Effects of flavonoid-induced oxidative stress on anti-H5N1 influenza a virus activity exerted by baicalein and biochanin A

BMC Res Notes. 2014 Jun 23:7:384. doi: 10.1186/1756-0500-7-384.

Abstract

Background: Different flavonoids are known to interfere with influenza A virus replication. Recently, we showed that the structurally similar flavonoids baicalein and biochanin A inhibit highly pathogenic avian H5N1 influenza A virus replication by different mechanisms in A549 lung cells. Here, we investigated the effects of both compounds on H5N1-induced reactive oxygen species (ROS) formation and the role of ROS formation during H5N1 replication.

Findings: Baicalein and biochanin A enhanced H5N1-induced ROS formation in A549 cells and primary human monocyte-derived macrophages. Suppression of ROS formation induced by baicalein and biochanin A using the antioxidant N-acetyl-L-cysteine strongly increased the anti-H5N1 activity of both compounds in A549 cells but not in macrophages.

Conclusions: These findings emphasise that flavonoids induce complex pharmacological actions some of which may interfere with H5N1 replication while others may support H5N1 replication. A more detailed understanding of these actions and the underlying structure-activity relationships is needed to design agents with optimised anti-H5N1 activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcysteine* / pharmacology
  • Anticarcinogenic Agents / pharmacology
  • Antioxidants / pharmacology
  • Antiviral Agents / pharmacology
  • Cell Line, Tumor
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Drug Synergism
  • Flavanones / pharmacology*
  • Flavonoids / pharmacology*
  • Genistein / pharmacology*
  • Host-Pathogen Interactions / drug effects
  • Humans
  • Influenza A Virus, H5N1 Subtype / drug effects*
  • Influenza A Virus, H5N1 Subtype / physiology
  • Lung Neoplasms / metabolism
  • Lung Neoplasms / pathology
  • Lung Neoplasms / virology
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Macrophages / virology
  • Monocytes / drug effects
  • Monocytes / metabolism
  • Monocytes / virology
  • Oxidative Stress / drug effects*
  • Reactive Oxygen Species / metabolism
  • Virus Replication / drug effects

Substances

  • Anticarcinogenic Agents
  • Antioxidants
  • Antiviral Agents
  • Flavanones
  • Flavonoids
  • Reactive Oxygen Species
  • baicalein
  • Genistein
  • biochanin A
  • Acetylcysteine