二苯胺衍生物对大鼠腹腔巨噬细胞花生四烯酸代谢的影响

Kazuo Ohuchi , Masako Watanabe , Yukari Fukui , Noriyasu Hirasawa , Tsuneo Ozeki , Susumu Tsurufuji
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引用次数: 5

摘要

研究了二苯胺衍生物双氯芬酸钠、甲氧胺酸和洛苯扎里特二钠对大鼠腹腔巨噬细胞花生四烯酸代谢的影响。通过放射免疫测定,洛苯扎里特二钠对前列腺素E2的产生没有影响,尽管另外两种二苯胺衍生物具有有效的抑制活性。三种二苯胺衍生物对(3H)花生四烯酸标记巨噬细胞的Ca2+离子载体刺激的放射性释放没有影响。HPLC分析表明,双氯芬酸钠和甲氧胺酸对脂氧合酶产物的合成没有影响。综上所述,虽然其基本化学结构类似于双氯芬酸钠和甲氧胺酸,但对花生四烯酸的代谢没有抑制作用,说明氯苯扎里特二钠的免疫调节作用并不干扰花生四烯酸的代谢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of diphenylamine derivatives on arachidonic acid metabolism in rat peritoneal macrophages

The effect of diphenylamine derivatives such as diclofenac sodium, mefenamic acid and lobenzarit disodium on arachidonic acid metabolism in rat peritoneal macrophages was examined. Lobenzarit disodium has no effect on prostaglandin E2 production as measured by radioimmunoassay although two other diphenylamine derivatives have a potent inhibito activity. Three diphenylamine derivatives have no effect on Ca2+ ionophore-stimulated release of radioactivity from (3H)arachidonic acid-labeled macrophages. HPLC analysis revealed that lobenzarit disodium had no effect on the synthesis of lipoxygenase products as observed in diclofenac sodium and mefenamic acid. It is concluded that lobenzarit disodium, although its fundamental chemical structure resembles diclofenac sodium and mefenamic acid, has no inhibitory activity on arachidonic acid metabolism, suggesting that immunomodulatory activities of lobenzarit disodium are manifested without interfering with arachidonic acid metabolism.

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