Abstract
Most of the anti-obesity drugs used over the past 50 years, and one (sibutramine) of the two globally licensed for long-term use today have acted centrally. With the exception of sibutramine (and the possible further approval of rimonabant), however, all of these have been withdrawn due to concerns over toxicity or abuse potential, or their use is greatly restricted. This is one reason why pharmaceutical companies are seeking drugs that act peripherally to influence energy expenditure, substrate utilisation or both. Fortunately, studies on genetically modified mice are revealing many new targets that fall into these categories [1].
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Clapham, J.C., Arch, J.R. (2008). Influencing energy expenditure and substrate utilisation. In: Wilding, J.P.H. (eds) Pharmacotherapy of Obesity. Milestones in Drug Therapy. Birkhäuser Basel. https://doi.org/10.1007/978-3-7643-7425-9_8
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