Sturm R J, Holloway D A, Buckley S, Osborne M C, Grimes D, Weichman B M, Rimele T J
Division of Immunopharmacology, Wyeth-Ayerst Research, Princeton, NJ 08543-8000.
Agents Actions. 1989 Jun;27(3-4):414-7. doi: 10.1007/BF01972838.
A neutrophil-derived relaxing factor (NDRF) from oyster glycogen (OG)-elicited rat PMN, which causes an endothelium independent relaxation of rat aorta, and which is pharmacologically indistinguishable from endothelium-derived relaxing factor (EDRF) has been described. Experiments were designed to evaluate the presence of NDRF in PMN from rat -whole blood, -carrageenan pleurisy, -OG peritonitis, and guinea pig (GP) -OG peritonitis, as well as in OG-elicited rat macrophages (M phi). Significant vascular relaxing activity was found using rat PMN from OG peritonitis and carrageenan pleurisy, as well as from OG-M phi. Little or no activity was found in rat whole blood PMN or PMN from GP-OG peritonitis. These results suggest that NDRF activity may be expressed upon cellular migration to an inflammatory site in the rat, and may not be present in all species. Also, all inflammatory cells examined were capable of reversing EDRF-dependent relaxations when stimulated to produce superoxide anion suggesting a dual regulatory role for these cells on local vascular tone.
已报道从牡蛎糖原(OG)诱导的大鼠多形核白细胞(PMN)中分离出一种嗜中性粒细胞衍生的舒张因子(NDRF),它可引起大鼠主动脉的非内皮依赖性舒张,并且在药理学上与内皮衍生的舒张因子(EDRF)无法区分。设计实验以评估大鼠全血、角叉菜胶性胸膜炎、OG性腹膜炎的PMN以及豚鼠(GP)OG性腹膜炎的PMN中NDRF的存在情况,同时也评估OG诱导的大鼠巨噬细胞(M phi)中NDRF的存在情况。使用来自OG性腹膜炎、角叉菜胶性胸膜炎以及OG-M phi的大鼠PMN发现了显著的血管舒张活性。在大鼠全血PMN或GP-OG性腹膜炎的PMN中几乎未发现或未发现活性。这些结果表明,NDRF活性可能在细胞迁移至大鼠炎症部位时表达,且可能并非在所有物种中都存在。此外,所有检测的炎症细胞在被刺激产生超氧阴离子时都能够逆转EDRF依赖性舒张,这表明这些细胞对局部血管张力具有双重调节作用。