E Köhler, G Varnai, S Knospe, W Förster, D Michaelis, H Wanka
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引用次数: 1
摘要
通过6小时的细胞毒试验,研究了血小板活化因子(PAF)拮抗剂BN 52021 (0.06-2.5 mM)对新诊断1型糖尿病患者单核细胞(MNC)对新生大鼠51cr标记朗格汉斯胰岛的细胞毒活性的影响。观察到BN 52021对抗胰岛细胞毒性的剂量依赖性抑制作用。在浓度为0.6 mM BN 52021时,对胰岛溶解的抑制是显著的。在4天的细胞培养过程中,BN 52021对抗原介导的具有抗胰岛细胞毒性的免疫细胞的触发没有抑制作用。结果表明,该药仅在MNC对胰岛的免疫细胞溶解反应中有效。目前不能排除BN 52021独立于paf的行动。
Effects of the platelet-activating factor antagonist BN 52021 on anti-islet cytotoxicity of mononuclear cells and serum from type 1 (insulin-dependent) diabetic patients.
The effect of platelet-activating factor (PAF) antagonist BN 52021 (0.06-2.5 mM) on the cytotoxic activity of mononuclear cells (MNC) from newly diagnosed type 1 diabetic patients against 51Cr-labeled Langerhans islets from neonatal rats was investigated in a 6-hour cytotoxicity test. A dose-dependent inhibition of anti-islet cytotoxicity by BN 52021 was observed. The suppression of the islet lysis was significant at a concentration of 0.6 mM BN 52021. During a 4-day cell culture, BN 52021 had no inhibitory effect on the antigen-mediated triggering of immunocytes with anti-islet cytotoxicity. The results suggest that the drug is only effective during immunocytolytic reactions of MNC against pancreatic islets. A PAF-independent action of BN 52021 can not be excluded at present.