脂氧合酶抑制剂而非位点特异性5-脂氧合酶阻滞剂可防止内毒素休克和抑制肿瘤坏死因子的产生。

Eicosanoids Pub Date : 1992-01-01
F U Schade, R Engel, D Jakobs
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引用次数: 0

摘要

在本研究中,我们发现脂氧合酶抑制剂可以预防LPS-,但不能预防肿瘤坏死因子α (TNF -)引起的致死。特异性5-脂氧合酶抑制剂(MK-886、CGS-8515)对内毒素性休克无效。5-脂氧合酶抑制剂干扰巨噬细胞中LTC4的形成,而它们不影响内毒素诱导的TNF α的形成,无论是在细胞培养中还是在小鼠中。其他特异性较低的脂氧合酶阻滞剂抑制TNF α形成的效力与它们干扰13-HODD合成的能力定量相关。基于TNF α合成抑制与13-HODD形成密切相关的事实,该产物可能对TNF α的形成很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lipoxygenase inhibitors but not site specific 5-lipoxygenase blockers protect against endotoxic shock and inhibit production of tumor necrosis factor.

In the present study it was found that lipoxygenase inhibitors prevent LPS-, but not tumor necrosis factor alpha (TNF alpha)-evoked lethality. The specific 5-lipoxygenase inhibitors (MK-886, CGS-8515) were uneffective in endotoxin-induced shock. The 5-lipoxygenase inhibitors interfered with LTC4 formation in macrophages while they did not affect endotoxin induced TNF alpha-formation, neither in cell cultures nor in mice. The potency of other, less specific lipoxygenase blockers to suppress TNF alpha formation correlated quantitatively with their ability to interfere with 13-HODD synthesis. Based on the fact that a tight correlation exists between inhibition of TNF alpha synthesis and 13-HODD formation, this product might be important for TNF alpha formation.

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