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组胺拮抗剂在实验性诱导瘙痒中作为止痒剂的疗效。

The efficacy of histamine antagonists as antipruritics in experimentally induced pruritus.

作者信息

Davies M G, Marks R, Horton R J, Storari F E

出版信息

Arch Dermatol Res. 1979 Oct;266(2):117-20. doi: 10.1007/BF00694619.

Abstract
  1. The antipruritic ability of histamine (H1 and H2) antagonists alone and in combination in experimentally induced pruritus has been investigated in 12 normal human volunteers. 2. A combination of cimetidine (H2 anatagonist) and chlorpheniramine (H1 antagonist) proved effective in suppressing itch that was artificially induced by the application of papain and histamine. 3. The combination was more effective than chlorpheniramine or cimetidine alone or placebo. 4. The results suggest that both H1 and H2 receptors are involved in the mediation of pruritus.
摘要
  1. 已在12名正常人类志愿者中研究了组胺(H1和H2)拮抗剂单独及联合使用对实验性诱导瘙痒的止痒能力。2. 西咪替丁(H2拮抗剂)和氯苯那敏(H1拮抗剂)联合使用被证明对抑制因涂抹木瓜蛋白酶和组胺而人工诱导的瘙痒有效。3. 该联合用药比单独使用氯苯那敏或西咪替丁或安慰剂更有效。4. 结果表明,H1和H2受体均参与瘙痒的介导。

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