IDENTIFICATION OF HYPOTHALAMIC NUCLEI INVOLVED IN OSMOREGULATION USING FOS IMMUNOCYTOCHEMISTRY IN THE DOMESTIC HEN (GALLUS-DOMESTICUS), RING DOVE (STREPTOPELIA-RISORIA), JAPANESE-QUAIL (COTURNIX JAPONICA) AND ZEBRA FINCH (TAENOPYGIA-GUTTATA)
Pj. Sharp et al., IDENTIFICATION OF HYPOTHALAMIC NUCLEI INVOLVED IN OSMOREGULATION USING FOS IMMUNOCYTOCHEMISTRY IN THE DOMESTIC HEN (GALLUS-DOMESTICUS), RING DOVE (STREPTOPELIA-RISORIA), JAPANESE-QUAIL (COTURNIX JAPONICA) AND ZEBRA FINCH (TAENOPYGIA-GUTTATA), Cell and tissue research, 282(2), 1995, pp. 351-361
Domestic hens were injected intraperitoneally with hypertonic or isoto
nic saline and killed 0.5, 1, 2, 6, 12 and 24 h later. Japanese quail,
Ring doves and Zebra finches were treated in the same way and killed
2 h later Using fos immunocytochemistry, fos-positive cells were visua
lized in the preoptic-anterior hypothalamus. In all species, two hours
after treatment with hypertonic but not with isotonic saline, a promi
nent cluster of fos-positive cells was seen close to the mid-line, dor
sal to the anterior part of the third ventricle, in and around the nuc
leus commissurae pallii. The cell cluster was associated with the dors
al region of the organum vasculosum laminae terminalis and passed caud
o-dorsally above the anterior commissure into the area of the subforni
cal organ, spreading diffusely into the nucleus septalis medialis and
the nucleus dorsomedialis anterior thalami. The maximal expression of
c-fos was seen 2 h after treatment with hypertonic saline: weak fos im
munoreactive product was seen at 0.5, 1 h and 6 h but not after 12 and
24 h. In all birds, 2 h after treatment with hypertonic but not with
isotonic saline, fos-positive cells were also seen in the nucleus para
ventricularis and nucleus supraopticus. Double immunocytochemistry in
the domestic hen with an antibody to vasotocin showed that these fos-p
ositive cells were classical magnocellular vasotocinergic neurones. Th
is study extends earlier studies in birds using lesioning and electrop
hysiological techniques to identify the precise cellular-localization
of the avian ''osmoreceptive complex'' projected onto a stereotaxic at
las.