Record Display for the EPA National Library Catalog


Main Title Effect of Pentamidine on Cytokine (IL-1Beta, TNFalpha, IL-6) Production by Human Alveolar Macrophages In vitro.
Author Quay, J. ; Rosenthal, G. ; Becker, S. ;
CORP Author TRC Environmental Corp., Chapel Hill, NC.;Health Effects Research Lab., Research Triangle Park, NC. Human Studies Div.
Publisher cJul 93
Year Published 1993
Report Number EPA-68-D0-0110; EPA/600/J-94/540;
Stock Number PB95-148029
Additional Subjects Pentamidine ; Pharmacology ; Interleukin-1 ; Tumor necrosis factor ; Interleukin-6 ; Alveolar macrophages ; Glyceraldehydephosphate dehydrogenase ; Biosynthesis ; In vitro analysis ; Cell survival ; Lipopolysaccharides ; Post-translational protein processing ; Genetic transcription ; Northern blotting ; Polymerase chain reaction ; Messenger RNA ; Ornithine decarboxylase ; Kinetics ; Reprints ;
Library Call Number Additional Info Location Last
NTIS  PB95-148029 Some EPA libraries have a fiche copy filed under the call number shown. 07/26/2022
Collation 16p
Pentamidine (Pe) is an aromatic diamidine drug used clinically to treat Pneumocystis carinii pneumonia by aerosol inhalation. Nothing has been reported about the effects of this drug on human alveolar macrophage (AM) properties. In the study AM were exposed in vitro to various concentrations of Pe along or in combination with bacterial endotoxin (LPS). Super-natants were collected at 3, 6, and 24 h and assayed for secreted IL-1beta, IL-6, and TNFalpha. While the drug did not induce release of these cytokines, LPS-induced secretion of all three cytokines was inhibited by Pe in a dose-dependent manner. Reduced steady-state mRNA levels were found as early as 3 h after LPS stimulation, with Pe concentrations corresponding to those that decreased cytokine secretion. At the later time points, Pe also inhibited beta-actin, ornithine decarboxylase, and GAPDH mRNA expression, indicating that pentamidine had a general toxic effect on mRNA transcription in the macrophages. It is concluded that Pe, at pharmaceutically relevant concentrations and with apparent low cytotoxicity as determined by dye uptake, nonspecifically inhibits cytokine production by a toxic effect on transcriptional events.