We have examined the distribution of 5-HT1A and 5-HT2A receptor mRNAs
in post-mortem human hippocampus, neocortex, raphe nuclei, cerebellum
and basal ganglia using in situ hybridization histochemistry. Receptor
transcripts in brains from two males and two females (mean age +/- S.
D. = 70 +/- 4 years; post-mortem interval = 29 +/- 6 h) were visualise
d with S-35-radiolabelled synthetic oligodeoxyribonucleic acid probes.
In the hippocampus, 5-HT1A receptor mRNA was present in all fields, e
specially CA1. In the parahippocampal gyrus and neocortical regions 5-
HT1A receptor mRNA was enhanced in superficial and middle laminae. 5-H
T1A receptor mRNA was particularly abundant in the raphe and other ser
otonergic cell groups of the brainstem. The analysis of emulsion dippe
d sections showed 5-HT1A receptor mRNA to be concentrated in pyramidal
neurons, together with the granule cells of the dentate gyrus. In neo
cortical areas lamina III pyramidal neurons were more heavily labelled
than those in lamina V. There was no evidence of glial expression of
5-HT1A receptor mRNA in grey matter or white matter compartments. 5-HT
2A receptor mRNA was present in all neocortical areas examined, where
it was located in pyramidal neurons, of lamina V more than in those of
lamina III, as well as in putative interneurons, especially within la
mina IVc of the striate cortex. 5-HT2A receptor mRNA was observed at m
inimal levels in the hippocampus and not in the raphe. Neither 5-HT1A
nor 5-HT2A receptor mRNA were detected in the cerebellum, substantia n
igra or striatum. The ability to detect these transcripts at the regio
nal and cellular level will help reveal important details of the 5-HT
receptor system in the human brain. This includes the investigation of
their putative roles in the normal chemoarchitecture and in pathophys
iological brain processes.