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体内激发人皮肤后,组胺在风团中释放但不在红晕中释放:一项微透析研究。

Histamine is released in the wheal but not the flare following challenge of human skin in vivo: a microdialysis study.

作者信息

Petersen L J, Church M K, Skov P S

机构信息

Department of Dermatology, Bispebjerg University Hospital, Southampton, UK.

出版信息

Clin Exp Allergy. 1997 Mar;27(3):284-95. doi: 10.1046/j.1365-2222.1997.d01-502.x.

Abstract

BACKGROUND

The mediator mechanisms of the cutaneous wheal and flare response, which underlies allergic skin and urticarial conditions, are controversial. The wheal results primarily from a direct effect of histamine on the local vascular bed but to what extent does histamine diffuse within the wheal? The flare is neurogenic, in origin, being disseminated within the dermis by axon reflexes, but do the neuropeptides released from the nerve endings cause the vasodilatation directly or do they induce the further release of histamine which then transduces the flare?

OBJECTIVE

We have addressed these questions by inserting 216 microns diameter microdialysis fibres into the dermis within the different areas of the wheal and flare to monitor changes in histamine levels provoked by intradermal injections of histamine, allergen, codeine and substance P. Twenty-one subjects participated in the investigations.

RESULTS

The histamine concentration in unprovoked skin was 10.5 +/- 0.6 nM. As the dialysis efficacy was approximately 50%, this equates to tissue concentrations of 20 nM. All provicants released large amounts of histamine at the injection site, maximum histamine levels being 337-1293 nM. Diffusion of histamine within the wheal was poor, levels at 2.3 mm and 3.7 mm from the site of injection being 4-22% and 0.2-3.7% respectively of those 1 mm from the injection site. No increased histamine levels were detected in the flare with any provicant. Atraumatic delivery to the skin of histamine in infusion concentrations of 30-10,000 nM caused concentration-related effects, at least 100 nM being necessary to induce a significant increase in skin blood flow, a threshold of 300-1000 being required to stimulate a visible flare and a measurable erythema, and 3000-10,000 nM being the minimum for induction of a wheal. Thus the skin blood vessels and nerves are responsive to histamine, but at relatively high concentrations.

CONCLUSIONS

These data support the theory that the flare reaction to focal histamine injection or release is a neurogenic reflex not involving histamine release at its effector end.

摘要

背景

作为过敏性皮肤和荨麻疹状况基础的皮肤风团及潮红反应的介质机制存在争议。风团主要是由组胺对局部血管床的直接作用所致,但组胺在风团内扩散的程度如何?潮红起源于神经源性,通过轴突反射在真皮内扩散,但是从神经末梢释放的神经肽是直接引起血管舒张,还是诱导组胺进一步释放,然后由组胺传导潮红?

目的

我们通过将直径216微米的微透析纤维插入风团和潮红不同区域的真皮内,以监测皮内注射组胺、变应原、可待因和P物质所引发的组胺水平变化,从而解决了这些问题。21名受试者参与了这些研究。

结果

未受刺激皮肤中的组胺浓度为10.5±0.6纳摩尔/升。由于透析效率约为50%,这相当于组织浓度为20纳摩尔/升。所有激发剂在注射部位均释放出大量组胺,组胺最高水平为337 - 1293纳摩尔/升。组胺在风团内的扩散较差,距离注射部位2.3毫米和3.7毫米处的水平分别为距离注射部位1毫米处水平的4 - 22%和0.2 - 3.7%。使用任何激发剂时,在潮红中均未检测到组胺水平升高。以30 - 10000纳摩尔/升的输注浓度将组胺无创伤性地递送至皮肤会产生浓度相关效应,至少100纳摩尔/升才会引起皮肤血流显著增加,刺激可见潮红和可测量红斑需要300 - 1000纳摩尔/升的阈值,诱导风团的最低浓度为3000 - 10000纳摩尔/升。因此,皮肤血管和神经对组胺有反应,但需要相对较高的浓度。

结论

这些数据支持这样一种理论,即对局部组胺注射或释放的潮红反应是一种神经源性反射,在其效应端不涉及组胺释放。

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