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Serotonin depletion attenuates cocaine seeking but enhances sucrose seeking and the effects of cocaine priming on reinstatement of cocaine seeking in rats

机译:5-羟色胺的耗竭减弱了可卡因的寻找,但增强了蔗糖的寻找以及可卡因引发对大鼠可卡因恢复作用的影响

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Rationale: Acute serotonin (5-HT) depletion by the tryptophan hydroxylase inhibitor, para-chlorophenylalanine, attenuates cocaine seeking in rats. Objective: The present study examined the effects of chronic 5-HT depletion on cocaine- and sucrose seeking using the 5-HT-selective neurotoxin 5,7-dihydroxytryptamine (5,7-DHT). Methods: Separate groups of rats were trained to lever press for cocaine infusions (0.33 mg/kg/0.1 ml, i.v.) or for sucrose pellets (45 mg Noyes) on a fixed ratio (FR) 1 schedule of reinforcement during daily 2-h sessions. Subsequently, animals received i.c.v. infusions of either vehicle or 5,7-DHT (150 µg/6 µl or 200 µg/20 µl). After a minimum of 10 days post-lesion, cocaine- and sucrose seeking were measured as lever presses in the absence of reinforcement (extinction). Some cocaine-trained animals were also assessed for the re-establishment of self-administration and reinstatement of extinguished cocaine seeking by i.v. cocaine priming injections and response-contingent presentations of cocaine-paired stimuli. Results: 5-HT depletion by the 150 µg/6 µl dose of 5,7-DHT failed to alter cocaine- and sucrose seeking despite producing a 42–77% depletion of 5-HT in limbic terminal regions. The 200 µg/20 µl dose of 5,7-DHT attenuated cocaine seeking but enhanced sucrose seeking during extinction and produced a 55–85% depletion of 5-HT. In addition, cocaine-paired cues and cocaine priming reinstated cocaine-seeking behavior, and responding was enhanced in 5,7-DHT-treated animals relative to vehicle-treated controls at the 1 mg/kg/0.1 ml priming dose. However, re-establishment of cocaine self-administration was not altered by 5,7-DHT. Conclusion: The results suggest that 5-HT depletion may attenuate cocaine seeking but may enhance sucrose seeking when animals are tested during extinction. Furthermore, 5-HT depletion may enhance cocaine seeking produced by cocaine itself. Together these findings suggest that 5-HT depletion may have opposite effects on incentive motivation for cocaine during abstinence versus relapse.
机译:原理:色氨酸羟化酶抑制剂对氯苯丙氨酸对急性5-羟色胺(5-HT)的消耗会减弱大鼠中的可卡因搜寻量。目的:本研究使用5-HT-选择性神经毒素5,7-二羟基色胺(5,7-DHT)研究了慢性5-HT消耗对可卡因和蔗糖寻求的影响。方法:分别对大鼠进行训练,使其在每天2小时内以固定比例(FR)1时间表进行加压按压以进行可卡因输注(0.33 mg / kg / 0.1 ml,静脉注射)或蔗糖小丸(45 mg Noyes)的加压会议。随后,动物接受了静脉内注射。输注媒介物或5,7-DHT(150 µg / 6 µl或200 µg / 20 µl)。病变后至少10天后,在没有增强作用(消光)的情况下,通过杠杆按压测量可卡因和蔗糖的寻找。 i.v.还对一些可卡因训练的动物进行了评估,以重新建立自我管理和恢复灭绝的可卡因。可卡因引发注射和可卡因配对刺激的反应性表现。结果:尽管在边缘区产生5-HT消耗42-77%,但以150 µg / 6 µl剂量的5,7-DHT消耗5-HT却无法改变可卡因和蔗糖的寻求。 200 µg / 20 µl剂量的5,7-DHT在灭绝过程中减弱了可卡因的寻味能力,但增强了蔗糖的寻味能力,使5-HT损耗了55-85%。此外,可卡因配对的提示和可卡因引发恢复了可卡因的寻找行为,相对于1 mg / kg / 0.1 ml引发剂量的媒介物对照,在5,7-DHT处理的动物中反应增强。但是,5,7-DHT并没有改变可卡因自我管理的重建。结论:结果表明,在灭绝过程中对动物进行测试时,5-HT耗竭可能会减弱可卡因的寻找,但可能会增强蔗糖的寻找。此外,5-HT消耗可能会增强可卡因本身产生的可卡因搜寻。这些发现共同表明,5-HT耗竭可能在节欲与复发期间对可卡因的激励动机产生相反的影响。

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