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natriuretic peptide receptor The anorexic effect observed wh
The anorexic effect observed when AR231630 is infused into the VTA could be the result of the DA release inhibition, as previously described [11]. However, there is also a hedonic aspect in feeding that possibly involves dopaminergic mechanisms of reward. Helm et al. showed a functional link between the motivational aspect of feeding and hypothalamic energy-control mechanisms [24]. An involvement of 5-HT2C receptors in mechanisms of reward has been suggested [13] and these receptors could possibly provide a link between homeostatic and hedonic eating [6]. Both are not independent, and while non-homeostatic eating is frequently attributed to dopamine, serotonin is largely recognized as a neurotransmitter within the homeostatic system. In this context, 5-HT2C receptor agonists generally inhibit reward-related behaviors [16], such as hedonic food intake. Another possible explanation for the hypophagic effect of AR231630 observed when injected into the VTA, but not into the ARC, could be the result of a non-specific hypoactive behavior. Several studies demonstrated hypophagic effects of intra-hypothalamic administration of 5-HT2C receptor agonists such as mCPP, TFMPP, and DOI [3]. However, DOI has an interruptive effect on feeding, mainly by inducing hypoactivity which decreases feeding by response natriuretic peptide receptor [25]. In our experiments, AR231630 reduces both locomotor activity and food intake when injected into the VTA, which raises the possibility that the resulting hypolocomotion could affect food intake in a non-specific manner. In addition, as Mosher et al. showed that administration of WAY161503 (a 5-HT2C receptor agonist) induced a state-dependent conditioned place aversion and a conditioned taste aversion to saccharin, we cannot exclude that AR231630 induces gustatory avoidance when injected into the VTA, leading to a decreased food intake [26]. On the other hand, although the ARC would seem to be a logical candidate due to 5-HT2C receptor expression on POMC neurons, local infusion of AR231630 into the ARC did not modify food intake. These findings are unexpected given the recent studies using 5-HT2C receptor deficient mice showing that 5-HT2C receptor re-expression in POMC neurons is sufficient to mediate the acute anorexigenic effects of 5-HT2C receptor agonists [27]. However, this study was done in mice and the role of 5-HT2C receptors on food intake in rat brain may not be as significant as it is in mouse brain. Another possibility that we cannot exclude is that 5-HT2C receptors may be expressed on nerve terminals of projections located on different nuclei, such as the paraventricular nucleus (PVN). Hence, an injection of 5-HT2C receptor agonists directly into the ARC would only reach receptors located on the cell bodies of these neurons, but not the ones potentially located at the terminals. In addition, even though the same dose of AR231630 was used in the VTA, it may not be enough to activate 5-HT2C receptors in the ARC, which would account for the absence of effect on food intake when injected into the ARC. Other potential regions implicated in the regulation of feeding behaviors, include the PVN, ventromedial nucleus, dorsomedial nucleus, lateral hypothalamic area, and parabrachial nucleus. These regions all receive serotoninergic projections [28]. The physiological relevance of 5-HT2C receptor expression in these sites is yet to be characterized. In summary, injection of AR231630 into the VTA is sufficient to inhibit the expression of amphetamine-induced and basal locomotor activity as well as food intake in rats. Blockade of the anorexic effect of peripheral AR231630 on feeding by intra-VTA SB242084 injections suggests the involvement of 5-HT2C receptors in these effects. While the ARC is a neuroanatomical site well known for its role in feeding, AR231630 had no effect on food consumption when injected into this brain region. Taken together, it is reasonable to suggest that the VTA is a primary locus for the suppressant effect of 5-HT2C receptor agonists on reward-related behaviors elicited by both amphetamine and food. This study further implies that the mechanisms preventing addiction may also participate to efficacy for treating obesity.’