Engleman E A, Murphy J M, Zhou F C, Hingtgen J N
Department of Psychiatry, Indiana University School of Medicine, Indianapolis.
Neurochem Res. 1992 May;17(5):483-8. doi: 10.1007/BF00969896.
Studies from this laboratory have demonstrated that administration of the selective 5-HT2/1C antagonist LY53857 can block 5-HTP-induced response suppression. To further investigate the serotonergic mechanisms involved in this effect, we decided to test the capacity of LY53857 to block response suppression induced with two selective 5-HT agonists. After a 15 minute baseline period, rats trained to press a lever for milk reinforcement on a VI 1' schedule were given IP injections of 1.0 mg/kg DOI, or 1.0 mg/kg 8-OH-DPAT to induce response suppression. Subsequently, rats were injected with 1.0 mg/kg LY53857 1 hour prior to DOI- or 8-OH-DPAT-induced response suppression. Preinjections with LY53857 resulted in a 100% blockade of DOI-induced response suppression whereas the same dose did not block response suppression induced with 8-OH-DPAT. These results indicate that the 5-HTP-induced response suppression shows some pharmacological similarity to DOI-induced response suppression and may be mediated through 5-HT2 and/or 5-HT1C receptors.
本实验室的研究表明,给予选择性5-HT2/1C拮抗剂LY53857可阻断5-羟色胺酸(5-HTP)诱导的反应抑制。为了进一步研究参与此效应的5-羟色胺能机制,我们决定测试LY53857阻断两种选择性5-羟色胺(5-HT)激动剂诱导的反应抑制的能力。在15分钟的基线期后,对按VI 1' 程序训练按压杠杆以获取牛奶强化物的大鼠腹腔注射1.0mg/kg DOI或1.0mg/kg 8-羟基二丙胺基四氢萘(8-OH-DPAT)以诱导反应抑制。随后,在DOI或8-OH-DPAT诱导反应抑制前1小时,给大鼠注射1.0mg/kg LY53857。预先注射LY53857可100%阻断DOI诱导的反应抑制,而相同剂量不能阻断8-OH-DPAT诱导的反应抑制。这些结果表明,5-HTP诱导的反应抑制与DOI诱导的反应抑制在药理学上有一些相似性,可能是通过5-HT2和/或5-HT1C受体介导的。