{"title":"2- br - α -麦角隐亭对氨基甲酸乙酯麻醉大鼠的心血管作用。","authors":"G Pesce, F J Stefano","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Experiments were designed to study the cardiovascular effects of Bromocriptine (2-Br-alpha-ergocriptine) in the normotensive anesthetized rats. The intravenous administration of bromocriptine (20 micrograms/kg and 200 micrograms/kg) produced a long-lasting and not dose-dependent fall in the mean blood pressure and heart rate. The pressor response to phenylephrine, an alpha adrenergic agonist, was antagonized by bromocriptine in a dose-dependent manner. At a dose of 20 micrograms/kg bromocriptine behaved as a competitive antagonist, whereas at the dose of 200 micrograms/kg produced an insurmountable blockade of the response to phenylephrine. Previous administration of phentolamine (5 mg/kg) prevented the insurmountable blockade of alpha adrenoceptors by bromocriptine. This observation suggests that both drugs compete for the same receptor. It is concluded that blockade of peripheral alpha-adrenoceptors may contribute to cardiovascular effects of bromocriptine.</p>","PeriodicalId":7131,"journal":{"name":"Acta physiologica latino americana","volume":"32 2","pages":"117-22"},"PeriodicalIF":0.0000,"publicationDate":"1982-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cardiovascular effects of 2-Br-alpha-ergocriptine in urethane anesthetized rats.\",\"authors\":\"G Pesce, F J Stefano\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Experiments were designed to study the cardiovascular effects of Bromocriptine (2-Br-alpha-ergocriptine) in the normotensive anesthetized rats. The intravenous administration of bromocriptine (20 micrograms/kg and 200 micrograms/kg) produced a long-lasting and not dose-dependent fall in the mean blood pressure and heart rate. The pressor response to phenylephrine, an alpha adrenergic agonist, was antagonized by bromocriptine in a dose-dependent manner. At a dose of 20 micrograms/kg bromocriptine behaved as a competitive antagonist, whereas at the dose of 200 micrograms/kg produced an insurmountable blockade of the response to phenylephrine. Previous administration of phentolamine (5 mg/kg) prevented the insurmountable blockade of alpha adrenoceptors by bromocriptine. This observation suggests that both drugs compete for the same receptor. It is concluded that blockade of peripheral alpha-adrenoceptors may contribute to cardiovascular effects of bromocriptine.</p>\",\"PeriodicalId\":7131,\"journal\":{\"name\":\"Acta physiologica latino americana\",\"volume\":\"32 2\",\"pages\":\"117-22\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1982-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta physiologica latino americana\",\"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":"Acta physiologica latino americana","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Cardiovascular effects of 2-Br-alpha-ergocriptine in urethane anesthetized rats.
Experiments were designed to study the cardiovascular effects of Bromocriptine (2-Br-alpha-ergocriptine) in the normotensive anesthetized rats. The intravenous administration of bromocriptine (20 micrograms/kg and 200 micrograms/kg) produced a long-lasting and not dose-dependent fall in the mean blood pressure and heart rate. The pressor response to phenylephrine, an alpha adrenergic agonist, was antagonized by bromocriptine in a dose-dependent manner. At a dose of 20 micrograms/kg bromocriptine behaved as a competitive antagonist, whereas at the dose of 200 micrograms/kg produced an insurmountable blockade of the response to phenylephrine. Previous administration of phentolamine (5 mg/kg) prevented the insurmountable blockade of alpha adrenoceptors by bromocriptine. This observation suggests that both drugs compete for the same receptor. It is concluded that blockade of peripheral alpha-adrenoceptors may contribute to cardiovascular effects of bromocriptine.