Role for insulin signaling in catecholaminergic neurons in control of energy homeostasis |
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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 |
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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. |
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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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