Cintra Rachel R, Lins Lívia C R F, Medeiros Katty A A L, Souza Marina F, Gois Auderlan M, Bispo José M M, Melo Mônica S, Leal Pollyana C, Meurer Ywlliane S R, Ribeiro Alessandra M, Silva Regina H, Marchioro Murilo, Santos José R
Laboratory of Neurophysiology, Department of Physiology, Federal University of Sergipe, São Cristovão, SE, Brazil.
Department of Health Education, Federal University of Sergipe, Lagarto, SE, Brazil.
Brain Res Bull. 2021 Jun;171:1-9. doi: 10.1016/j.brainresbull.2021.03.001. Epub 2021 Mar 3.
Nociception alterations are frequent non-motor symptoms of the prodromal phase of Parkinson's disease (PD). The period for the onset of symptoms and the pathophysiological mechanisms underlying these alterations remain unclear. We investigated the course of nociception alterations in a progressive model of parkinsonism induced by reserpine (RES) in rats. Male Wistar rats (6-7 months) received 5 or 10 subcutaneous injections of RES (0.1 mg/kg) or vehicle daily for 20 days. Motor evaluation and nociceptive assessment were performed throughout the treatment. At the end of the treatment rats were euthanized, the brains removed and processed for immunohistochemical analysis (TH and c-Fos). The RES-treated rats exhibited an increased nociceptive response to mechanical and chemical stimulation in the electronic von Frey and formalin tests, respectively. Moreover, these alterations preceded the motor impairment observed in the catalepsy test. In addition, the RES treatment reduced the TH-immunoreactivity in the ventral tegmental area (VTA) and increased the c-Fos expression in the ventral-lateral periaqueductal gray (vlPAG), rostral ventral medulla (RVM) and dorsal raphe nucleus (DRN) after noxious stimuli induced by formalin. Taken together, our results reinforce that nociceptive changes are one of the early signs of PD and monoamine depletion in basal ganglia can be involved in the abnormal processing of nociceptive information in PD.
伤害感受改变是帕金森病(PD)前驱期常见的非运动症状。症状出现的时期以及这些改变背后的病理生理机制仍不清楚。我们在利血平(RES)诱导的大鼠帕金森病进行性模型中研究了伤害感受改变的过程。雄性Wistar大鼠(6 - 7个月)每天皮下注射5或10次RES(0.1 mg/kg)或溶剂,持续20天。在整个治疗过程中进行运动评估和伤害感受评估。治疗结束时,对大鼠实施安乐死,取出大脑并进行免疫组织化学分析(TH和c - Fos)。RES处理的大鼠在电子von Frey试验和福尔马林试验中分别对机械和化学刺激表现出伤害感受反应增加。此外,这些改变先于在僵住试验中观察到的运动障碍。另外,RES处理降低了腹侧被盖区(VTA)的TH免疫反应性,并在福尔马林诱导的伤害性刺激后增加了腹外侧导水管周围灰质(vlPAG)、延髓头端腹内侧区(RVM)和中缝背核(DRN)中的c - Fos表达。综上所述,我们的结果强化了伤害感受改变是PD的早期迹象之一,并且基底神经节中的单胺耗竭可能参与了PD中伤害性信息的异常处理。