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利用皮肤微透析技术在体测量完整人体皮肤中P物质诱导的组胺释放。

The use of cutaneous microdialysis to measure substance P-induced histamine release in intact human skin in vivo.

作者信息

Petersen L J, Poulsen L K, Søndergaard J, Skov P S

机构信息

Department of Dermatology, Bispebjerg Hospital, University of Copenhagen, Denmark.

出版信息

J Allergy Clin Immunol. 1994 Oct;94(4):773-83. doi: 10.1016/0091-6749(94)90186-4.

Abstract

BACKGROUND

The purpose of this study was to introduce a microdialysis technique, which makes it possible to measure the release of small inflammatory mediators into the extracellular water space in intact human skin in vivo. Using this technique, we have studied the histamine releasing properties of substance P, a putative skin mast cell releasing agent.

METHODS

Small hollow fibers were inserted into the upper dermis of nine healthy subjects. Each fiber was perfused with Kreb's Ringer bicarbonate buffer at a rate of 3.0 microliters/min. After establishment of a baseline, each fiber was challenged intracutaneously with substance P (0 to 4 mumol/L). Samples were collected at 2-minute intervals for 18 minutes. Histamine was measured by a fluorometric method, which correlated with an enzyme immunoassay (r = 0.96).

RESULTS

Baseline dialysate histamine concentration was 1.7 +/- 0.3 ng/ml. Peak histamine release after injection of vehicle, 0.5, 1, 2, and 4 mumol/L substance P was 0.0, 1.0, 6.0, 44.5, and 88.5 ng/ml, respectively (p = 0.00002). Statistically significant histamine release was demonstrated with 1.0 mumol/L substance P and greater. Most peak values were seen 2 to 4 minutes after injection. The histamine elimination showed a monoexponential decline; dialysate histamine half-life was 3.81 +/- 0.28 minutes.

CONCLUSIONS

This study showed that substance P releases histamine in a dose-dependent manner from intact human skin in normal subjects. We suggest that microdialysis may be a promising technique for the evaluation of mediator levels in intact human skin after intradermal injection of an inflammatory or allergenic stimulus.

摘要

背景

本研究的目的是介绍一种微透析技术,该技术能够在体内完整的人体皮肤中测量小炎症介质向细胞外水间隙的释放。利用该技术,我们研究了P物质(一种假定的皮肤肥大细胞释放剂)的组胺释放特性。

方法

将小空心纤维插入9名健康受试者的上真皮层。每根纤维以3.0微升/分钟的速率用克雷布斯林格碳酸氢盐缓冲液灌注。在建立基线后,每根纤维经皮内注射P物质(0至4微摩尔/升)进行激发。每隔2分钟收集样本,共收集18分钟。组胺通过荧光法测量,该方法与酶免疫测定法相关(r = 0.96)。

结果

基线透析液组胺浓度为1.7±0.3纳克/毫升。注射赋形剂、0.5、1、2和4微摩尔/升P物质后的组胺释放峰值分别为0.0、1.0、6.0、44.5和88.5纳克/毫升(p = 0.00002)。1.0微摩尔/升及更高浓度的P物质显示出统计学上显著的组胺释放。大多数峰值出现在注射后2至4分钟。组胺消除呈单指数下降;透析液组胺半衰期为3.81±0.28分钟。

结论

本研究表明,在正常受试者中,P物质从完整的人体皮肤中以剂量依赖方式释放组胺。我们认为,微透析可能是一种有前景的技术,用于评估皮内注射炎症或变应原刺激后完整人体皮肤中的介质水平。

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