Lloret S, Moreno J J
Departamento de Ciencias Fisiológicas Humanas y de la Nutrición, Fac. Farmacia, Univ. Barcelona, Spain.
Eur J Pharmacol. 1994 Nov 3;264(3):379-84. doi: 10.1016/0014-2999(94)00500-1.
The anti-inflammatory action of nonapeptide fragments of uteroglobin or lipocortin I known as antiflammins, was tested in the carrageenan or phospholipase A2 rat paw oedema model. The development of carrageenan-induced oedema in rats was significantly inhibited during the early and late phases of the oedema by the local administration of antiflammins 1 and 2. However, the peptides were not able to inhibit phospholipase A2-induced oedema. The time course of the anti-oedematous activity of nonapeptides after intradermal carrageenan injection may be attributed to their effect on mast cell degranulation and accumulation and activation of leukocytes. Naja naja phospholipase A2 exhibited strong histamine release-inducing activity, which may have contributed to the rat paw oedema induction. Surprisingly, antiflammins had a limited but significant inhibitory effect on histamine secretion.
子宫珠蛋白或脂皮质素I的九肽片段(即抗炎症蛋白)的抗炎作用,在角叉菜胶或磷脂酶A2诱导的大鼠足爪水肿模型中进行了测试。在水肿的早期和晚期,通过局部给予抗炎症蛋白1和2,角叉菜胶诱导的大鼠水肿的发展受到显著抑制。然而,这些肽不能抑制磷脂酶A2诱导的水肿。皮内注射角叉菜胶后九肽的抗水肿活性的时间进程可能归因于它们对肥大细胞脱颗粒以及白细胞聚集和激活的影响。眼镜蛇磷脂酶A2表现出很强的组胺释放诱导活性,这可能对角叉菜胶诱导的大鼠足爪水肿有作用。令人惊讶的是,抗炎症蛋白对组胺分泌有有限但显著的抑制作用。