Abstract Obesity contributes to the development of type 2 diabetes and other chronic diseases, while weight loss ameliorates the risk for these maladies. Current medical therapies remain inadequate to combatting the ongoing US obesity epidemic, however- in part because some of the most promising obesity drugs promote aversive responses (e.g., nausea) that limit their therapeutic utility. To design improved obesity therapies, we must understand the mechanisms of action for and relationships among circuits that control food intake and that mediate nausea. The area postrema (AP) senses nutrients and potentially harmful substances and contains receptors that represent important targets for obesity therapy. Single-cell analysis reveals that the AP contains two major populations of glutamatergic (GLU) neurons: The first (GLU10) contains Calcr-expressing (CalcrAP) neurons that also contain RAMP3 (and thus AmyR). The other (termed GLU4) consists of multiple subpopulations, including one marked by Prlhr (PrlhrAP cells) and another marked by Gfral (the receptor for GDF15; GfralAP cells); both subpopulations express Glp1r. A single population of GABAergic AP neurons contains Gipr-expressing (GiprAP) cells. We hypothesize that CalcrAP neurons respond to amylin and other nutrient-stimulated signals and promote non-aversive satiation, while pathologic signals stimulate GLU4 cells (including Glp1rAP, PrlhrAP, and GfralAP neurons) to promote aversive anorexia. Together with the ability of GIPR agonists to blunt some aversive responses, the predominantly local projection pattern of AP GABA neurons leads us to hypothesize that nutrient-responsive GiprAP cells represent “anti-nausea” neurons that inhibit GLU4 cells, attenuating their aversive effects. We also postulate that GiprAP neurons inhibit only specific GLU4 subpopulations and thus modify only a subset of AP-mediated aversive signals. While the mouse represents the most common mammalian genetic system, rats provide richer behavioral assays and permit the precise manipulation of AP neurons by stereotaxic methods. Rats also more closely model the human response to AmyR agonists. Hence, we have developed a panel of genetically-modified rat lines to target AP neurons that express receptors for key pharmacologic agents, enabling us to define the functions and mechanisms of action for distinct subsets of AP neurons. The results of these studies will permit the rational design of agents for the therapy of obesity that target the most advantageous components of these circuits.