Abstract
We studied the distribution of NADPH-diaphorase activity in the visual cortex of normal adult New World monkeys (Saimiri sciureus) using the malic enzyme "indirect" method. NADPH-diaphorase neuropil activity had a heterogeneous distribution. In coronal sections, it had a clear laminar pattern that was coincident with Nissl-stained layers. In tangential sections, we observed blobs in supragranular layers of V1 and stripes throughout the entire V2. We quantified and compared the tangential distribution of NADPH-diaphorase and cytochrome oxidase blobs in adjacent sections of the supragranular layers of V1. Although their spatial distributions were rather similar, the two enzymes did not always overlap. The histochemical reaction also revealed two different types of stained cells: a slightly stained subpopulation and a subgroup of deeply stained neurons resembling a Golgi impregnation. These neurons were sparsely spined non-pyramidal cells. Their dendritic arbors were very well stained but their axons were not always evident. In the gray matter, heavily stained neurons showed different dendritic arbor morphologies. However, most of the strongly reactive cells lay in the subjacent white matter, where they presented a more homogenous morphology. Our results demonstrate that the pattern of NADPH-diaphorase activity is similar to that previously described in Old World monkeys.
Highlights
NADPH-diaphorase (NADPHd) activity in the central nervous system has been studied since Thomas and Pearse [1] described the “solitary cells” that survive various neurodegenerative and ischemic insults [2,3]
The bluish appearance of formazan was dispersed as a background activity that revealed NADPHd-reactive neuropil
Particulate NOS can be demonstrated histochemically using glutaraldehyde as a fixative, this isoform seems to predominate in brain regions other than the neocortex [22]
Summary
NADPH-diaphorase (NADPHd) activity in the central nervous system has been studied since Thomas and Pearse [1] described the “solitary cells” that survive various neurodegenerative and ischemic insults [2,3]. The identification of NADPHd as the enzyme responsible for NO synthesis was accomplished by biochemical and immunohistochemical procedures [7,8,9] This finding led to the utilization of histochemical methods for localizing NOS in neural tissue [10]. NOS utilizes NADPH as a cofactor to reduce the chromogen nitroblue tetrazolium, a yellowish salt, to diformazan that has a bluish appearance. This approach has been widely used to study the central nervous system of many non-primate species including rats [10,11], guinea pigs [12], opossums [13] and cats [14]. Until recently there were no data on the distribution of this enzyme in the visual cortex of New World monkeys
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