Using in vivo microdialysis techniques, the effects of RTI-55 and/or cocaine on extracellular dopamine (DA) concentrations were measured in the nucleus accumbens (NACC) of freely moving rats. In control animals, cocaine (20 mg/kg) increased NACC DA approximately 458% 60 minutes following administration, returning to baseline values within 200 minutes. Similarly, RTI-55 administration (0.25 mg/kg) increased NACC DA levels approximately 347%. When combined, however, cocaine further increased NACC DA to 705% of baseline values when given 4 hours following RTI-55. This increase was significantly larger than cocaine alone (P < 0.05). In addition, chronic RTI-55 administration (5 days) further potentiated cocaine's ability to increase NACC DA (783%) but this did not reach statistical significance (P > 0.1) compared to acute RTI55/cocaine animals. These findings indicate that RTI-55, a drug that binds directly to the dopamine transporter (DAT) with higher affinity than cocaine, does not appear to be effective in attenuating cocaine's effects on NACC dopamine levels. In fact, acute RTI-55 potentiates cocaine's effects on NACC DA.

译文

使用体内微透析技术,在自由移动的大鼠伏伏核(NACC)中测量了RTI-55和/或可卡因对细胞外多巴胺(DA)浓度的影响。在对照动物中,可卡因(20 mg / kg)在给药60分钟后可使NACC DA升高约458%,在200分钟内恢复至基线值。同样,RTI-55的给药(0.25 mg / kg)使NACC DA水平升高约347%。但是,当联合使用时,可卡因在RTI-55后4小时给予时,NACC DA进一步增加至基线值的705%。这一增加比单独使用可卡因要大得多(P <0.05)。此外,长期RTI-55给药(5天)进一步增强了可卡因增加NACC DA的能力(783%),但与急性RTI55 /可卡因动物相比,这没有统计学意义(P> 0.1)。这些发现表明,RTI-55是一种比可卡因具有更高亲和力的直接结合多巴胺转运蛋白(DAT)的药物,在减轻可卡因对NACC多巴胺水平的影响方面似乎并不有效。实际上,急性RTI-55增强了可卡因对NACC DA的作用。

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