Greenberg R
Br J Pharmacol. 1974 Sep;52(1):61-8. doi: 10.1111/j.1476-5381.1974.tb09687.x.
1 The effects of indomethacin and eicosa-5,8,11,14-tetraynoic acid (ETYA) on the contractile response of the transmurally stimulated rabbit portal vein were studied in vitro.2 When the veins were stimulated for 240 pulses at 1 and 2 Hz, the responses were potentiated by indomethacin and ETYA. However, responses to 4 and 8 Hz were not potentiated. The responses to continuous electrical stimulation at 2 Hz were also potentiated by indomethacin and ETYA. This potentiating effect was attenuated when the veins were pretreated with alpha-methyl-p-tyrosine. The responses of the veins to noradrenaline were not altered by either indomethacin or ETYA.3 Prostaglandin E(2) inhibited the responses of the portal vein to electrical stimulation. The magnitude of this inhibition was inversely related to the frequency of stimulation. The responses of the vein to noradrenaline were not altered by prostaglandin E(2).4 It is concluded that potentiation by indomethacin and ETYA of the response of the isolated portal vein is due to an increased release of newly synthesized noradrenaline as a result of inhibition of prostaglandin synthesis.
体外研究了吲哚美辛和5,8,11,14-二十碳四炔酸(ETYA)对经壁刺激兔门静脉收缩反应的影响。
当静脉在1Hz和2Hz频率下接受240次脉冲刺激时,吲哚美辛和ETYA可增强反应。然而,对4Hz和8Hz的反应并未增强。吲哚美辛和ETYA也可增强静脉在2Hz频率下连续电刺激的反应。当静脉用α-甲基对酪氨酸预处理后,这种增强作用减弱。吲哚美辛和ETYA均未改变静脉对去甲肾上腺素的反应。
前列腺素E2抑制门静脉对电刺激的反应。这种抑制的程度与刺激频率呈负相关。前列腺素E2未改变静脉对去甲肾上腺素的反应。
得出结论,吲哚美辛和ETYA对离体门静脉反应的增强作用是由于抑制前列腺素合成导致新合成的去甲肾上腺素释放增加。