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特应性皮炎患者皮损皮肤中组胺诱导瘙痒的神经元致敏作用。

Neuronal sensitization for histamine-induced itch in lesional skin of patients with atopic dermatitis.

作者信息

Ikoma Akihiko, Rukwied Roman, Ständer Sonja, Steinhoff Martin, Miyachi Yoshiki, Schmelz Martin

机构信息

Departments of Dermatology, Kyoto University, Kyoto, Japan.

出版信息

Arch Dermatol. 2003 Nov;139(11):1455-8. doi: 10.1001/archderm.139.11.1455.

Abstract

OBJECTIVE

Lowered threshold of neurons (ie, neuronal sensitization) in atopic dermatitis was investigated by testing sensitivity to histamine.

DESIGN

Comparative study.

SETTING

A dermatological clinic and a research laboratory.

PARTICIPANTS

Eighteen patients with atopic dermatitis (AD) and 6 patients with chronic plaque-type psoriasis as well as 14 healthy control subjects.

INTERVENTIONS

Histamine prick was performed in lesional and nonlesional skin of patients and in control subjects.

MAIN OUTCOME MEASURES

Axon reflex flare and wheal were measured planimetrically, and the itch intensity was rated on a numerical scale (0-10).

RESULTS

In nonlesional skin of patients with AD, itch intensity and axon reflex flare were both significantly smaller compared with controls (mean +/- SEM maximum itch, 1.5 +/- 0.3 vs 3.1 +/- 0.2 [P<.05]; mean +/- SEM diameter, 12.3 +/- 2.0 vs 25.3 +/- 2.5 mm [P<.01]). In lesional skin of patients with AD, on the contrary, massive itch was provoked (maximum itch, 4.4 +/- 0.3), although flare was relatively small (diameter, 16.1 +/- 3.4 mm). Itch ratings in patients with psoriasis were low both in lesional and nonlesional skin (maximum itch, 1.3 +/- 0.6 and 1.0 +/- 0.4, respectively).

CONCLUSION

As the area of axon reflex flare is an indirect measure of activity in primary afferent neurons, our results suggest a decreased activation of peripheral pruriceptors in patients with AD. The massively increased itch in lesional skin of patients with AD might therefore be based on sensitization for itch in the spinal cord rather than in primary afferent neurons. This sensitization does not appear to be simply based on skin inflammation because histamine-induced itch was not augmented in lesional skin of psoriasis.

摘要

目的

通过检测对组胺的敏感性,研究特应性皮炎患者神经元阈值降低(即神经元致敏)情况。

设计

对比研究。

地点

皮肤科诊所和研究实验室。

参与者

18例特应性皮炎(AD)患者、6例慢性斑块型银屑病患者以及14名健康对照者。

干预措施

对患者的皮损及非皮损皮肤和对照者进行组胺点刺。

主要观察指标

采用平面测量法测量轴突反射性风团和红斑,并对瘙痒强度进行数字评分(0 - 10分)。

结果

与对照组相比,AD患者非皮损皮肤的瘙痒强度和轴突反射性红斑均显著较小(平均±标准误最大瘙痒评分,1.5±0.3 对3.1±0.2 [P<0.05];平均±标准误直径,12.3±2.0对25.3±2.5 mm [P<0.01])。相反,AD患者皮损皮肤虽红斑相对较小(直径,16.1±3.4 mm),但引发了剧烈瘙痒(最大瘙痒评分,4.4±0.3)。银屑病患者皮损及非皮损皮肤的瘙痒评分均较低(最大瘙痒评分分别为1.3±0.6和1.0±0.4)。

结论

由于轴突反射性红斑面积是初级传入神经元活动的间接指标,我们的结果提示AD患者外周瘙痒感受器的激活减少。因此,AD患者皮损皮肤中瘙痒的大幅增加可能基于脊髓而非初级传入神经元对瘙痒的致敏。这种致敏似乎并非简单基于皮肤炎症,因为组胺诱导的瘙痒在银屑病皮损皮肤中并未增强。

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