Institute of Pharmacology, Polish Academy of Sciences, Department of Neuro-Psychopharmacology, Kraków, Poland.
Institute of Pharmacology, Polish Academy of Sciences, Department of Neuro-Psychopharmacology, Kraków, Poland.
Pharmacol Rep. 2017 Oct;69(5):985-994. doi: 10.1016/j.pharep.2017.05.016. Epub 2017 Jun 3.
Although Parkinson's disease (PD) is characterized by progressive neurodegeneration of multiple neurotransmitter systems, 6-hydroxydopamine (6-OHDA) as a model substance is mainly used to selectively damage the nigrostriatal dopaminergic neurons and induce parkinsonian-like motor disturbances in rats. We hypothesized that high doses of this neurotoxin affecting other monoaminergic systems may also evoke the depressive-like behavior.
The impact of 6-OHDA (8, 12, 16μg/4μl) administered unilaterally into the medial forebrain bundle on the sucrose solution intake (a measure of anhedonia) and on the tissue levels of noradrenaline (NA), dopamine (DA) and serotonin (5-HT) in the striatum (STR), substantia nigra (SN), prefrontal cortex (PFC) and hippocampus (HIP) was examined in rats pretreated or non-pretreated with desipramine.
The highest dose of 6-OHDA reduced the preference for 3% sucrose solution both in rats without and with desipramine pretreatment. All used doses of 6-OHDA dramatically decreased DA content in the studied brain structures on the ipsilateral side. NA levels were severely decreased in the ipsilateral STR, HIP and PFC of rats non-pretreated with desipramine and to a much lesser extent in those pretreated with desipramine. In the SN, moderate decreases in NA level were found both in rats pretreated and non-pretreated with desipramine. Higher doses of 6-OHDA reduced 5-HT content in the ipsilateral STR, HIP and PFC, but not in the SN, only in rats non-pretreated with desipramine.
Administration of the highest dose of 6-OHDA without desipramine pretreatment evoked neurochemical and behavioral changes resembling the advanced PD with coexisting depression.
尽管帕金森病(PD)的特征是多种神经递质系统的进行性神经退行性变,但 6-羟多巴胺(6-OHDA)作为一种模型物质主要用于选择性损伤黑质纹状体多巴胺能神经元,并在大鼠中诱导类似帕金森病的运动障碍。我们假设,这种影响其他单胺能系统的高剂量神经毒素也可能引起类似抑郁的行为。
将单侧内侧前脑束中给予的 6-OHDA(8、12、16μg/4μl)对蔗糖溶液摄入(快感缺失的衡量标准)以及纹状体(STR)、黑质(SN)、前额叶皮层(PFC)和海马(HIP)中去甲肾上腺素(NA)、多巴胺(DA)和 5-羟色胺(5-HT)的组织水平的影响,在预先用或未用去甲丙咪嗪预处理的大鼠中进行了检查。
最高剂量的 6-OHDA 降低了未用和用去甲丙咪嗪预处理的大鼠对 3%蔗糖溶液的偏好。所有使用剂量的 6-OHDA 都显著降低了研究大脑结构中同侧 DA 的含量。未用去甲丙咪嗪预处理的大鼠的同侧 STR、HIP 和 PFC 中 NA 水平严重降低,而用去甲丙咪嗪预处理的大鼠则降低较少。在 SN 中,用去甲丙咪嗪预处理和未预处理的大鼠中均发现 NA 水平中度降低。较高剂量的 6-OHDA 降低了同侧 STR、HIP 和 PFC 中的 5-HT 含量,但 SN 中未用去甲丙咪嗪预处理的大鼠则没有。
未经去甲丙咪嗪预处理给予最高剂量的 6-OHDA 会引起类似于并发抑郁的晚期 PD 的神经化学和行为变化。