Mchedlishvili G, Ormotsadze L
Blood Vessels. 1979;16(3):126-34. doi: 10.1159/000158199.
In order to study the action of serotonin (5-HT), noradrenaline (NA), hypertensin (HT), prostaglandins A1, B1 and E2 (PGA1, PGB1 and PGE2) and vasopressin (VP), internal carotid arteries were isolated in situ from both cerebral and general circulation and perfused continuously with oxygenated Ringers' bicarbonate solution. The order of potencies of the vasoactive substances when administered intra-arterially was: 5-HT greater than HT greater than PGE2- greater than PGB1 greater than NA. The relative duration of the constrictor effects was: 5-HT less than PGA1-less than HT and PGE2 less than PGB1 and NA less than VP. The relaxation index of these substances on the vascular wall was: 5-HT less than PGE2 less than HT less than PGB1-less than NA less than PGA1 less than VP. Some of these substances, specifically PGB1, PGE2 and VP, frequently caused a residual constriction of the smooth muscle following their dilator effect. The role of these vasoactive substances in the development of vasospasm is discussed.
为了研究血清素(5-羟色胺,5-HT)、去甲肾上腺素(NA)、高血压素(HT)、前列腺素A1、B1和E2(PGA1、PGB1和PGE2)以及血管加压素(VP)的作用,从脑循环和体循环中原位分离出颈内动脉,并用含氧的林格氏碳酸氢盐溶液持续灌注。动脉内给药时血管活性物质的效力顺序为:5-HT>HT>PGE2>PGB1>NA。收缩效应的相对持续时间为:5-HT<PGA1<HT和PGE2<PGB1且NA<VP。这些物质对血管壁的舒张指数为:5-HT<PGE2<HT<PGB1<NA<PGA1<VP。其中一些物质,特别是PGB1、PGE2和VP,在其舒张作用后常导致平滑肌残余收缩。讨论了这些血管活性物质在血管痉挛发生中的作用。