Hwang S B, Lam M H, Li C L, Shen T Y
Eur J Pharmacol. 1986 Jan 14;120(1):33-41. doi: 10.1016/0014-2999(86)90636-9.
Platelet activating factor (PAF), a potent lipid-like vasoactive agent, induced rat foot edema when it was injected subplantarly. The edema reached its maximum 1 h after PAF challenge. Indomethacin did not inhibit the peak edematous response whereas both PAF antagonists, kadsurenone and L-652,731, inhibit the PAF-induced rat foot edema (PFE). Both PAF antagonists also partially block the first phase of the carrageenin-induced rat foot edema (CFE). Using the inhibition of [3H]PAF receptor binding to prepared rabbit platelet membranes, release of PAF or PAF-like materials in carrageenin-injected rat hindpaw was observed. These results suggest that the released PAF or PAF-like materials together with the released histamine and kinin evoke the first phase hindpaw edema in the rats. Indomethacin or PAF antagonist, administered alone, does not block the first phase or the second phase of CFE, respectively. However, PAF antagonist potentiated the inhibitory effects of indomethacin suggesting that the released PAF may also be involved in the biosynthesis of prostaglandins to initiate the second phase of rat CFE.
血小板活化因子(PAF)是一种强效的类脂血管活性物质,足底皮下注射时可诱导大鼠足部水肿。PAF激发后1小时水肿达到最大值。吲哚美辛不抑制水肿反应峰值,而两种PAF拮抗剂海风藤酮和L-652,731可抑制PAF诱导的大鼠足部水肿(PFE)。两种PAF拮抗剂还可部分阻断角叉菜胶诱导的大鼠足部水肿(CFE)的第一阶段。通过抑制[3H]PAF与制备的兔血小板膜的受体结合,观察到角叉菜胶注射的大鼠后爪中PAF或类PAF物质的释放。这些结果表明,释放的PAF或类PAF物质与释放的组胺和激肽一起引发大鼠后爪水肿的第一阶段。单独给予吲哚美辛或PAF拮抗剂分别不阻断CFE的第一阶段或第二阶段。然而,PAF拮抗剂增强了吲哚美辛的抑制作用,表明释放的PAF也可能参与前列腺素的生物合成,从而引发大鼠CFE的第二阶段。