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地氯雷他定和左西替利嗪对组胺诱导的人体皮肤风团、潮红及瘙痒作用的比较。

Comparison of the effects of desloratadine and levocetirizine on histamine-induced wheal, flare and itch in human skin.

作者信息

Denham K J, Boutsiouki P, Clough G F, Church M K

机构信息

Division of Infection, Inflammation and Repair, School of Medicine, University of Southampton, Southampton, UK.

出版信息

Inflamm Res. 2003 Oct;52(10):424-7. doi: 10.1007/s00011-003-1193-5.

Abstract

OBJECTIVE

A previous study showed the inhibitory effects of loratadine on histamine-induced wheal, flare and itch in human skin to be very variable between individuals. It was hypothesised that this variability may have been due to differences in the rates of metabolism of loratadine to its active form, desloratadine. This double blind, crossover study examined the effects of desloratadine in 12 healthy volunteers. Levocetirizine was used as a comparator.

METHODS

Desloratadine (5 mg), levocetirizine (5 mg) or placebo was taken orally 4 h before an intradermal injection of histamine (20 microL, 100 microM) or vehicle control into the forearm skin. Flare areas were assessed by scanning laser Doppler imaging before and at 30 s intervals for a period of 9 min. Wheal areas were measured by planimetry at 10 min. Itch was scored every 30 s for 5 min using a visual analogue scale.

RESULTS

Following placebo administration, the mean (+/- SEM) wheal area at 10 min was 79.3 +/- 6.9 mm(2), mean flare area for the first 5 min following challenge 26.6 +/- 2.7 cm(2), and itch score for the same period 48.5 +/- 7.6%. The effects of desloratadine were variable between individuals, mean reductions in the wheal and flare areas being 17% (P = 0.033) and 12% (P = 0.036). Desloratadine did not reduce itch significantly. Levocetirizine was more consistent in its effects, mean reductions in wheal, flare and itch being 51%, 67% 78% respectively (all P < 0.001).

CONCLUSIONS

A single dose of 5 mg levocetirizine produced more consistent and greater inhibitory effects on histamine-induced wheal, flare and itch than did 5 mg desloratadine. The difference is suggested to reflect the basic pharmacokinetics of the two drugs.

摘要

目的

先前的一项研究表明,氯雷他定对组胺诱导的人体皮肤风团、红晕和瘙痒的抑制作用在个体间差异很大。据推测,这种差异可能是由于氯雷他定代谢为其活性形式地氯雷他定的速率不同所致。这项双盲、交叉研究检测了地氯雷他定对12名健康志愿者的影响。左西替利嗪用作对照。

方法

在皮内注射组胺(20微升,100微摩尔)或在前臂皮肤注射溶媒对照前4小时,口服地氯雷他定(5毫克)、左西替利嗪(5毫克)或安慰剂。在9分钟内,每隔30秒通过扫描激光多普勒成像评估红晕面积,在10分钟时通过平面测量法测量风团面积。使用视觉模拟量表每30秒对瘙痒进行评分,共5分钟。

结果

服用安慰剂后,10分钟时平均(±标准误)风团面积为79.3±6.9平方毫米,激发后前5分钟平均红晕面积为26.6±2.7平方厘米,同期瘙痒评分为48.5±7.6%。地氯雷他定的效果在个体间存在差异,风团和红晕面积的平均减少率分别为17%(P = 0.033)和12%(P = 0.036)。地氯雷他定未显著减轻瘙痒。左西替利嗪的效果更一致,风团、红晕和瘙痒的平均减少率分别为51%、67%和78%(均P < 0.001)。

结论

单剂量5毫克左西替利嗪对组胺诱导的风团、红晕和瘙痒产生的抑制作用比5毫克地氯雷他定更一致且更强。这种差异提示反映了两种药物的基本药代动力学情况。

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