Weitzell R, Steppeler A, Starke K
Eur J Pharmacol. 1978 Nov 1;52(1):137-41. doi: 10.1016/0014-2999(78)90033-x.
Strips of the rabbit pulmonary artery were preincubated with 3H-noradrenaline and then superfused and stimulated electrically at 2 or 4 Hz. PGE2 and PGI2 reduced the stimulation-evoked overflow of total tritium and 3H-noradrenaline. PGI2 was about 10 times less potent than PGE2. High concentrations of 6-keto-PGF 1alpha also diminished the evoked overflow, but the effect was small. It is concluded that PGI2, in comparison with PGs of the E series, is a relatively weak inhibitor of noradrenaline release.
将兔肺动脉条与3H-去甲肾上腺素预孵育,然后以2或4Hz的频率进行灌流并电刺激。前列腺素E2(PGE2)和前列环素(PGI2)减少了刺激诱发的总氚和3H-去甲肾上腺素的溢出。PGI2的效力约为PGE2的十分之一。高浓度的6-酮-前列腺素F1α(6-keto-PGF1α)也减少了诱发的溢出,但作用较小。得出的结论是,与E系列前列腺素相比,PGI2是去甲肾上腺素释放的相对较弱的抑制剂。