Lipoxygenase inhibitors suppress formation of tumor necrosis factor in vitro and in vivo.

Lymphokine research Pub Date : 1989-01-01
U F Schade, I Burmeister, R Engel, M Reinke, D T Wolter
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Abstract

The LPS induced synthesis of tumor necrosis factor in macrophage cultures, as determined in a fibroblast cytolysis assay was found to be effectively blocked by inhibitors of lipoxygenases. Likewise, the presence of tumor necrosis factor in serum of D-galactosamine sensitized mice after challenge with endotoxin was suppressed by the lipoxygenase inhibitors. Indomethacin, a blocker of cycclooxygenase was neither in vivo nor in vitro effective in the prevention of the endotoxin-induced synthesis of TNF. From LPS-treated macrophages we were able to isolate 13-hydroxylinoleic acid, a lipoxygenase product, which is significantly increased after LPS treatment of the cells, covalently bound to cellular constituents and may, therefore, be possibly involved in the formation of TNF.

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脂氧合酶抑制剂体外和体内抑制肿瘤坏死因子的形成。
在成纤维细胞溶解实验中,脂多糖诱导巨噬细胞中肿瘤坏死因子的合成被脂氧合酶抑制剂有效阻断。同样,脂氧合酶抑制剂可抑制内毒素刺激后d -半乳糖胺致敏小鼠血清中肿瘤坏死因子的存在。吲哚美辛,一种环氧化酶阻滞剂,在体内和体外都不能有效预防内毒素诱导的TNF合成。从LPS处理的巨噬细胞中,我们能够分离出13-羟基亚油酸,这是一种脂氧合酶产物,在细胞LPS处理后显著增加,与细胞成分共价结合,因此可能参与TNF的形成。
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