Hetem L A, de Souza C J, Guimarães E S, Zuardi A W, Graeff F G
Departamento de Neurologia, Psiquiatria e Psicologia Médica, Universidade de São Paulo, Ribeirão Preto, Brazil.
Psychopharmacology (Berl). 1996 Oct;127(3):276-82.
To investigate the role of 5-HT in human anxiety, the 5-HT releaser and uptake blocker d-fenfluramine (FEN) was administered to healthy volunteers under two models of experimental anxiety. The first was a simulated public speaking (SPS) test consisting of talking in front of a video camera, anxiety being evaluated mainly by self-rating scales. The second was a conditioned fear test, in which the changes in skin electrical conductance caused by a tone associated once with an aversive white noise were measured. The doses of 15 and 30 mg FEN, PO, decreased anxiety induced by SPS in a dose-dependent way, as indicated by the anxiety factor of Norris Visual Analogue Mood Scale. In the conditioned fear test, however, the amplitude and level of skin conductance responses to the conditioned aversive stimulus were not significantly changed by FEN. The differential effects of FEN in these human experimental models of anxiety, together with similar results reported in rats, support the view that 5-HT exerts a dual action on brain mechanisms regulating anxiety, facilitating conditioned while inhibiting unconditioned fear. The presumed reduction in unconditioned fear caused by FEN may have implications for the treatment of panic disorder.
为研究5-羟色胺(5-HT)在人类焦虑中的作用,在两种实验性焦虑模型下,对健康志愿者施用5-HT释放剂及摄取阻滞剂右旋芬氟拉明(FEN)。第一种是模拟公开演讲(SPS)测试,即对着摄像机讲话,主要通过自评量表评估焦虑程度。第二种是条件性恐惧测试,测量由曾与厌恶的白噪声相关联的音调所引起的皮肤电导率变化。口服15毫克和30毫克剂量的FEN,诺里斯视觉模拟情绪量表的焦虑因子显示,其以剂量依赖方式减轻了SPS诱导的焦虑。然而,在条件性恐惧测试中,FEN并未使对条件性厌恶刺激的皮肤电导率反应的幅度和水平发生显著变化。FEN在这些人类实验性焦虑模型中的不同作用,以及在大鼠中报告的类似结果,支持了以下观点:5-HT对调节焦虑的脑机制发挥双重作用,促进条件性恐惧,同时抑制非条件性恐惧。FEN引起的非条件性恐惧的假定减轻可能对惊恐障碍的治疗具有启示意义。