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在恒河猴中,δ-9-四氢大麻酚和CP 55,940在固定间隔给药方案下维持静脉自我给药失败。

Failure of Delta(9)-tetrahydrocannabinol and CP 55,940 to maintain intravenous self-administration under a fixed-interval schedule in rhesus monkeys.

作者信息

Mansbach R.S., Nicholson K.L., Martin B.R., Balster R.L.

机构信息

Department of Pharmacology and Toxicology, Medical College of Virginia, Virginia Commonwealth University, Richmond, VA 23298-0613, USA.

出版信息

Behav Pharmacol. 1994 Apr;5(2):219-225. doi: 10.1097/00008877-199404000-00014.

Abstract

The lack of procedures which can unequivocally demonstrate cannabinoid self-administration in animals has been an obstacle to the study of the neural basis for the reinforcing effects of this drug class. Because delta(9)-tetrahydrocannabinol (delta(9)-THC) produce a relatively slow-onset, long-lasting behavioral effect, a self-administration procedure with widely spaced drug deliveries was evaluated as an alternative to fixed-ratio schedules which typically require frequent, closely spaced injections to demonstrate reinforcing effects. Three adult male rhesus monkeys were surgically implanted with intravenous catheters and trained to self-administer phencyclidine (PCP) under a 10min fixed-interval schedule of reinforcement. Three injections were available each day, separated by 2h periods during which responding had no programmed consequences. In an attempt to link the effect of the drug with the response which produced it, each 20s injection was paired with a red light which remained illuminated for 10min. PCP (100µg/kg/injection) maintained steady rates of responding during each availability period, ranging from approximately 0.2 to 0.7 responses/s. During 7 day substitution periods, Delta(9)-THC (17-100µg/kg/injection) maintained low rates of responding which occasionally surpassed those during vehicle substitutions, but fell far below rates maintained by PCP. Substitution tests with the potent Delta(9)-THC analog CP 55,940 also resulted in low rates of responding. These results demonstrate that Delta(9)-THC is a poor reinforcer in animals, even under conditions where some of its unfavourable biodispositional properties are taken into consideration.

摘要

缺乏能够明确证明动物存在大麻素自我给药行为的实验程序,一直是研究这类药物强化作用神经基础的障碍。由于Δ⁹-四氢大麻酚(Δ⁹-THC)会产生相对起效缓慢、持续时间长的行为效应,因此评估了一种给药间隔时间长的自我给药程序,作为固定比率给药方案的替代方法,固定比率给药方案通常需要频繁、间隔时间短的注射来证明强化作用。三只成年雄性恒河猴通过手术植入静脉导管,并在10分钟固定间隔强化程序下训练自我给药苯环己哌啶(PCP)。每天有三次注射机会,每次注射间隔2小时,在此期间的反应没有预设结果。为了将药物的效果与产生该效果的反应联系起来,每次20秒的注射都与一盏红灯配对,红灯持续亮10分钟。PCP(100μg/kg/次注射)在每个可注射时间段内维持稳定的反应率,范围约为0.2至0.7次反应/秒。在7天的替代期内,Δ⁹-THC(17 - 100μg/kg/次注射)维持较低的反应率,偶尔超过给予赋形剂时的反应率,但远低于PCP维持的反应率。用强效的Δ⁹-THC类似物CP 55,940进行的替代试验也导致反应率较低。这些结果表明,即使在考虑了Δ⁹-THC一些不利的生物处置特性的情况下,它在动物中仍是一种较差的强化剂。

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