| Literature DB >> 21641553 |
A Christine Könner1, Simon Hess, Sulay Tovar, Andrea Mesaros, Carmen Sánchez-Lasheras, Nadine Evers, Linda A W Verhagen, Hella S Brönneke, André Kleinridders, Brigitte Hampel, Peter Kloppenburg, Jens C Brüning.
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.Entities:
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Year: 2011 PMID: 21641553 DOI: 10.1016/j.cmet.2011.03.021
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287