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Title
Control of sensory neuron excitability by serotonin involves 5HT2C receptors and Ca2+-activated chloride channels
AuthorBoehm, Stefan ; Yousuf, Arsalan ; Gantumur, Enkhbileg ; Salzer, Isabella
Published in
Neuropharmacology, Oxford, 2016, Vol. 110, page 277-286
PublishedOxford : Elsevier, 2016
LanguageEnglish
Document typeJournal Article
Keywords (EN)dorsal root ganglion neurons / 5ht2 receptors / trpv1 channels / ca2+-activated chloride channels / ttx-resistant na+ channels / kv7 k+ channels / molecular-mechanisms / analgesic flupirtine / sodium current / anoctamin 1 / activation / pain / trpv1 / nociceptors
Project-/ReportnumberW 1205-B09
ISSN0028-3908
URNurn:nbn:at:at-ubmuw:3-1393 Persistent Identifier (URN)
DOI10.1016/j.neuropharm.2016.08.006 
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Control of sensory neuron excitability by serotonin involves 5HT2C receptors and Ca2+-activated chloride channels [1.43 mb]
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Abstract (English)

Serotonin (5HT) is a constituent of the so-called "inflammatory soup" that sensitizes nociceptors during inflammation. Nevertheless, receptors and signaling mechanisms that mediate an excitation of dorsal root ganglion (DRG) neurons by 5HT remained controversial. Therefore, capsaicin-sensitive nociceptive neurons dissociated from rat DRGs were used to investigate effects of 5HT on membrane excitability and currents through ligand- as well as voltage-gated ion channels. In 58% of the neurons tested, 5HT increased action potential firing, an effect that was abolished by the 5HT2 receptor antagonist ritanserin, but not by the 5HT3 antagonist tropisetron. Unlike other algogenic mediators, such as PGE2 and bradykinin, 5HT did not affect currents through TTX-resistant Na+ channels or Kv7 K+ channels. In all neurons investigated, 5HT potentiated capsaicin-evoked currents through TRPV1 channels, an effect that was attenuated by antagonists at 5HT2A (4 F 4 PP), 5HT2B (SB 204741), as well as 5HT2C (RS 102221) receptors. 5HT triggered slowly arising inward Cl- currents in 53% of the neurons. This effect was antagonized by the 5HT2C receptor blocker only, and the current was prevented by an inhibitor of Ca2+-activated chloride channels (CaCC). The 5HT-induced increase in action potential firing was also abolished by this CaCC blocker and by the TRPV1 inhibitor capsazepine. Amongst the subtype selective 5HT2 antagonists, only RS 102221 (5HT2C-selectively) counteracted the rise in action potential firing elicited by 5HT. These results show that 5HT excites DRG neurons mainly via 5HT2C receptors which concomitantly mediate a sensitization of TRPV1 channels and an opening of CaCCs. (C) 2016 The Authors. Published by Elsevier Ltd.

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