Baumann Thomas K, Burchiel Kim J, Ingram Susan L, Martenson Melissa E
Division of Neurosurgery, Oregon Health Sciences University, Portland, OR 97201-3098 USA Department of Pharmacology, Oregon Health Sciences University, Portland, OR 97201-3098 USA.
Pain. 1996 Apr;65(1):31-38. doi: 10.1016/0304-3959(95)00145-X.
This study examined the responses of cultured adult human dorsal root ganglion (hDRG) neurons to protons and capsaicin, two substances known to produce pain and hyperalgesia in humans. Both substances were applied to each neuron and responses were examined under both voltage- and current-clamp recording conditions. Sensitivity to protons was tested with rapid acidification of the extracellular fluid from pH 7.35 to 6.0. In neurons nominally clamped near -60 mV, low pH evoked a transient inward current which, in all 40 hDRG neurons tested, was followed by a more sustained inward current. The sustained current was associated with an increase in membrane conductance in 10 neurons, a decrease in 27 neurons, and no overt change in conductance (< 10%) in 3 neurons. Current-clamp recordings in the same neurons showed that the proton-induced sustained net inward current caused a prolonged depolarization of the membrane potential in all 40 hDRG neurons. The prolonged depolarization was associated with action potential discharge in 5 neurons. Unlike low pH, capsaicin evoked a sustained net inward current in only a subset of neurons tested (10 nM: 1/4, 30 nM: 4/8, 100 nM: 11/18, and 10 microM: 10/10 neurons tested). The capsaicin-evoked currents were accompanied by an increase in membrane conductance in 15 neurons, a decrease in 2, and no overt change in conductance in 9 neurons. Capsaicin currents, like proton-induced currents, resulted in prolonged depolarizations (10 nM: 0/4, 30 nM: 5/8, 100 nM: 8/18, and 10 microM: 10/10 neurons tested). The depolarization resulted in the discharge of action potentials in 14 neurons. It is concluded that, while both protons and capsaicin exert excitatory effects on human sensory neurons, multiple membrane mechanisms lead to the depolarization of cultured hDRG neurons by low pH. Inhibition of resting membrane conductances contributes to the responses to low pH in some hDRG neurons.
本研究检测了培养的成人人类背根神经节(hDRG)神经元对质子和辣椒素的反应,这两种物质在人类中均会引起疼痛和痛觉过敏。将这两种物质分别作用于每个神经元,并在电压钳和电流钳记录条件下检测反应。通过将细胞外液从pH 7.35快速酸化至pH 6.0来测试对质子的敏感性。在名义上钳制在-60 mV附近的神经元中,低pH值诱发了一个短暂的内向电流,在所测试的所有40个hDRG神经元中,随后是一个更持续的内向电流。在10个神经元中,持续电流与膜电导增加有关,在27个神经元中与膜电导降低有关,在3个神经元中电导无明显变化(<10%)。在相同神经元上进行的电流钳记录显示,质子诱导的持续净内向电流在所有40个hDRG神经元中导致膜电位的长时间去极化。在5个神经元中,长时间去极化与动作电位发放有关。与低pH不同,辣椒素仅在一部分测试神经元中诱发持续的净内向电流(10 nM:1/4,30 nM:4/8,100 nM:11/18,10 μM:10/10测试神经元)。辣椒素诱发的电流在15个神经元中伴随着膜电导增加,在2个神经元中伴随着膜电导降低,在9个神经元中电导无明显变化。辣椒素电流与质子诱导的电流一样,导致长时间去极化(10 nM:0/4,30 nM:5/8,100 nM:8/18,10 μM:10/10测试神经元)。去极化在14个神经元中导致动作电位发放。结论是,虽然质子和辣椒素都对人类感觉神经元发挥兴奋作用,但多种膜机制导致培养的hDRG神经元因低pH而发生去极化。静息膜电导的抑制在一些hDRG神经元对低pH的反应中起作用。