Artigo
Distribution of NADPH-diaphorase-positive neurons in the prefrontal cortex of the Cebus monkey
Fecha
2006-04-14Registro en:
Brain Research. Amsterdam: Elsevier B.V., v. 1083, p. 118-133, 2006.
0006-8993
10.1016/j.brainres.2006.01.098
WOS:000237374200013
4408095517346846
6273648007883637
8487462626931877
0000-0003-4859-0583
0000-0003-4859-0583
0000-0003-4859-0583
0000-0001-5650-7343
Autor
Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
Resumen
We studied the distribution of NADPH-diaphorase (NADPH-d) activity in the prefrontal cortex of normal adult Cebus apella monkeys using NADPH-d histochemical protocols. The following regions were studied: granular areas 46 and 12, dysgranular areas 9 and 13, and agranular areas 32 and Oap. NADPH-d-positive neurons were divided into two distinct types, both non-pyramidal. Type I neurons had a large soma diameter (17.24 +/- 1.73 pm) and were densely stained. More than 90% of these neurons were located in the subcortical white matter and infragranular layers. The remaining type I neurons were distributed in the supragranular layers. Type II neurons had a small, round or oval soma (9.83 +/- 1.03 mu m), and their staining pattern varied markedly. Type II neurons were distributed throughout the cortex, with their greatest numerical density being observed in layers II and III. In granular areas, the number of type II neurons was up to 20 times that of type I neurons, but this proportion was smaller in agranular areas. Areal density of type II neurons was maximum in the supragranular layers of granular areas and minimum in agranular areas. Statistical analysis revealed that these areal differences were significant when comparing some specific areas. In conclusion, our results indicate a predominance of NADPH-d-positive cells in supragranular layers of granular areas in the Cebus prefrontal cortex. These findings support previous observations on the role of type II neurons as a new cortical nitric oxide source in supragranular cortical layers in primates, and their potential contribution to cortical neuronal activation in advanced mammals. (c) 2006 Elsevier B.V. All rights reserved.