Complex modulation of the cold receptor TRPM8 by volatile anaesthetics and its role in complications of general anaesthesia

Author:

Vanden Abeele Fabien1,Kondratskyi Artem1,Dubois Charlotte1,Shapovalov George1,Gkika Dimitra1,Busserolles Jérôme2,Shuba Yaroslav34,Skryma Roman1,Prevarskaya Natalia1

Affiliation:

1. Inserm U1003, Equipe labellisée par la Ligue Nationale Contre le Cancer, Laboratory of Excellence, Ion Channels Science and Therapeutics; Université des Sciences et Technologies de Lille (USTL), Villeneuve d'Ascq, France

2. Inserm UMR 1107, Clermont Université, Université d'Auvergne, Pharmacologie Fondamentale et Clinique de la Douleur, Faculté de Médecine, Clermont-Ferrand, France

3. Bogomoletz Institute of Physiology and International Centre of Molecular Physiology of the National Academy of Sciences of Ukraine, Kiev, Ukraine

4. State Key Laboratory of Molecular and Cellular Physiology, Kiev 01024, Ukraine

Abstract

Summary The mechanisms by which volatile general anaesthetics (VAs) produce a depression of central nervous system are beginning to be better understood, but little is known about a number of side effects. Here, we show that the cold receptor transient receptor potential melastatin 8 (TRPM8) undergoes a complex modulation by clinical concentrations of VAs in dorsal root ganglion neurons and HEK-293 cells heterologously expressing TRPM8. VAs produced a transient enhancement of TRPM8 through a depolarizing shift of its activation towards physiological membrane potentials, followed by a sustained TRPM8 inhibition. The stimulatory action of VAs engaged molecular determinants distinct from those used by the TRPM8 agonist. Transient TRPM8 activation by VAs could explain side effects such as inhibition of respiratory drive, shivering and the cooling sensation during the beginning of anaesthesia, whereas the second phase of VA action, that associated with sustained TRPM8 inhibition, might be responsible for hypothermia. Consistent with this, both hypothermia and the inhibition of respiratory drive induced by VAs are partially abolished in Trpm8-knockout animals. Thus, we propose TRPM8 as a new clinical target for diminishing common and serious complications of general anaesthesia.

Publisher

The Company of Biologists

Subject

Cell Biology

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