Modulation of the cold-activated channel TRPM8 by lysophospholipids and polyunsaturated fatty acids

David A. Andersson, Mark Nash, Stuart Bevan

Research output: Contribution to journalArticlepeer-review

149 Scopus citations


We investigated the role of phospholipase A2 (PLA2) and the effects of PLA2 products (polyunsaturated fatty acids and lysophospholipids) on the cold-sensitive channel transient receptor potential (melastatin)-8 (TRPM8), heterologously expressed in Chinese hamster ovary cells. TRPM8 responses to cold and the agonist icilin were abolished by inhibitors of the calcium-independent (iPLA2) form of the enzyme, whereas responses to menthol were less sensitive to iPLA2 inhibition. Inhibition of PLA2 similarly abolished the cold responses of the majority of cold-sensitive dorsal root ganglion neurons. The products of PLA2 had opposing effects on TRPM8. Lysophospholipids (LPLs) (lysophosphatidylcholine, lysophosphatidylinositol, and lysophosphatidylserine) altered the thermal sensitivity of TRPM8, raising the temperature threshold toward normal body temperature. Polyunsaturated fatty acids (PUFAs), such as arachidonic acid, inhibited the activation of TRPM8 by cold, icilin, and menthol. The relative potencies of lysophospholipids and PUFAs are such that lysophosphatidylcholine is able to modulate TRPM8 in the presence of an equimolar concentration of arachidonic acid. Positive modulation by LPLs provides a potential physiological mechanism for sensitizing and activating TRPM8 in the absence of temperature variations.

Original languageEnglish (US)
Pages (from-to)3347-3355
Number of pages9
JournalJournal of Neuroscience
Issue number12
StatePublished - Mar 21 2007
Externally publishedYes


  • Arachidonic acid
  • Icilin
  • Lysophospholipid
  • Menthol
  • Phospholipase A2
  • TRPM8

ASJC Scopus subject areas

  • Neuroscience(all)


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