Current address: Merck & Co. Inc., Rahway, NJ 07065, USA.
Thymol and related alkyl phenols activate the hTRPA1 channel
Article first published online: 29 JAN 2009
2008 British Pharmacological Society
British Journal of Pharmacology
Volume 153, Issue 8, pages 1739–1749, April 2008
How to Cite
Lee, S. P., Buber, M. T., Yang, Q., Cerne, R., Cortés, R. Y., Sprous, D. G. and Bryant, R. W. (2008), Thymol and related alkyl phenols activate the hTRPA1 channel. British Journal of Pharmacology, 153: 1739–1749. doi: 10.1038/bjp.2008.85
- Issue published online: 29 JAN 2009
- Article first published online: 29 JAN 2009
- (Received December 4, 2007, Revised February 4, 2008, Accepted February 12, 2008)
- alkyl-substituted phenols;
- FLIPR assay;
- whole-cell electrophysiology;
- calcium imaging;
Background and purpose: Thymol, a major component of thyme and oregano, has medical uses in oral care products as an astringent and antibiotic. Its distinctive sharp odour and pungent flavour are considered aversive properties. The molecular basis of these aversive properties is not well understood.
Experimental approach: The ability of thymol to activate human transient receptor potential channel A1 (hTRPA1) expressed in stably transfected human embryonic kidney 293 (HEK293) cells was measured by membrane potential and calcium-sensitive dyes in a fluorescence-imaging plate reader (FLIPR) assay. Direct activation of hTRPA1 currents was measured by whole-cell voltage clamp recording. Intracellular calcium changes were measured using fura-2 dye. The FLIPR assay was also used to measure membrane potential changes elicited by thymol after pretreatment with camphor, a known TRPA1 inhibitor. The ability of related alkyl phenols to activate hTRPA1 was also determined.
Key results: Thymol potently activated a membrane potential response and intracellular calcium increase in hTRPA1-expressing HEK293 cells in a concentration-dependent manner. Activation by thymol desensitized hTRPA1 to further exposure to thymol or the known ligand allyl isothiocyanate (AITC). The related phenols 2-tert-butyl-5-methylphenol, 2,6-diisopropylphenol (propofol) and carvacrol also activated hTRPA1. Phenols with less bulky carbon substitutions and lower logP values were less potent in general. The response to thymol was blocked by camphor.
Conclusions and implications: These results suggest a role for hTRPA1 activation in the reported pungent and aversive properties of some of these pharmaceutically important phenols.
British Journal of Pharmacology (2008) 153, 1739–1749; doi:10.1038/bjp.2008.85; published online 10 March 2008