Luebbert, Matthias and Kyereme, Jessica and Schoebel, Nicole and Beltran, Leopoldo and Wetzel, Christian Horst and Hatt, Hanns (2013) Transient Receptor Potential Channels Encode Volatile Chemicals Sensed by Rat Trigeminal Ganglion Neurons. PLOS ONE, 8 (10): e77998. ISSN 1932-6203,
Full text not available from this repository. (Request a copy)Abstract
Primary sensory afferents of the dorsal root and trigeminal ganglia constantly transmit sensory information depicting the individual's physical and chemical environment to higher brain regions. Beyond the typical trigeminal stimuli (e. g. irritants), environmental stimuli comprise a plethora of volatile chemicals with olfactory components (odorants). In spite of a complete loss of their sense of smell, anosmic patients may retain the ability to roughly discriminate between different volatile compounds. While the detailed mechanisms remain elusive, sensory structures belonging to the trigeminal system seem to be responsible for this phenomenon. In order to gain a better understanding of the mechanisms underlying the activation of the trigeminal system by volatile chemicals, we investigated odorant-induced membrane potential changes in cultured rat trigeminal neurons induced by the odorants vanillin, heliotropyl acetone, helional, and geraniol. We observed the dose-dependent depolarization of trigeminal neurons upon application of these substances occurring in a stimulus-specific manner and could show that distinct neuronal populations respond to different odorants. Using specific antagonists, we found evidence that TRPA1, TRPM8, and/or TRPV1 contribute to the activation. In order to further test this hypothesis, we used recombinantly expressed rat and human variants of these channels to investigate whether they are indeed activated by the odorants tested. We additionally found that the odorants dose-dependently inhibit two-pore potassium channels TASK1 and TASK3 heterologously expressed In Xenopus laevis oocytes. We suggest that the capability of various odorants to activate different TRP channels and to inhibit potassium channels causes neuronal depolarization and activation of distinct subpopulations of trigeminal sensory neurons, forming the basis for a specific representation of volatile chemicals in the trigeminal ganglia.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | DOMAIN POTASSIUM CHANNELS; BACKGROUND K+ CHANNEL; TRP CHANNELS; SENSORY NEURONS; CAPSAICIN RECEPTOR; ION-CHANNEL; DIRECT ACTIVATION; CATION CHANNEL; CALCIUM-IONS; PAIN; |
| Subjects: | 600 Technology > 610 Medical sciences Medicine |
| Divisions: | Medicine > Lehrstuhl für Psychiatrie und Psychotherapie |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 31 Mar 2020 07:20 |
| Last Modified: | 31 Mar 2020 07:20 |
| URI: | https://pred.uni-regensburg.de/id/eprint/15837 |
Actions (login required)
![]() |
View Item |

