Amiodarone and bepridil inhibit anthrax toxin entry into host cells

作者：Sanchez, Ana M.; Thomas, Diane; Gillespie, Eugene J.; Damoiseaux, Robert; Rogers, Joseph; Saxe, Jonathan P.; Huang, Jing; Manchester, Marianne; Bradley, Kenneth A.^*

来源：Antimicrobial Agents and Chemotherapy, 2007, 51(7): 2403-2411.

DOI：10.1128/AAC.01184-06

• T-LYMPHOCYTE ACTIVATION
• PROTEIN-KINASE-C
• LETHAL TOXIN
• EDEMA TOXIN
• ALVEOLAR MACROPHAGES
• PROTECTIVE ANTIGEN
• ADENYLATE-CYCLASE
• DENDRITIC CELLS
• RECEPTOR
• PHARMACOKINETICS

Anthrax lethal toxin is one of the fundamental components believed to be responsible for the virulence of Bacillus anthracis. In order to find novel compounds with anti-lethal toxin properties, we used a cell-based assay to screen a collection of approximately 500 small molecules. Nineteen compounds that blocked lethal toxin-mediated killing of RAW 264.7 macrophages were identified, and we report here on the characterization of the two most potent antitoxic compounds, amiodarone and bepridil. These drugs are used to treat cardiac arrhythmia or angina in humans at doses similar to those that provide protection against lethal toxin in vitro. Our results support a model whereby the antitoxic properties of both drugs result from their ability to block endosomal acidification, thereby blocking toxin entry. Amiodarone was tested in vivo and found to significantly increase survival of lethal toxin-challenged Fischer rats.

• 出版日期2007-7