Joordens R J, Hijzen T H, Olivier B
Department of Psychopharmacology, Faculty of Pharmacy, Utrecht University, The Netherlands.
Life Sci. 1998;63(25):2227-32. doi: 10.1016/s0024-3205(98)00507-4.
In the present study, the effects of alprazolam, chlordiazepoxide, ethanol and haloperidol in the strychnine-potentiated startle response paradigm were investigated. Because strychnine increases control startle levels without fear-conditioning, no central state of fear exists. When anxiolytic drugs reduce the fear-induced potentiation of the startle response without reducing the strychnine-induced startle potentiation, their attenuating effect on startle potentiation in the fear-potentiated startle response paradigm can more likely be attributed to their anxiolytic properties. The selected drugs, which effectively reduced the fear-induced startle potentiation in an earlier study, indeed did not selectively affect the strychnine-induced startle potentiation, supporting the notion that the dose-dependent reduction of startle potentiation due to anxiolytic drugs in the fear-potentiated startle response paradigm does not reflect a "non-specific" disruption of startle behavior.
在本研究中,我们调查了阿普唑仑、氯氮卓、乙醇和氟哌啶醇在士的宁增强惊吓反应范式中的作用。由于士的宁在无恐惧条件下会提高对照惊吓水平,因此不存在恐惧的中枢状态。当抗焦虑药物在不降低士的宁诱导的惊吓增强的情况下,减少恐惧诱导的惊吓反应增强时,它们在恐惧增强惊吓反应范式中对惊吓增强的减弱作用更可能归因于其抗焦虑特性。在早期研究中有效降低恐惧诱导的惊吓增强的所选药物,确实没有选择性地影响士的宁诱导的惊吓增强,这支持了以下观点:在恐惧增强惊吓反应范式中,抗焦虑药物导致的惊吓增强的剂量依赖性降低并不反映惊吓行为的“非特异性”破坏。