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Nucleus accumbens neuronal maturation differences in young rats bred for low versus high voluntary running behaviour

机译:低自愿性行为与高自愿性行为相育的幼鼠伏伏核神经元成熟差异

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摘要

We compared the nucleus accumbens (NAc) transcriptomes of generation 8 (G8), 34-day-old rats selectively bred for low (LVR) versus high voluntary running (HVR) behaviours in rats that never ran (LVRnon-run and HVRnon-run), as well as in rats after 6 days of voluntary wheel running (LVRrun and HVRrun). In addition, the NAc transcriptome of wild-type Wistar rats was compared. The purpose of this transcriptomics approach was to generate testable hypotheses as to possible NAc features that may be contributing to running motivation differences between lines. Ingenuity Pathway Analysis and Gene Ontology analyses suggested that ‘cell cycle’-related transcripts and the running-induced plasticity of dopamine-related transcripts were lower in LVR versus HVR rats. From these data, a hypothesis was generated that LVR rats might have less NAc neuron maturation than HVR rats. Follow-up immunohistochemistry in G9–10 LVRnon-run rats suggested that the LVR line inherently possessed fewer mature medium spiny (Darpp-32-positive) neurons (P < 0.001) and fewer immature (Dcx-positive) neurons (P < 0.001) than their G9–10 HVR counterparts. However, voluntary running wheel access in our G9–10 LVRs uniquely increased their Darpp-32-positive and Dcx-positive neuron densities. In summary, NAc cellularity differences and/or the lack of running-induced plasticity in dopamine signalling-related transcripts may contribute to low voluntary running motivation in LVR rats.
机译:我们比较了第8代(G8),34天大的大鼠伏隔核(NAc)转录组的选择,这些大鼠分别针对永不跑动的大鼠(LVRnon-run和HVRnon-run)低(LVR)与高自愿跑(HVR)行为进行了繁殖),以及在自愿进行轮转运动6天(LVRrun和HVRrun)后的大鼠中。另外,比较了野生型Wistar大鼠的NAc转录组。该转录组学方法的目的是针对可能的NAc特征生成可检验的假设,这些特征可能有助于品系之间的运行动机差异。创造力途径分析和基因本体分析表明,与HVR大鼠相比,LVR大鼠的“细胞周期”相关转录本和多巴胺相关转录本的运行诱导可塑性较低。从这些数据得出的假设是,LVR大鼠可能比HVR大鼠具有更少的NAc神经元成熟。 G9-10 LVR非流产大鼠的后续免疫组织化学表明,LVR系固有地具有较少的成熟中棘(Darpp-32阳性)神经元(P <0.001)和较少的未成熟(Dcx阳性)神经元(P <0.001)比他们的G9-10 HVR同行要高。但是,在我们的G9-10 LVR中,主动行走轮访问会独特地增加其Darpp-32阳性和Dcx阳性的神经元密度。总之,NAc细胞性差异和/或多巴胺信号相关转录物中缺乏跑步诱导的可塑性可能会导致LVR大鼠的自愿跑步动机降低。

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