Effect of chronic chloroquine administration on iron loading in the liver and reticuloendothelial system and on oxidative responses by the alveolar macrophages

• Published in: Biochemical pharmacology 1999-04, Vol.57 (8), p.907-911
• Main Authors: Legssyer, Rachida, Ward, Roberta J., Crichton, Robert R., Boelaert, Johan R.
• Format: Article
• Language: English
• Subjects: Animals; Antibiotics. Antiinfectious agents. Antiparasitic agents; Antiparasitic agents; Biological and medical sciences; Chloroquine - administration & dosage; Chloroquine - pharmacology; Iron - metabolism; iron loading, iron depletion, chloroquine, alveolar macrophages; Lipopolysaccharides; Liver - drug effects; Liver - metabolism; Macrophages, Alveolar - drug effects; Macrophages, Alveolar - metabolism; Male; Medical sciences; Mononuclear Phagocyte System - drug effects; Mononuclear Phagocyte System - metabolism; Nitrites - metabolism; Oxidation-Reduction; Pharmacology. Drug treatments; Rats; Rats, Wistar; Superoxide Dismutase - metabolism
• ISSN: 0006-2952; 1873-2968
• DOI: 10.1016/S0006-2952(98)00368-2

The ability of chloroquine to alter iron loading in the liver, spleen, and alveolar macrophages was investigated in iron-loaded or -depleted rats. Chloroquine significantly reduced incorporation of iron into the liver, spleen, and alveolar macrophages of animals loaded in vivo with iron dextran. The ability of these macrophages to respond to oxidative stress was assayed by their capacity to release reactive nitrogen intermediates after lipopolysaccharide (LPS) stimulation. A significant reduction in nitrite release was observed in primary cultures of macrophages isolated from chloroquine/iron dextran-administered rats in comparison to macrophages lavaged from rats iron-loaded alone. Macrophages isolated from iron-deficient rats showed a significant increase in nitrite after LPS stimulation, whereas nitrite release in the macrophages lavaged from the rats which had also received chloroquine during the iron depletion regime was much lower. These results indicate that the use of agents which decrease the iron content and diminish the oxidative response of the cell to altered iron status may be of therapeutic value in patients with iron loading, particularly of the reticuloendothelial system.