Handa J, Koyama T, Yoneda S, Matsuda M, Handa H
No Shinkei Geka. 1975 Jul;3(7):577-84.
Effects of topical and intravenous administration of phenoxybenzamine (PBZ) on the experimental vasospasm were studied in cats. Cerebral vasospasm was produced by a topical application of blood, prostaglandin (PG) E2 or PGF2alpha to be exposed basilar artery. Topical PBZ caused a significant dilatation of the basilar artery and the occurrence of vasospasm was completely prevented either with blood, PGE2 or PGF2alpha. Intravenous administration of PBZ in the dosage with which the pressor response to phenylephrine was completely blocked, or three times that dosage, failed to show any preventive effect on the vasospasm. From these experimental results, it seems that the antispasmogenic action of topically applied PBZ is due largely to the non-spacific vasodilator action of PBZ and not to its alpha adrenergic blocking action. It is also suggested that the role of alpha adrenergic mechanism in the genesis of vasospasm in this experimental design is not significant.
在猫身上研究了局部和静脉注射苯氧苄胺(PBZ)对实验性血管痉挛的影响。通过向暴露的基底动脉局部应用血液、前列腺素(PG)E2或PGF2α来诱发脑血管痉挛。局部应用PBZ可使基底动脉显著扩张,并且无论是血液、PGE2还是PGF2α诱发的血管痉挛均能被完全预防。静脉注射能完全阻断对去氧肾上腺素升压反应剂量的PBZ,或该剂量的三倍,均未显示出对血管痉挛有任何预防作用。从这些实验结果来看,局部应用PBZ的抗痉挛作用很大程度上是由于PBZ的非特异性血管舒张作用,而非其α肾上腺素能阻断作用。这也表明在该实验设计中,α肾上腺素能机制在血管痉挛发生过程中的作用并不显著。