Baumeister Alan A
Department of Psychology, Louisiana State University, Baton Rouge, LA 70803, USA.
J Hist Neurosci. 2013;22(1):14-29. doi: 10.1080/0964704X.2012.664087.
Two revolutionary drugs were introduced into psychiatry in the early 1950s for the treatment of agitated mental patients - reserpine and chlorpromazine. These drugs initiated the modern era of drug treatment for schizophrenia and other psychoses. Early research revealed that, although the pharmacological profiles of the two drugs overlapped considerably, they had different mechanisms of action. The mechanism of action of reserpine was determined first: it depletes monoamines from the brain and other tissues. By contrast, chlorpromazine has little or no effect on brain monoamine concentrations. The mystery created by two drugs that have similar pharmacological profiles but different mechanisms of action is the chlorpromazine enigma. For about eight years after the mechanism of action of reserpine was determined, researchers followed several false leads about the mechanism of action of chlorpromazine. Then, in 1963, Arvid Carlsson and Margit Lindqvist proposed that chlorpromazine (and haloperidol) work by blocking "monoaminergic" receptors. It was quickly determined that dopamine receptor blockade was the most important action. Although the idea of chemical communication between central neurons had yet to gain wide acceptance, this idea was central to resolving the chlorpromazine enigma.
20世纪50年代初,两种革命性药物被引入精神病学领域,用于治疗躁动不安的精神病人——利血平和氯丙嗪。这些药物开启了精神分裂症和其他精神病药物治疗的现代时代。早期研究表明,尽管这两种药物的药理学特征有很大重叠,但它们的作用机制不同。利血平的作用机制首先被确定:它使大脑和其他组织中的单胺类物质耗竭。相比之下,氯丙嗪对大脑单胺浓度几乎没有影响。两种药物药理学特征相似但作用机制不同所产生的谜团就是氯丙嗪之谜。在利血平的作用机制被确定后的大约八年时间里,研究人员在氯丙嗪的作用机制上沿着几条错误线索进行了研究。然后,在1963年,阿尔维德·卡尔森(Arvid Carlsson)和玛吉特·林德qvist(Margit Lindqvist)提出氯丙嗪(和氟哌啶醇)通过阻断“单胺能”受体起作用。很快就确定多巴胺受体阻断是最重要的作用。尽管中枢神经元之间化学通讯的想法尚未得到广泛认可,但这个想法是解开氯丙嗪之谜的关键。