Graeff Frederico G
Department of Neurology, Psychiatry and Medical Psychology, Faculty of Medicine of Ribeirão Preto, University of São Paulo, 14049-900, Brazil.
Neurosci Biobehav Rev. 2004 May;28(3):239-59. doi: 10.1016/j.neubiorev.2003.12.004.
This article reviews experimental evidence and theoretical constructs that implicate serotonin (5-HT) modulation of defensive behavior within the midbrain periaqueductal gray in panic disorder (PD). Evidence with conflict tests in experimental animals indicates that 5-HT enhances anxiety, whereas results with aversive stimulation of the dorsal periaqueductal gray point to an anxiolytic role of 5-HT. To solve this contradiction, it has been suggested that the emotional states determined by the two types of animal model are different. Conflict tests would generate conditioned anxiety, whereas periaqueductal gray stimulation would produce unconditioned fear, as evoked by proximal threat. Clinically, the former would be related to generalized anxiety while the latter to PD. Thus, 5-HT is supposed to facilitate anxiety, but to inhibit panic. This hypothesis has been tested in the animal model of anxiety and panic named the elevated T-maze, in two procedures of human experimental anxiety applied to healthy volunteers or panic patients, and in CO2-induced panic attacks. Overall, the obtained results have shown that drugs that enhance 5-HT function increase different indexes of anxiety, but decrease indexes of panic. Drugs that impair 5-HT function have the opposite effects. Thus, so far the predictions derived from the above hypothesis have been fulfilled.
本文综述了与惊恐障碍(PD)中脑导水管周围灰质内防御行为的5-羟色胺(5-HT)调节相关的实验证据和理论结构。实验动物冲突试验的证据表明,5-HT会增强焦虑,而对导水管周围灰质背侧进行厌恶刺激的结果则表明5-HT具有抗焦虑作用。为了解决这一矛盾,有人提出两种动物模型所确定的情绪状态不同。冲突试验会产生条件性焦虑,而导水管周围灰质刺激会产生由近端威胁引发的无条件恐惧。临床上,前者与广泛性焦虑有关,而后者与惊恐障碍有关。因此,5-HT被认为会促进焦虑,但会抑制惊恐。这一假设已在名为高架T迷宫的焦虑和惊恐动物模型中、在应用于健康志愿者或惊恐障碍患者的两种人类实验性焦虑程序中以及在二氧化碳诱发的惊恐发作中得到检验。总体而言,所获得的结果表明,增强5-HT功能的药物会增加不同的焦虑指标,但会降低惊恐指标。损害5-HT功能的药物则有相反的效果。因此,到目前为止,上述假设所做出的预测已得到证实。