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[吡罗昔康对过敏性炎症的作用]

[Action of piroxicam on allergic inflammation].

作者信息

Abe N, Tanaka K, Kanaoka K, Egawa M, Watanabe I, Hirai S

出版信息

Nihon Yakurigaku Zasshi. 1983 May;81(5):431-40.

PMID:6629214
Abstract

Effects of piroxicam on allergic inflammation were investigated with allergic air pouch inflammation and antigen-induced arthritis in rats. In allergic air pouch inflammation, piroxicam exerted a dose-dependent inhibition (1-10 mg/kg, p.o.) of the exudate production, the migration of leukocytes and the release of lysosomal enzyme into the exudate; and its potency was superior to that of indomethacin and equivalent to that observed with prednisolone. In contrast with this, the suppressive effect of piroxicam on non-allergic air pouch inflammation was as weak as indomethacin. Prednisolone showed a similar effect on both types of air pouch inflammation. In antigen-induced arthritis, piroxicam showed a dose-dependent (0.3-3 mg/kg, p.o.) inhibitory effect on knee joint swelling and an improving action on the functional disorder of the inflamed joint. On this model, piroxicam was 3 to 4 times more active than both indomethacin and prednisolone. In non-allergic joint inflammation induced with croton oil in rats, however, the anti-inflammatory potency of piroxicam was almost equal to those of indomethacin and prednisolone. Piroxicam showed more potent inhibition than indomethacin on heterologous passive cutaneous anaphylaxis in rats, but showed only a slight inhibition on the increased vascular permeability caused by histamine and bradykinin. Piroxicam had no influence upon the plaque-forming cell response and the delayed hypersensitivity reaction in mice; furthermore, the hemolytic activity of complement in guinea-pig serum was scarcely affected by piroxicam in vitro. These results indicate that piroxicam possesses prominent efficiency on allergic inflammation and may function on several activities of inflammatory cells.

摘要

通过大鼠过敏性气囊炎症和抗原诱导性关节炎模型,研究了吡罗昔康对过敏性炎症的影响。在过敏性气囊炎症模型中,吡罗昔康(1 - 10毫克/千克,口服)对渗出物产生、白细胞迁移以及溶酶体酶释放到渗出物中均有剂量依赖性抑制作用;其效力优于吲哚美辛,与泼尼松龙相当。与此相反,吡罗昔康对非过敏性气囊炎症的抑制作用与吲哚美辛一样弱。泼尼松龙对两种类型的气囊炎症均有类似作用。在抗原诱导性关节炎模型中,吡罗昔康(0.3 - 3毫克/千克,口服)对膝关节肿胀有剂量依赖性抑制作用,并对炎症关节的功能障碍有改善作用。在该模型中,吡罗昔康的活性比吲哚美辛和泼尼松龙高3至4倍。然而,在大鼠巴豆油诱导的非过敏性关节炎症中,吡罗昔康的抗炎效力与吲哚美辛和泼尼松龙几乎相当。吡罗昔康对大鼠异种被动皮肤过敏反应的抑制作用比吲哚美辛更强,但对组胺和缓激肽引起的血管通透性增加仅有轻微抑制作用。吡罗昔康对小鼠的空斑形成细胞反应和迟发型超敏反应没有影响;此外,在体外,吡罗昔康对豚鼠血清中补体的溶血活性几乎没有影响。这些结果表明,吡罗昔康对过敏性炎症具有显著疗效,可能作用于炎症细胞的多种活性。

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