Depolarization of mouse DRG neurons by GABA does not translate into acute pain or hyperalgesia in healthy human volunteers

The majority of somatosensory DRG neurons express GABAA receptors (GABAAR) and depolarise in response to its activation based on the high intracellular chloride concentration maintained by the Na-K-Cl cotransporter type 1 (NKCC1). The translation of this response to peripheral nerve terminals in peo...

Full description

Saved in:
Bibliographic Details
Main Authors: Sohns, Kyra (Author) , Kostenko, Anna (Author) , Behrendt, Marc (Author) , Schmelz, Martin (Author) , Rukwied, Roman (Author) , Carr, Richard (Author)
Format: Article (Journal)
Language:English
Published: August 26, 2024
In: PLOS ONE
Year: 2024, Volume: 19, Issue: 8, Pages: 1-19
ISSN:1932-6203
DOI:10.1371/journal.pone.0307668
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1371/journal.pone.0307668
Verlag, kostenfrei, Volltext: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0307668
Get full text
Author Notes:Kyra Sohns, Anna Kostenko, Marc Behrendt, Martin Schmelz, Roman Rukwied, Richard Carr
Description
Summary:The majority of somatosensory DRG neurons express GABAA receptors (GABAAR) and depolarise in response to its activation based on the high intracellular chloride concentration maintained by the Na-K-Cl cotransporter type 1 (NKCC1). The translation of this response to peripheral nerve terminals in people is so far unclear. We show here that GABA (EC50 = 16.67μM) acting via GABAAR produces an influx of extracellular calcium in approximately 20% (336/1720) of isolated mouse DRG neurons. In contrast, upon injection into forearm skin of healthy volunteers GABA (1mM, 100μl) did not induce any overt sensations nor a specific flare response and did not sensitize C-nociceptors to slow depolarizing electrical sinusoidal stimuli. Block of the inward chloride transporter NKCC1 by furosemide (1mg/100μl) did not reduce electrically evoked pain ratings nor did repetitive GABA stimulation in combination with an inhibited NKCC1 driven chloride replenishment by furosemide. Finally, we generated a sustained period of C-fiber firing by iontophoretically delivering codeine or histamine to induce tonic itch. Neither the intensity nor the duration of histamine or codeine itch was affected by prior injection of furosemide. We conclude that although GABA can evoke calcium transients in a proportion of isolated mouse DRG neurons, it does not induce or modify pain or itch ratings in healthy human skin even when chloride gradients are altered by inhibition of the sodium coupled NKCC1 transporter.
Item Description:Gesehen am 11.02.2025
Physical Description:Online Resource
ISSN:1932-6203
DOI:10.1371/journal.pone.0307668