Experimental Pain Research, MCTN, Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany.
PLoS One. 2024 Aug 26;19(8):e0307668. doi: 10.1371/journal.pone.0307668. eCollection 2024.
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.
大多数躯体感觉 DRG 神经元表达 GABAA 受体(GABAAR),并基于由 Na-K-Cl 共转运蛋白 1(NKCC1)维持的高细胞内氯离子浓度,对其激活产生去极化反应。迄今为止,这种反应在人体周围神经末梢的转化尚不清楚。我们在这里表明,GABA(EC50=16.67μM)通过 GABAAR 作用会导致大约 20%(336/1720)的分离小鼠 DRG 神经元中外源钙内流。相比之下,当将 GABA(1mM,100μl)注入健康志愿者的前臂皮肤时,既不会引起任何明显的感觉,也不会引起特定的红斑反应,也不会使 C-伤害感受器对缓慢去极化正弦电刺激敏感。用呋塞米(1mg/100μl)阻断内向氯离子转运体 NKCC1 并不能降低电诱发的疼痛评分,也不能结合抑制 NKCC1 驱动的氯离子补充来重复 GABA 刺激。最后,我们通过离子电渗法递送可待因或组氨酸来产生持续的 C 纤维放电,以诱导持续性瘙痒。在预先注射呋塞米的情况下,组胺或可待因瘙痒的强度和持续时间均不受影响。我们的结论是,尽管 GABA 可以在一定比例的分离小鼠 DRG 神经元中引发钙瞬变,但即使通过抑制钠偶联 NKCC1 转运体改变氯离子梯度,它也不会引起或改变健康人皮肤的疼痛或瘙痒评分。