This study examined the influence of pretreatment with N-[2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl]-N-(2-pyridinyl)
cyclohexane carboxamide
maleate (WAY100635, full
5-HT1A receptor antagonist, 37 nmol) on feeding effects evoked by local
injections of 8-hydroxy-2-(di-n-propylamino)-tetralin (8-
OH-DPAT, 5-HT(1A) and 5-HT(7) receptor agonist, 6 nmol) into the LH and into the
ARC of female rats adapted to a wet mash diet (enriched with 10%
sucrose), during diestrus or estrus. The results showed that the LH-pretreatment with WAY100635 suppressed the hypophagic effects evoked by
8-OH-DPAT during estrus as well as diestrus. The
ARC pretreatment with WAY100635 blockaded the hypophagia evoked by
8-OH-DPAT in estrus rats. The previous treatment with WAY100635 in the
ARC also suppressed the feeding duration decrease evoked by
8-OH-DPAT in estrus. The latency to start feeding, the drinking behavior and the durations of other non-ingestive behaviors were not affected by the different treatments, hypothalamic regions (LH or
ARC), and/or estrous cycle stages (diestrus and estrus), except for the locomotion duration increase after 8-OH-DAPT in LH-pretreated rats in diestrus. The present findings confirm our previous suggestion that
ARC- and the LH-5-HT(1A) receptors participate in the serotonergic control of feeding and that these feeding-related serotonergic circuits in LH are affected by ovarian
hormones, since the treatment with WAY100635 evoked a hypophagia response during the diestrus phases.