Jh. Mclean et al., LOCALIZATION OF 5-HT2A RECEPTOR MESSENGER-RNA BY IN-SITU HYBRIDIZATION IN THE OLFACTORY-BULB OF THE POSTNATAL RAT, Journal of comparative neurology, 353(3), 1995, pp. 371-378
The olfactory bulb receives a dense serotonergic input and appears to
require serotonergic input in early olfactory associational learning.
However, it is not known which cell types receive the serotonergic inp
ut or whether the cells express markers for the input throughout life.
These issues need resolution in order for the mechanisms of serotoner
gic interactions to be better understood. The mRNA for the 5-HT2A rece
ptor was localized in the olfactory bulb of postnatal day 1, 2, 14 and
9-month-old Sprague-Dawley rats as well as in the bulb of adult (6 mo
nths) and aged (22-30 month) Fisher 344 rats by in situ hybridization
using an S-35-labelled 5-HT2A-specific oligonucleotide probe mixture.
In all animals, hybridization was observed in mitral cells which are t
he major output cells of the main olfactory bulb. Tufted cells, locate
d in the external plexiform layer and juxtaglomerular region, were rea
dily observed in adult and aged animals and were also observed, albeit
not as readily, in neonate pups. Quantitative analysis of the silver
grain density over cells confirmed qualitative observations and showed
that mitral and tufted cells were labelled in the neonate as well as
in adult and aged animals. Labelled cells were also numerous in the ex
ternal division of the anterior olfactory nucleus in all animals. 5-HT
2A receptor mRNA could not be detected either qualitatively or quantit
atively by in situ hybridization in the accessory olfactory bulb, nor
could it be observed in the olfactory epithelium. The results suggest
that the output cells of the main olfactory bulb receive serotonergic
input via 5-HT2A receptors and that the serotonergic input onto these
cells could influence olfactory functioning at all postnatal ages. (C)
1995 Wiley-Liss, Inc.