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首页> 外文期刊>Japanese Journal of Pharmacology >A COMPARISON OF THE EFFECTS OF TYRAMINE AND EPHEDRINE ON ATRIAL CONTRACTIONS IN RABBITS AND GUINEA-PIGS
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A COMPARISON OF THE EFFECTS OF TYRAMINE AND EPHEDRINE ON ATRIAL CONTRACTIONS IN RABBITS AND GUINEA-PIGS

机译:酪氨酸和麻黄碱对家兔和几内亚猪心房收缩作用的比较

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References(10) Bertler, Carlsson and Rosengren (1) found that the pressor effect of tyramine is decreased in animals that have previously been reserpinized, and Burn and Rand (2) have reported that in such animals the change in blood pressure, response of vessel wall, or nictitating membrane to tyramine recovers after the treatment of noradrenaline. It has also been reported that the catecholamine content of various organs decreases after the administration of reserpine (3-5). The generally accepted explanation of these findings has been that the decreased response to tyranime in reserpinized animals may be due to the decrease in endogenous catecholamine available to tyramine after reserpine administration. On the other hand, tyramine and ephedrine show similar pharmacological effects both in vivo and in vitro. The action mechanism of ephedrine also remains to be clarified, despite the many investigations that have been carried out since Chen and Schmidt (6) reported on the pharmacological effects of this drug. Ephedrine is also effective as a bronchodilator and, in some cases, as a pressor drug. Clinically, however, a decrease in response to ephedrine after repeated administration has often been encountered, especially in blood pressure response, but tyramine yields to tachyphylaxis scarcely. It is generally held that mechanism of this so-called “tachyphylaxis” phenomenon is due to receptor occupation by ephedrine (7). We have previously carried out a series of experiments on rabbit and guinea-pig atria with a number of drugs assumed to have the ability to mobilize and activate endogenous catecholamine (8, 9). We have used the similar experimental procedure in our attempt to clarify the action mechanisms of tyramine and ephedrine, and to explain the mechanism of tachyphylaxis phenomenon that displays following repeated administration of ephedrine. In the present experiments also, reserpine and nicotine were used as experimental means, reserpine for its reduction of endogenous catecholamine, and nicotine for its indirect activation.
机译:参考文献(10)Bertler,Carlsson和Rosengren(1)发现酪胺的升压作用在先前被重新固定化的动物中降低了,Burn和Rand(2)报道了这类动物的血压变化,去甲肾上腺素治疗后血管壁或酪氨酸的硝化膜恢复。也有报道称,利血平给药后各器官的儿茶酚胺含量降低(3-5)。这些发现的普遍接受的解释是,在利血平化的动物中对酪氨酸的反应降低可能是由于利血平给药后可用于酪胺的内源性儿茶酚胺减少。另一方面,酪胺和麻黄碱在体内和体外均显示出相似的药理作用。尽管自Chen和Schmidt(6)报道了该药的药理作用以来进行了许多研究,但麻黄碱的作用机理仍有待阐明。麻黄碱还可用作支气管扩张药,在某些情况下还可用作加压药。然而,在临床上,经常遇到重复给药后对麻黄碱的反应下降,特别是在血压反应中,但是酪胺几乎不会产生速激肽。通常认为,这种所谓的“速动性”现象的机制是由于麻黄碱对受体的占领(7)。我们之前已经对兔子和豚鼠心房进行了一系列实验,使用了许多具有动员和激活内源性儿茶酚胺能力的药物(8、9)。我们尝试使用类似的实验程序来阐明酪胺和麻黄碱的作用机制,并解释重复服用麻黄碱后出现的速激肽现象的机制。在本实验中,利血平和尼古丁也用作实验手段,利血平用于减少内源性儿茶酚胺,尼古丁用于间接激活。

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