LTB4受体拮抗剂抑制钙霉素诱导的人PMN胞质钙的刺激。

Eicosanoids Pub Date : 1992-01-01
R Heckenberger, K Schrör
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引用次数: 0

摘要

本研究通过使用选择性LTB4拮抗剂(SC 41930)来研究PMN衍生的LTB4对PMN激活的意义。血小板活化因子(PAF, 3微米),受体依赖的激动剂,或钙霉素(a 23187, 10微米),受体独立的激动剂,刺激人PMN。PMN的激活是通过LTB4的释放和游离细胞质ca2 +水平的变化来确定的。用SC 41930(0.1-10微米)预处理PMN, PAF和钙霉素对激动剂诱导的细胞内钙离子升高均有浓度依赖性抑制。有趣的是,在相同浓度的SC 41.930下,对LTB4的释放有浓度依赖性的抑制作用。用无细胞5-脂氧合酶制备的对照实验显示,在去甲二氢胍有活性的条件下,SC 41930对5-脂氧合酶没有直接影响。这些数据表明,LTB4受体拮抗剂SC 41930对激动剂诱导的PMN激活具有非选择性抑制作用,并表明内源性LTB4的形成参与了一个正反馈回路,即使是钙离子载体也需要这个正反馈回路来最大限度地刺激PMN功能。
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Inhibition of calcimycin-induced stimulation of cytosolic calcium in human PMN by a LTB4 receptor antagonist.

This study investigates the significance of PMN-derived LTB4 for PMN activation by using a selective LTB4 antagonist (SC 41930). Human PMN were stimulated by platelet-activating-factor (PAF, 3 microM), a receptor dependent agonist, or by calcimycin (A 23187, 10 microM), a receptor independent agonist. PMN activation was determined by LTB4 release and changes in free cytosolic Ca++ levels. Pretreatment of the PMN with SC 41930 (0.1-10 microM) caused a concentration-dependent inhibition of agonist induced rise in cytosolic Ca++ with both PAF and calcimycin. Interestingly, at the same concentrations of SC 41.930, there was a concentration-dependent inhibition of LTB4 release. Control experiments with a cell-free 5-lipoxygenase preparation did not show any direct effect of SC 41930 on the enzyme under conditions when nordihydroguiaretic acid was active. The data demonstrate a nonselective inhibition of agonist induced PMN activation by the LTB4 receptor antagonist SC 41930 and suggest that formation of endogenous LTB4 is involved in a positive feed-back loop that is required for maximum stimulation of PMN function even by a calcium ionophore.

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