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不含甲硫氨酸的抗炎肽(抗炎症素)对血小板活化因子合成的抑制作用。

Inhibition of the synthesis of platelet-activating factor by anti-inflammatory peptides (antiflammins) without methionine.

作者信息

Tetta C, Camussi G, Bussolino F, Herrick-Davis K, Baglioni C

机构信息

Laboratorio di Immunopatologia della Cattedra di Nefrologia, Università di Torino, Italy.

出版信息

J Pharmacol Exp Ther. 1991 May;257(2):616-20.

PMID:2033508
Abstract

Antiflammins are synthetic peptides corresponding to a region of similarity between uteroglobin and lipocortin I. These peptides inhibit synthesis of platelet-activating factor and release of arachidonic acid from neutrophils and macrophages stimulated by phagocytosis or tumor necrosis factor. Antiflammins containing methionine are inactivated readily in the absence of reducing agents. Novel antiflammins containing alanine or norleucine in place of methionine are inhibitory without added reducing agents, but only when stock solutions are heated to 45 degrees C. Heating may favor hydrophobic interactions between peptide molecules, thereby activating the antiflammins. These peptides are less inhibitory when added after cell stimulation, suggesting that they interfere with the activation of phospholipase A2.

摘要

抗炎症蛋白是与子宫珠蛋白和脂皮质蛋白I之间的相似区域相对应的合成肽。这些肽可抑制血小板活化因子的合成以及吞噬作用或肿瘤坏死因子刺激的中性粒细胞和巨噬细胞中花生四烯酸的释放。含有甲硫氨酸的抗炎症蛋白在没有还原剂的情况下很容易失活。用丙氨酸或正亮氨酸取代甲硫氨酸的新型抗炎症蛋白在不添加还原剂时具有抑制作用,但前提是储备溶液需加热至45摄氏度。加热可能有利于肽分子之间的疏水相互作用,从而激活抗炎症蛋白。这些肽在细胞受到刺激后添加时抑制作用较小,这表明它们会干扰磷脂酶A2的激活。

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