。
J Cell Physiol. 1995 Nov;165(2):254-60. doi: 10.1002/jcp.1041650206.
6
Contractile properties of isolated frog skeletal muscles under the influence of Na-octanoate.辛酸钠作用下离体青蛙骨骼肌的收缩特性
Acta Biol Med Ger. 1982;41(2-3):205-13.
7
Inhibitory effects of salicylate on contractility in skeletal muscle.水杨酸盐对骨骼肌收缩性的抑制作用。
J Pharmacol Exp Ther. 1984 Aug;230(2):478-82.
8
Mechanism of action of cobra cardiotoxin in the skeletal muscle.眼镜蛇心脏毒素在骨骼肌中的作用机制。
J Pharmacol Exp Ther. 1976 Mar;196(3):758-70.
9
Porcine malignant hyperthermia: effects of temperature and extracellular calcium concentration on halothane-induced contracture of susceptible skeletal muscle.猪恶性高热:温度和细胞外钙浓度对氟烷诱导的易感骨骼肌挛缩的影响。
Anesthesiology. 1975 Mar;42(3):301-6.
10
Studies on contractures induced in mouse diaphragm by caffeine and cupric and selenite ions.
Arch Int Pharmacodyn Ther. 1989 Jul-Aug;300:265-80.