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Role for insulin signaling in catecholaminergic neurons in control of energy homeostasis
Authors:Könner A Christine  Hess Simon  Tovar Sulay  Mesaros Andrea  Sánchez-Lasheras Carmen  Evers Nadine  Verhagen Linda A W  Brönneke Hella S  Kleinridders André  Hampel Brigitte  Kloppenburg Peter  Brüning Jens C
Affiliation:Department of Mouse Genetics and Metabolism, Institute for Genetics, Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases, Center of Molecular Medicine, University of Cologne,Cologne, Germany.
Abstract:Dopaminergic midbrain neurons integrate signals on food palatability and food-associated reward into the complex control of energy homeostasis. To define the role of insulin receptor (IR) signaling in this circuitry, we inactivated IR signaling in tyrosine hydroxylase (Th)-expressing cells of mice (IR(ΔTh)). IR inactivation in Th-expressing cells of mice resulted in increased body weight, increased fat mass, and hyperphagia. While insulin acutely stimulated firing frequency in 50% of dopaminergic VTA/SN neurons, this response was abolished in IR(ΔTh) mice. Moreover, these mice exhibited an altered response to cocaine under food-restricted conditions. Taken together, these data provide in?vivo evidence for a critical role of insulin signaling in catecholaminergic neurons to control food intake and energy homeostasis.
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