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Ghrelin Receptor Antagonism of Methamphetamine-Induced Conditioned Place Preference and Intravenous Self-Administration in Rats

机译:甲基苯丙胺诱导的条件性位置偏爱和大鼠静脉内自我管理的Ghrelin受体拮抗作用。

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摘要

Methamphetamine abuse imposes a significant burden on individuals and society worldwide, and an effective therapy of methamphetamine addiction would provide distinguished social benefits. Ghrelin significantly participates in reinforcing neurobiological mechanisms of stimulants, including amphetamines; thus, ghrelin antagonism is proposed as a promising addiction treatment. The aim of our study was to elucidate whether the pretreatment with growth hormone secretagogue receptor (GHS-R1A) antagonist, substance JMV2959, could reduce the methamphetamine intravenous self-administration (IVSA) and the tendency to relapse, and whether JMV2959 could reduce or prevent methamphetamine-induced conditioned place preference (CPP) in rats. Following an adequate maintenance period, JMV2959 3 mg/kg was administered intraperitoneally 20 min before three consequent daily 180 min sessions of methamphetamine IVSA under a fixed ratio FR1, which significantly reduced the number of active lever-pressings, the number of infusions, and the amount of the consumed methamphetamine dose. Pretreatment with JMV2959 also reduced or prevented relapse-like behavior tested in rats on the 12th day of the abstinence period. Pretreatment with JMV2959 significantly reduced the expression of methamphetamine-induced CPP. Simultaneous administration of JMV2959 with methamphetamine during the conditioning period significantly reduced the methamphetamine-CPP. Our results encourage further research of the ghrelin antagonism as a potential new pharmacological tool for methamphetamine addiction treatment.
机译:甲基苯丙胺的滥用给全世界的个人和社会带来了沉重负担,有效的甲基苯丙胺成瘾疗法将提供显着的社会效益。 Ghrelin显着参与增强兴奋剂(包括苯丙胺)的神经生物学机制。因此,提出了生长素释放肽拮抗作用作为有前途的成瘾疗法。本研究的目的是阐明用生长激素促分泌素受体(GHS-R1A)拮抗剂JMV2959进行的预处理是否可以减少甲基苯丙胺的静脉内自用(IVSA)和复发的趋势,以及JMV2959是否可以减少或预防甲基苯丙胺诱导的大鼠条件性位置偏爱(CPP)。经过足够的维护期后,在固定的FR1比率下,在连续三天每天180分钟的甲基安非他明静脉注射IVSA前20分钟腹膜内注射JMV2959 3 mg / kg,这显着减少了主动杠杆按压次数,输注次数和消耗的甲基苯丙胺剂量。在禁欲期的第12天,用JMV2959进行预处理还可以减少或预防大鼠的复发样行为。用JMV2959预处理可显着降低甲基苯丙胺诱导的CPP的表达。在调节期间,将JMV2959与甲基苯丙胺同时给药可显着降低甲基苯丙胺-CPP。我们的结果鼓励对生长素释放肽拮抗作用的进一步研究,以作为甲基苯丙胺成瘾治疗的潜在新药理学工具。

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