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马来酸氯苯那敏对倍他米松抑制内源性氢化可的松合成效力的影响。

The influence of dimetindene maleate on the endogenous hydrocortisone synthesis suppressing potency of betamethasone.

作者信息

Rehn D, Haack D, Vecsei P, Hennings G

出版信息

Arzneimittelforschung. 1985;35(6):970-2.

PMID:2862878
Abstract

Plasma hydrocortisone (cortisol) levels in 7 healthy volunteers were measured following administration of 0.25 mg betamethasone or 0.25 mg betamethasone and 1 mg dimetindene maleate. The H1-receptor antagonist dimetindene maleate did not influence the hydrocortisone suppressing activity of betamethasone, which was proved by comparison with the published plasma hydrocortisone levels of 162 young healthy untreated volunteers.

摘要

在7名健康志愿者服用0.25毫克倍他米松或0.25毫克倍他米松与1毫克马来酸氯苯那敏后,测量其血浆氢化可的松(皮质醇)水平。通过与162名未接受治疗的年轻健康志愿者已发表的血浆氢化可的松水平进行比较,证明H1受体拮抗剂马来酸氯苯那敏不会影响倍他米松的氢化可的松抑制活性。

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1
The influence of dimetindene maleate on the endogenous hydrocortisone synthesis suppressing potency of betamethasone.马来酸氯苯那敏对倍他米松抑制内源性氢化可的松合成效力的影响。
Arzneimittelforschung. 1985;35(6):970-2.
2
[Effect of a betamethasone-dimethidine-maleate combination on dermatologic diseases. Determination of plasma cortisol levels before, during and after several days' therapy].[倍他米松 - 马来酸二甲替啶组合对皮肤病的疗效。数天治疗前、治疗期间及治疗后的血浆皮质醇水平测定]
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