{"title":"l - n6 -苯异丙腺苷(L-PIA)对大鼠离体半膈肌的影响。","authors":"V M Varagić, 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":"{\"title\":\"The effect of L-N6-phenylisopropyladenosine (L-PIA) on the isolated hemidiaphragm of the rat.\",\"authors\":\"V M Varagić, 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}","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}
The effect of L-N6-phenylisopropyladenosine (L-PIA) on the isolated hemidiaphragm of the rat.
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.