Effects of acute administration of O,O,S-trimethyl phosphorothioate on the respiratory burst and phagocytic activity of splenic and peritoneal leukocytes
- 1 June 1988
- journal article
- research article
- Published by Springer Nature in Inflammation Research
- Vol. 24 (1-2) , 152-160
- https://doi.org/10.1007/bf01968094
Abstract
An impurity in malathion, O,O,S-trimethyl phosphorothioate (OOS-TMP), was previously shown to be immunosuppressive. The immune cell type which induced immune suppression caused by OOS-TMP at 24 hrs after administration was found to be splenic macrophages. Further characterization of macrophages from OOS-TMP treated mice indicated that OOS-TMP led to macrophage differentiation. In this study, these initial studies were continued and extended to examine the effects of OOS-TMP on splenic and peritoneal macrophages at various times following exposure. Administration of OOS-TMP increased the size heterogeneity of cell volume, phagocytic capability and respiratory burst activity of splenic and peritoneal macrophages. However, by day 7 splenic and peritoneal macrophages from similar to control. These data would suggest that macrophages not previously exposed to OOS-TMP migrated to the spleen and peritoneum of treated animals. This migration may allow the restoration of the ability of splenocytes from treated animals to generate an immune response. Alternatively, these data may indicate that 7 days following exposure to OOS-TMP, the differentiative state of the splenic and peritoneal macrophages of treated mice had decayed and hence these cells had regained resident characteristics.Keywords
This publication has 28 references indexed in Scilit:
- Investigations into the mechanism of immunosuppression caused by acute treatment with O,O,S-trimethyl phosphorothioate: Generation of suppressive macrophages from treated animals*1Toxicology and Applied Pharmacology, 1987
- Macrophage membrane proteins: Possible role in the regulation of priming for enhanced respiratory burst activityCellular Immunology, 1986
- Evidence for role of hydroxyl radical in complement and neutrophil-dependent tissue injury.Journal of Clinical Investigation, 1983
- Effect of drug metabolism inducer and inhibitor on O,O,S-trimethyl phosphorothioate-induced delayed toxicity in ratsChemico-Biological Interactions, 1983
- Demonstration of a soluble mediator that induces exudates rich in Ia-positive macrophages.The Journal of Experimental Medicine, 1980
- Toxicity of O,O,S-trimethyl and triethyl phosphorothioate to the ratJournal of Agricultural and Food Chemistry, 1979
- Hepatic and extrahepatic malathion carboxylesterases. Assay and localization in the ratToxicology and Applied Pharmacology, 1979
- Increased superoxide anion production by immunologically activated and chemically elicited macrophagesThe Journal of Experimental Medicine, 1978
- Hydrogen peroxide release from mouse peritoneal macrophages: dependence on sequential activation and triggering.The Journal of Experimental Medicine, 1977
- Effect of impurities on the mammalian toxicity of technical malathion and acephateJournal of Agricultural and Food Chemistry, 1977