Ravindran Lakshmi N, Stein Murray B
Department of Psychiatry, University of California San Diego, La Jolla, CA, USA; VA San Diego Health Care System, La Jolla, CA 92037, USA.
Brain Res. 2009 Oct 13;1293:24-39. doi: 10.1016/j.brainres.2009.03.037. Epub 2009 Mar 28.
Post-traumatic stress disorder (PTSD) is a prevalent anxiety disorder that results in multiple disabling symptoms. Research into the underlying neurobiology has implicated dysregulation in multiple neurotransmitter systems including norepinephrine, serotonin, and glutamate as well as the hypothalamic-pituitary axis. Understanding how these biological systems interact with each other and how they may affect key neural structures, such as the amygdala, hippocampus, and prefrontal cortex, to produce post-traumatic symptoms is critical for the development of effective pharmacological treatments. We briefly discuss the proposed biological dysfunctions underlying PTSD and how agents that target these dysfunctions may be utilized in PTSD. We then provide a review of the different pharmacological agents that have been investigated in PTSD. These drugs include: antidepressants, anti-adrenergic agents, anticonvulsants, benzodiazepines, atypical antipsychotics, and novel agents.
创伤后应激障碍(PTSD)是一种常见的焦虑症,会导致多种致残症状。对其潜在神经生物学的研究表明,包括去甲肾上腺素、血清素和谷氨酸在内的多种神经递质系统以及下丘脑-垂体轴存在失调。了解这些生物系统如何相互作用,以及它们如何影响关键神经结构(如杏仁核、海马体和前额叶皮质)以产生创伤后症状,对于开发有效的药物治疗至关重要。我们简要讨论了PTSD潜在的生物功能障碍,以及针对这些功能障碍的药物如何用于PTSD治疗。然后,我们综述了在PTSD研究中所探究的不同药物。这些药物包括:抗抑郁药、抗肾上腺素能药物、抗惊厥药、苯二氮䓬类药物、非典型抗精神病药物和新型药物。