Kurosawa Motohiro, Ishizuka Tamotsu
Int Arch Allergy Immunol. 1993;100(1):28-34. doi: 10.1159/000236383.
Effects of vasoactive intestinal peptide (VIP) on superoxide anion (O2-) formation by N-formyl-methionyl-leucyl-phenylalanine (fMLP)-activated inflammatory cells from healthy volunteers were investigated using 2-methyl-6-[p-methoxyphenyl]-3,7-dihydroimidazo [1,2-a]pyrazin-3-one (MCLA) as a chemiluminescence probe. VIP inhibited the maximal light intensity of MCLA-dependent luminescence in a dose-dependent manner by the activated peripheral blood neutrophils, mononuclear cells and also by the human monoblast cell line U937, the capacity of which for O2- formation was induced by pretreatment with interferon-gamma. 3 x 10(-6) M VIP also inhibited O2- formation by the activated peripheral blood eosinophils and alveolar macrophages obtained by bronchoalveolar lavage.
采用2-甲基-6-[对甲氧基苯基]-3,7-二氢咪唑并[1,2-a]吡嗪-3-酮(MCLA)作为化学发光探针,研究了血管活性肠肽(VIP)对健康志愿者来源的经N-甲酰甲硫氨酰亮氨酰苯丙氨酸(fMLP)激活的炎症细胞产生超氧阴离子(O2-)的影响。VIP以剂量依赖的方式抑制了活化的外周血中性粒细胞、单核细胞以及人单核细胞系U937(其产生O2-的能力经γ干扰素预处理诱导)所引起的依赖MCLA的发光的最大光强度。3×10(-6) M的VIP还抑制了活化的外周血嗜酸性粒细胞以及通过支气管肺泡灌洗获得的肺泡巨噬细胞产生O2-。