Zhang Zhang-Jin, Jiang Xiao-Long, Zhang Steven E, Hough Christopher J, Li He, Chen Jian-Guo, Zhen Xue-Chu
Department of Psychiatry, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814, USA.
Neurosci Lett. 2005;382(1-2):134-8. doi: 10.1016/j.neulet.2005.03.001. Epub 2005 Mar 17.
While the benzazepine SKF83959 elicits classical behavioral responses associated with dopamine D1 receptors, it also acts as a D1 receptor antagonist biochemically. The paradoxical properties of this agent remain an enigma. In the present study, we sought to determine the behavioral effects of SKF83959 in the rat acoustic startle reflex test. Systemic administration of SKF83959 produced a dose-related increase in the startle amplitude with a stimulus of 105 dB, and a significant group difference was observed between animals treated with 1 mg/kg SKF83959 and vehicle controls. SKF83959 also significantly reduced the latency to startle response to stimuli of 95 dB and 105 dB in a dose-dependent manner. However, unlike classical dopamine D1-like receptor agonists, SKF83959 failed to disrupt prepulse inhibition (PPI) of either the startle amplitude or the latency to startle response; rather, the agent dose-dependently increased the PPI latency to startle response of 105 dB stimulus. These results suggest that the behavioral effects of SKF83959 in the rat acoustic startle reflex paradigm are paradoxical, and these paradoxical effects may be associated with its distinct pharmacological properties.
虽然苯并氮杂卓类药物SKF83959会引发与多巴胺D1受体相关的典型行为反应,但它在生化方面也可作为一种D1受体拮抗剂。该药物这种矛盾的特性仍是一个谜。在本研究中,我们试图确定SKF83959在大鼠听觉惊吓反射试验中的行为效应。全身性给予SKF83959会使105分贝刺激下的惊吓幅度呈剂量依赖性增加,并且在给予1毫克/千克SKF83959的动物与溶剂对照组之间观察到显著的组间差异。SKF83959还以剂量依赖性方式显著缩短了对95分贝和105分贝刺激的惊吓反应潜伏期。然而,与经典的多巴胺D1样受体激动剂不同,SKF83959未能破坏惊吓幅度或惊吓反应潜伏期的前脉冲抑制(PPI);相反,该药物剂量依赖性地增加了对105分贝刺激的惊吓反应的PPI潜伏期。这些结果表明,SKF83959在大鼠听觉惊吓反射范式中的行为效应是矛盾的,并且这些矛盾效应可能与其独特的药理学特性有关。