Retinal afferents to the dorsal raphe nucleus in rats and Mongolian gerbils

J Comp Neurol. 1999 Nov 29;414(4):469-84. doi: 10.1002/(sici)1096-9861(19991129)414:4<469::aid-cne4>3.0.co;2-p.

Abstract

A direct pathway from the retina to the dorsal raphe nucleus (DRN) has been demonstrated in both albino rats and Mongolian gerbils. Following intraocular injection of cholera toxin subunit B (CTB), a diffuse stream of CTB-positive, fine-caliber optic axons emerged from the optic tract at the level of the pretectum/anterior mesencephalon. In gerbils, CTB-positive axons descended ventromedially into the periaqueductal gray, moving caudally and arborizing extensively throughout the DRN. In rats, the retinal-DRN projection comprised fewer, but larger caliber, axons, which arborized in a relatively restricted region of the lateral and ventral DRN. Following injection of CTB into the lateral DRN, retrogradely labeled ganglion cells (GCs) were observed in whole-mount retinas of both species. In gerbils, CTB-positive GCs were distributed over the entire retina, and a nearest-neighbor analysis of CTB-positive GCs showed significant regularity (nonrandomness) in their distribution. The overall distribution of gerbil GC soma diameters ranged from 8 to 22 micrometer and was skewed slightly towards the larger soma diameters. Based on an adaptive mixtures model statistical analysis, two Gaussian distributions appeared to comprise the total GC distribution, with mean soma diameters of 13 (SEM +/-1.7) micrometer, and 17 (SEM +/-1.5) micrometer, respectively. In rats, many fewer CTB-positive GCs were labeled following CTB injections into the lateral DRN, and nearly all occurred in the inferior retina. The total distribution of rat GC soma diameters was similar to that in gerbils and also was skewed towards the larger soma diameters. Major differences observed in the extent and configuration of the retinal-DRN pathway may be related to the diurnal/crepuscular vs. nocturnal habits of these two species.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Axons / ultrastructure*
  • Cell Count
  • Cell Size
  • Cholera Toxin
  • Dendrites / ultrastructure*
  • Gerbillinae / anatomy & histology*
  • Immunohistochemistry
  • Peptide Fragments
  • Raphe Nuclei / cytology*
  • Rats
  • Rats, Sprague-Dawley / anatomy & histology*
  • Retinal Ganglion Cells / cytology*
  • Visual Pathways / cytology*

Substances

  • Peptide Fragments
  • cholera toxin, B subunit (50-64)
  • Cholera Toxin