JMF2-1, a lidocaine derivative acting on airways spasm and lung allergic inflammation in rats

J Allergy Clin Immunol. 2007 Jan;119(1):219-25. doi: 10.1016/j.jaci.2006.08.037. Epub 2006 Oct 13.


Background: Prior reports show that nebulized lidocaine might be an effective treatment for asthma.

Objective: We sought to determine the anti-inflammatory and spasmolytic effects of lidocaine and its analogue, JMF2-1, which we have synthesized for reduced local anesthetic activity.

Methods: Blockade of Na(+) currents was assayed in cultured GH(3) cells by using the patch-clamp technique, whereas anesthesia was assessed in a cutaneous pinching test in rats. Lidocaine and its analogue were nebulized into sensitized rats for evaluation of their effectiveness on airways spasm and inflammation induced by methacholine and allergen, respectively. Tissue histamine release and tracheal spasm triggered by allergen challenge in the absence and presence of these treatments were also examined in vitro.

Results: The 50% inhibitory concentration values for blockade of Na(+) currents after treatment with JMF2-1 (25.4 mM) was remarkably higher than that of lidocaine (0.18 mM), which is consistent with the weak anesthetic capacity of this analogue. In contrast, JMF2-1 was more potent than lidocaine in inhibiting allergen-induced histamine release and tracheal spasm. In in vivo settings methacholine-induced increase in lung resistance (145%) significantly reduced to 72% and 47% after lidocaine and JMF2-1 treatment, respectively. Both treatments inhibited by about 81% allergen-evoked eosinophil accumulation into the lung tissue.

Conclusion: Replacement of the 2,6-dimethyl radicals by the 2-trifluormethyl group on the benzene ring of lidocaine significantly reduces anesthetic activity, preserving its ability to prevent key aspects of the allergic inflammatory response in the lung.

Clinical implications: Nebulized JMF2-1 might be a means of achieving the antiasthmatic effects of lidocaine without the anesthetic effects.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anesthetics / pharmacology
  • Animals
  • Anti-Asthmatic Agents / pharmacology*
  • Anti-Inflammatory Agents / pharmacology*
  • Cell Line
  • Histamine / metabolism
  • Leukocyte Count
  • Lidocaine / analogs & derivatives*
  • Lidocaine / pharmacology*
  • Lung / drug effects
  • Lung / immunology
  • Lung / physiopathology
  • Mice
  • Ovalbumin
  • Rats
  • Rats, Wistar
  • Respiratory Hypersensitivity / chemically induced
  • Respiratory Hypersensitivity / drug therapy*
  • Respiratory Hypersensitivity / immunology
  • Respiratory Hypersensitivity / physiopathology
  • Seizures / chemically induced
  • Sodium Channel Blockers / pharmacology
  • Sodium Channels / physiology
  • Trachea / drug effects
  • Trachea / physiopathology


  • Anesthetics
  • Anti-Asthmatic Agents
  • Anti-Inflammatory Agents
  • Sodium Channel Blockers
  • Sodium Channels
  • Histamine
  • Ovalbumin
  • Lidocaine