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组织活力成像:离子电渗疗法诱导的微血管对血管活性药物的反应。

Tissue viability imaging: microvascular response to vasoactive drugs induced by iontophoresis.

作者信息

Henricson Joakim, Nilsson Anders, Tesselaar Erik, Nilsson Gert, Sjöberg Folke

机构信息

Department of Experimental and Clinical Medicine, Linköping University Hospital, Linköping, Sweden.

出版信息

Microvasc Res. 2009 Sep;78(2):199-205. doi: 10.1016/j.mvr.2009.04.008. Epub 2009 May 4.

Abstract

When one is studying the physiology of the cutaneous microcirculation there is a need for relevant non-invasive and versatile techniques. In this study we used a new optical device, the tissue viability imager (TiVi), to map changes in cutaneous microvascular concentrations of red blood cells during iontophoresis of vasoactive substances (noradrenaline (NA) and phenylephrine (Phe) for vasoconstriction and acetylcholine (ACh) and sodium nitroprusside (SNP) for vasodilatation). We aimed to present data both individually and pooled, using a four-variable logistic dose response model that is commonly used in similar in vitro vascular studies. The accuracy of the TiVi was also investigated by calculating the coefficient of variation and comparing it with similar tests previously done using laser Doppler imaging. Tests were also performed using the TiVi and LDPI simultaneously to further compare the two methods. Results showed that the TiVi is capable of quantifying vascular responses to iontophorised noradrenaline and phenylephrine without the need to increase background flow first. Fitting the TiVi data to the dose response model resulted in ED(50)-values with narrow confidence intervals and acceptable r(2) values. Mean ED(50)-values for the TiVi did not differ significantly from similar values obtained using laser Doppler. Results further seem to suggest that when the blood perfusion increases during vasodilatation in skin the initial phase relies mainly on an increase in red blood cell concentration whereas the further perfusion increase is due to an increase in red blood cell velocity.

摘要

在研究皮肤微循环的生理学时,需要相关的非侵入性且通用的技术。在本研究中,我们使用了一种新的光学设备——组织活力成像仪(TiVi),来绘制血管活性物质离子电渗疗法(用于血管收缩的去甲肾上腺素(NA)和苯肾上腺素(Phe),以及用于血管舒张的乙酰胆碱(ACh)和硝普钠(SNP))过程中皮肤微血管中红细胞浓度的变化。我们旨在单独呈现数据并进行汇总,使用一种在类似体外血管研究中常用的四变量逻辑剂量反应模型。还通过计算变异系数并将其与先前使用激光多普勒成像进行的类似测试进行比较,来研究TiVi的准确性。还同时使用TiVi和激光多普勒血流成像(LDPI)进行测试,以进一步比较这两种方法。结果表明,TiVi能够在无需先增加背景血流的情况下,量化血管对离子电渗的去甲肾上腺素和苯肾上腺素的反应。将TiVi数据拟合到剂量反应模型中,得到的半数有效剂量(ED(50))值具有较窄的置信区间和可接受的r(2)值。TiVi的平均ED(50)值与使用激光多普勒获得的类似值没有显著差异。结果进一步似乎表明,当皮肤血管舒张期间血液灌注增加时,初始阶段主要依赖于红细胞浓度的增加,而进一步的灌注增加则是由于红细胞速度的增加。

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