Effects of eye enucleation on NADPH-diaphorase positive neurons in the superficial layers of the rat superior colliculus.

Dihydronicotinamide adenine-dinucleotide phosphate diaphorase (NADPH-d) positive neurons in the superficial layers of superior colliculus (SC) were studied in the adult rat after eye enucleation at postnatal day 5 (P5). Bilaterally, NADPH-d histochemistry revealed either weakly or intensely labeled neurons. In the SC contralateral to the enucleation, the volume of superficial layers decreased significantly, whereas the total number of NADPH-d positive neurons was only slightly reduced, thus resulting in an increased cell density. Bilaterally, the number of NADPH-d positive neurons was around 20% of Nissl-stained neurons. While the number of neurons which were weakly positive for NADPH-d was unchanged contralateral to the enucleation (thus resulting in a significant increase in their percentage on the overall NADPH-d population), the number of intensely labeled neurons decreased by 30%. Intensely labeled neurons were classified with respect to cell size and dendritic distribution. Some (126) were reconstructed and analyzed on the computer, in order to quantitate morphological differences in dendritic distribution in the denervated and control SC. The percent of neurons which could be assigned to some classes (marginal, stellate, narrow field vertical and wide field vertical) was reduced contralateral to the enucleation. In addition, vertically-oriented neurons (narrow field vertical, wide field vertical and pyriform) showed a significant decrease in soma size, dendritic length and number of branch points. And finally, the overall orientation of dendrites on narrow and wide field vertical neurons was more dispersed, when compared to the control colliculus. Thus, P5 eye enucleation affects the adult morphology of NADPH-d positive neurons in the superficial layers of the rat SC, resulting in increased cell density, changed relative number of cells in each morphological type, and altered soma size, dendritic length and orientation in specific neurons.