The Yerkes National Primate Research Center of Emory University, 954 Gatewood Road NE, Atlanta, GA 30329, USA.
Brain Res. 2012 Oct 30;1482:47-54. doi: 10.1016/j.brainres.2012.09.005. Epub 2012 Sep 11.
In order to examine the effect of cocaine and amphetamine regulated transcript (CART) peptide depletion in adult rats, CART shRNAs or scrambled control shRNAs were administered bilaterally into the nucleus accumbens (NAc). There was an increase in body weight of the shRNA injected rats compared with the rats injected with the scrambled RNA. This is compatible with the data showing a role for the peptide in body weight and food intake. Also at this time, there was about a two-and-a-half fold increase in cocaine-mediated locomotion in the shRNA injected rats compared to the control rats. This finding is critical support for the hypothesis that endogenous CART peptides in the NAc inhibit the actions of cocaine and other psychostimulants. In immunohistochemical experiments on these same animals, there was a decrease in the staining density of CART peptide in the NAc of the shRNA injected rats. These data show that shRNA can reduce CART peptides in the NAc and that endogenous CART peptides influence body weight and cocaine-induced locomotor activity (LMA).
为了研究可卡因和安非他命调节转录物(CART)肽在成年大鼠中的耗竭效应,将 CART shRNA 或乱序对照 shRNA 双侧注入伏隔核(NAc)。与注射乱序 RNA 的大鼠相比,注射 shRNA 的大鼠体重增加。这与肽在体重和食物摄入中的作用的数据一致。此外,在同一时间,与对照大鼠相比,注射 shRNA 的大鼠对可卡因介导的运动的反应增加了约 2.5 倍。这一发现为内源性 CART 肽在 NAc 中抑制可卡因和其他精神兴奋剂作用的假设提供了关键支持。在对这些相同动物进行的免疫组织化学实验中,注射 shRNA 的大鼠 NAc 中 CART 肽的染色密度降低。这些数据表明,shRNA 可以减少 NAc 中的 CART 肽,而内源性 CART 肽影响体重和可卡因诱导的运动活动(LMA)。