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World J Biol Chem. May 26, 2011; 2(5): 98-104
Published online May 26, 2011. doi: 10.4331/wjbc.v2.i5.98
Published online May 26, 2011. doi: 10.4331/wjbc.v2.i5.98
Figure 2 Survival of B.
anthracis Sterne-challenged DBA/2 mice after treatment. Mice challenged with B. anthracis Sterne spores (i.p.) were treated (s.c.) with indicated daily bolus doses. A: A3R agonist Cl-IB-MECA (0.05, 0.15 and 0.3 mg/kg); B: combination of Cl-IB-MECA (0.05, 0.15 and 0.3 mg/kg) with ciprofloxacin (50 mg/kg); C, D: Caspase-1 inhibitor YVAD (C: 2.5 mg/kg; D: 12.5 mg/kg) in combination with ciprofloxacin (50 mg/kg); E: Triple combination of caspase-1 inhibitor YVAD (2.5 mg/kg), A3AR agonist Cl-IB-MECA (0.15 mg/kg) and ciprofloxacin (50 mg/kg); F: Triple combination of caspase-1 inhibitor YVAD (12.5 mg/kg), A3AR agonist Cl-IB-MECA (0.3 mg/kg) and ciprofloxacin (50 mg/kg). Kaplan–Meier statistical log-rank analysis was used for survival data.
- Citation: Popov SG, Popova TG, Kashanchi F, Bailey C. Targeting the inflammasome and adenosine type-3 receptors improves outcome of antibiotic therapy in murine anthrax. World J Biol Chem 2011; 2(5): 98-104
- URL: https://www.wjgnet.com/1949-8454/full/v2/i5/98.htm
- DOI: https://dx.doi.org/10.4331/wjbc.v2.i5.98