EFFECTS OF THE SELECTIVE TACHYKININ NK3 RECEPTOR AGONIST NH2-SENKTIDEON INTRAORAL INTAKE AND TASTE REACTIVITY RESPONSES ELICITED BY NACL IN SODIUM-REPLETE RATS
C. Polidori et al., EFFECTS OF THE SELECTIVE TACHYKININ NK3 RECEPTOR AGONIST NH2-SENKTIDEON INTRAORAL INTAKE AND TASTE REACTIVITY RESPONSES ELICITED BY NACL IN SODIUM-REPLETE RATS, Regulatory peptides, 66(1-2), 1996, pp. 101-104
Our previous studies have shown that i.c.v, injections of the selectiv
e tachykinin NK3 receptor agonist [Asp(5,6),MePhe(8)]substance P(5,11)
, also referred to as NH2-senktide (NH2-SENK), inhibit salt intake in
rats in a two-bottle intake test. The present study evaluated the effe
ct of i,c,v, injections of NH2-SENK on intraoral intake and taste reac
tivity responses elicited by intraoral infusions of water or NaCl solu
tions (0.03, 0.15, 0.25 and 0.5 M) in sodium-replete rats. The effect
of NH2-SENK on the intake of 0.03, 0.15 and 0.25 M NaCl solutions and
of water was also evaluated in a two-bottle intake test. In this test,
31 ng/rat of NH2-SENK significantly reduced the intake of 0.15 and 0.
25 M NaCl, but not that of water or of 0.03 M NaCl. The dose of 31 ng/
rat of NH2-SENK reduced the intraoral intake of 0.25 acid 0.5 M NaCl,
while 125 ng/rat reduced the intraoral intake of 0.15, 0.25 and 0.5 M
NaCl; neither dose reduced the intraoral intake of water or of 0.03 M
NaCl. Taken together, these findings indicate that the effect of H-2-S
ENK on salt intake is dependent on the concentration of the NaCl solut
ion offered; moreover, the intraoral intake data suggest that the effe
ct of NH2-SENK on salt intake may be exerted to a large extent on the
consummatory processes of salt ingestion. NH2-SENK, 31 or 125 ng/rat,
altered taste reactivity responses shortly after the beginning of the
intraoral infusion. The most peculiar effect was an increase in passiv
e dripping during the first min of intraoral infusion of 0.15, 0.25 an
d 0.5 M, but not of water or of 0.03 M NaCl, This finding suggests tha
t NH2-SENK elicits a prompt alteration of taste mechanisms for salt, w
hich may account for its antinatriorexic action.