Maturation of the olfactory epithelium was studied in the rat. As a de
velopmental index of the olfactory epithelium, quantitation was based
on the thickness and the number of cell layers of the epithelium. Mean
epithelial thicknesses were 84 mu m on embryonic day (E) 19, 94 mu m
on postnatal day (P) 0, 98 mu m on P10 and 57 mu m in adult. Average n
umbers of cell layers were 7 (E19), 8 (P0), 10 (P10) and 7 (adult). Th
us the olfactory epithelium progressively increased in thickness betwe
en P0-P10, and later decreased in thickness as well as in number of ce
ll layers toward adult. To clarify the number of mature receptor cells
sending their axons to the olfactory bulb, the percentages of recepto
r cell labeling (number of labeled cells/total number of receptor cell
s) were estimated with an aid of retrograde fluorescent tracer injecte
d into the olfactory bulb. As a result, their percentages were 34% (P1
-P3), 50% (P8-P10) and 78% (adult). The ablation experiment of the bul
b on P1 pups and adult rats revealed that the percentages of receptor
cell degeneration were 31% in neonates (P1) and 76% in adults, confirm
ing the results obtained from the retrograde tracing. Thus the present
study shows the substantial increase of mature receptor cells during
development and may provide a morphological basis in understanding of
the functional maturity of olfaction.