Ikoma A, Fartasch M, Heyer G, Miyachi Y, Handwerker H, Schmelz M
Department of Dermatology, Kyoto University, Japan.
Neurology. 2004 Jan 27;62(2):212-7. doi: 10.1212/wnl.62.2.212.
Central sensitization for pain is important for patients with chronic pain. The authors investigated a possible role of central sensitization for itch in patients with chronic pruritus.
Noxious stimuli were applied in lesional and visually nonlesional skin areas of 25 patients with atopic dermatitis, in lesional skin areas of 9 patients with psoriasis vulgaris, and in 20 healthy subjects. The stimuli included mechanical pinpricks, electrical stimuli, contact heat, and injection of low-pH solution. Intensities of itch and pain were assessed separately on a numeric rating scale.
All the noxious stimuli primarily evoked pain in control subjects and patients with psoriasis vulgaris. In patients with atopic dermatitis, however, itch was evoked instead of burning pain. In their lesional skin, itch was the predominant sensation. Chemical stimuli evoked intense itch in lesional and visually healthy skin areas (the area under the curve of itch rating compared with the control, mean +/- SEM, 668 +/- 166 and 625 +/- 192 vs 38 +/- 23; p < 0.001; p < 0.01). Chemically induced itch also was observed in healthy subjects after a conditioning histamine stimulus of 15 minutes, but not after a conditioning histamine stimulus of 2 minutes.
The chronic barrage of pruriceptive input may elicit central sensitization for itch so that nociceptive input no longer inhibits itch but on the contrary is perceived as itch. In contrast to the well-known A-fiber-mediated alloknesis and hyperknesis, this type of central sensitization appears to be elicited by C-nociceptors.
疼痛的中枢敏化对慢性疼痛患者很重要。作者研究了中枢敏化在慢性瘙痒患者瘙痒中的可能作用。
对25例特应性皮炎患者的皮损及视觉上无皮损的皮肤区域、9例寻常型银屑病患者的皮损区域以及20名健康受试者施加有害刺激。刺激包括机械针刺、电刺激、接触热和注射低pH溶液。分别用数字评分量表评估瘙痒和疼痛的强度。
所有有害刺激在对照组和寻常型银屑病患者中主要诱发疼痛。然而,在特应性皮炎患者中,诱发的是瘙痒而非灼痛。在他们的皮损中,瘙痒是主要感觉。化学刺激在皮损及视觉上健康的皮肤区域诱发强烈瘙痒(瘙痒评分曲线下面积与对照组相比,均值±标准误,分别为668±166和625±192,而对照组为38±23;p<0.001;p<0.01)。在健康受试者中,15分钟的组胺预处理刺激后也观察到化学诱导的瘙痒,但2分钟的组胺预处理刺激后未观察到。
瘙痒性传入的慢性刺激可能引发瘙痒的中枢敏化,从而使伤害性传入不再抑制瘙痒,反而被感知为瘙痒。与众所周知的A纤维介导的异感症和感觉过敏不同,这种类型的中枢敏化似乎是由C伤害感受器引发的。