Whittle B J, Morishita T, Ohya Y, Leung F W, Guth P H
Am J Physiol. 1986 Dec;251(6 Pt 1):G772-8. doi: 10.1152/ajpgi.1986.251.6.G772.
Intravenous infusion of platelet-activating factor (PAF or AGEPC) induces extensive acute hemorrhagic damage in the ra gastric mucosa. The effects of PAF have now been investigated on several microcirculatory parameters in the rat gastric mucosa. Infusion of PAF (25-100 ng X kg-1 X min-1 iv) dose-dependently reduced systemic arterial blood pressure and mucosal blood flow, as determined by hydrogen gas clearance. Microscopic observation likewise indicated a dose-dependent slowing of mucosal capillary blood flow, as determined by red blood cell velocity after PAF infusion with stasis of flow at the highest dose. These actions were not the consequence of vasoconstriction, since there was no significant change in arteriolar and venular vessel diameter in the submucosa during PAF infusion, although a dose-related slowing and stasis of blood flow was observed. There was no capillary leakage of plasma protein in the gastric mucosa during PAF infusion, as determined by a fluorescence marker (FITC-BSA) technique. The precursor and breakdown product, lyso-PAF (200 ng X kg-1 X min-1) had no significant action on any of these microcirculatory parameters. These observations support the suggestion that microvascular changes leading to stasis may contribute to the ulcerogenic actions of PAF.
静脉输注血小板活化因子(PAF 或乙酰基甘油醚磷酸胆碱)可在大鼠胃黏膜中引发广泛的急性出血性损伤。现已研究了 PAF 对大鼠胃黏膜多种微循环参数的影响。输注 PAF(25 - 100 ng·kg⁻¹·min⁻¹,静脉注射)可使体循环动脉血压和黏膜血流呈剂量依赖性降低,这是通过氢气清除率测定的。显微镜观察同样显示黏膜毛细血管血流呈剂量依赖性减慢,这是通过在输注 PAF 后红细胞速度测定的,在最高剂量时血流出现停滞。这些作用并非血管收缩的结果,因为在输注 PAF 期间黏膜下层的小动脉和小静脉血管直径没有显著变化,尽管观察到血流有剂量相关的减慢和停滞。通过荧光标记物(异硫氰酸荧光素 - 牛血清白蛋白)技术测定,在输注 PAF 期间胃黏膜中没有血浆蛋白的毛细血管渗漏。PAF 的前体和分解产物溶血磷脂酰胆碱(200 ng·kg⁻¹·min⁻¹)对这些微循环参数中的任何一个均无显著作用。这些观察结果支持这样的观点,即导致血流停滞的微血管变化可能促成了 PAF 的致溃疡作用。