神经药理学报 ›› 2011, Vol. 1 ›› Issue (5): 49-55.

• 综述 • 上一篇    下一篇

α2-肾上腺素受体激动剂右旋美托嘧啶对缺血性脑血管病的保护作用

胡敏1,2,何治1,2   

  1. 1. 三峡大学医学院药学系,宜昌,443002,中国
    2. 三峡大学国家中药药理三级实验室,宜昌,443002,中国
  • 出版日期:2011-10-26 发布日期:2013-03-24
  • 通讯作者: 何治,男,神经药理学博士,副教授,硕士研究生导师;研究方向:神经药理学;E-mail:hezhi2003@163.com
  • 作者简介:胡敏,女,在读硕士研究生;E-mail:humin71325@163.com
  • 基金资助:

    国家自然科学基金青年科学基金项目(No.81100873),湖北省卫生厅青年科技人才项目(No.QJX2012-27),宜昌市科学技术研究与开发项目(No.A01301-02)

Neuroprotective role of the Alpha 2-Adrenergic Agonist Dexmedetomidine in Ischemic Cerebrovascular Disease

HU Min 1,2,HE Zhi 1,2   

  1. 1. Pharmacy Department, Medical School of China Three Gorges University,Yichang,443002,China
    2. Third-grade Pharmacological Laboratory for Traditional Chinese Medicine research, State Administration of Traditional Chinese Medicine,Three Gorges University,Yichang,443002,China
  • Online:2011-10-26 Published:2013-03-24
  • Contact: 何治,男,神经药理学博士,副教授,硕士研究生导师;研究方向:神经药理学;E-mail:hezhi2003@163.com
  • About author:胡敏,女,在读硕士研究生;E-mail:humin71325@163.com
  • Supported by:

    国家自然科学基金青年科学基金项目(No.81100873),湖北省卫生厅青年科技人才项目(No.QJX2012-27),宜昌市科学技术研究与开发项目(No.A01301-02)

摘要: 缺血性脑血管病是常见病、多发病,其致残率和死亡率均高,严重影响着人类的身体健康和生活质量。而脑缺血缺氧时,神经元会出现损伤和死亡。现有大量研究证明α2-肾上腺素受体激动剂能保护大脑神经元免受缺血/再灌注的损伤,但其发挥神经保护作用的确切机制尚不完全清楚,可能与α2-肾上腺素受体的激活有关。右旋美托嘧啶就是一种高选择性的α2-肾上腺素受体激动剂,具有一定的神经保护作用。本文就缺血性脑血管病病理生理演变过程、右旋美托嘧啶的分子药理学及其发挥神经保护作用的机制作一综述。

关键词: &, alpha, 2-肾上腺素受体激动剂, 右旋美托嘧啶, 缺血性脑血管病, 神经保护作用

Abstract: Ischemic cerebrovascular disease is a common and frequently encountered disease with high disability and mortality rates, and has severe effects on human’s health and quality of life. Cerebral hypoxic ischemia leads to an increase in the number of damaged or dead neurons. Recent studies have provided considerable evidence that alpha 2-adrenergic agonists can protect the brain neuron from cerebral ischemia/reperfusion injury. However, the exact mechanisms of this protection remain unknown. Activation of the alpha 2-adrenergic receptor may be involved. Dexmedetomidine is a highly selective agonist of the alpha 2-adrenergic receptors with neuroprotective effects. This article reviews the pathophysiological process of ischemic cerebrovascular disease, the molecular pharmacology and the neuroprotective mechanisms of dexmedetomidine.

Key words: alpha 2-adrenergic agonists, dexmedetomidine, ischemic cerebrovascular disease, neuroprotection

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