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依那普利对变应原诱导的皮肤过敏反应的影响。

Effect of enalapril on allergen-induced cutaneous hypersensitivity reaction.

作者信息

Snyman J R, Sommers D K

机构信息

Department of Pharmacology, University of Pretoria, South Africa.

出版信息

Br J Clin Pharmacol. 1991 Dec;32(6):713-6.

Abstract
  1. To test the hypothesis that the in vivo inhibition of angiotensin converting enzyme in a patient who presents atopy, results in a significant increase in cutaneous bradykinin and prostaglandin production, the effect of enalapril on the cutaneous hypersensitivity reaction was examined in 10 atopic volunteers. 2. A crossover study design was used and volunteers were randomly allocated to treatment with either enalapril (10 mg) alone, or in combination with indomethacin (75 mg), with and without ketotifen (1 mg). Drugs were administered twice daily for 2 days. 3. Allergen (Southern Grass Mix) was administered intradermally 2 h after last drug dosage and the surface areas of the immediate wheal-and-flare-reactions were measured 15 min later. The late phase of the cutaneous response was evaluated 6 h later by determining skinfold thickness and surface area. 4. Enalapril alone had no effect on any of the parameters measured. 5. The cutaneous hypersensitivity reaction was significantly reduced with regard to both immediate and late cutaneous responses when the indomethacin and ketotifen combination was added to enalapril therapy. 6. When only indomethacin was added to enalapril pretreatment the flare reaction was significantly reduced, but whealing was unaffected. 7. This study presents further evidence that mast cell mediators other than prostaglandins are involved in the cutaneous hypersensitivity reaction. Furthermore, that endogenous bradykinin production after enalapril pretreatment either never reaches the supraphysiological concentrations used in previous experiments, or that bradykinin is rapidly and effectively broken down to inactive peptides by other carboxypeptidase enzymes.
摘要
  1. 为了验证以下假设:在患有特应性的患者体内抑制血管紧张素转换酶会导致皮肤缓激肽和前列腺素生成显著增加,在10名特应性志愿者中研究了依那普利对皮肤过敏反应的影响。2. 采用交叉研究设计,志愿者被随机分配接受单独使用依那普利(10毫克)治疗,或与吲哚美辛(75毫克)联合使用,以及联合或不联合酮替芬(1毫克)。药物每日服用两次,共服用2天。3. 在最后一次给药后2小时皮内注射过敏原(南方草混合剂),15分钟后测量即刻风团和潮红反应的表面积。6小时后通过测定皮褶厚度和表面积评估皮肤反应的晚期阶段。4. 单独使用依那普利对所测量的任何参数均无影响。5. 当依那普利治疗中加入吲哚美辛和酮替芬联合用药时,即刻和晚期皮肤反应的皮肤过敏反应均显著降低。6. 当仅在依那普利预处理中加入吲哚美辛时,潮红反应显著降低,但风团形成未受影响。7. 本研究进一步证明,除前列腺素外的肥大细胞介质参与了皮肤过敏反应。此外,依那普利预处理后内源性缓激肽的生成要么从未达到先前实验中使用的超生理浓度,要么缓激肽被其他羧肽酶迅速有效地分解为无活性肽。

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本文引用的文献

1
Familial carboxypeptidase N deficiency.
Ann Intern Med. 1980 Sep;93(3):443-5. doi: 10.7326/0003-4819-93-3-443.
5
Angiotensin-converting enzyme inhibition and prostaglandins.血管紧张素转换酶抑制作用与前列腺素
Am J Cardiol. 1982 Apr 21;49(6):1405-9. doi: 10.1016/0002-9149(82)90351-4.

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