The effect of L-N6-phenylisopropyladenosine (L-PIA) on the isolated hemidiaphragm of the rat.

Journal de pharmacologie Pub Date : 1986-10-01
V M Varagić, M Prostran
{"title":"The effect of L-N6-phenylisopropyladenosine (L-PIA) on the isolated hemidiaphragm of the rat.","authors":"V M Varagić,&nbsp;M Prostran","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The effect of L-N6-phenylisopropyladenosine (L-PIA) on the maximum tension developed (Td) and the maximum rate of rise of tension (dT/dt max) of the isolated hemidiaphragm of the rat was investigated during direct electrical stimulation. L-PIA itself (0.07-5.5 mumol l-1) did not produce significant changes in either Td, or dT/dt max. In the presence of a standard concentration of dipyridamole (26.4 mumol l-1), L-PIA produced a significant and concentration-dependent increase in both Td and dT/dt max. In the presence of a standard concentration of aminophylline (640 mumol l-1), L-PIA produced a small and insignificant, but concentration-dependent decrease of both Td and dT/dt max. In the presence of both dipyridamole (26.4 mumol l-1) and of aminophylline (640 mumol l-1), L-PIA (0.07-5.5 mumol l-1) produced a small and insignificant potentiation of the isometric contraction of the isolated hemidiaphragm. It is concluded that antagonistic action between L-PIA and aminophylline probably takes place at A1-receptors. The inhibitory action of L-PIA, observed after blockade of adenosine receptors by aminophylline, is presumably realized through some other mechanism(s) independent of adenosine receptor sites.</p>","PeriodicalId":14817,"journal":{"name":"Journal de pharmacologie","volume":"17 4","pages":"707-11"},"PeriodicalIF":0.0000,"publicationDate":"1986-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal de pharmacologie","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The effect of L-N6-phenylisopropyladenosine (L-PIA) on the maximum tension developed (Td) and the maximum rate of rise of tension (dT/dt max) of the isolated hemidiaphragm of the rat was investigated during direct electrical stimulation. L-PIA itself (0.07-5.5 mumol l-1) did not produce significant changes in either Td, or dT/dt max. In the presence of a standard concentration of dipyridamole (26.4 mumol l-1), L-PIA produced a significant and concentration-dependent increase in both Td and dT/dt max. In the presence of a standard concentration of aminophylline (640 mumol l-1), L-PIA produced a small and insignificant, but concentration-dependent decrease of both Td and dT/dt max. In the presence of both dipyridamole (26.4 mumol l-1) and of aminophylline (640 mumol l-1), L-PIA (0.07-5.5 mumol l-1) produced a small and insignificant potentiation of the isometric contraction of the isolated hemidiaphragm. It is concluded that antagonistic action between L-PIA and aminophylline probably takes place at A1-receptors. The inhibitory action of L-PIA, observed after blockade of adenosine receptors by aminophylline, is presumably realized through some other mechanism(s) independent of adenosine receptor sites.

l - n6 -苯异丙腺苷(L-PIA)对大鼠离体半膈肌的影响。
研究了l - n6 -苯异丙基腺苷(L-PIA)对直接电刺激大鼠离体半膈最大张力(Td)和最大张力上升速率(dT/ dT max)的影响。L-PIA本身(0.07-5.5 μ mol l-1)对Td和dT/ dT max均无显著影响。在标准浓度的双嘧达莫(26.4 μ mol l-1)存在下,L-PIA产生了Td和dT/ dT max的显著且浓度依赖性的增加。在标准浓度的氨茶碱(640 μ mol l-1)存在下,L-PIA对Td和dT/ dT max的影响较小且不显著,但具有浓度依赖性。在双嘧达莫(26.4 μ mol l-1)和氨茶碱(640 μ mol l-1)存在的情况下,L-PIA (0.07-5.5 μ mol l-1)对离体半膈肌的等距收缩产生微弱且不显著的增强作用。因此,L-PIA与氨茶碱的拮抗作用可能发生在a1受体上。在氨茶碱阻断腺苷受体后观察到的L-PIA的抑制作用,可能是通过一些独立于腺苷受体位点的其他机制实现的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信