Márquez M T, de Mikulic L E, Aramendía P
Acta Physiol Lat Am. 1979;29(4-5):245-54.
The beta-blocking activity of propranolol was studied on the positive inotropic effect of norepinephrine, epinephrine, isoproterenol, dopamine and ethylephrine, in the left atrium driven at different rates. Dose of the antagonist of 10(-8) and 10(-7) M did not block the norepinephrine dose-response curve at 1 and 2.8 Hz, but a shift to the right was observed at 1.6 Hz. Although epinephrine showed a significant increase in its pD2 (p less than 0.001) at the lower stimulation frequency, the blockade increased progressively the higher the rates. On the other hand, propranolol antagonized isoproterenol at all the frequencies tested, in spite of an increase in the maxima at 2.8 Hz. This latter behavior was also true for dopamine and ethylephrine. Both sympathomimetic amines were blocked by propranolol at 1 and 1.6 Hz. The complex effect of propranolol on Ca2+ movements and its effects on cAMP and ATPase seem to be superimposed to the beta-blocking activity. Thus, the various actions on the sympathomimetic amines change according to the agonist considered and the stimulation frequency employed.
在不同频率驱动的左心房中,研究了普萘洛尔对去甲肾上腺素、肾上腺素、异丙肾上腺素、多巴胺和乙基肾上腺素正性肌力作用的β受体阻断活性。10^(-8)和10^(-7)M的拮抗剂剂量在1Hz和2.8Hz时未阻断去甲肾上腺素的剂量反应曲线,但在1.6Hz时观察到曲线右移。尽管肾上腺素在较低刺激频率下其pD2显著增加(p<0.001),但阻断作用随频率升高而逐渐增强。另一方面,普萘洛尔在所有测试频率下均拮抗异丙肾上腺素,尽管在2.8Hz时最大值有所增加。多巴胺和乙基肾上腺素也有同样的表现。这两种拟交感胺在1Hz和1.6Hz时均被普萘洛尔阻断。普萘洛尔对Ca2+运动的复杂作用及其对cAMP和ATP酶的影响似乎叠加在β受体阻断活性上。因此,对拟交感胺的各种作用根据所考虑的激动剂和所用的刺激频率而变化。