[Possible mechanisms of the anti-inflammatory action of polyamines].

Y Azuma, S Ohtani, Y Matsunaga, Y Ueda, K Tajima, N Takagi
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Abstract

Carrageenin paw edema of rats was inhibited in a dose-dependent manner by subcutaneous administration of polyamines. The latter had to be administered at least 2 hr before carrageenin challenge to achieve such inhibition. Moreover, inhibition was blocked by the simultaneous injection of actinomycin D. Polyamines also inhibited local bluing reactions to histamine in rats and similarly had to be administered 3 hr previously to achieve inhibition. Polyamines were shown to be glucocorticoid-type anti-inflammatory drugs, and may be glucocorticoids mediators of the synthesis of the postulated vascular permeability inhibitory protein that do not inhibit phospholipase A2 activity. Neutrophil chemotaxis was inhibited by polyamines in a concentration-dependent manner. In contrast to the experience with carrageenin paw edema, simultaneous addition to actinomycin D did not block the inhibitory action of polyamines on neutrophil chemotaxis. These results suggest that polyamines possess at least 2 different anti-inflammatory mechanisms. The first is mediated by the synthesis of an anti-inflammatory protein, and the second consist of direct action on leukocytes.

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[多胺抗炎作用的可能机制]。
多胺皮下给药对大鼠角叉菜胶足部水肿有剂量依赖性抑制作用。后者必须在角叉菜胶攻击前至少2小时给予以达到这种抑制。此外,同时注射放线菌素d可以阻断抑制作用。多胺也可以抑制大鼠对组胺的局部变蓝反应,同样必须在3小时前给药才能达到抑制作用。多胺被证明是糖皮质激素类型的抗炎药物,并且可能是糖皮质激素介质合成假定的血管通透性抑制蛋白,不抑制磷脂酶A2的活性。中性粒细胞趋化性受多胺抑制呈浓度依赖性。与角叉菜胶足跖水肿相比,同时添加放线菌素D并没有阻断多胺对中性粒细胞趋化性的抑制作用。这些结果表明,多胺具有至少两种不同的抗炎机制。第一种是由一种抗炎蛋白的合成介导的,第二种是直接作用于白细胞。
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