...
首页> 外文期刊>Behavioural Brain Research: An International Journal >Anterior ventral tegmental area dopaminergic neurons are not involved in the motivational effects of bromocriptine, pramipexole and cocaine in drug-free rats
【24h】

Anterior ventral tegmental area dopaminergic neurons are not involved in the motivational effects of bromocriptine, pramipexole and cocaine in drug-free rats

机译:前腹侧被盖区多巴胺能神经元不参与溴隐亭,普拉克索和可卡因对无药大鼠的刺激作用

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Dopamine dysregulation syndrome in Parkinson's disease has been attributed to dopamine replacement therapies and/or a lesion of the dopaminergic system. Dopaminergic neuronal loss targets the substantia nigra and the ventral tegmental area (VTA). We hypothesize that dopamine replacement therapy is responsible for the potential reinforcement effect in Parkinson's disease, by acting on the neuronal reward circuitry. We previously demonstrated that the posterior (p) VTA, which projects to the nucleus accumbens (NAc), is implicated in the motivational effect of dopamine receptor agonists in 6-OHDA bilateral pVTA-lesioned drug-free animals. In the present study we investigated the implication of the anterior (a) VTA in the potential reinforcement effect of dopamine receptor agonists. Using the conditioned place preference (CPP) behavioral paradigm, we investigated the motivational effects of dopamine receptor agonists (bromocriptine and pramipexole), and cocaine in rats with a 6-OHDA bilateral lesion of the aVTA. Bromocriptine and pramipexole did not induce a significant CPP at 1. mg/kg in both sham and bilateral 6-OHDA-lesioned rats. However bromocriptine induced CPP only at a dose of 3. mg/kg in both animal groups. Moreover cocaine, which is known to increase dopamine release, induced reinforcing effects in both 6-OHDA-lesioned and sham rats. Our data show a lack of involvement of aVTA dopamine neurons in the motivational effects of bromocriptine, pramipexole and cocaine.
机译:帕金森氏病中的多巴胺失调综合症已归因于多巴胺替代疗法和/或多巴胺能系统病变。多巴胺能神经元损失的目标是黑质和腹侧被盖区(VTA)。我们假设多巴胺替代疗法通过作用于神经元奖赏回路来负责帕金森氏病的潜在增强作用。我们先前证明,向伏伏核(NAc)突出的后部(p)VTA与多巴胺受体激动剂对6-OHDA患双侧pVTA病变的无药动物的刺激作用有关。在本研究中,我们研究了前(a)VTA对多巴胺受体激动剂的潜在增强作用的影响。使用条件性位置偏爱(CPP)行为范式,我们研究了多巴胺受体激动剂(溴隐亭和普拉克索)和可卡因对aVTA 6-OHDA双侧病变的大鼠的刺激作用。在假手术和双侧6-OHDA损伤大鼠中,溴隐亭和普拉克索在1 mg / kg时均未诱导明显的CPP。但是在两个动物组中,溴隐亭仅以3 mg / kg的剂量诱导CPP。此外,已知可卡因会增加多巴胺的释放,在6-OHDA损伤和假手术大鼠中均会引起增强作用。我们的数据表明aVTA多巴胺神经元缺乏对溴隐亭,普拉克索和可卡因的刺激作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号