Andersen P, Kubota K, Lo E S, Huttinot G, Maibach H
Department of Dermatology, University of California, School of Medicine, San Francisco 94143-0989, USA.
Br J Dermatol. 1995 Jan;132(1):59-65. doi: 10.1111/j.1365-2133.1995.tb08625.x.
Although cutaneous vasoconstriction assays are used as a primary screen for ranking the in vivo efficacy of new corticosteroids and in vivo human drug delivery studies, little is known about the relationship between the blanching reaction and corticosteroid tissue or plasma concentrations. We measured cutaneous vascular reactions in five volunteers, using an improved reflectance spectroscopic method, and a sensitive radioimmunoassay technique was employed to measure plasma betamethasone concentrations. Using a specially developed betamethasone-17-valerate patch prepared in BIO-PSA, constant corticosteroid release was ensured, and correlations between cutaneous blanching and plasma corticosteroid concentrations were calculated. Maximal skin blanching was documented 12 h post-application, whereas plasma corticosteroid concentrations peaked later, at 32 h post-application, when a paradoxical telangiectatic vasodilatation occurred. At 72 h post-application, when the plasma corticosteroid concentration was still above the 12 h level, this paradoxical vasodilatation was maximal. The corticosteroid-induced vascular reactions were mainly due to arterial haemoglobin (Oxy Haem), and both vasoconstriction and vasodilatation were related to changes in Oxy Haem. Our results suggest a dual, probably both time and concentration related, interaction between corticosteroids and dermal vessels in which lower concentrations at 6-12 h exposure caused vasoconstriction, but as the exposure time increased (> or = 24 h) paradoxical vasodilatation was induced, although plasma corticosteroid concentrations were still rising.
尽管皮肤血管收缩试验被用作对新型皮质类固醇的体内疗效进行排名的主要筛选方法以及体内人体药物递送研究,但对于变白反应与皮质类固醇组织或血浆浓度之间的关系却知之甚少。我们使用一种改进的反射光谱法测量了五名志愿者的皮肤血管反应,并采用灵敏的放射免疫测定技术测量血浆倍他米松浓度。使用在生物粘贴剂中制备的特制倍他米松-17-戊酸酯贴片,确保了皮质类固醇的持续释放,并计算了皮肤变白与血浆皮质类固醇浓度之间的相关性。施用后12小时记录到最大皮肤变白,而血浆皮质类固醇浓度在施用后32小时达到峰值,此时出现了矛盾的毛细血管扩张性血管舒张。施用后72小时,当血浆皮质类固醇浓度仍高于12小时水平时,这种矛盾的血管舒张最为明显。皮质类固醇诱导的血管反应主要归因于动脉血红蛋白(氧合血红蛋白),血管收缩和血管舒张均与氧合血红蛋白的变化有关。我们的结果表明皮质类固醇与真皮血管之间存在双重相互作用,可能与时间和浓度都相关,其中在6至12小时暴露时较低浓度会导致血管收缩,但随着暴露时间增加(≥24小时),尽管血浆皮质类固醇浓度仍在上升,但会诱导出矛盾的血管舒张。