Department of Pharmacology, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, SP, Brazil.
Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, SP, Brazil.
Exp Neurol. 2018 Apr;302:46-56. doi: 10.1016/j.expneurol.2018.01.003. Epub 2018 Jan 4.
Parkinson's disease (PD) is characterized by a reduction in the number of dopaminergic neurons of the substantia nigra (SNpc), accompanied by motor and non-motor deficiencies such as respiratory failure. Here, our aim was to investigate possible neuronal communications between the SNpc and chemoreceptor neurons within the retrotrapezoid nucleus (RTN), in order to explain neurodegeneration and the loss of breathing function in the 6-OHDA PD animal model. Male Wistar rats received tracer injections in the SNpc, RTN and periaqueductal gray (PAG) regions to investigate the projections between those regions. The results showed that neurons of the SNpc project to the RTN by an indirect pathway that goes through the PAG region. In different groups of rats, reductions in the density of neuronal markers (NeuN) and the number of catecholaminergic varicosities in PAG, as well as reductions in the number of CO-activated PAG neurons with RTN projections, were observed in a 6-OHDA model of PD. Physiological experiments showed that inhibition of the PAG by bilateral injection of muscimol did not produce resting breathing disturbances but instead reduced genioglossus (GG) and abdominal (Abd) muscle activity amplitude induced by hypercapnia in control rats that were urethane-anesthetized, vagotomized, and artificially ventilated. However, in a model of PD, we found reductions in resting diaphragm muscle activity (Dia) and GG frequencies, as well as in hypercapnia-induced Dia, GG and Abd frequencies and GG and Abd amplitudes. Therefore, we can conclude that there is an indirect pathway between neurons of the SNpc and RTN that goes through the PAG and that there is a defect of this pathway in an animal model of PD.
帕金森病(PD)的特征是黑质(SNpc)中的多巴胺能神经元数量减少,伴有运动和非运动缺陷,如呼吸衰竭。在这里,我们的目的是研究 SNpc 和位于梯形核(RTN)内的化学感受器神经元之间可能存在的神经元通讯,以解释在 6-OHDA PD 动物模型中神经退行性变和呼吸功能丧失的原因。雄性 Wistar 大鼠在 SNpc、RTN 和导水管周围灰质(PAG)区域接受示踪剂注射,以研究这些区域之间的投射。结果表明,SNpc 的神经元通过间接途径投射到 RTN,该途径穿过 PAG 区域。在不同的 PD 动物模型组中,PAG 中的神经元标志物(NeuN)密度和儿茶酚胺能末梢密度降低,以及具有 RTN 投射的 PAG 中 CO 激活的神经元数量减少。生理实验表明,双侧注射 muscimol 抑制 PAG 不会引起静息呼吸紊乱,但会降低在麻醉、切断迷走神经和人工通气的对照大鼠中,由高碳酸血症诱导的颏舌肌(GG)和腹部(Abd)肌肉活动幅度。然而,在 PD 模型中,我们发现静息膈肌肌肉活动(Dia)和 GG 频率以及高碳酸血症诱导的 Dia、GG 和 Abd 频率和 GG 和 Abd 幅度降低。因此,我们可以得出结论,SNpc 和 RTN 之间存在一条通过 PAG 的间接通路,并且在 PD 动物模型中存在该通路的缺陷。