Graeff F G, Zuardi A W, Giglio J S, Lima Filho E C, Karniol I G
Psychopharmacology (Berl). 1985;86(3):334-8. doi: 10.1007/BF00432224.
In order to assess the role played by serotonin (5-HT) in subjective anxiety, three groups of 12 healthy volunteers were given 12 mg metergoline (MET), 10 mg diazepam (DZ) or placebo (PB), under double-blind conditions, and submitted to a simulated public speaking (SPS) test. MET increased state-anxiety scores, measured by Spielberg's State-Trait Anxiety Inventory. The effect of MET was significantly different from both the PB and DZ groups immediately before the SPS test (prestress) as well as 24 h after medication, and from the DZ group only, 2.5 h after the test (poststress). In contrast, DZ did not significantly affect subjective anxiety. The SPS test significantly increased anxiety in DZ- or PB-treated subjects as compared to prestress scores, whereas the increases in the MET group were not significant, probably because pretest levels were already high. No drug effect on heart rate, skin electrical conductance and quality of sleep during the night following medication was found. In addition, the drugs did not cause bodily symptoms that could secondarily affect mood. Since MET is a 5-HT receptor antagonist, active on the central nervous system, an inhibitory role of 5-HT on subjective anxiety might be suggested.
为了评估血清素(5-羟色胺,5-HT)在主观焦虑中所起的作用,在双盲条件下,将三组各12名健康志愿者分别给予12毫克甲麦角林(MET)、10毫克地西泮(DZ)或安慰剂(PB),并让他们接受模拟公开演讲(SPS)测试。通过斯皮尔伯格状态-特质焦虑量表测得,MET增加了状态焦虑得分。在SPS测试前(应激前)以及用药后24小时,MET的效果与PB组和DZ组均有显著差异,而在测试后2.5小时(应激后),仅与DZ组有显著差异。相比之下,DZ对主观焦虑没有显著影响。与应激前得分相比,SPS测试显著增加了接受DZ或PB治疗的受试者的焦虑程度,而MET组的增加不显著,这可能是因为测试前的水平已经很高。未发现药物对用药后夜间的心率、皮肤电导率和睡眠质量有影响。此外,这些药物没有引起可能继发影响情绪的身体症状。由于MET是一种对中枢神经系统有活性的5-HT受体拮抗剂,因此可能提示5-HT对主观焦虑具有抑制作用。