WEB 2086 and WEB 2170 are potent platelet-activating factor (PAF) receptor antagonists and have been used widely as pharmacological tools to investigate the actions of PAF in a variety of biological systems. 2. Low concentrations of WEB 2086 and WEB 2170 blocked the vasoconstrictor action of PAF in the rat perfused heart. In this study, we observed that moderate concentrations of WEB 2086 and WEB 2170 increased the perfusion pressure in rat isolated hearts under constant flow perfusion. The vasoconstrictor actions of WEB 2086 and WEB 2170 were not observed with a structurally different PAF receptor antagonist, FR-900452. 3. To determine whether this vasoconstrictor action of WEB 2086 involved non-specific effects or was via the activation of PAF receptors, hearts were pretreated with 1000 pmol PAF or 50 microM FR-900452. These pretreatments attenuated the vasoconstrictor action of 1 microM WEB 2086, suggesting that the action of WEB 2086 may be mediated via PAF receptors. Pretreatment with the leukotriene receptor antagonist (L-649,923, 5 microM) and the leukotriene synthesis inhibitor (MK-886, 10 microM) that are known to block the vasoconstrictor action of PAF receptor activation also attenuated the vasoconstrictor action of WEB 2086. Pretreatment with PAF or MK-886 attenuated the vasoconstrictor action of 0.5 microM WEB 2170. 4. When PAF receptors were activated by PAF in the perfused heart, significant amounts of leukotriene C4 and leukotriene C4/D4/E4 were detected in the coronary effluent. However, no significant amount of these leukotrienes was detected in the coronary effluent when hearts were perfused with 1 microM WEB 2086 or 0.5 microM WEB 2170. 5. In summary, our results indicate that WEB 2086 and WEB 2170 possess partial agonist effects in the rat perfused heart where they produced vasoconstriction via the activation of PAF receptor. This action could be attenuated by PAF pretreatment or a PAF receptor antagonist. The vasoconstrictor action of WEB 2086 and WEB 2170 involved the production of leukotrienes. But unlike the vasoconstrictor action of PAF, no significant amount of leukotrienes was detected in the effluent suggesting that the vasoconstrictor action of WEB 2086 and WEB 2170 may be explained on the basis of intracellularly or locally produced leukotrienes.
摘要
WEB 2086和WEB 2170是强效的血小板激活因子(PAF)受体拮抗剂,已被广泛用作药理学工具,以研究PAF在各种生物系统中的作用。2. 低浓度的WEB 2086和WEB 2170可阻断PAF在大鼠离体心脏中的血管收缩作用。在本研究中,我们观察到中等浓度的WEB 2086和WEB 2170在恒流灌注下可增加大鼠离体心脏的灌注压力。而结构不同的PAF受体拮抗剂FR-900452未观察到WEB 2086和WEB 2170的血管收缩作用。3. 为了确定WEB 2086的这种血管收缩作用是涉及非特异性效应还是通过PAF受体的激活,心脏先用1000 pmol PAF或50 microM FR-900452进行预处理。这些预处理减弱了1 microM WEB 2086的血管收缩作用,表明WEB 2086的作用可能是通过PAF受体介导的。用已知可阻断PAF受体激活的血管收缩作用的白三烯受体拮抗剂(L-649,923,5 microM)和白三烯合成抑制剂(MK-886,10 microM)进行预处理也减弱了WEB 2086的血管收缩作用。用PAF或MK-886预处理减弱了0.5 microM WEB 2170的血管收缩作用。4. 当在灌注心脏中PAF激活PAF受体时,在冠状动脉流出液中检测到大量的白三烯C4和白三烯C4/D4/E4。然而,当心脏用1 microM WEB 2086或0.5 microM WEB 2170灌注时,在冠状动脉流出液中未检测到大量的这些白三烯。5. 总之,我们的结果表明,WEB 2086和WEB 2170在大鼠灌注心脏中具有部分激动剂作用,它们通过激活PAF受体产生血管收缩。这种作用可被PAF预处理或PAF受体拮抗剂减弱。WEB 2086和WEB 2170的血管收缩作用涉及白三烯的产生。但与PAF的血管收缩作用不同,在流出液中未检测到大量的白三烯,这表明WEB 2086和WEB 2170的血管收缩作用可能基于细胞内或局部产生的白三烯来解释。