Literature DB >> 22858652

Limitations in anti-obesity drug development: the critical role of hunger-promoting neurons.

Marcelo O Dietrich1, Tamas L Horvath.   

Abstract

Current anti-obesity drugs aim to reduce food intake by either curbing appetite or suppressing the craving for food. However, many of these agents have been associated with severe psychiatric and/or cardiovascular side effects, highlighting the need for alternative therapeutic strategies. Emerging knowledge on the role of the hypothalamus in enabling the central nervous system to adapt to the changing environment - by managing peripheral tissue output and by regulating higher brain functions - may facilitate the discovery of new agents that are more effective and have an acceptable benefit-risk profile. Targeting the molecular pathways that mediate the beneficial effects of calorie restriction and exercise may represent an alternative therapeutic approach for the treatment of chronic metabolic disorders such as obesity.

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Year:  2012        PMID: 22858652     DOI: 10.1038/nrd3739

Source DB:  PubMed          Journal:  Nat Rev Drug Discov        ISSN: 1474-1776            Impact factor:   84.694


  258 in total

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  50 in total

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Review 3.  Molecular and cellular regulation of hypothalamic melanocortin neurons controlling food intake and energy metabolism.

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6.  Hypocretin neuron-specific transcriptome profiling identifies the sleep modulator Kcnh4a.

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