Nature MetabolismNeurosciencePeer-reviewed journal article
Hypothalamic GABRA5-positive Neurons Control Obesity via Astrocytic GABA
Moonsun SaiD, Eun-Seon YooiD, Wuhyun KohiD, Mingu Gordon ParkiD, Hyun‐Jun JangiD, Yong Ryoul YangiD, Mridula BhallaiD, Jae‐Hun LeeiD, Jiwoon LimiD, Woojin WoniD, Jea KwoniD, Joon-Ho KwoniD, Yejin SeongiD, Byungeun Kim, Heeyoung AniD, Seung Eun LeeiD, Ki Duk ParkiD, Pann‐Ghill SuhiD, Jong‐Woo SohniD, Changjoon Justin LeeiD
Abstract
The lateral hypothalamic area (LHA) regulates food intake and energy expenditure. Although LHA neurons innervate adipose tissues, the identity of neurons that regulate fat is undefined. Here we identify that Gabra5-positive neurons in LHA (GABRA5LHA) polysynaptically project to brown and white adipose tissues in the periphery. GABRA5LHA are a distinct subpopulation of GABAergic neurons and show decreased pacemaker firing in diet-induced obesity (DIO) mouse model. Chemogenetic inhibition of GABRA5LHA suppresses energy expenditure and increases weight gain, whereas gene-silencing of Gabra5 in LHA decreases weight gain. In DIO mouse model, GABRA5LHA are tonically inhibited by nearby reactive astrocytes releasing GABA, which is synthesized by MAOB. Gene-silencing of astrocytic MAOB in LHA reduces weight gain significantly without affecting food intake, which is recapitulated by administration of a MAOB inhibitor, KDS2010. We propose that firing of GABRA5LHA facilitates energy expenditure and selective inhibition of astrocytic GABA is a molecular target for treating obesity.
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