Coffin V L, Spealman R D
J Pharmacol Exp Ther. 1985 Dec;235(3):724-8.
The effects of chlordiazepoxide (CDAP) on suppressed behavior of squirrel monkeys were determined alone and in combination with selected methylxanthines (caffeine, theophylline, 8-phenyltheophylline, theobromine, 3-isobutyl-1-methylxanthine) and analogs of adenosine (L-PIA, N6-cyclohexyladenosine, NECA). Monkeys responded under a fixed-interval schedule of food presentation in which responding was suppressed by a concurrent fixed-ratio schedule of response-produced electric shock. Dose-effect curves were determined by administering cumulative doses i.v. during timeout periods that preceded sequential components of the schedule. When administered alone, CDAP produced dose-related increases in the rate of suppressed responding at doses up to 17.8 mg/kg and decreased responding at a higher dose of 32.0 mg/kg. Under the same conditions, the methylxanthines usually had only small effects on responding over the range of doses studied, whereas L-PIA and NECA usually decreased responding in a dose-related manner. After presession treatment with intermediate doses of caffeine, 8-phenyltheophylline or 3-isobutyl-1-methylxanthine, the increases is suppressed responding produced by CDAP often were larger than those produced by CDAP alone. In contrast, after presession treatment with low doses of L-PIA, NECA or N6-cyclohexyladenosine the increases in suppressed responding normally produced by CDAP were either reduced or eliminated. Although L-PIA, NECA and N6-cyclohexyladenosine attenuated the rate-increasing effects of CDAP, there was no indication that they produced an overall rightward shift in the CDAP dose-effect curve, suggesting that the adenosine analogs did not act simply as competitive antagonists of CDAP.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了氯氮䓬(CDAP)单独以及与选定的甲基黄嘌呤(咖啡因、茶碱、8-苯基茶碱、可可碱、3-异丁基-1-甲基黄嘌呤)和腺苷类似物(L-PIA、N6-环己基腺苷、NECA)联合使用时对松鼠猴抑制行为的影响。猴子在固定间隔的食物呈现时间表下做出反应,在此期间,反应会因同时出现的固定比率的反应产生电击而受到抑制。通过在时间表的连续组成部分之前的超时期间静脉注射累积剂量来确定剂量效应曲线。单独给药时,CDAP在剂量高达17.8mg/kg时会产生与剂量相关的抑制反应率增加,而在32.0mg/kg的较高剂量时反应会减少。在相同条件下,在所研究的剂量范围内,甲基黄嘌呤通常对反应只有很小的影响,而L-PIA和NECA通常会以剂量相关的方式减少反应。在用中等剂量的咖啡因、8-苯基茶碱或3-异丁基-1-甲基黄嘌呤进行会前治疗后,CDAP产生的抑制反应增加通常比单独使用CDAP时更大。相比之下,在用低剂量的L-PIA、NECA或N6-环己基腺苷进行会前治疗后,CDAP通常产生的抑制反应增加要么减少要么消除。尽管L-PIA、NECA和N6-环己基腺苷减弱了CDAP的速率增加作用,但没有迹象表明它们使CDAP剂量效应曲线整体向右移动,这表明腺苷类似物并非简单地作为CDAP的竞争性拮抗剂起作用。(摘要截断于250字)