Humphrey D M, McManus L M, Satouchi K, Hanahan D J, Pinckard R N
Lab Invest. 1982 Apr;46(4):422-7.
Intradermal injection of 0.1 pmole (52 pg.) of acetyl glyceryl ether phosphorylcholine (AGEPC) in guinea pigs induced increased vascular permeability as assessed by a skin-blueing model. Rabbits and rats showed increased vascular permeability with 1.0 pmole (520 pg.) of AGEPC. On a molar basis, from 1,000 to 10,000 times more histamine was required to induce skin blueing in the same animals. In rabbits and guinea pigs, the increased vascular permeability induced by AGEPC occurred as an early, transient phase and as a delayed, prolonged phase. The early, transient phase was not inhibited by chlorpheniramine doses which markedly reduced or abrogated histamine-induced blueing. AGEPC was 100 to 1000 times more potent than histamine on a molar basis for the induction of vasoconstriction in a blued skin assay in guinea pigs. These studies demonstrate that AGEPC has potent vasoactive properties and provide additional information that implicates this acetylated alkyl phosphoglyceride as a mediator of the acute inflammatory process.
通过皮肤变蓝模型评估,在豚鼠皮内注射0.1皮摩尔(52皮克)的乙酰甘油醚磷酸胆碱(AGEPC)可诱导血管通透性增加。兔子和大鼠在注射1.0皮摩尔(520皮克)的AGEPC后血管通透性增加。以摩尔为基础,在相同动物中诱导皮肤变蓝所需的组胺量是AGEPC的1000到10000倍。在兔子和豚鼠中,AGEPC诱导的血管通透性增加分为早期短暂阶段和延迟延长阶段。早期短暂阶段不受氯苯那敏剂量的抑制,而氯苯那敏剂量可显著降低或消除组胺诱导的皮肤变蓝。在豚鼠的皮肤变蓝试验中,以摩尔为基础,AGEPC诱导血管收缩的效力比组胺强100至1000倍。这些研究表明AGEPC具有强大的血管活性特性,并提供了更多信息,表明这种乙酰化烷基磷酸甘油酯是急性炎症过程的介质。