E. Ohare et al., UTILIZATION OF A NOVEL MODEL OF FOOD REINFORCED BEHAVIOR INVOLVING NEUROPEPTIDE-Y, INSULIN, 2-DEOXY-D-GLUCOSE AND NALOXONE, Behavioural pharmacology, 7(8), 1996, pp. 742-753
The cyclic-ratio schedule methodology exposes animals to an ascending
followed by a descending sequence of ratio values over six consecutive
cycles. The response functions, obtained by plotting response rates a
gainst reinforcement rates at each schedule value, are argued to provi
de features useful in the evaluation of drug effects on feeding behavi
or. In the present study the effects of s.c. insulin (5.0 IU/kg), i.c.
v. neuropeptide Y (NPY) (5.0 mu g/5.0 mu l), i.c.v. insulin (0.5 mU/5.
0 mu l), i.c.v. 2-deoxyglucose (2-DG) (10.0 mu g/5.0 mu l), i.c.v. nal
oxone (NLX) (50.0 mu g/5.0 yl) in conjuction with i.c.v. NPY (5.0 mu g
/5.0 mu l), and i.c.v. NLX alone (50.0 mu g/5.0 mu l) were assessed. i
.c.v. NPY, insulin and 2-DG caused an elevation of the response functi
on obtained by plotting response rates against reinforcement rates but
did not affect the slope of the function. This elevation was similar
to that observed after increasing the incentive value of the reinforce
r (i.e., similar to increasing a 5.0% sucrose concentration reinforcer
to 10.0%, and to substituting 45 mg sweet food pellets for 45 mg grai
n pellets). S.c. insulin produced no shift in the function from baseli
ne, and i.c.v. NLX blocked the effect of i.c.v, NPY. I.c.v. NLX given
alone reduced the slope of the response function, by selectively reduc
ing response rates at the higher schedule values, a shift in the funct
ion similar to that observed following an increase in body weight. Sin
ce the literature on NPY and insulin would suggest that their effects
are mediated through mechanisms associated with internal regulation, t
hese findings were not predicted.