The aim of this study was to examine the involvement of the hypothalamic ox
ytocin (OXT) and vasopressin (AVP) neurons in acute phase reaction using qu
antitative dual-labeled immunostaining with Fos and either OXT and AVP in s
everal hypothalamic regions. Administration of low dose (5 mu g/kg) and hig
h dose (125 mu g/kg) of LPS induced intense nuclear Fos immunoreactivity in
many OXT and AVP neurons in all the observed hypothalamic regions. The per
centage of Fos-positive nuclei in OXT magnocellular neurons was higher than
that of AVP magnocellular neurons in the supraoptic nucleus (SON), the mag
nocellular neurons in the paraventricular nucleus (magPVN), rostral SON (rS
ON), and nucleus circularis (NC), whose axons terminate at the posterior pi
tuitary for peripheral release. The percentage of Fos-positive nuclei in AV
P parvocellular neurons in the paraventricular nucleus (parPVN) was higher
than that of OXT parvocellular neurons, whose axons terminate within the br
ain for central release. Moreover, the percentage of Fos-positive nuclei in
AVP magnocellular neurons of the SON and rSON was significantly higher tha
n that of the magPVN and NC when animals were given LPS via intraperitoneal
(i.p.)-injection. This regional heterogeneity was not observed in OXT magn
ocellular neurons of i.p.-injected rats or in either OXT or AVP magnocellul
ar neurons of intravenous (i.v.)-injected rats. The present data suggest th
at LPS-induced peripheral release of AVP and OXT is due to the activation o
f the magnocellular neurons in the SON, magPVN, NC, and rSON, and the centr
al release of those hormones is in part derived from the activation of parv
ocellular neurons in the PVN. It is also suggested that the activation of A
VP magnocellular neurons is heterogeneous among the four hypothalamic regio
ns, but that of OXT magnocellular neurons is homogenous among these brain r
egions in response to LPS administration. (C) 2000 Elsevier Science B.V. Al
l rights reserved.