Prostaglandin EP3 receptor–expressing preoptic neurons bidirectionally control body temperature via tonic GABAergic signaling

Abstract

The bidirectional controller of the thermoregulatory center in the preoptic area (POA) is unknown. Using rats, here, we identify prostaglandin EP3 receptor–expressing POA neurons (POA ^EP3R neurons) as a pivotal bidirectional controller in the central thermoregulatory mechanism. POA ^EP3R neurons are activated in response to elevated ambient temperature but inhibited by prostaglandin E ₂, a pyrogenic mediator. Chemogenetic stimulation of POA ^EP3R neurons at room temperature reduces body temperature by enhancing heat dissipation, whereas inhibition of them elicits hyperthermia involving brown fat thermogenesis, mimicking fever. POA ^EP3R neurons innervate sympathoexcitatory neurons in the dorsomedial hypothalamus (DMH) via tonic (ceaseless) inhibitory signaling. Although many POA ^EP3R neuronal cell bodies express a glutamatergic messenger RNA marker, their axons in the DMH predominantly release γ-aminobutyric acid (GABA), and their GABAergic terminals are increased by chronic heat exposure. These findings demonstrate that tonic GABAergic inhibitory signaling from POA ^EP3R neurons is a fundamental determinant of body temperature for thermal homeostasis and fever.

Abstract

Abstract

Tonic GABAergic signaling from EP3 receptor-expressing preoptic neurons determines the control level of body temperature.