Pituitary cells transport secretory products from deep cytoplasmic por
tions towards the subplasmalemmal region (SPL) by two mechanisms: (a)
the regulated, secretagogue-dependent and (b) the secretagogue-indepen
dent constitutive pathway. Since thyrotropin (TSH) secretion is impair
ed in diabetes, we studied both pathways in the thyrotropes of control
and streptozocin (STZ)-treated male rats. By electron microscopy, we
measured the nucleus and cytoplasm area and counted the secretory gran
ules. In 4 selected SPL (500 nm deep) areas per cell we also counted t
he marginated secretory granules and measured their area. Moreover, af
ter TSH indirect immunogold labelling we counted immunogold particles
on (a) the secretory granules of the SPL and (b) the intergranular SPL
cytoplasm. To check the background staining we also counted immunogol
d particles on nonthyrotropic cells. In diabetic compared with control
thyrotropes we found: (a) cytoplasmic atrophy and increased number of
secretory granules per cytoplasm unit area, (b) reduced number of sec
retory granules in the SPL (blunted regulated secretion), (c) larger s
ecretory granules in the SPL (abnormal secretory granule maturation),
(d) decreased immunogold labelling of secretory granules in the SPL (r
educed TSH transported by each secretory granule towards the cell memb
rane) and (e) decreased immunogold labelling of the intergranular SPL
cytoplasm (blunted constitutive secretion). Our data suggest reduced r
egulated and constitutive TSH secretion and may thus contribute to a b
etter understanding of the hypothyroidism in STZ-diabetic rats.