J. Philopena et al., NALOXONE DECREASES INTAKE OF 10-PERCENT SUCROSE IN PREWEANLING RATS, Pharmacology, biochemistry and behavior, 54(2), 1996, pp. 333-337
To investigate the role of opioids in the mediation of sucrose intake
in the preweanling rat pup, we measured the effect of naloxone on inta
ke of pups licking 10% sucrose from the floor of a beaker (independent
ingestion test) and of pups ingesting 10% sucrose that was continuous
ly infused through an anterior, sublingual oral catheter (oral cathete
r test). Pups were tested only once to eliminate the possible effect o
f test experience. Pups were tested in the second postnatal week (PN7,
9, 10, 11, and 14 days) with naloxone (1 mg/kg) or vehicle controls.
Fourteen-day-old pups were also tested with 0.1 and 0.5 mg/kg. Naloxon
e began to be efficacious for inhibiting intake on PN10 in the oral ca
theter test and on PN11 in the independent ingestion test. On PN14, th
e inhibition of intake was dose related and naloxone was more potent f
or inhibiting intake in independent ingestion tests than in oral cathe
ter tests. Naloxone not only decreased intake, it also decreased the i
ncidence of licking, increased mouthing and resting, and had no signif
icant effect on locomotion. The site of the inhibitory effect of nalox
one on intake was in the central nervous system, presumably in the bra
in, because naloxonemethiodide, an analogue of naloxone that does not
cross the blood-brain barrier, did not inhibit sucrose in either test.
These results demonstrate that the intake of 10% sucrose depends on e
ndogenous opioids as early as PN10 and that this opioid mechanism oper
ates when pups have not had prior test experience and in a test (oral
catheter test) where intake is not dependent on appetitive behaviors.