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Nitrergic neurons of the forepaw representation in the rat somatosensory and motor cortices: A quantitative study.

Bárbara de Paula Pires Franco GuimaraesMarco Rocha CuradoAnaelli Aparecida Nogueira-CamposJean Christophe HouzelRicardo Gattass
Published in: The Journal of comparative neurology (2021)
Nitrergic neurons (NNs) are inhibitory neurons capable of releasing nitric oxide (NO) that are labeled with nicotinamide adenine dinucleotide phosphate diaphorase histochemistry. The rat primary somatosensory (S1) and motor (M1) cortices are a favorable model to investigate NN populations by comparing their morphology, since these areas share the border of forepaw representation. The distribution of the Type I NN of the forepaw representation in the S1 and M1 cortices of the rat in different laminar compartments and the morphological parameters related to the cell body and dendritic arborization were measured and compared. We observed that the neuronal density in the S1 (130 NN/mm3 ) was higher than the neuronal density in the M1 (119 NN/mm3 ). Most NN neurons were multipolar (S1 with 58%; M1 with 69%), and a minority of the NN neurons were horizontal (S1 with 6%; M1 with 12%). NN found in S1 had a higher verticality index than NN found in M1, and no significant differences were observed for the other morphological parameters. We also demonstrated significant differences in most of the morphological parameters of the NN between different cortical compartments of S1 and M1. Our results indicate that the NN of the forepaw in S1 and M1 corresponds to a neuronal population, where the functionality is independent of the different types of sensory and motor processing. However, the morphological differences found between the cortical compartments of S1 and M1, as well as the higher density of NNs found in S1, indicate that the release of NO varies between the areas.
Keyphrases
  • spinal cord
  • nitric oxide
  • oxidative stress
  • high resolution
  • stem cells
  • computed tomography
  • cell therapy
  • cerebral ischemia
  • mesenchymal stem cells
  • brain injury
  • subarachnoid hemorrhage
  • bone marrow