PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 8675151-4 1996 Dose-dependent increases in superoxide release, interleukin-1 (IL-1) release, and, within a relatively narrow range, prostaglandin-E2 (PGE2) release were observed in opsonized zymosan (oz)-stimulated HHMphi derived from both cirrhotic and noncirrhotic patients. Zymosan 176-183 interleukin 1 alpha Homo sapiens 63-67 8678906-2 1996 We demonstrate here that tenidap inhibits the zymosan-induced expression of both interleukin 1 and tumor necrosis factor alpha in macrophages, at the mRNA and protein levels. Zymosan 46-53 interleukin 1 alpha Homo sapiens 81-126 8386286-2 1993 In our basic studies, HHM phi increased dose dependently the release of superoxide (O2-) and interleukin-1 (IL-1) when stimulated by opsonized zymosan, up to 1000 micrograms/dish. Zymosan 143-150 interleukin 1 alpha Homo sapiens 93-112 8025949-10 1994 PB-PMNs in culture also showed mRNA expression for IL-1 alpha, IL-1 beta, and TNF alpha in a time- and dose-dependent manner, especially after stimulation with zymosan. Zymosan 160-167 interleukin 1 alpha Homo sapiens 51-61 8131658-4 1993 The production of IL-1 was tested through human monocytes stimulated with zymosan and measured by ELISA method; the activity of IL-1 was measured by its effect on the proliferation of murine thymocytes. Zymosan 74-81 interleukin 1 alpha Homo sapiens 18-22 2113649-9 1990 Zymosan or LPS stimulation of splenic cells from silicone- and PVC-loaded animals also secreted increased quantities of IL 1 as compared to controls. Zymosan 0-7 interleukin 1 alpha Homo sapiens 120-124 2357213-2 1990 Using overnight adherent macrophages, stimulation with lipopolysaccharide or zymosan caused a time-dependent increase in IL-1 production. Zymosan 77-84 interleukin 1 alpha Homo sapiens 121-125 2357213-3 1990 LTC4 was detected and preceded IL-1 production only in zymosan-treated macrophages. Zymosan 55-62 interleukin 1 alpha Homo sapiens 31-35 2999234-4 1985 Similarly, IL 1 production by monocytes stimulated with the known IL 1 inducers muramyl dipeptide, silica, or zymosan was also enhanced by LTB4. Zymosan 110-117 interleukin 1 alpha Homo sapiens 11-15 2801317-3 1989 E-5110 also inhibited the IL-1 generation induced by antigen-antibody complexes, opsonized zymosan and silica particles. Zymosan 91-98 interleukin 1 alpha Homo sapiens 26-30 3500253-6 1987 Pretreatment of the neutrophils with IL-1a augmented neutrophil oxygen radical production induced by opsonized zymosan, and this synergistic effect was evident as early as 10 min after IL-1a was added to the neutrophil culture. Zymosan 111-118 interleukin 1 alpha Homo sapiens 37-42 3500253-6 1987 Pretreatment of the neutrophils with IL-1a augmented neutrophil oxygen radical production induced by opsonized zymosan, and this synergistic effect was evident as early as 10 min after IL-1a was added to the neutrophil culture. Zymosan 111-118 interleukin 1 alpha Homo sapiens 185-190 3500253-7 1987 Phagocytosis of opsonized particles by neutrophils, and degranulation induced by opsonized zymosan were also enhanced by IL-1a in a dose-dependent manner. Zymosan 91-98 interleukin 1 alpha Homo sapiens 121-126 2999234-4 1985 Similarly, IL 1 production by monocytes stimulated with the known IL 1 inducers muramyl dipeptide, silica, or zymosan was also enhanced by LTB4. Zymosan 110-117 interleukin 1 alpha Homo sapiens 66-70 6325057-2 1984 The addition of bacterial lipopolysaccharides (LPS), quartz silica particles, zymosan, or phorbol myristate acetate (PMA) enhanced 3 to 50 times the overall production and 25 to 2000 times the release of IL-1. Zymosan 78-85 interleukin 1 alpha Homo sapiens 204-208 6325057-4 1984 During the same period of time, the addition of silica particles or PMA had clearly less effect while the addition of LPS or zymosan produced high levels of intracellular IL-1 but only a modest release of it. Zymosan 125-132 interleukin 1 alpha Homo sapiens 171-175