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Activation of TRESK channels by the inflammatory mediator lysophosphatidic acid balances nociceptive signalling

Please always quote using this URN: urn:nbn:de:bvb:20-opus-148312
  • In dorsal root ganglia (DRG) neurons TRESK channels constitute a major current component of the standing outward current IK\(_{SO}\). A prominent physiological role of TRESK has been attributed to pain sensation. During inflammation mediators of pain e.g. lysophosphatidic acid (LPA) are released and modulate nociception. We demonstrate co-expression of TRESK and LPA receptors in DRG neurons. Heterologous expression of TRESK and LPA receptors in Xenopus oocytes revealed augmentation of basal K\(^{+}\) currents upon LPA application. In DRGIn dorsal root ganglia (DRG) neurons TRESK channels constitute a major current component of the standing outward current IK\(_{SO}\). A prominent physiological role of TRESK has been attributed to pain sensation. During inflammation mediators of pain e.g. lysophosphatidic acid (LPA) are released and modulate nociception. We demonstrate co-expression of TRESK and LPA receptors in DRG neurons. Heterologous expression of TRESK and LPA receptors in Xenopus oocytes revealed augmentation of basal K\(^{+}\) currents upon LPA application. In DRG neurons nociception can result from TRPV\(_{1}\) activation by capsaicin or LPA. Upon co-expression in Xenopus oocytes LPA simultaneously increased both depolarising TRPV\(_{1}\) and hyperpolarising TRESK currents. Patch-clamp recordings in cultured DRG neurons from TRESK[wt] mice displayed increased IK\(_{SO}\) after application of LPA whereas under these conditions IK\(_{SO}\) in neurons from TRESK[ko] mice remained unaltered. Under current-clamp conditions LPA application differentially modulated excitability in these genotypes upon depolarising pulses. Spike frequency was attenuated in TRESK[wt] neurons and, in contrast, augmented in TRESK[ko] neurons. Accordingly, excitation of nociceptive neurons by LPA is balanced by co-activation of TRESK channels. Hence excitation of sensory neurons is strongly controlled by the activity of TRESK channels, which therefore are good candidates for the treatment of pain disorders.show moreshow less

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Metadaten
Author: Sina Kollert, Benjamin Dombert, Frank Döring, Erhard Wischmeyer
URN:urn:nbn:de:bvb:20-opus-148312
Document Type:Journal article
Faculties:Medizinische Fakultät / Institut für Klinische Neurobiologie
Medizinische Fakultät / Physiologisches Institut
Language:English
Parent Title (English):Scientific Reports
Year of Completion:2015
Volume:5
Issue:12548
Source:Scientific Reports 5:12548 (2015). DOI: 10.1038/srep12548
DOI:https://doi.org/10.1038/srep12548
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Tag:2-pore potassium channel; cells; domain K\(^{+}\) channels; initiation; migraine; modulation; molecular mechanisms; neuropathic pain; protein coupled receptors; sensory neurons
Release Date:2018/11/13
Licence (German):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International