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表皮生长因子受体抑制剂致相关皮肤瘙痒的机制研究

彭艳梅 刘青 邓博 崔慧娟 段桦 邱钰芹

中国比较医学杂志2018,Vol.28Issue(5):28-33,6.
中国比较医学杂志2018,Vol.28Issue(5):28-33,6.DOI:10.3969/j.issn.1671-7856.2018.05.006

表皮生长因子受体抑制剂致相关皮肤瘙痒的机制研究

Mechanistic study of epidermal growth factor receptor inhibitor-related pruritus

彭艳梅 1刘青 2邓博 2崔慧娟 2段桦 1邱钰芹1

作者信息

  • 1. 北京中医药大学,北京 100029
  • 2. 中日友好医院,北京 100029
  • 折叠

摘要

Abstract

Objective The aim of this study was to investigate the mechanism underlying pruritus by comparing the epidermal growth factor receptor inhibitor(EGFRI)-erlotinib mouse model with the substance P(SP)-induced pruritus mouse model. Methods Two randomized groups of mice were treated with erlotinib or SP to induce pruritus. Behavioral and skin manifestations were observed. Pathological images and neurokinin 1 receptor(NK-1R)expression of the skin were determined. Concentration of interleukin(IL)-31, IL-33, histamine, leukotriene B4, and SP was analyzed by enzyme-linked immunosorbent assay. Nitric oxide was analyzed by colorimetry. Results Transient pruritus induced by erlotinib appeared 2 to 5 days after treatment. In contrast, continuous pruritus was observed during the first hour, but was then gradually relieved. These two shared similar scratching behavior. Concentration of neurotransmitters showed similar trends in changes among the erlotinib group and SP group. Immunohistochemical expression was also consistent between the erlotinib group and SP group. Conclusions Erlotinib-associated pruritus is related to release of signaling factors through the SP/NK-1R signaling pathway.

关键词

表皮生长因子受体抑制剂/皮肤不良反应/P物质/NK-1R/阿瑞匹坦

Key words

epidermal growth factor receptor inhibitors/EGFRIs/dermatologic adverse effect/substance P/NK-1R/aprepitant

分类

医药卫生

引用本文复制引用

彭艳梅,刘青,邓博,崔慧娟,段桦,邱钰芹..表皮生长因子受体抑制剂致相关皮肤瘙痒的机制研究[J].中国比较医学杂志,2018,28(5):28-33,6.

基金项目

北京市科委"首都特色应用研究"专项(编号:Z151100004015168) (编号:Z151100004015168)

国家自然基金青年项目(编号:81603462). (编号:81603462)

中国比较医学杂志

OA北大核心CSTPCD

1671-7856

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