Re. Blackburn et al., CENTRAL OXYTOCIN AND ANP RECEPTORS MEDIATE OSMOTIC INHIBITION OF SALTAPPETITE IN RATS, American journal of physiology. Regulatory, integrative and comparative physiology, 38(2), 1995, pp. 245-251
These studies evaluated the involvement of central oxytocin (OT) and a
trial natriuretic peptide (ANP) receptors in the osmotic inhibition of
hypovolemia-induced salt appetite. Rats were pretreated centrally wit
h the A chain of the cytotoxin ricin conjugated to OT (rAOT) or ANP (r
AANP) to selectively inactivate cells bearing these respective recepto
rs, or rats were pretreated with the unconjugated A chain (rA) as a co
ntrol. Hypovolemia was induced with subcutaneous colloid injections, a
nd rats then were given either 2 M mannitol, which raises plasma osmol
ality but lowers plasma sodium, or 1 M NaCl, which raises both. Hypert
onic mannitol inhibited saline ingestion in rA-treated control rats bu
t stimulated ingestion in rAOT- and rAANP-treated rats, whereas hypert
onic NaCl blunted saline ingestion in rA- and rAOT-treated rats but st
imulated ingestion in rAANP-treated rats. Angiotensin II-induced salin
e intake was similarly potentiated in rAOT- and rAANP-treated rats, in
dicating that this treatment also activates central inhibitory OT and
ANP pathways. These data suggest that central ANP receptors mediate bo
th Na+- and osmolality-induced inhibition of NaCl ingestion, whereas c
entral OT receptors primarily mediate osmolality-induced inhibition of
NaCl ingestion in rats.