TY - JOUR
T1 - Central infusion of melanocortin agonist MTII in rats
T2 - assessment of c-Fos expression and taste aversion
AU - Thiele, Todd E.
AU - Dijk, Gertjan van
AU - Yagaloff, Keith A.
AU - Fisher, Stewart L.
AU - Schwartz, Michael
AU - Burn, Paul
AU - Seeley, Randy J.
N1 - Relation: http://www.rug.nl/fwn/onderzoek/programmas/cbn/index
Rights: University of Groningen, Centre for Behaviour and Neurosciences
PY - 1998
Y1 - 1998
N2 - Like leptin (OB protein), central infusion of the nonspecific melanocortin agonist MTII reduces food intake for relatively long periods of time (i.e., 12 h). To test the hypothesis that MTII may influence ingestive behavior via mechanisms similar to those that mediate the effects of leptin, we infused a single dose of MTII into the third ventricle (i3vt) of Long-Evans rats and examined three dependent measures that have been studied following i3vt infusion of leptin: 1) effects on long-term food intake and body weight (48 h), 2) patterns of c-Fos expression in the brain, and 3) conditioned taste aversion learning. Similar to leptin, MTII reduced 48-h food intake (1.0 nmol dose), reduced body weight at 24 and 48 h (0.1 and 1.0 nmol doses, respectively), and induced c-Fos expression in the paraventricular nucleus of the hypothalamus and the central nucleus of the amygdala. In contrast to leptin, MTII was found to produce conditioned taste aversions. These results are consistent with the hypothesis that MTII may influence regulatory behavior via mechanisms similar to those that mediate the effects of leptin.
AB - Like leptin (OB protein), central infusion of the nonspecific melanocortin agonist MTII reduces food intake for relatively long periods of time (i.e., 12 h). To test the hypothesis that MTII may influence ingestive behavior via mechanisms similar to those that mediate the effects of leptin, we infused a single dose of MTII into the third ventricle (i3vt) of Long-Evans rats and examined three dependent measures that have been studied following i3vt infusion of leptin: 1) effects on long-term food intake and body weight (48 h), 2) patterns of c-Fos expression in the brain, and 3) conditioned taste aversion learning. Similar to leptin, MTII reduced 48-h food intake (1.0 nmol dose), reduced body weight at 24 and 48 h (0.1 and 1.0 nmol doses, respectively), and induced c-Fos expression in the paraventricular nucleus of the hypothalamus and the central nucleus of the amygdala. In contrast to leptin, MTII was found to produce conditioned taste aversions. These results are consistent with the hypothesis that MTII may influence regulatory behavior via mechanisms similar to those that mediate the effects of leptin.
M3 - Article
SN - 1522-1490
VL - 274
SP - R248-R254
JO - American Journal of Physiology - Regulatory, Integrative and Comparative Physiology
JF - American Journal of Physiology - Regulatory, Integrative and Comparative Physiology
IS - 1
ER -