Hartman D A, Ochalski S J, Carlson R P
Wyeth-Ayerst Research, Princeton, NJ 08543, USA.
Inflamm Res. 1995 Jul;44(7):269-74. doi: 10.1007/BF02032567.
IL-1 beta, IL-8, IL-6 and TNF alpha, derived from infiltrating leukocytes, are important mediators of inflammation in arthritic and allergic diseases. Heparinized human whole blood was evaluated as a model to study the effects of various classes of antiinflammatory drugs on cytokine release/biosynthesis from leukocytes. Whole blood was stimulated with zymosan A (1.5 mg/ml) or LPS (5 micrograms/ml) for 4 h to induce cytokine release. Dexamethasone was the most potent inhibitor of TNF alpha, IL-1 beta, IL-6 and IL-8 release from LPS stimulated blood leukocytes (IC50s of 0.19, 0.11 microM, 0.16 and 0.07 respectively). In LPS stimulated blood, SKF-86002, a 5-lipoxygenase/cytooxygenasae inhibitor, and rolipram, a PDE IV inhibitor, also inhibited the release of TNF alpha (IC50s of 33 and 11 microM, respectively), IL-1 beta (IC50s of 11 and 30 microM, respectively), IL-6 (IC50s of 56 and > 30, respectively) and IL-8 (IC50s of 6.7 and 15, respectively), whereas isoproterenol (1 microM) inhibited significantly only TNF alpha release. Nonsteroidal antiinflammatory drugs, 5-lipoxygenase inhibitors and immuno-suppressive drugs were inactive at 30 microM against LPS and zymosan A stimulation of cytokine release. Using zymosan A as the stimulus, only SKF-86002 (30 microM) showed significant inhibition of IL-1 beta (-59%). This 4 h human blood assay has the potential to identify novel inhibitors and sites of actions (e.g. transcription, post-transcriptional and secretion) of new antiinflammatory drugs.
源自浸润白细胞的白细胞介素-1β、白细胞介素-8、白细胞介素-6和肿瘤坏死因子α是关节炎和过敏性疾病炎症的重要介质。肝素化人全血被用作一种模型,以研究各类抗炎药物对白细胞细胞因子释放/生物合成的影响。用酵母聚糖A(1.5毫克/毫升)或脂多糖(5微克/毫升)刺激全血4小时以诱导细胞因子释放。地塞米松是脂多糖刺激的血液白细胞中肿瘤坏死因子α、白细胞介素-1β、白细胞介素-6和白细胞介素-8释放的最有效抑制剂(IC50分别为0.19、0.11微摩尔/升、0.16和0.07)。在脂多糖刺激的血液中,5-脂氧合酶/环氧化酶抑制剂SKF-86002和磷酸二酯酶IV抑制剂咯利普兰也抑制肿瘤坏死因子α(IC50分别为33和11微摩尔/升)、白细胞介素-1β(IC50分别为11和30微摩尔/升)、白细胞介素-6(IC50分别为56和>30)和白细胞介素-8(IC50分别为6.7和15)的释放,而异丙肾上腺素(1微摩尔/升)仅显著抑制肿瘤坏死因子α的释放。非甾体抗炎药、5-脂氧合酶抑制剂和免疫抑制药物在30微摩尔/升时对脂多糖和酵母聚糖A刺激的细胞因子释放无活性。以酵母聚糖A作为刺激物时,只有SKF-86002(30微摩尔/升)对白细胞介素-1β有显著抑制作用(-59%)。这种4小时的人体血液检测有潜力识别新型抗炎药物的抑制剂和作用位点(如转录、转录后和分泌)。