NONSTEROID ANTI-INFLAMMATORY AGENTS - REGULATORS OF PHAGOCYTIC SECRETION OF LYSOSOMAL ENZYMES FROM GUINEA-PIG NEUTROPHILS

  • 1 January 1978
    • journal article
    • research article
    • Vol. 207  (2) , 618-629
Abstract
Several nonsteroid anti-inflammatory agents were evaluated for their capacity to modulate phagocytosis by and lysosomal enzyme secretion from polymorphonuclear neutrophils. During cell contact with and phagocytosis of serum-treated zymosan particles, guinea-pig neutrophils demonstrated a selective extracellular release of lysosome granule-associated .beta.-glucuronidase and acid protease but not cytoplasmic lactate dehydrogenase. Ketoprofen, suprofen, diftalone, benoxaprofen and Abbott 29590 [2,3-dihydro-1H-pyridino-(2,3-b)(1,4)thiazine-2-one] inhibited particle uptake by and lysosomal enzyme release from neutrophils incubated with zymosan in Krebs-Ringer phosphate medium containing 7.5 mM glucose, pH 7.4, at 37.degree. C. Flazalone and sulindac were inactive. In the presence of cytochalasin B, an agent which inhibits phagocytosis while having no effect on the selective discharge of lysosomal enzymes, ketoprofen, suprofen, diftalone, benoxaprofen and Abbott 29590 continued to inhibit the release of .beta.-glucuronidase and acid protease from neutrophils. An investigation of the properties of guinea pig neutrophil acid protease activity revealed a pH optimum of 3.5. Activity was inhibited by diazoacetyl-DL-norleucine methyl ester and p-hydroxyphenylpyruvic acid. Sulfhydryl inhibitors, chelating agents and soybean trypsin inhibitor had no effect on neutrophil acid protease activity. Certain nonsteroid anti-inflammatory agents may function as regulators of the phagocytic secretion of lysosomal enzymes from neutrophils; these neutrophils apparently contain an acid protease which resembles an enzyme known to mediate tissue destruction in several inflammatory diseases.