4.7 Article

The involvement of the pathway connecting the substantia nigra, the periaqueductal gray matter and the retrotrapezoid nucleus in breathing control in a rat model of Parkinson's disease

Journal

EXPERIMENTAL NEUROLOGY
Volume 302, Issue -, Pages 46-56

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.expneurol.2018.01.003

Keywords

Central chemoreflex; Retrotrapezoid nucleus; Ventilation; Periaqueductal gray

Categories

Funding

  1. Sao Paulo Research Foundation (FAPESP) [2014/22406-1, 2016/23281-3, 2015/23376-1]
  2. Conselho Nacional de Desenvolvimento Cientffico e Tecnologico (CNPq) [471263/2013-3]
  3. FAPESP fellowship [2015/18842-3, 2013/00103-4]
  4. CNPq fellowship [301904/2015-4, 301219/2016-8]
  5. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

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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 6OHDA 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 CO2-activated PAG neurons with RTN projections, were observed in a 6OHDA 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(EMG)) and abdominal (Abd(EMG)) 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(EMG)) and GG(EMG) frequencies, as well as in hypercapnia-induced Dia(EMG), GG(EMG) and Abd(EMG) frequencies and GG(EMG) and Abd(EMG) 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.

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