Kantak Kathleen M, Black Yolanda, Valencia Eric, Green-Jordan Kristen, Eichenbaum Howard B
Laboratory of Behavioral Neuroscience, Department of Psychology, Boston University, 64 Cummington Street, MA 02215, USA.
Psychopharmacology (Berl). 2002 May;161(3):278-87. doi: 10.1007/s00213-002-1036-z. Epub 2002 Mar 28.
To investigate potential neurocognitive mechanisms underlying drug-seeking and drug-taking behavior, the effects of reversible lidocaine-induced inactivation of the lateral dorsal striatum (DST) on behavior studied in a drug maintenance/cue reinstatement model were evaluated. This region of the DST was investigated because it selectively regulates stimulus-response learning that is disrupted by 10 microg of bilaterally infused lidocaine.
Rats ( n=6) were trained to self-administer 1 mg/kg per infusion cocaine under a second-order schedule of drug delivery. The effects of bilateral lidocaine (30-100 microg) inactivation of the lateral DST were evaluated during drug maintenance tests as well as during tests in which responding was reinstated by cocaine-associated cues presented in combination with a cocaine priming injection. The lower 10 microg dose was used to examine the effects of lidocaine on reinstatement of responding induced by presentation of cues alone.
During drug maintenance tests, drug-seeking behavior was significantly increased after inactivation by 100 microg lidocaine. The number of infusions earned did not change. During cue-induced reinstatement tests preceded by a cocaine priming injection, 100 microg lidocaine significantly decreased both drug-seeking behavior and the number of infusion-paired light deliveries earned. During reinstatement tests with cues presented alone, inactivation of the lateral DST by 10 microg lidocaine did not influence either behavior.
These findings suggest that stimulus-response functions of the lateral DST may regulate the dose-related effects of self-administered cocaine because the lidocaine-induced changes in behavior during the maintenance and cocaine priming tests resembled the effects of exposure to increasingly lower doses of cocaine, respectively. Given the lack of an effect of lidocaine during the cues-alone tests, the lateral DST does not appear to regulate drug-seeking behavior per se (i.e., responding maintained by drug-associated cues at times when drug is not available).
为了研究寻求药物和服药行为背后潜在的神经认知机制,评估了利多卡因可逆性诱导外侧背侧纹状体(DST)失活对药物维持/线索恢复模型中行为的影响。之所以研究DST的这个区域,是因为它选择性地调节刺激-反应学习,而双侧注入10微克利多卡因会破坏这种学习。
训练大鼠(n = 6)在二阶给药方案下自我给药每注射一次1毫克/千克的可卡因。在药物维持测试期间以及通过与可卡因启动注射联合呈现的可卡因相关线索恢复反应的测试期间,评估双侧利多卡因(30 - 100微克)使外侧DST失活的效果。使用较低的10微克剂量来检查利多卡因对仅由线索呈现诱导的反应恢复的影响。
在药物维持测试期间,100微克利多卡因失活后,寻求药物行为显著增加。获得的注射次数没有变化。在可卡因启动注射后的线索诱导恢复测试期间,100微克利多卡因显著降低了寻求药物行为和获得的与注射配对的光刺激次数。在仅呈现线索的恢复测试期间,10微克利多卡因使外侧DST失活对两种行为均无影响。
这些发现表明,外侧DST的刺激-反应功能可能调节自我给药可卡因的剂量相关效应,因为利多卡因在维持和可卡因启动测试期间引起的行为变化分别类似于暴露于越来越低剂量可卡因的效果。鉴于在仅线索测试中利多卡因没有效果,外侧DST似乎本身并不调节寻求药物行为(即,在没有药物时由药物相关线索维持的反应)。