Broadbent J, Cunningham C L
Department of Behavioral Neuroscience, Oregon Health Sciences University, Portland 97201-3098, USA.
Psychopharmacology (Berl). 1996 Jul;126(2):156-64. doi: 10.1007/BF02246351.
The present study examined the effect of interstimulus interval on acquisition of conditioned thermal responses produced by trials in which a light/noise stimulus (CS) was repeatedly paired with infusion of morphine sulphate (US). Rats were implanted with a chronic intravenous catheter for drug delivery and a biotelemetry device for remote monitoring of core body temperature. In experiment 1, different groups received morphine either 0.5 (group P0.5) or 15 min (group P15) after onset of the 15-min CS. A third group was exposed to an identical number of CS and US presentations but in an explicitly unpaired manner (group UP). After repeated exposure to morphine, all groups showed a more rapid rise in body temperature in response to drug infusion. Test presentations of CS alone revealed conditioned hyperthermic responses to CS in groups P0.5 and P15. However, the response of the P15 group was smaller than that of the P0.5 group, suggesting weaker conditioning at the longer interstimulus interval. The contribution of CS-US overlap to the diminished associative strength observed in the P15 group was assessed in experiment 2. Groups P0.5/15 and P0.5/30 received infusions of morphine 0.5 min after onset of a 15- or 30-min CS, respectively. Group P15/30 received morphine 15 min after onset of a 30 min CS, whereas group UP/30 received explicitly unpaired presentations of the US and a 30-min CS. Enhancement of the hyperthermic effect of morphine was observed in all groups after ten conditioning trials. Test presentations of the CS without drug revealed that all paired groups had acquired conditioned hyperthermic responses. These results support the conclusion that drug-induced conditioning can occur at relatively long interstimulus intervals when there is sufficient temporal overlap between the CS and unconditioned response evoked by the drug US.
本研究考察了刺激间隔对条件性热反应习得的影响,该条件性热反应通过将光/噪声刺激(条件刺激,CS)与硫酸吗啡注入(非条件刺激,US)反复配对的试验产生。给大鼠植入一根用于药物递送的慢性静脉导管和一个用于远程监测核心体温的生物遥测装置。在实验1中,不同组在15分钟的条件刺激开始后0.5分钟(P0.5组)或15分钟(P15组)接受吗啡。第三组接受相同次数的条件刺激和非条件刺激呈现,但呈现方式明显为非配对(UP组)。反复接触吗啡后,所有组在药物注入时体温上升更快。单独的条件刺激测试呈现显示P0.5组和P15组对条件刺激有条件性体温过高反应。然而,P15组的反应小于P0.5组,表明在较长的刺激间隔下条件作用较弱。在实验2中评估了条件刺激-非条件刺激重叠对P15组中观察到的联想强度减弱的影响。P0.5/15组和P0.5/30组分别在15分钟或30分钟的条件刺激开始后0.5分钟接受吗啡注入。P15/30组在30分钟的条件刺激开始后15分钟接受吗啡,而UP/30组接受非条件刺激和30分钟条件刺激的明显非配对呈现。经过十次条件作用试验后,所有组均观察到吗啡热效应增强。无药物时条件刺激的测试呈现显示所有配对组均获得了条件性体温过高反应。这些结果支持以下结论:当药物非条件刺激诱发的条件刺激和非条件反应之间存在足够的时间重叠时,药物诱导的条件作用可以在相对较长的刺激间隔下发生。