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奈多罗米钠和色甘酸钠对中性粒细胞和嗜酸性粒细胞诱导趋化作用的抑制

Inhibition of neutrophil and eosinophil induced chemotaxis by nedocromil sodium and sodium cromoglycate.

作者信息

Bruijnzeel P L, Warringa R A, Kok P T, Kreukniet J

机构信息

Department of Pulmonary Disease, State University Hospital Utrecht, The Netherlands.

出版信息

Br J Pharmacol. 1990 Apr;99(4):798-802. doi: 10.1111/j.1476-5381.1990.tb13009.x.

DOI:10.1111/j.1476-5381.1990.tb13009.x
PMID:2163279
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1917545/
Abstract
  1. Neutrophils and eosinophils infiltrate the airways in association with the allergen-induced late phase asthmatic reaction. Mobilization of these cells takes place via lipid-like and protein-like chemotactic factors. In this study platelet-activating factor (PAF), leukotriene B4 (LTB4), zymosan-activated serum (ZAS) and N-formyl-methionyl-leucyl-phenylalanine (FMLP) were used as illustrative examples of both groups. Chemotaxis was studied in human neutrophils and eosinophils. The inhibitory effects of nedocromil sodium and sodium cromoglycate were evaluated. 2. All chemotactic factors tested attracted neutrophils with the following rank order of activity: ZAS greater than PAF identical to FMLP identical to LTB4. Eosinophils were only mobilized by PAF, LTB4 and ZAS with the following rank order of activity: ZAS greater than PAF greater than LTB4. 3. Nedocromil sodium and sodium cromoglycate were equally active as the PAF antagonist BN 52021 in inhibiting the PAF-induced chemotaxis of neutrophils (IC50 approximately 10(-8) M). Both drugs were also equally active in inhibiting the chemotaxis of neutrophils induced by ZAS (IC50 approximately 10(-7)-10(-6) M), FMLP (IC50 approximately 10(-7) M) and LTB4 (IC50 approximately 10(-6) M). 4. Nedocromil sodium significantly inhibited the chemotaxis of eosinophils induced by PAF (IC50 approximately 10(-6) M) and LTB4 (IC50 approximately 10(-7) M). The inhibitory potency of BN 52021 was similar to that of nedocromil sodium on the PAF-induced chemotaxis of eosinophils. Sodium cromoglycate was incapable of eliciting significant inhibition of these chemotactic responses. However, sodium cromoglycate significantly inhibited the chemotaxis of eosinophils induced by ZAS (IC50 approximately 10(-7) M), whereas nedocromil sodium was ineffective.
摘要
  1. 中性粒细胞和嗜酸性粒细胞与变应原诱导的迟发性哮喘反应相关,浸润气道。这些细胞的动员通过脂类和蛋白类趋化因子发生。在本研究中,血小板活化因子(PAF)、白三烯B4(LTB4)、酵母聚糖激活血清(ZAS)和N-甲酰甲硫氨酰亮氨酰苯丙氨酸(FMLP)被用作这两类因子的示例。研究了人中性粒细胞和嗜酸性粒细胞的趋化作用。评估了奈多罗米钠和色甘酸钠的抑制作用。2. 所有测试的趋化因子均能吸引中性粒细胞,其活性顺序如下:ZAS>PAF=FMLP=LTB4。嗜酸性粒细胞仅被PAF、LTB4和ZAS动员,其活性顺序如下:ZAS>PAF>LTB4。3. 奈多罗米钠和色甘酸钠在抑制PAF诱导的中性粒细胞趋化作用方面,与PAF拮抗剂BN 52021活性相当(IC50约为10⁻⁸ M)。两种药物在抑制ZAS(IC5约为10⁻⁷ - 10⁻⁶ M)、FMLP(IC50约为10⁻⁷ M)和LTB4(IC50约为10⁻⁶ M)诱导的中性粒细胞趋化作用方面也同样有效。4. 奈多罗米钠显著抑制PAF(IC50约为10⁻⁶ M)和LTB4(IC50约为10⁻⁷ M)诱导的嗜酸性粒细胞趋化作用。BN 52021对PAF诱导的嗜酸性粒细胞趋化作用的抑制效力与奈多罗米钠相似。色甘酸钠不能对这些趋化反应产生显著抑制。然而,色甘酸钠显著抑制ZAS诱导的嗜酸性粒细胞趋化作用(IC50约为10⁻⁷ M),而奈多罗米钠无效。

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