Freye E, Kuschinsky K
Pharmacology. 1976;14(1):1-7. doi: 10.1159/000136573.
Fentanyl in low doses (0.02-0.05 mg/kg) had no significant effect on the dopamine turnover 20 min after intraperitoneal (i.p.) injection and raised the homovanillic acid (HVA) concentration in the rat striatum with a maximum at 60 min after i.p. injection. Higher doses (0.1-0.2 mg/kg)reduced the HVA content after 20 min and raised it after 60 min. Naloxone (1 mg/kg) given shortly (5min) after high doses of fentanyl (0.2 mg/kg) was able to eliminate the early (i.e., 20 min after i.p. injection) decrease and the late (i.e., 60 min after i.p. injection)increase of HVA content in the striatum. Naloxone (1mg/kg) alone slightly increased the HVA concentration, after 20 as well as after 60 min. Droperidol (3-12 mg/kg) and haloperidol (6-12 mg/kg) markedly increased the HVA content in the rat striatum 90 min after i.p. injection. These effects were dose-dependent. Naloxone (1 mg/kg) did not significantly inhibit the rise of HVA induced by droperidol.
低剂量(0.02 - 0.05毫克/千克)的芬太尼腹腔注射20分钟后对多巴胺周转率无显著影响,腹腔注射60分钟后使大鼠纹状体中的高香草酸(HVA)浓度升高至最大值。较高剂量(0.1 - 0.2毫克/千克)在20分钟后降低HVA含量,60分钟后升高。大剂量芬太尼(0.2毫克/千克)注射后不久(5分钟)给予纳洛酮(1毫克/千克)能够消除纹状体中HVA含量早期(即腹腔注射后20分钟)的降低和晚期(即腹腔注射后60分钟)的升高。单独使用纳洛酮(1毫克/千克)在20分钟和60分钟后均使HVA浓度略有升高。氟哌利多(3 - 12毫克/千克)和氟哌啶醇(6 - 12毫克/千克)腹腔注射90分钟后显著增加大鼠纹状体中的HVA含量。这些作用呈剂量依赖性。纳洛酮(1毫克/千克)并未显著抑制氟哌利多诱导的HVA升高。