Hepatic changes produced by 30-day administration of a novel aminocyclitol antibiotic, trospectomycin sulfate, to laboratory animals

• Published in: Fundamental and applied toxicology Vol. 14; no. 1; p. 60
• Main Authors: Ulrich, R G, Petrella, D K, Larsen, E R, Cox, J W, Cramer, C T, Piper, R C, Gray, J E
• Format: Journal Article
• Language: English
• Published: United States 01-01-1990
• Subjects: Acid Phosphatase - analysis; Alanine Transaminase - blood; Animals; Anti-Infective Agents - toxicity; Aspartate Aminotransferases - blood; Dogs; Female; Liver - drug effects; Liver - ultrastructure; Male; Rats; Rats, Inbred Strains; Spectinomycin - analogs & derivatives; Spectinomycin - toxicity
• ISSN: 0272-0590
• DOI: 10.1016/0272-0590(90)90231-8

The studies described here were done to characterize the hepatic response to a new aminocyclitol antibiotic, trospectomycin sulfate, administered intravenously (beagle dog) or subcutaneously (Sprague-Dawley rat) at a variety of dose levels, to investigate reversibility of observed changes, and to document any untoward effects of subchronic trospectomycin sulfate administration. Both species showed significant elevations in serum levels of alanine and aspartate transaminases in higher dose groups. In the dog only, a transient neuromuscular blockade was also observed within higher dose groups. No other functional, morphological, or serum chemical changes were observed. Examination of liver by electron microscopy revealed the presence of cytoplasmic lamellar inclusion bodies, concentrated in the bile canalicular region of the hepatocytes. Occurrence of the lamellar bodies and coincident transaminase increases were found to be reversible upon discontinuance of treatment (studied in the dog). Electron microscopy of acid phosphatase cytochemistry in the rat indicated that most, but not all, of the lamellar bodies contained this enzyme. This observation suggests that they may be derived from the lysosome, or once formed become lysosomal.