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Effects of Vancomycin and Ciprofloxacin on the NMRI Mouse Metabolism.

Abstract
The reduction in gut microbiota diversity is associated with a range of human diseases. Overuse of antibiotics has been associated with a diminished gut-microbial diversity in humans and may promote microbiota-associated negative effects to physical health, such as the metabolic syndrome-cluster of diseases and mental illnesses. There is a pressing need to deepen the understanding of the effects of antibiotics at the biochemical level. The current study investigated metabolic effects of two widely prescribed antibiotics-vancomycin and ciprofloxacin-on biofluids and brain tissue samples of NMRI female mice using a 1H nuclear magnetic resonance (NMR) spectroscopy-based metabolic profiling approach. While both antibiotics significantly affected the host metabolic signatures of urine and feces, only ciprofloxacin induced metabolic changes in plasma. Metabolic perturbations were pronounced 1 day post-treatment, reverting back to baseline at day 20 post-treatment. Both antibiotics induced changes in the choline metabolism, host-microbial cometabolites, short chain fatty acid production, and protein/purine degradation. The metabolic profiles of brain tissue aqueous extracts did not show any antibiotics-related changes by day 20 post-treatment. The data suggest that the metabolic disruptions in biofluids caused by antibiotics are reversed by day 20 post-treatment when compared to the pre-treatment profiles.
AuthorsZhigang Liu, Bing Xia, Jasmina Saric, Jürg Utzinger, Elaine Holmes, Jennifer Keiser, Jia V Li
JournalJournal of proteome research (J Proteome Res) Vol. 17 Issue 10 Pg. 3565-3573 (10 05 2018) ISSN: 1535-3907 [Electronic] United States
PMID30183313 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Anti-Bacterial Agents
  • Ciprofloxacin
  • Vancomycin
Topics
  • Animals
  • Anti-Bacterial Agents (pharmacology)
  • Body Fluids (drug effects)
  • Brain (drug effects, metabolism)
  • Ciprofloxacin (pharmacology)
  • Female
  • Gastrointestinal Microbiome (drug effects, physiology)
  • Humans
  • Magnetic Resonance Spectroscopy
  • Metabolome (drug effects)
  • Metabolomics (methods)
  • Mice
  • Mice, Inbred Strains
  • Vancomycin (pharmacology)

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