Katz J L, Witkin J M
Psychobiology Laboratory, NIDA Addiction Research Center, Baltimore, MD 21224.
Psychopharmacology (Berl). 1991;103(1):33-40. doi: 10.1007/BF02244070.
Effects of cocaine, alone and in combination with the dopaminergic antagonists, SCH 23390 and haloperidol were studied in squirrel monkeys trained to respond under fixed-interval schedules of electric-shock presentation. Cocaine at intermediate doses (0.1 and 0.3 mg/kg) increased rates of responding under the fixed-interval schedule and during 1-min timeout periods that separated each fixed-interval component. Higher doses (1.0 - 3.0 mg/kg) decreased response rates. Cocaine also dose-dependently altered the temporal pattern of responding characteristic of behavior under fixed-interval schedules. Haloperidol (0.003-0.1 mg/kg) and SCH 23390 (0.001-0.03 mg/kg) dose-dependently decreased rates of responding. A low dose (0.001 mg/kg) of the selective D1 antagonist, SCH 23390, did not appreciably alter the effects of cocaine. Higher doses (0.003-0.01 mg/kg), which when given alone decreased rates of responding, attenuated the increases in response rates produced by cocaine. In addition, the decreases in response rates produced by the higher dose of cocaine were attenuated by 0.01 mg/kg SCH 23390. The alterations in temporal patterning of responding under the fixed-interval schedule were not antagonized by any dose of SCH 23390. Haloperidol (0.003 mg/kg) did not appreciably alter the effects of cocaine; higher doses (0.01-0.03 mg/kg), which when given alone decreased rates of responding, attenuated the increases in response rates produced by 0.1 mg/kg cocaine. The decreases in response rates under the fixed-interval schedule that were produced by higher doses, or the changes in temporal patterning of responding at any dose of cocaine, were not antagonized by any dose of haloperidol that was studied.(ABSTRACT TRUNCATED AT 250 WORDS)
在经过训练能在电击呈现的固定间隔时间表下做出反应的松鼠猴中,研究了可卡因单独使用以及与多巴胺能拮抗剂SCH 23390和氟哌啶醇联合使用的效果。中等剂量(0.1和0.3毫克/千克)的可卡因增加了在固定间隔时间表下以及在分隔每个固定间隔成分的1分钟超时期间的反应率。更高剂量(1.0 - 3.0毫克/千克)降低了反应率。可卡因还剂量依赖性地改变了固定间隔时间表下行为反应的时间模式。氟哌啶醇(0.003 - 0.1毫克/千克)和SCH 23390(0.001 - 0.03毫克/千克)剂量依赖性地降低了反应率。低剂量(0.001毫克/千克)的选择性D1拮抗剂SCH 23390并未明显改变可卡因的效果。更高剂量(0.003 - 0.01毫克/千克)单独使用时会降低反应率,可减弱可卡因产生的反应率增加。此外,0.01毫克/千克的SCH 23390减弱了高剂量可卡因产生的反应率降低。固定间隔时间表下反应时间模式的改变未被任何剂量的SCH 23390拮抗。氟哌啶醇(0.003毫克/千克)并未明显改变可卡因的效果;更高剂量(0.01 - 0.03毫克/千克)单独使用时会降低反应率,可减弱0.1毫克/千克可卡因产生的反应率增加。高剂量产生的固定间隔时间表下反应率的降低,或任何剂量可卡因下反应时间模式的变化,均未被所研究的任何剂量的氟哌啶醇拮抗。(摘要截断于250字)