神经药理学报››2011,Vol. 1››Issue (3): 55-64.

• 综述 •上一篇

情感性精神障碍疾病治疗药物的研究现状

薛占霞1,彭亮2

  1. 1. 欧宝平台登录 药学系,张家口,075000,中国
    2. 中国医科大学药学院,沈阳,110001,中国
  • 出版日期:2011-06-26发布日期:2012-06-28
  • 通讯作者:彭亮,女,教授,博士生导师;研究方向:神经药理学;联系电话:+86-24-23256666-5130
  • 作者简介:薛占霞,女,讲师,博士;研究方向:神经药理学;E-mail:xuezhanxia412@163.com
  • 基金资助:

    国家自然科学基金项目(No.30670651)

Research Status of the Drugs Uesed in the Treatment of Affective Disorders Diseases

XUE Zhan-xia1,PENG Liang2

  1. 1. Department of Pharmacology,Hebei North University,Zhangjiakou,075000, China
    2. Department of Clinical Pharmacology,China Medical University,Shenyang, China
  • Online:2011-06-26Published:2012-06-28

摘要:情感性精神障碍包括抑郁症(又称单向情感精神障碍)和躁郁症(双相情感精神障碍),是最为常见的精神疾病,其发病率高、复发率高,社会危害严重。目前临床上治疗单向情感精神障碍的主要药物是以氟西汀、度罗西汀为代表的5-羟色胺选择性再摄取抑制剂(serotonin-specific reuptake inhibitors,SSRIs)和5-羟色胺/去甲肾上腺素双重再摄取抑制剂(serotonin/norepinephrine dual reuptake inhibitor,SNRIs)。治疗双相情感精神障碍的药物主要有碳酸锂、丙戊酸钠和卡马西平等。目前,关于这些药物的机制研究主要有以下几方面:①SSRIs上调细胞溶质型磷脂酶A2(cytosolic phospholipase A2,cPLA2)、细胞外信号调控激酶(extracellular-signal regulated kinases,ERK)及c-Fos和FosB 基因表达增加;②腺苷酸脱氨酶(adenosine deaminase,ADAR2)介导氟西汀对5-HT2B受体RNA编辑的调节作用;③碳酸锂、丙戊酸钠和卡马西平对cPLA2a基因表达的长期调节作用及碱化细胞的作用。但现存的理论都不能明确解释药物的作用机制,并且有些研究结果仍存在尚待解决的问题。

关键词:抑郁症,5-羟色胺特异性再摄取抑制剂,碳酸锂,丙戊酸钠,卡马西平,细胞溶质型磷脂酶A2,腺苷酸脱氨酶,细胞碱化

Abstract:Affective disorders including depression (also known as unipolar depression) and bipolar disorder (unipolar depression),are the most common psychiatric disorders, which have high incidence ratio, high recurrence ratio, and is harmful to the society. Clinically, anti-unipolar depression drugs are mainly serotonin-specific reuptake inhibitors (SSRIs), fluoxetine as represented, and serotonin/norepinephrine dual reuptake inhibitor (SNRIs), duloxetine as represented. And lithium salts (Li+), valproate sodium, and carbamazepine are the three classical anti-bipolar drugs. At present, researches concerning these drugs propose following major mechanisms: ①The expression of cytosolic phospholipase A2 (cPLA2), extracellular-signal regulated kinases (ERK) and c-Fos and FosB is increased by SSRIs; ②Chronic administration of Fluoxetine could induce 5-HT2Breceptor pre-mRNA editing, with the help of adenosine deaminase (ADAR2) activity; ③Lithium carbonate, carbamazepine, valproate sodium could upregulate the mRNA and protein of cPLA2aand induce alkalinization of cell. But the accurate pharmacological mechanisms of these drugs have not been fully elucidated and are needed to be further investigated.

Key words:depression,serotonin-specific reuptake inhibitors (SSRIs),lithium carbonate,carbamazepine,valproate sodium,cytosolic phospholipase A2(cPLA2),adenosine deaminase (ADAR2),intracellular alkalinization

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