Strauss R R, Paul B B, Sbarra A J
J Bacteriol. 1968 Dec;96(6):1982-90. doi: 10.1128/jb.96.6.1982-1990.1968.
The anti-inflammatory drug phenylbutazone has been found to inhibit both engulfment and intracellular killing of E. coli by guinea pig peritoneal polymorphonuclear (PMN) leukocytes. The bactericidal activity of leukocytic homogenates was also inhibited by the drug. Addition of the drug at various time intervals to a phagocytic reacting system caused an almost immediate cessation of bactericidal activity. Metabolic studies showed that the drug sharply curtailed glucose-l-(14)C and (14)C-formate oxidation of both resting and phagocytizing PMN leukocytes. These data indicated an effect upon the hexose monophosphate shunt and H(2)O(2) formation. Further investigation showed that the sites of inhibition were on glucose-6-phosphate and 6-phosphogluconate dehydrogenase. These inhibitions resulted in decreased H(2)O(2) production. It is suggested that H(2)O(2) activates lysosomes and subsequently complexes with the lysosomal enzyme, myeloperoxidase. This complex is a potent bactericidal agent in the phagocyte.
已发现抗炎药保泰松可抑制豚鼠腹腔多形核(PMN)白细胞对大肠杆菌的吞噬及细胞内杀伤作用。该药物还能抑制白细胞匀浆的杀菌活性。在吞噬反应系统的不同时间间隔添加该药物,几乎会立即导致杀菌活性停止。代谢研究表明,该药物显著减少了静息及吞噬状态下PMN白细胞对葡萄糖 - l -(14)C和(14)C - 甲酸的氧化。这些数据表明其对磷酸己糖旁路和H₂O₂形成有影响。进一步研究表明,抑制位点位于葡萄糖 - 6 - 磷酸脱氢酶和6 - 磷酸葡萄糖酸脱氢酶。这些抑制导致H₂O₂生成减少。有人提出,H₂O₂可激活溶酶体,并随后与溶酶体酶髓过氧化物酶结合。这种复合物是吞噬细胞中一种有效的杀菌剂。