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Atrial natriuretic peptide inhibits nitric oxide synthesis in mouse macrophages
Institution:1. Research Centre on Aging, University of Sherbrooke, Sherbrooke, Faculty of Medicine and Health Sciences, Quebec J1H 5N4, Canada;2. Dept. Physiology and Biophysics, University of Sherbrooke, Sherbrooke, Faculty of Medicine and Health Sciences, Quebec J1H 5N4, Canada;3. Dept. of Orthopedic Surgery, University of Sherbrooke, Sherbrooke, Faculty of Medicine and Health Sciences, Quebec J1H 5N4, Canada;4. CHUS Research Center, University of Sherbrooke, Sherbrooke, Faculty of Medicine and Health Sciences, Quebec J1H 5N4, Canada
Abstract:The atrial natriuretic peptide (ANP) affects cardiovascular physiology, and, as has been suggested more recently, exerts immunomodulatory activities. In this context, we examined the effect of ANP on nitric oxide (NO) synthesis in murine bone marrow derived macrophages as well as in peritoneal macrophages. Cultured macrophages were stimulated with lipopolysaccharides (LPS 0.1–10 μg/ml) and NO synthesis was monitored by measuring increased concentrations of NO2 in the medium. In initial experiments employment of NG-monomethyl-L-arginine (L-NMMA) and dexamethasone, two specific inhibitors of nitric oxide synthase (NOS), confirmed the presence of inducible NOS activity in the cells. Exposure of cells to rat ANP99–126 in the range of 10?8 to 10?6 M significantly decreased LPS induced NO synthesis over 24 hours of incubation. Thus, ANP may alter macrophage function by affecting their nitric oxide synthesizing pathway.
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