作者: George Ku , Niall S. Doherty , Lisa F. Schmidt , Richard L. Jackson , Robert J. Dinerstein
DOI: 10.1096/FASEBJ.4.6.2318380
关键词: Lipopolysaccharide 、 Interleukin 、 Immunology 、 Prostaglandin 、 Pharmacology 、 Interleukin 2 、 Probucol 、 Interleukin 3 、 Secretion 、 Chemistry 、 Tumor necrosis factor alpha 、 Biotechnology 、 Genetics 、 Biochemistry 、 Molecular biology
摘要: Probucol, 4,4'-(isopropylidenedithio)bis(2,6-di-tert-butyl-phenol), has been shown to inhibit atherogenesis in genetically hypercholesterolemic (Watanabe) rabbits. Since atherosclerotic lesions contain macrophages capable of screting interleukin 1 (IL 1) and other cytokines that could contribute the pathogenesis disease, we have investigated whether probucol affects IL secretion. Resident peritoneal from mice dosed with secreted 40-80% less than control animals when stimulated vitro lipopolysaccharide (LPS). The inhibitory effect was observed assayed by standard bioassay, thymocyte proliferation assay, or a competitive receptor binding assay. Probucol treatment had no on LPS-induced membrane expression; secretion tumor necrosis factor (TNF); Con A-induced splenic 2 2) 3 3) release; prostaglandin- zymosan-induced prostacyclin, leukotrie...