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2-(2-吡啶基)乙胺(PEA)对离体豚鼠心脏的作用。

Effects of 2-(2-pyridyl)ethylamine (PEA) on the isolated guinea-pig heart.

作者信息

Laher I, McNeill J H

出版信息

Agents Actions. 1980 Nov;10(5):417-21. doi: 10.1007/BF01968039.

Abstract

The effect of 2-(2-pyridyl)ethylamine (PEA) on the rate and force of contraction of cardiac tissues from untreated and reserpine-pretreated guinea-pigs was examined. PEA produced changes in rate of spontaneously beating right atria without activation of H1 or H2-receptors. The positive chronotropic effect of PEA was eliminated when atria from reserpine-pretreated animals were used, indicating an entirely indirect mode of action of PEA in the right atrium. The positive inotropic effect of low doses of PEA in left atria was antagonized by promethazine, whereas the inotropic effect of higher doses of PEA was reduced either by propranolol or following reserpine pretreatment. In the right ventricle strip, the inotropic effect of high doses of PEA was blocked equally by propranolol and promethazine. The results obtained indicate that in the guinea-pig heart, PEA either produces it effects through catecholamine release (right atrium) or through a combination of both H1-receptor stimulation and catecholamine release (left atrium and right ventricle strip). The direct inotropic effects of PEA produced only small increases in force of contraction. The study indicates that caution should be used in ascribing all of the effects of PEA to histamine receptor stimulation.

摘要

研究了2-(2-吡啶基)乙胺(PEA)对未处理及经利血平预处理的豚鼠心脏组织收缩速率和力量的影响。PEA可使自发性搏动的右心房速率发生变化,且未激活H1或H2受体。当使用经利血平预处理动物的心房时,PEA的正性变时作用消失,这表明PEA在右心房的作用完全是间接的。左心房中低剂量PEA的正性变力作用可被异丙嗪拮抗,而高剂量PEA的变力作用则可被普萘洛尔减弱,或在利血平预处理后减弱。在右心室条带中,高剂量PEA的变力作用被普萘洛尔和异丙嗪同等程度地阻断。所得结果表明,在豚鼠心脏中,PEA要么通过释放儿茶酚胺产生作用(右心房),要么通过刺激H1受体和释放儿茶酚胺两者的联合作用产生作用(左心房和右心室条带)。PEA的直接变力作用仅使收缩力量有小幅增加。该研究表明,将PEA的所有作用都归因于组胺受体刺激时应谨慎。

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