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血小板活化因子拮抗剂WEB 2086对小鼠腹腔巨噬细胞肿瘤坏死因子产生的影响。

Effect of platelet activating factor antagonist WEB 2086 on the production of TNF from murine peritoneal macrophages.

作者信息

Ju D W, Zheng Q Y, Wang H B, Wang X F, Fang J

机构信息

Department of Pharmacology, School of Pharmacy, Second Military Medical University, Shanghai.

出版信息

Yao Xue Xue Bao. 1993;28(10):721-7.

PMID:8009983
Abstract

In the present study the effect of platelet activating factor (PAF) antagonist WEB 2086 on the production of tumor necrosis factor (TNF) from primed murine peritoneal macrophages was investigated. At 10(-6) and 10(-5) mol/L, WEB 2086 was found to significantly inhibit LPS induced TNF production from macrophages by activated thioglycollate solution. WEB 2086 inhibition of TNF release began 4 h after LPS stimulation and lasted 22 h with a peek at 16 h. The results showed that PAF might play an important role in the production of TNF. Four methods were compared in the bioassay of TNF. The data demonstrated that L-929 cells treated with actinomycin D and sodium fluoride were the most sensitive for the assay of TNF. This method was employed in this study.

摘要

在本研究中,研究了血小板活化因子(PAF)拮抗剂WEB 2086对经预处理的小鼠腹腔巨噬细胞肿瘤坏死因子(TNF)产生的影响。在10^(-6)和10^(-5) mol/L浓度下,发现WEB 2086能显著抑制由活化的巯基乙酸盐溶液诱导的巨噬细胞产生LPS诱导的TNF。WEB 2086对TNF释放的抑制作用在LPS刺激后4小时开始,持续22小时,在16小时达到峰值。结果表明,PAF可能在TNF的产生中起重要作用。在TNF的生物测定中比较了四种方法。数据表明,用放线菌素D和氟化钠处理的L-929细胞对TNF测定最为敏感。本研究采用了该方法。

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