Coupar I M, McLennan P L
Br J Pharmacol. 1978 Jan;62(1):51-9. doi: 10.1111/j.1476-5381.1978.tb07005.x.
1 The report of the depression by indomethacin of vasoconstrictor responses to noradrenaline and their partial restoration by prostaglandin E(2) (PGE(2)) and PGE(1) in rat isolated perfused mesenteric blood vessels was investigated. The further suggestion that prostaglandins may be necessary for the combination of noradrenaline with the alpha-adrenoceptor in this tissue was also studied.2 The reported depression by indomethacin was confirmed and was further shown to be in the form of a concentration-dependent flattening of the noradrenaline concentration-effect curve.3 A concentration-dependent restorative effect was observed for all prostaglandins studied. The decreasing order of potency for the restoration towards normal of the indomethacin-depressed responses to noradrenaline was: PGE(2), PGE(1), PGA(1), PGF(2alpha), PGA(2).4 The prostaglandins studied were not uniform in their restorative actions and could be separated into two groups. PGE(2) and PGE(1) restored responses towards the control level whereas PGA(1), PGA(2) and PGF(2alpha) increased responses to an above control level and did so over a smaller concentration range. The possibility of several prostaglandin receptors is discussed.5 At concentrations equi-effective in restoring depressed responses to control levels PGA(1) but not PGE(2), caused a parallel shift of the noradrenaline concentration-effect curve to the left and a small, gradual rise in the basal perfusion pressure.6 The reason for the differing effects remains obscure but does not seem to involve a change in the alpha-adrenoceptor as indicated by the pA(2) of phentolamine. Furthermore, the restorative and potentiating effect of PGA(1) is not mediated by blockade of neuronal uptake of noradrenaline.7 It appears that prostaglandins are required for the vasoconstrictor action of noradrenaline in rat mesenteric blood vessels and that this effect is distal to the drug-receptor interaction. The possible involvement of prostaglandins with intracellular calcium ions is discussed.
1 研究了消炎痛对大鼠离体灌注肠系膜血管中去甲肾上腺素血管收缩反应的抑制作用,以及前列腺素E(2)(PGE(2))和PGE(1)对其部分恢复作用。还研究了前列腺素可能是该组织中去甲肾上腺素与α-肾上腺素受体结合所必需的这一进一步的推测。
2 消炎痛所报道的抑制作用得到证实,并且进一步表明其表现为去甲肾上腺素浓度-效应曲线呈浓度依赖性变平。
3 对所研究的所有前列腺素均观察到浓度依赖性的恢复作用。消炎痛抑制的去甲肾上腺素反应恢复至正常的效力递减顺序为:PGE(2)、PGE(1)、PGA(1)、PGF(2α)、PGA(2)。
4 所研究的前列腺素在其恢复作用方面并不一致,可分为两组。PGE(2)和PGE(1)将反应恢复至对照水平,而PGA(1)、PGA(2)和PGF(2α)则使反应增加至高于对照水平,且在较小的浓度范围内如此。讨论了几种前列腺素受体的可能性。
5 在恢复抑制反应至对照水平等效的浓度下,PGA(1)而非PGE(2)导致去甲肾上腺素浓度-效应曲线平行左移,且基础灌注压有小幅度的逐渐升高。
6 不同作用的原因仍不清楚,但似乎不涉及酚妥拉明的pA(2)所表明的α-肾上腺素受体的变化。此外,PGA(1)的恢复和增强作用不是由去甲肾上腺素的神经元摄取阻断介导的。
7 看来前列腺素是大鼠肠系膜血管中去甲肾上腺素血管收缩作用所必需的,且这种作用在药物-受体相互作用的远端。讨论了前列腺素与细胞内钙离子可能的关系。