Cardiotoxic effect of levofloxacin and ciprofloxacin in rats with/without acute myocardial infarction: Impact on cardiac rhythm and cardiac expression of Kv4.3, Kv1.2 and Nav1.5 channels

Biomed Pharmacother. 2017 Aug:92:196-206. doi: 10.1016/j.biopha.2017.05.049. Epub 2017 May 22.

Abstract

Prolongation of QT interval is possible with fluoroquinolones, yet the underlying contributing factors have not been elucidated. Two widely used fluoroquinolone drugs were at the focus of this study in rats with/without acute myocardial dysfunction (AMI) induced by isoproterenol. The effects of levofloxacin and ciprofloxacin on the cardiac mRNA expression of rat Kv4.3, Kv1.2 and Nav1.5 mRNAs were determined. Administration of the two antibiotics produced dose-dependent changes in ECG parameters that were more prominent in rats with AMI than healthy rats; this was accompanied by elevations in serum lactate dehydrogenase and creatine kinase-MB. Histopathological examination indicated some loss of striations, edema and fibrotic changes in rats with AMI; however the two antibiotics did not further exacerbate the cardiac histopathology. mRNA expression of the ion channels was altered in rats with AMI and healthy rats. In conclusion, long-term administration of levofloxacin and ciprofloxacin produced deleterious effects on the ECG pattern of rats with/without AMI. The effect was generally baseline-dependent and therefore, rats with AMI showed greater ECG disturbances and increases in cardiac enzymes. Taken together, these data make it advisable to monitor patients with a history of acute AMI requiring treatment with these antibiotics until data from human studies are available.

Keywords: Acute myocardial infarction; Cardiac ion channels; Ciprofloxacin; ECG; Levofloxacin; Rat.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Anti-Bacterial Agents / toxicity
  • Cardiotoxins / toxicity*
  • Ciprofloxacin / toxicity*
  • Dose-Response Relationship, Drug
  • Electrocardiography / drug effects
  • Gene Expression
  • Heart Rate / drug effects
  • Heart Rate / physiology
  • Kv1.2 Potassium Channel / biosynthesis*
  • Kv1.2 Potassium Channel / genetics
  • Levofloxacin / toxicity*
  • Male
  • Myocardial Infarction / chemically induced
  • Myocardial Infarction / genetics
  • Myocardial Infarction / physiopathology*
  • NAV1.5 Voltage-Gated Sodium Channel / biosynthesis*
  • NAV1.5 Voltage-Gated Sodium Channel / genetics
  • Rats
  • Rats, Wistar
  • Shal Potassium Channels / biosynthesis*
  • Shal Potassium Channels / genetics

Substances

  • Anti-Bacterial Agents
  • Cardiotoxins
  • Kv1.2 Potassium Channel
  • NAV1.5 Voltage-Gated Sodium Channel
  • Scn5a protein, rat
  • Shal Potassium Channels
  • Ciprofloxacin
  • Levofloxacin