Pleiotropic Effects of the NSAID Fenamates on Chloride Channels: Opportunity for Ion Channelopathies?

Paola Laghetti1, Ilaria Saltarella1, Simone Dell'Atti1

  • 1Section of Pharmacology, Department of Precision and Regenerative Medicine, School of Medicine, University of Bari Aldo Moro, Bari, Italy.

Insights

Fenamates show diverse effects on chloride channels, offering potential for treating channelopathies. These drugs may activate or inhibit chloride channels, making them promising for new therapeutic development.

Area of Science:

  • Molecular biology
  • Pharmacology
  • Physiology

Background:

  • Chloride channels regulate vital cellular functions like volume, excitability, and secretion.
  • Dysfunction of chloride channels causes diseases known as channelopathies, including cystic fibrosis and epilepsy.
  • Fenamates, known for anti-inflammatory effects, are being investigated for repurposing to treat channelopathies.

Purpose of the Study:

  • To review the effects of specific fenamates (niflumic acid, flufenamic acid, mefenamic acid, meclofenamic acid, tolfenamic acid) on various chloride channels.
  • To explore the potential of fenamates as therapeutic agents for channelopathies.

Main Methods:

  • Narrative review of existing literature on fenamate activity on chloride channels.
  • Analysis of fenamate effects across different channel isoforms, cellular conditions, and tissue types.

Main Results:

  • Fenamates exhibit a broad spectrum of activity on multiple chloride channel types.
  • Their effects can be either activating or inhibitory, depending on concentration, channel isoform, and cellular context.
  • Niflumic acid, flufenamic acid, mefenamic acid, meclofenamic acid, and tolfenamic acid demonstrate varied modulatory actions.

Conclusions:

  • Fenamates possess versatile modulatory activity on chloride channels.
  • Their broad-spectrum effects suggest potential as lead compounds for developing novel drugs targeting channelopathies.
  • Further research into fenamate mechanisms could unlock new therapeutic strategies for these diseases.

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