Thomas G
Prostaglandins. 1980 Jan;19(1):39-50. doi: 10.1016/0090-6980(80)90152-5.
In rats pretreated with indomethacin, injection of PGE1 (prostaglandin E1) with carrageenan potentiated the carrageenan paw oedema. This effect of PGE1, was maximal when it was injected together with carrageenan, there being a reduction in the action of PGE1 if carrageenan injection was delayed after PGE1 injection. PGE1 induced potentiation of increase in plasma protein leakage induced by intradermal injections of bradykinin and histamine also depended on the injection of PGE1 along with these agents. Thus oedema enhancement by PGE1 differs from its action in pain, where PGs cause a long lasting sensitization of the injected area for the actions of other algesics. Since vasodilation may be a mechanism of oedema enhancement by PGs, the ability of adenosine and papaverine to mimic PGE1 in paws and skins of rats were examined. Adenosine was active whereas papaverine was inactive in this respect. To clarify this difference, the vasodilatory properties of PGE1, adenosine and papaverine were assessed by their ability to antagonize NA response in perfused rat mesenteric blood vessels. Only papaverine was effective in antagonising the NA response. Thus, PGE1 and adenosine which potentiated the oedema inducing actions of other agents showed no vasodilatory properties and papaverine, a vasodilator, had no oedema potentiating actions.
在用吲哚美辛预处理的大鼠中,注射前列腺素E1(PGE1)和角叉菜胶会增强角叉菜胶所致的爪部水肿。PGE1的这种作用在与角叉菜胶同时注射时最为明显,如果在注射PGE1后延迟注射角叉菜胶,PGE1的作用会减弱。PGE1对皮内注射缓激肽和组胺所致血浆蛋白渗漏增加的增强作用也取决于与这些药物同时注射PGE1。因此,PGE1所致的水肿增强作用与其在疼痛中的作用不同,在疼痛中PG会使注射部位对其他镇痛药的作用产生持久的敏化。由于血管舒张可能是PG增强水肿的一种机制,因此研究了腺苷和罂粟碱在大鼠爪部和皮肤中模拟PGE1的能力。在这方面,腺苷有活性而罂粟碱无活性。为了阐明这种差异,通过它们拮抗灌注大鼠肠系膜血管中去甲肾上腺素(NA)反应的能力来评估PGE1、腺苷和罂粟碱的血管舒张特性。只有罂粟碱能有效拮抗NA反应。因此,增强其他药物致水肿作用的PGE1和腺苷没有血管舒张特性,而血管舒张剂罂粟碱没有水肿增强作用。