Suppr超能文献

D - 600及其光学异构体对猫乳头肌和豚鼠心房收缩力的影响。

Effects of D-600 and its optical isomers on force of contraction in cat papillary muscles and guinea-pig auricles.

作者信息

Ludwig C, Nawrath H

出版信息

Br J Pharmacol. 1977 Mar;59(3):411-7. doi: 10.1111/j.1476-5381.1977.tb08394.x.

Abstract

1 (--)-D-600 and (+)-D-600 exerted concentration-dependent negative inotropic effects in papillary muscles from cats, the potency of (--)-D-600 being about 100 times greater than that of (+)-D-600. The action was more pronounced at high than at low frequencies of stimulation. Time to peak force, relaxation time and therefore also total duration of contraction were not significantly affected by the drugs. 2 The negative inotropic effects of both drugs were not reversible after washing in drug-free solution for 60 min at all concentrations tested. 3 The same negative inotropic effects were seen in guinea-pig left auricles with the racemic mixture of both isomers. 4 Uptake measurements of D-600-[nitrile-14C] in isolated left auricles of guinea-pigs showed the drug to be accumulated in the myocardial tissue; tissue-medium ratios from 1.25 to 6.0 were found at exposure times from 1 to 100 minutes. Preparations which were loaded first with D-600-[nitrile-14C] for 100 min and then washed in drug-free solution for different times lost up to about 80% of the initial radioactivity, whereas the depression of force of contraction was not reversible. 5 The results show that there are marked quantitative differences between the actions of (--)-D-600 and (+)-D-600 on isometric force of contraction in cat papillary muscles. Although the time course of the uptake of D-600-[nitrile-14C] and the development of the negative inotropy in guinea-pit left auricles were reasonably well related, the magnitude of the negative inotropy does not seem to be dependent on the total tissue concentration once the negative inotropic effect has been fully developed.

摘要
  1. (-)-D-600和(+)-D-600对猫乳头肌产生浓度依赖性负性肌力作用,(-)-D-600的效力比(+)-D-600约大100倍。在高刺激频率下该作用比低刺激频率时更明显。药物对达峰力时间、舒张时间以及因此收缩的总持续时间均无显著影响。2. 在所有测试浓度下,在无药溶液中冲洗60分钟后,两种药物的负性肌力作用均不可逆。3. 在豚鼠左心房中,两种异构体的外消旋混合物也呈现相同的负性肌力作用。4. 对豚鼠离体左心房中D-600-[腈-14C]的摄取测量显示该药物在心肌组织中蓄积;在暴露1至100分钟时,组织-介质比为1.25至6.0。首先用D-600-[腈-14C]加载100分钟,然后在无药溶液中冲洗不同时间的制剂,损失了高达约80%的初始放射性,而收缩力的降低是不可逆的。5. 结果表明,(-)-D-600和(+)-D-600对猫乳头肌等长收缩力的作用存在显著的量的差异。尽管豚鼠左心房中D-600-[腈-14C]的摄取时间进程与负性肌力作用的发展有较好的相关性,但一旦负性肌力作用充分发展,负性肌力的大小似乎并不依赖于总组织浓度。

相似文献

10
Effect of verapamil and D 600 on cardiac transmembrane potentials.
Acta Physiol Acad Sci Hung. 1978;51(1-2):51-9.

引用本文的文献

1
Structural model for phenylalkylamine binding to L-type calcium channels.苯烷基胺与L型钙通道结合的结构模型。
J Biol Chem. 2009 Oct 9;284(41):28332-28342. doi: 10.1074/jbc.M109.027326. Epub 2009 Aug 21.
6
On the mechanism of slow calcium channel block in heart.
Pflugers Arch. 1980 May;385(2):175-9. doi: 10.1007/BF00588699.

本文引用的文献

4
A dissociation of positive staircase (Bowditch) from ouabain-induced positive inotropism.
Circ Res. 1974 Sep;35(3):439-47. doi: 10.1161/01.res.35.3.439.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验